Next Article in Journal
Amaranth Oil Increases Total and LDL Cholesterol Levels without Influencing Early Markers of Atherosclerosis in an Overweight and Obese Population: A Randomized Double-Blind Cross-Over Study in Comparison with Rapeseed Oil Supplementation
Next Article in Special Issue
Anti-Aging Effects of Calorie Restriction (CR) and CR Mimetics Based on the Senoinflammation Concept
Previous Article in Journal
Nonalcoholic Fatty Liver Disease Induced by High-Fat Diet in C57bl/6 Models
Previous Article in Special Issue
The Effects of Calorie Restriction on Autophagy: Role on Aging Intervention
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Nutrients
Volume 11
Issue 12
10.3390/nu11123068
nutrients-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Mechanisms of Calorie Restriction: A Review of Genes Required for the Life-Extending and Tumor-Inhibiting Effects of Calorie Restriction

by
Toshimitsu Komatsu
1,
Seongjoon Park
1,
Hiroko Hayashi
1,
Ryoichi Mori
1,
Haruyoshi Yamaza
2 and
Isao Shimokawa
1,*
1
Department of Pathology, Nagasaki University School of Medicine and Graduate School of Biomedical Sciences, Nagasaki 852-8521, Japan
2
Section of Pediatric Dentistry, Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan
*
Author to whom correspondence should be addressed.
Nutrients 2019, 11(12), 3068; https://0-doi-org.brum.beds.ac.uk/10.3390/nu11123068
Submission received: 8 November 2019 / Revised: 12 December 2019 / Accepted: 13 December 2019 / Published: 16 December 2019
(This article belongs to the Special Issue The Effect of Calorie Restriction and Intermittent Fasting on Health and Disease)
Browse Figures
Review Reports Versions Notes

Abstract

:
This review focuses on mechanisms of calorie restriction (CR), particularly the growth hormone (GH)/insulin-like growth factor-1 (IGF-1) axis as an evolutionary conserved signal that regulates aging and lifespan, underlying the effects of CR in mammals. Topics include (1) the relation of the GH-IGF-1 signal with chronic low-level inflammation as one of the possible causative factors of aging, that is, inflammaging, (2) the isoform specificity of the forkhead box protein O (FoxO) transcription factors in CR-mediated regulation of cancer and lifespan, (3) the role for FoxO1 in the tumor-inhibiting effect of CR, (4) pleiotropic roles for FoxO1 in the regulation of disorders, and (5) sirtuin (Sirt) as a molecule upstream of FoxO. From the evolutionary view, the necessity of neuropeptide Y (Npy) for the effects of CR and the pleiotropic roles for Npy in life stages are also emphasized. Genes for mediating the effects of CR and regulating aging are context-dependent, particularly depending on nutritional states.

1. Introduction

Laboratory rodents often continue to gain body weight after puberty until certain age points under standard husbandry conditions in which animals can freely access food, often called ad libitum (AL) feeding. In contrast, restriction of food intake in mice by 30% to 40%, when initiated at young age, e.g., 12 weeks of age, limits the gain in body weight [1]. Dietary regimens involving food restriction, here referred to as calorie restriction (CR), reduce morbidity and mortality in experimental animals compared with AL feeding animals [1]. Since the original report on the effects of CR in 1935 [2], many laboratories have confirmed the effects of CR and investigated the underlying molecular mechanisms. Notably, a recent meta-analysis of lifespan studies in laboratory rodents described various responses to CR, that is, no extension or even shortened lifespans in CR rodents [3]. The analysis also suggested potentially substantial effects of the genotypes of animals as well as husbandry on experimental outcomes in CR studies. A genome-scale metabolic model and transcriptome data in the male Sprague Dawley rat liver also revealed varied metabolic responses of the liver with different levels and durations of CR [4]. Recent studies have also identified sexual dimorphism in physiological responses to CR [5,6]. Kane et al. [6] found that female rodents may have a greater response to CR than male rodents, with modulated sensitivities to mechanistic target of rapamycin (Mtor), growth hormone (GH), insulin-like growth factor-1 (IGF-1) or fibroblastic growth factor 21 and greater inflammatory and mitochondrial health responses [6]. Therefore, the effects of CR may not be universal as originally expected. Nonetheless, CR models in a range of organisms have contributed to our understanding of the aging process.
Epistasis analyses using mutant strains in lower organisms such as Caenorhabditis elegans (C. elegans) have revealed genes required for the effects of CR (referred to here as CR genes) and the signal pathways mediating the effects of CR. In C. elegans, a number of genes such as aak-2, daf-16, skin-1, clk-1, and pha-4 have been reported to be associated with the life-prolonging effect of CR [7]. Some of these genes also mediate the effects of CR in mice. Previous studies also reported that mutations of single genes (referred to here as longevity genes) can extend lifespan even in AL feeding animals. Many of these genes can be functionally categorized into genes associated with nutrient sensing or metabolic responses [8]. Among these gene mutations, reduction- or loss-of-function mutations of genes in the growth hormone (GH)-insulin-like growth factor-1 (IGF-1) signaling consistently extend lifespan in a range of organisms [8]. Since CR is known to decrease the plasma concentration of GH and IGF-1, the GH-IGF-1 pathway is considered an evolutionary conserved pathway for longevity and a main aspect of the mechanism of CR [9].
Thus far, a total of 112 CR genes in yeast, 62 in nematode, 27 in drosophila, and seven in mice have been identified and are listed in the database [10]. Among these genes, forkhead box protein O 3 (Foxo3) and sirtuin 1 (Sirt1) genes are common in mice, nematodes, and flies. CR and longevity gene models have elucidated signal pathways for the extension of lifespan, although the signal pathways are context dependent. This review will focus on FoxO transcription factors and the sirtuin deacetylases that are upstream of FoxO. We also discuss roles for neuropeptide Y (Npy), which is essential for the effects of CR in mice and thus mammals.

2. A Central Role for GH and IGF-1 in the Regulation of Lifespan

Previous studies reported that a single gene mutation can prolong the lifespan of experimental animals under AL conditions of standard diets. Genetic analyses of long-lived strains of nematodes identified a mutation in a single gene, age-1 [11]. This gene was later found to encode a component of phosphoinositide 3-kinase (PI3K) that is important for growth factor signals such as those modulated by IGF-1 [12]. Kenyon et al. showed that mutation of daf-2, which is associated with resistance larval development, prolongs the lifespan of C. elegans, and daf-16 is required [13]. Daf-2 and Daf-16 correspond to the receptor for IGF-1 and the FoxO transcription factor in mammals, respectively. Thus, in C. elegans, attenuated IGF-1 signaling promotes activation of Daf-16, leading to transcriptional modulation of its target genes and extended lifespan. Even in Drosophila, mutations in genes in insulin-like signaling such as Inr (insulin-like receptor) and chico (insulin-receptor substrate) can extend the lifespan [14]. In these conditions, dFoxo is also required.
The lifespan of C. elegans can also be extended by suppression of target of rapamycin (Tor in mammalians, mechanistic target of rapamycin, Mtor), which is downstream of IGF-1 signaling and promotes cell proliferation and division when nutrients are abundant [15]. Mtor forms complexes (mTORC1 and mTORC2) with other molecules in nutrition and energy rich conditions. These complexes activate transcription and translation when insulin and growth factors concomitantly rise. Mtor complexes promote protein synthesis and cell division while inhibiting autophagy. All genetic manipulations that suppress Mtor identified thus far can extend the lifespan of Drosophila [16].
In mammals, GH is upstream of the IGF-1 signal. GH is competitively controlled by Somatostatin and GH-releasing hormone (Ghrh), which are secreted from hypothalamic neurons. In mice, reduction-of-function gene mutations in molecules involved in the signal between Ghrh and IGF-1 consistently prolong lifespan [17]. Furthermore, longevity is achieved by inhibition of mTORC1 by rapamycin [18], deletion of the S6K gene [19], and suppression of Mtor [15,20].
Together these results in a range of experimental animals indicate that signal attenuation of the IGF-1 signal, activation of FoxO transcription factor, and suppression of Mtor are key mechanisms for slowing aging and prolonging lifespan (Figure 1). However, it should be noted that the life-extending effect of the reduced IGF-1 signaling could be sexually dimorphic. In Igf1 receptor (Igf1r) gene heterozygotic knockout (Igf1+/−) mouse models of different genetic backgrounds (129/SvPas and C57BL/6J) [21,22], only female Igf1r+/− mice significantly outlived controls, whereas this was not observed for males. Genetic studies in humans also indicate that genetic variations causing reduced IGF-1 signaling are beneficial for survival in old age only in females but not in males [23,24,25]. The mechanisms underlying the sexual dimorphism for longevity in the context of reduction of IGF-1 signaling remain to be explored.

3. Possible Relation of the GH-IGF-1 Axis with Inflammaging

Generalized chronic low-level inflammation may be a causative factor for aging and related diseases. This low-level inflammation associated with the aging process is called inflammaging [26]. It is also called sterile inflammation because it is not caused by infection.
Senescent cells that increase in tissues with age not only stop undergoing cell division but also express inflammatory cytokines such as IL-1α, IFNβ, chemokines, matrix metalloproteases, and growth factors, inducing local inflammation in tissues. This phenomenon is called the senescence-accelerated secretory phenotype (SASP) [27]. A recent report showed that the average lifespan of mice can be extended by selectively removing senescent cells expressing p16 Ink4a from tissues [28]. The removal of senescent cells also suppresses age-related lipodystrophy, tumorigenesis, glomerulosclerosis of the kidney, and so on. This report indicates that senescent cells are involved in the progression of aging in animals.
SASP was reported to be caused by induction of type I interferon (IFN-I) signal by activating transcription of the retrotransposable element long-interspersed element-1 (L1) [29]. In normally proliferating cells, L1 is suppressed by a cell monitoring mechanism, e.g., three prime repair exonuclease 1 (Trex1) and the RB transcriptional corepressor 1 (Rb1). In senescent cells, these repression mechanisms are disrupted, leading to activation of L1 via activation of FoxA1 [29].
During exposure of cells to harmful stimuli and conditions, such as chemicals and ischemia, the injured cells excrete or secrete various molecules such as ATP, uric acid, oxidatively modified DNA, and aggregated proteins, which are called damage-associated molecular pattern molecules (DAMPs) [30]. DAMPs bind to receptors, such as Toll-like receptors, in the cell membrane and cytoplasm of resident macrophages and elicit innate immune and inflammatory responses. The sensor of innate immunity, called the nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3 (NLRP3) inflammasome, is activated, and macrophages secrete inflammatory cytokines and exacerbate inflammatory responses. These inflammatory signals have been reported to damage surrounding parenchymal cells. As with senescent cells, this minor but chronic inflammatory response at the cellular level is thought to be the main factor driving aging and disease, including cancer.
GH is not only secreted from anterior pituitary cells but is also expressed in various cells including immune cells. The GH receptor (Ghr) is also expressed in a wide range of cells, and the GH signaling system is activated by endocrine action as well as by autocrine and paracrine actions. Recent studies suggested that the sensitivity of the GH-IGF-1 signal increases with age and that DAMP inflammasome is likely to be activated [31]. This activation of the inflammasome is suppressed in long-lived Ghr-deficient mice [31]. Since CR also attenuates GH-IGF-1 signals, suppression of the inflammasome could be a main component of the anti-aging mechanism of CR.

4. Differential Regulation of Cancer and Lifespan by CR via FoxO Transcription Factors

Although multiple studies have used a variety of CR regimens in invertebrates and vertebrates, most of the CR regimens extend lifespans in these organisms. To analyze the signal pathways mediating the life-prolonging effects of CR, epistasis experiments in which mutation of a single gene causes attenuation or abrogation of the life-prolonging effect of CR have been conducted, mostly in C. elegans. These experiments have identified CR genes such as daf-16, skn-1, pha-4, clk-1, aak-2, and hsf-1, although the genes required for the effect of CR may differ depending on methods of CR [7]. These CR genes suggest the importance of regulation of insulin-like signaling, stress response, and mitochondrial bioenergetics.
CR is known to lower plasma concentrations of insulin and IGF-1 in mammals [9]. Therefore, IGF-1 signaling and thus FoxO transcription factors, the mammalian orthologs of Daf-16, were considered to play roles in the effects of CR. As mentioned, loss of Daf-16 abrogates the life-extending effects of CR in C. elegans [7]. In mammals, the FoxO transcription factor family includes four isoforms, FoxO1, FoxO3, FoxO4, and FoxO6 [32]. We tested the hypothesis that FoxOs are involved in the effects of CR by two lifespan studies using Foxo1 and Foxo3 knockout mice.
For the FoxO1 study, we used Foxo1 + /− mice, because Foxo1−/− mice died around embryonic day 11 due to defects in the branchial arches and remarkably impaired vascular development of embryos and yolk sacs, indicating the necessity of Foxo1 in development of the cardiovascular system [33]. In comparison, Foxo1+/− mice grow normally through pre- and post-natal stages. In Foxo1+/− mice, expression levels of Foxo1 mRNA in the examined tissues were reduced by 50% compared with levels in wild-type (WT) mice [34]. Results of the lifespan study indicated that CR extended lifespan in Foxo1+/− mice to the same extent as in WT mice; however, unlike CR in WT mice, CR did not significantly reduce the proportion of Foxo1+/− mice bearing spontaneously occurring tumors. By contrast, in Foxo3+/− and Foxo3−/− mice, CR did not extend lifespan [35], indicating the requirement of the Foxo3 gene in the life-extending effect of CR in mice. With AL feeding, Foxo3+/− mice displayed no reduction of lifespan compared with WT mice, while Foxo3−/− mice showed a slight reduction of lifespan [35]. Although the effect of CR in Foxo1-null mice should be investigated, our lifespan studies suggest a differential regulation of cancer and lifespan by CR via Foxo1 and Foxo3 (Figure 1).
In early studies using mice with germline-deleted Foxo1, -3, and -4 genes, deletion of a single gene had little effect on longevity or cancer development in postnatal life under AL conditions [36]. One exception was female Foxo3−/− mice, in which occurrence of pituitary adenoma was accelerated compared with WT and Foxo3+/− mice. Conditional, widespread somatic Foxo deletion in adult tissues was also achieved using an interferon-inducible Mx-Cre transgene to circumvent embryonic lethality of FoxO1 deficiency [36]. When the three Foxo genes were deleted in mice at the same time, tumor incidences were elevated, while lifespan was shortened. In particular, the incidences of thymic lymphoma and hemangioma were increased, compared with groups of mice retaining at least one Foxo allele [36]. Foxo1, -3, and -4 gene-deleted mice showed premature death due to the tumors. These experiments indicated that FoxO transcription factor genes are complementary as for development of cancers [36]. In other words, even if one Foxo gene is deleted, the other Foxo genes can substitute in AL conditions. However, our lifespan studies [34,35] indicate differential roles for FoxO1 and FoxO3 in the effects of CR.
The Daf-16 isoform-specific extension of lifespan in the context of reduction of IGF signaling has been also reported in C. elegans. The daf-16 genomic locus encodes three groups of transcripts (a, b, d/f/h) that are transcribed from distinct promoters [37,38,39]. Depending on the experimental setting, Daf-16a and/or Daf-16d/f/h, but not Daf-16b, play a major role in the extension of lifespan [39,40].
Numerous human genetic studies have indicated a correlation of the minor alleles of the FOXO3 gene with longevity [41]. However, there is no significant correlation of FOXO1 genotypes with longevity. A genome-wide meta-analysis of 30844 adults of European ancestry from 21 studies confirmed that the known longevity-associated FOXO3 variant rs2153960 is a genome-wide significant SNP for lowering IGF-1 concentrations [42].
The isoform specificity of FoxO and Daf-16 in the life-extending effect of CR as well as the human genomic studies for longevity suggest that the mechanism of lifespan control has been evolutionarily conserved. A recent study showed that FoxO6 functions in age-related insulin resistance and inflammation in rats with AL feeding, although CR was not investigated [43]. Thus, potential roles for FoxO4 and FoxO6 in the effects of CR remain to be elucidated.
How FoxO3 regulates lifespan remains unclear. Our microarray analysis in Foxo1+/− and Foxo3+/− CR mouse liver show that many genes are differentially regulated in these mice under conditions of CR (Tables S1 and S2). The pathway analysis of the differentially expressed genes between WT-CR and Foxo1+/− CR mice as well as WT-CR and Foxo3+/− CR mice also suggests that a number of inflammation and immune response pathways are activated in Foxo3+/− CR mice. By contrast, in Foxo1+/− CR mice, some T-cell functions may be down-regulated. FoxO3 is reported to prevent excess activation of interferone (IFN)-I in response to viral infection [44]. A ternary complex consisting of FoxO3, nuclear co-repressor 2 (Ncor2) and histone deacetylase 3 (Hdac3) exists on the promoter of interferon regulatory factor 7 (Irf7); a loss of FoxO3 enhances histone acetylation in the promoter of Irs7 gene, resulting in increased levels of Irf7 mRNA in macrophages [44]. An experimental stimulation of IFN-I activated the PI3K/Akt pathway, which in turn led to FoxO3 degradation. FoxO3 could play a role in optimizing host defense mechanisms against harmful stimuli as well as under unstimulated conditions by limiting the transcription of Irf7 and then Irf7-induced target inflammatory genes. This process could minimize activation of the inflammasome. Reduction of FoxO3 may disrupt the FoxO3-Irf7 regulatory circuit under CR conditions.

5. FoxO1 Mediates the Tumor-Inhibiting Effect of CR

A tumor-inhibiting but not life-extending effect of CR has been reported in Nrf2−/− mice [45]. The Nrf2 transcription factor belongs to the cap’n’collar basic-leucine zipper (CNC-bZIP) family. Under unstressed cellular conditions, Nrf2 binds to Keap1 in the cytoplasm and is degraded by the ubiquitin-proteasome system [46]. When the redox environment changes due to oxidative stress, Nrf2 and Keap1 dissociate and Nrf2 moves into the nucleus. Nrf2 forms heterodimers with other transcription factor cofactors such as Maf, binds to the antioxidant response element (ARE) in the promoter of target genes, and promotes the gene expressions of antioxidants and phase II detoxification enzymes.
The role of Nrf2 in the tumor-inhibiting effect of CR was tested in a two-stage skin carcinogenesis model using 7,12-dimethyl-benz (a) anthracene (DMBA) and 12-O-tetradecanoyl phorbol 13-acetate (TPA) [45]. In WT mice, CR significantly suppressed the development of skin tumors; in Nrf2−/− mice, the CR-mediated inhibitory effect on tumor growth was absent. In Nrf2+/− mice, the inhibitory effect was attenuated, suggesting a gene-dose dependency of Nrf2 in the inhibition of tumor formation by CR. However, even in Nrf2−/− mice, the life-extending effect of CR was preserved [45]. These results suggest that Nrf2 plays a major role in the tumor-inhibiting effect of CR but not for lifespan extension.
We also conducted a two-stage skin carcinogenesis model experiment to confirm the potential role for FoxO1 in the effect of CR, following the protocol of Pearson et al. [46] Appendix A. Briefly, DMBA was applied in the dorsal skin of mice at 31 weeks of age; after two weeks, TPA treatment was initiated. Skin papilloma started occurring six weeks after DMBA application, and thus four weeks later starting TPA treatment (Figure 2A). Our findings showed that haploinsufficiency of Foxo1 accelerated the occurrence of skin papilloma, particularly in CR conditions (WT-CR vs. Foxo1+/− CR, p = 0.0103 by log-rank test; Figure 2A), confirming the role for FoxO1 in the tumor-inhibiting effect of CR, as in Nrf2.
TPA promotes epidermal hyperplasia in the pre-neoplastic phase via reactive oxygen species (ROS) production and inflammation [47]. We assessed the epidermal thickness during TPA treatment and the proliferative activity of epidermal cells after TPA treatment. Epidermal thickness was greater in Foxo1+/− mice than in WT mice (genotype, p = 0.0331 by 3-f ANOVA: Figure 2B), although diet did not affect the thickness (diet, p = 0.2993 by 3-f ANOVA). Epidermal cell proliferation was greater in Foxo1+/− mice (genotype, p = 0.0193 by 3-f ANOVA; Figure 2C); the rate of apoptosis did not differ between WT and Foxo1+/− mice (data not shown). Thus, the reduced FoxO1 promotes epidermal cell proliferation in response to TPA.
We also evaluated macrophage infiltration in the dermis as an index of inflammation. Although the number of macrophages was less in the CR groups compared with the AL groups, indicating an effect of CR (diet, p = 0.0001 by 3-f ANOVA: Figure 2D), the number of macrophages did not significantly differ between WT and Foxo1+/− mice (genotype, p = 0.1374 by 3-f ANOVA).
We further analyzed the expression of genes associated with inflammatory stimuli. TPA induces cyclooxygenase-2 (COX-2), an enzyme that catalyzes arachidonic acid to prostaglandin G2, i.e., produces chemical mediators of inflammation, in the mouse skin [48]. The mRNA expression levels of COX-2 were elevated after TPA treatment (Figure 2E). The expression levels were significantly lower in WT-DR mice compared than other groups of mice; the effect is diminished in Foxo1+/− CR mice (diet; p = 0.0123; genotype x diet; p = 0.0399 by 3f-ANOVA). Although other inflammatory responses induced by TPA were mostly reduced in response to CR, even in Foxo1+/− CR mouse skin (data not shown), reduction of FoxO1 in the CR condition might affect the regulation of prostaglandins formation and then impair the tumor-inhibiting effect of CR.
The above results indicate that both FoxO1 and Nrf2 are necessary for the tumor-inhibiting effect of CR. Some Nrf2 target genes are also regulated by FoxO1 [49], such as heme oxygenasae (decycling) 1 (Hmox-1), glutamate-cysteine ligase, and catalytic subunit (Gclc) genes. Gclc is the rate-limiting enzyme in the synthesis of Glutathione (GSH). We also analyzed the expression of Nrf2-target genes and found that Gclc and Hmox-1 mRNA expression levels were lower in Foxo1+/− mice than in WT mice (only the data of Gclc mRNA are shown in Figure 2F; genotype; p = 0.0207: diet; p = 0.0175: genotype x diet; p = 0.5809 by 3f-ANOVA). In a study in C. elegans, Daf-16 and Skn-1 target genes were also reported to be preferentially regulated to induce conditions of mitohormesis [49], which could be a mechanism of CR.

6. Pleiotropic Roles for Foxo1 in Disorders

As indicated above, reduction of FoxO1 diminishes the anti-tumor effect of CR. However, reduction of FoxO1 does not affect lifespans in AL and CR conditions [34]. Multiple studies have reported beneficial effects of reduced FoxO1 on lesions or disorders, although these results depended on nutritional states. In AL conditions, Foxo1+/− mice showed accelerated skin wound healing with enhanced keratinocyte migration, reduced granulation tissue formation, and decreased collagen density, accompanied by an attenuated inflammatory response, compared with WT mice [50]. Foxo3−/− mice did not show any significant phenotypes for skin wound healing and inflammation. Reduction of FoxO1 also ameliorates glucose intolerance and insulin insensitivity in diabetic models [51], probably due to diminution of gluconeogenesis. Indeed, FoxO1 is reported to increase hepatic gluconeogenesis through upregulation of glucose 6-phosphatase (G6pc) and phosphoenolpyruvate carboxykinase (Pck1) in CR and fasting conditions [42].
Stress resistance is one of the hallmarks in CR animals, although whether this trait directly causes the extension of lifespan remains unclear. We tested stress resistance in Foxo1+/− mice using the endotoxin shock model following the procedures of Kamohara [52]. The survival rates and endoplasmic reticulum (ER) stress were monitored after lipopolysaccharide (LPS) injection. ER stress-responsive alkaline phosphatase (ESTRAP) mice [53] were used to monitor ER stress in vivo (details are described elsewhere [52]). In ESTRAP mice, secreted alkaline phosphatase (SEAP) is constitutively expressed, and SEAP activity in the blood is reduced by ER stress [53]. The experiment was performed using mice at six months of age. The results showed that the survival rate was extended by CR, particularly in Foxo1+/− mice (diet, p = 0.0263; genotype × diet, p = 0.0498 by likelihood ratio test: Figure 3A). After LPS injection, SEAP activity decreased until 8 h in each group and then stayed constant or recovered between 8 and 24 h (Figure 3B). Between 2 and 8 h after LPS injection, that is, in the acute phase of ER stress, CR attenuated ER stress (diet, p < 0.0001 by 3-f ANOVA), and the attenuating effect was greater in Foxo1+/− mice compared with Ctrl mice (genotype, p = 0.0093 by 3-f ANOVA: Figure 3B). These data indicate that reduction of FoxO1 enhances stress resistance in both AL and CR conditions. Therefore, in the present experimental setting, reduction of FoxO1 could enhance stress resistance, particularly in the CR condition.
In summary, these findings demonstrate that FoxO1 exerts pleiotropic effects on disorders depending on nutritional conditions.

7. Sirtuin as a Molecule Upstream of FoxO

Sirtuins (Sirts) are evolutionarily conserved proteins that catalyze the deacetylation and adenosine diphosphate (ADP) ribosylation of target proteins using the oxidized from of nicotinamide adenine dinucleotide (NAD+) as a coenzyme [54]. Since overexpression of Sir2p, one of the sirtuin genes in budding yeast, was reported to extend replicative lifespan of yeast, many studies have been conducted to demonstrate the importance of Sirts in the regulation of aging in various experimental models. Although findings in the early phase of investigation were controversial, re-examinations have confirmed Sirts as key molecules in the regulation of aging [55].
Although results in epistasis analyses using mutant strains in lower organisms are sometime affected by experimental settings such as CR or CR-like regimens [7,55], a number of studies have indicated the necessity of Sirt1 in the life-extending effect of CR. In Drosophila, deletion of Sirt1 (dSir2) in the fat body abolishes the life-extending effect of CR [56].
There are seven mammalian orthologs of nematode Sir2 (Sirt1–7) [54]. Sirt1, Sirt6, and Sirt7 exist mainly in the nucleus; Sirt2 is localized in the cytoplasm and Sirt3, Sirt4, and Sirt5 are in mitochondria [54]. Sirt targets in the nucleus include histones, transcription factors, and transcriptional regulators, which control gene expression by deacetylation. One example is the deacetylation of FoxO1 and PGC-1α by Sirt1 in the liver and increased expression of target genes related to gluconeogenesis and fatty acid oxidation [54].
Sirt in mitochondria regulates mitochondrial function, that is, energy metabolism, by deacetylating mitochondrial constituent proteins, energy metabolic pathway proteins, and mitochondrial transcription factors. Previous studies have shown that Sirt3 is deeply involved in the deacetylation of mitochondrial proteins [57].
SIRT4 and SIRT6 mainly function as ADP-ribosylating enzymes [44]. Accumulated evidence has indicated the importance of Sirts in the regulation of energy metabolism and genome instability.
Several studies have indicated the necessity of Sirt1 for the effects of CR in mice. Aged mouse kidney displays pathology such as glomerular and interstitial fibrosis, which is improved by CR [58]. However, this effect of CR is abrogated in Sirt1+/− mice. From this model, Kume et al. reported Sirt1-dependent deacetylation of FoxO3 as a key mechanism that promotes mitochondrial autophagy and then reduces oxidative insult in kidneys. Finally, CR extends lifespan in Sirt1+/− mice but not in Sirt1−/− mice [59]. These findings indicate that one of the mechanisms underlying the effect of CR involves epigenetic regulation of FoxO3 by Sirt1 (Figure 1).

8. Roles for Npy in the Effect of CR

An evolutionary perspective predicted that the effect of CR is derived from adaptive responses in animals to harsh conditions such as a famine [60]. Animals should have acquired a system(s) to survive in famine, which frequently occurs in the wild. If not, a species could undergo extinction. When food resources are abundant, animals consume as much food to promote growth and reproduction, while simultaneously storing the remaining energy as fat in the body. In starvation, animals use the stored fat as an energy source by activation of the lipolytic pathway. During food shortage, physiological functions such as reproduction, growth, and heat are suppressed to inhibit excessive consumption of energy. The transition to Dauer states in nematodes and hibernation in some mammals could be extreme examples. The effects of CR may derive from these adaptive processes.
A previous study in C. elegans showed that two ciliated neurons that are part of the amphid sensilla (ASI neurons) in the head, in which chemosensitive receptors are present, are necessary for the lifespan extension by CR [61]. These neurons express skn-1 as described above and are activated when dietary energy is reduced to promote the development of Dauer via the endocrine system [62]. The evolutionary view of CR and the finding in C. elegans suggest a possible implication of hypothalamic neurons in the effect of CR in vertebrates.
We focused on Npy, an orexigenic neuropeptide expressed in neurons in the arcuate nuclei of the hypothalamus and the sympathetic nervous system (SNS). Published data indicate that Npy plays a role in neuroendocrine adaptation to negative energy balance in mammals by suppressing activities of growth, reproduction, and heat, whereas it stimulates the glucocorticoid system [63,64]. Npy-overexpressing rats show improvements of cardiac function by regulation of the SNS and marginal extension of lifespan [65]. Npy is also known as a neuroprotective peptide [66]. These traits induced by Npy are consistent with the hallmarks of CR animals. Our previous study also confirmed that CR elevated mRNA levels of Npy in the arcuate nuclei in rats [67].
We tested a potential role for Npy in the effects of CR using Npy−/− mice. The life-extending effect in Npy−/− mice was attenuated to about one-third compared with WT mice [68]. Oxidative stress tolerance and tumor suppressive effects were also diminished. Initially, Npy deficiency was predicted to compromise neuroendocrine adaptative processes to CR, especially the inhibition of the GH-IGF-1 system, because experiments have shown that Npy is required to suppress Ghrh in fasting [69]. However, hypothalamic Ghrh mRNA, plasma IGF-1, insulin, and downstream Mtor in tissues, which could be related to the anti-aging effect of CR, were inhibited as in the WT mice [68]. In addition, plasma concentrations of leptin, adiponectin, and corticosterone in Npy−/− mice were also altered similarly as in WT mice [68]. These results indicate the complementary action of the neuroendocrine system in response to CR even without Npy. These findings also suggest that the Npy-related anti-aging mechanism of CR does not overlap with previously noted IGF-1, Mtor, adiponectin, and corticosteroids [68].
Npy−/− mice showed a slight increase of food intake normalized body weight in both AL and CR conditions during the lifespan study, indicating a reduction of food efficiency (a unit amount of food or calorie to gain or maintain body weight) compared with WT mice [59], suggesting an increment of energy expenditure in Npy−/− mice. In male mice, Npy deficiency increased mortality in CR condition until middle age, probably due to an excess loss of body fat [68]. Indeed, in male Npy−/− CR mice, lipolysis and/or thermogenesis was elevated through significant activation of the adrenergic receptor β3 and hormone-sensitive lipase pathway [70]. The premature death in CR mice was inhibited by administration of acipimox, a lipolysis inhibitor [71]. These findings suggest that the life-extending effect of CR requires inhibition of an excess loss of body energy through antagonizing the SNS. The study also emphasized the substantial role for Npy in the SNS in maintaining fat tissue under CR conditions in male mice. The extent of lifespan extension by CR negatively correlates with rates of white adipose tissue reduction by CR [72], i.e., mouse strains with less reduction of body fat by CR live longer than other strains in which fat is reduced greatly in response to CR. Therefore, the ability of energy preservation by Npy is essential for the life-extending effect of CR.
By contrast, deficiency of Npy may act beneficially in the life-stage under AL conditions. In female Npy−/−mice with AL feeding, the aging-related increase in body fat was minimized, leading to an improvement of insulin sensitivity via inhibition of inflammation in the fat [70]. Antagonism of Npy may be a promising target for drug discovery to prevent obesity in middle age, although Npy deficiency may cause unintentional weight loss in aged people.
Together these studies indicate that Npy exerts pleiotropic effects in health conditions depending on nutritional conditions.

9. Role for Npy in the Tumor-Inhibiting Effect of CR

Npy is expressed abundantly in the brain, adrenal gland, and adipose tissue. Npy circulates in the blood and is secreted locally from the SNS. Minor et al. reported that the tumor-inhibiting effect of CR was diminished in Npy−/− mice using a chemically induced skin tumor model [73]. The authors also suggested a role for hypothalamic arcuate nuclei (ARC) in the tumor-inhibiting effect of CR in a model of monosodium glutamate (MSG)-injected mice. MSG induces neuronal cell death in the ARC when injected subcutaneously on postnatal day five. In MSG-injected mice, no Npy-mRNA expression was observed in the ARC but serum Npy was detectable, suggesting a major role for hypothalamic Npy in the tumor-inhibiting effect of CR [73].
Our lifespan study also demonstrated a diminution of the tumor-inhibiting effect of CR in Npy−/− mice, suggesting a role for Npy in the tumor-inhibiting effect of CR [68]. The SNS not only releases catecholamines such as norepinephrine (NE) but also secretes Npy [74]. Recent studies have indicated that activation of the SNS exacerbates steatohepatitis, which is now recognized as one of the predisposing conditions of hepatocellular carcinoma (HCC) in obese people [75]. An experimental study also suggested that the SNS promotes HCC via activation of hepatic stellate cells and Kupffer cells [76,77]. Therefore, we investigated a potential role for Npy in a carcinogen-induced HCC model in different nutritional settings including CR as well as high calorie-intake regimens [78].
The complete details of the experiment are described elsewhere [78]. Briefly, HCC was induced by an intraperitoneal injection of diethylnitrosamine (DEN) in male C57BL6/J mice null for Npy (Npy−/−) and their haplotype (Npy+/−) as a control (Ctrl) on postnatal day 15 [78]. Npy+/− mice showed increased lifespan and reduced incidence of spontaneously occurring tumors in response to CR to the same extent as WT mice, indicating that one allele of the Npy gene is enough for the effects of CR [69]. Experimental mice, fed a standard diet AL after weaning, were subjected to three dietary regimens at 12 weeks of age and thereafter, that is, standard diet fed AL, 30% CR with the standard diet, and a high fat diet (HFD) fed AL. Mice were killed at 28 and 48 weeks to analyze the occurrence of HCC and growth of HCC in the liver.
CR inhibited the occurrence of microscopic HCC at 28 weeks in Npy−/− mice as well as Ctrl mice, compared to the AL and HFD groups (diet, p = 0.0195 by logistic regression; CR vs. AL, p = 0.0192; CR vs. HFD, p = 0.0310: Figure 4A), although the baseline proportion of mice bearing microscopic HCC at 28 weeks was slightly but significantly greater in Npy−/− mice (genotype, p = 0.0426 by logistic regression). Since DEN was administered at 15 days of age before initiating CR, Npy might exert an inhibitory effect on initiation of the carcinogen. At 48 weeks, many mice in the AL and the HFD groups showed macroscopic (≤1 mm in diameter) HCC [78], and thus the liver weight alone or the liver weight normalized by the body weight (Lw/Bw) represents an index of growth of HCC [78]. In the CR groups, the Lw/Bw was not increased between 28 and 48 weeks in Npy−/− and Ctrl mice, indicating that CR almost completely inhibits the growth of HCC even in the absence of Npy (Figure 4B). The AL and HFD feedings promoted the growth of HCC between 28 and 48 weeks more in Npy−/− mice than in Ctrl mice (genotype x age, p < 0.0001 by 3-f ANOVA; Npy−/− (48) vs. Ctrl (48), p < 0.0001 by Tukey’s honestly significant difference (HSD) test), although there was no significant difference in the tumor growth between the AL and HFD feedings (Figure 4B). These findings suggest a role for Npy in tumor growth in conditions of overnutrition, but not for CR. This HCC model indicates that Npy is not necessary for the tumor-inhibiting effect of CR.
Steatohepatitis, which was quantitated by the number of inflammatory foci/unit area, was exacerbated between 28 and 48 weeks (age, p = 0.0117 by 3-f ANOVA; Figure 4C). CR consistently inhibited steatohepatitis, compared with the AL and HFD groups, in both Ctrl and Npy−/− mice (CR vs. AL, p < 0.0001; CR vs. HFD, p < 0.0001 by Tukey’s HSD test). Therefore, CR might inhibit the occurrence and growth of HCC via suppressing steatohepatitis, one of the predisposing conditions for HCC even in the absence of Npy. Overall, steatohepatitis was less progressed in Npy−/− mice compared with Ctrl mice (genotype, p = 0.0069 by 3-f ANOVA), although the degree of steatohepatitis was differently altered by the diets between 28 and 48 weeks (Figure 4C). These findings suggest that Npy is involved in inhibition of growth of HCC but not simply through preventing steatohepatitis in AL and HFD conditions.
Npy is reported to counterbalance the actions of NE in stressed conditions [74]. In a Npy-overexpressing rat model, Npy attenuated sympathetic signals at baseline and diminished the immediate sympathetic response to stress [65]. Npy was also reported to minimize stress-induced bone loss through a suppression of NE circuits [79]. These findings indicated a counteracting role for Npy over NE in the activation of the SNS, a potentially exacerbating factor of many types of disorders in well-fed conditions (Figure 4D).

10. Conclusions

We reviewed and discussed underlying mechanisms of CR from an aspect of CR genes. It should be stressed that the isoform specificity of FoxO transcription factors for longevity becomes apparent under CR conditions but not AL conditions. Npy and FoxO1 both play pleiotropic roles in aging and related disorders, depending on the nutritional state. As briefly described in Section 1 and Section 2, the life-extending effects of CR and reduced IGF-1 signaling are also sexually dimorphic. Genes associated with regulation of the aging process should be investigated carefully in a context-dependent manner, i.e., abilities of physiological adaptation for individuals against environmental challenges, particularly food shortage.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/2072-6643/11/12/3068/s1, Table S1: Pathways signified by differentially regulated genes between WT-CR and Foxo3+/− CR livers in the fasting phase, Table S2: Pathways signified by differentially regulated genes between WT-CR and Foxo1+/− CR livers in the fasting phase.

Author Contributions

I.S. organized the review as a corresponding author and wrote most of the manuscript. T.K. and R.M. provided the data of skin carcinogenesis and critically reviewed the corresponding sections. H.Y. provided the data of ER stress and reviewed the sections related to stress response. S.P. and H.H. discussed and reviewed the sections on Npy.

Funding

This research was funded by JSPS KAKENHI Grant Numbers JP15H04682, JP19H04033.

Acknowledgments

We thank Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

Appendix A

Appendix A.1. Microarray Analysis

The microarray analysis using mouse liver tissues at six months of age was conducted, following the procedure published elsewhere [50]. Total RNA was extracted from liver tissues harvested from wild type (WT)-calorie restricted (CR), Foxo1+/− CR, and Foxo3+/− CR mice in the fasting phase, i.e., 3 to 4 h prior to the feeding. The details for isolation of RNA are also described in the Appendix A.2.3. The animal husbandry was described elsewhere [34,35]. Cyanine 3-labeled complementary RNA was generated from 200 ng of total RNA using the Low Input Quick AmpLabeling Kit, one color (Agilent Technologies, Santa Clara, CA), and then those was purified by the RNeasy mini kit (Qiagen), according to the manufacturer’s instructions. Fragmented cyanine 3-labeled complementary RNA (600 ng) was hybridized to SurePrint G3 mouse GE microarray, 8 × 60 K (Agilent Technologies), at 65 °C for 17 h. Subsequently, the microarray was washed and scanned using the DNA microarray scanner (Agilent Technologies). Data analysis was entrusted to Ingenuity Systems, Inc (Redwood City, CA) with Ingenuity iReport. We compared the gene expression in the liver, between WT and Foxo1+/− CR groups and between WT-CR and Foxo3+/− CR groups. The filtering standard was a fold change cutoff of 1.5, with statistical significance of p < 0.05. Bio-data mining processes were executed by iReport based ingenuity knowledge base to identify enriched canonical pathways for the differentially expressed genes with p < 0.05 by Fisher’s exact tests.

Appendix A.2. The Multistage Skin Tumorigenesis Model

Appendix A.2.1. Experimental Protocol

We followed the experimental procedure of Pearson et al. [36] for the multistage skin tumorigenesis model. Briefly, the number of mice in each group was 18 at the start of the experiment. At 31 weeks of age, a single dose of 25 µg of 7,12-dimethybenz(a)anthracene (DMBA, Sigma, St. Louis, MO) dissolved in 100 µl of acetone was applied topically in a dorsal area shaved in each mouse. Two weeks later, a topical treatment of 12-O-tetradecanoylphorbol-13-acetate (TPA, Sigma, St. Louis, MO, 4 µg dissolved in 100 µl of acetone) began and continued twice a week to the dorsal skin area until one papilloma with a diameter ≥ 1 mm was identified. Skin biopsy was done at the following time points: 0, 2, 3, 4, 5, and 6 weeks after DMBA treatment. Collected skin samples were cut in two specimens. One was immediately frozen in liquid nitrogen and stored at −80 °C. The other one was fixed in 4% formaldehyde for histological and immunohistochemical analyses. Once a skin tumor was identified, TPA treatment was stopped and left mice without any treatment. The experiment was terminated at 32 weeks after DMBA application. At the termination, mice were euthanized at 2 and 6 h after TPA or acetone treatment. The skin tissues without tumors were collected from each mouse, frozen in liquid nitrogen, and stored at −80 °C in order to analyze mRNA and protein expression.

Appendix A.2.2. Histology and Immunohistochemistry

Skin biopsy samples, fixed in 4% formaldehyde, were routinely processed and embedded in paraffin. Epidermal thickness was measured in hematoxylin and eosin (H.E.) stained sections under microscope. Details of immunohistochemical staining for proliferating cell nuclear antigen (PCNA) and F4/80 are described in elsewhere [41]. The primary antibodies for PCNA and for F4/80 were purchased from Abcam (Cambridge, U.K.). PCNA-positive cells in the epidermis and F4/80-positive cells in the dermis were counted for 10 high power views in each skin sample with microscope.

Appendix A.2.3. RNA Isolation and Quantitative Polymerase Chain Reaction

Total RNA was purified from skin using a RNeasy lipid tissue Mini kit (Qiagen). The quality of extracted RNA was evaluated as the densitometric ratio of 28S and 18S ribosomal RNA. The extracted RNA was converted to cDNA using RevaTra Ace® qPCR RT kit (TOYOBO, Tokyo, JAPAN) according to the manufacturer’s instructions and amplified using THUNDERBIRD SYBR qPCR Mix (TOYOBO) with Light Cycler 480 (Roche Diagnostics Japan, Tokyo, Japan). All of the primers used in the present analysis were purchased from TAKARA with reference to the Perfect Real time Support System (TAKARA, Siga, Japan). All samples and standard curves were tested in duplicate. We confirmed that expression levels of a housekeeping gene, Atp5f1-mRNA, were not significantly affected by the diet or the genotype or TPA treatment, and then used for normalization of specific mRNA expression levels.

Appendix A.2.4. Statistical Analysis

Difference in the fraction of mice bearing skin papilloma between groups was tested with the log-rank test. Epidermal thickness, proliferating cell nuclear antigen (PCNA)-positive cells, the number of dermal macrophages, and the expression levels of Cox2 and Gclc-mRNAs were analyzed using 3-factor ANOVA with Tukey’s honestly significant difference (HSD) test.

References

  1. Weindruch, R.; Walford, R.L. The Retardation of Aging and Disease by Dietary Restriction; Charles C Thomas Publisher: Springfield, IL, USA, 1988; pp. 31–115. [Google Scholar]
  2. McCay, C.M.; Crowell, M.F.; Maynard, L.A. The effect of retarded growth upon the length of life span and upon the ultimate body size. J. Nutr. 1935, 10, 63–79. [Google Scholar] [CrossRef]
  3. Swindle, W.R. Dietary restriction in rats and mice: A meta-analysis and review of the evidence fro genotype-dependent effects on lifespan. Ageing Res. Rev. 2012, 11, 254–270. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Baloni, P.; Sangar, V.; Yurkovich, J.; Robinson, M.; Taylor, S.; Karbowski, C.; Hamadeh, H.; He, Y.; Price, N. Genome-scale metabolic model of the rat liver predicts effects of diet restriction. Sci. Rep. 2019, 9, 9807. [Google Scholar]
  5. Mitchell, S.; Madrigal-Matute, J.; Scheibye-Knudsen, M.; Fang, E.; Aon, M.; González-Reyes, J.; Cortassa, S.; Kaushik, S.; Gonzalez-Freire, M.; Patel, B.; et al. Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice. Cell Metab. 2016, 23, 1093–1112. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Kane, A.; Sinclair, D.; Mitchell, J.; Mitchell, S. Sex differences in the response to dietary restriction in rodents. Curr. Opin. Physiol. 2018, 6, 28–34. [Google Scholar] [CrossRef]
  7. Greer, E.L.; Brunet, A. Different dietary restriction regimens extend lifespan by both independent and overlapping genetic pathways in C. elegans. Aging Cell 2009, 8, 113–127. [Google Scholar] [CrossRef] [Green Version]
  8. Shimokawa, I.; Chiba, T.; Yamaza, H.; Komatsu, T. Longevity genes: Insights from calorie restriction and genetic longevity models. Mol. Cells 2008, 26, 427–435. [Google Scholar]
  9. Longo, V.D.; Finch, C.E. Evolutionary medicine: From dwarf model systems to healthy centenarians? Science 2003, 299, 1342–1346. [Google Scholar] [CrossRef] [Green Version]
  10. Available online: http://genomics.senescence.info/diet/ (accessed on 6 November 2019).
  11. Johnson, T.E. Increased life-span of age-1 mutants in Caenorhabditis elegans and lower Gompertz rate of aging. Science 1990, 249, 908–912. [Google Scholar] [CrossRef]
  12. Morris, J.Z.; Tissenbaum, H.A.; Ruvkun, G. A phosphatidylinositol-3-OH kinase family member regulating longevity and diapause in Caenorhabditis elegans. Nature 1996, 382, 536–539. [Google Scholar] [CrossRef]
  13. Kenyon, C.; Chang, J.; Gensch, E.; Rudner, A.; Tabtiang, R. A C. elegans mutant that lives twice as long as wild type. Nature 1993, 366, 461–464. [Google Scholar] [CrossRef] [PubMed]
  14. Slack, C.; Foley, A.; Partridge, L. Activation of AMPK by the Putative Dietary Restriction Mimetic Metformin Is Insufficient to Extend Lifespan in Drosophila. PLoS ONE 2012, 7, e47699. [Google Scholar] [CrossRef] [PubMed]
  15. Vellai, T.; Takacs-Vellai, K.; Zhang, Y.; Kovacs, A.L.; Orosz, L. Influence of TOR kinase on lifespan in C. elegans. Nature 2003, 426, 620. [Google Scholar] [CrossRef] [PubMed]
  16. Kapahi, P.; Zid, B.M.; Harper, T.; Koslover, D.; Sapin, V.; Benzer, S. Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway. Curr. Biol. 2004, 14, 885–890. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Shimokawa, I. Growth hormone and IGF-1 axis in aging and longevity. In Hormones in Ageing and Longevity, 1st ed.; Rattan, S., Sharma, R., Eds.; Springer International Publishing AG: Cham, Switzerland, 2017; pp. 91–106. [Google Scholar]
  18. Harrison, D.E.; Strong, R.; Sharp, Z.D.; Nelson, J.F.; Astle, C.M.; Flurkey, K.; Nadon, N.L.; Wilkinson, J.E.; Frenkel, K.; Carter, C.S.; et al. Rapamycin fed late in life extends lifespan in genetically heterogeneous mice. Nature 2009, 460, 392–395. [Google Scholar] [CrossRef] [Green Version]
  19. Selman, C.; Tullet, J.M.A.; Wieser, D.; Irvine, E.; Lingard, S.J.; Choudhury, A.I.; Claret, M.; Al-Qassab, H.; Carmignac, D.; Ramadani, F.; et al. Ribosomal Protein S6 Kinase 1 Signaling Regulates Mammalian Life Span. Science 2009, 326, 140–144. [Google Scholar] [CrossRef] [Green Version]
  20. Wu, J.J.; Liu, J.; Chen, E.B.; Wang, J.J.; Cao, L.; Narayan, N.; Fergusson, M.M.; Rovira, I.I.; Allen, M.; Springer, D.A.; et al. Increased mammalian lifespan and a segmental and tissue-specific slowing of aging after genetic reduction of mTOR expression. Cell Rep. 2013, 4, 913–920. [Google Scholar] [CrossRef] [Green Version]
  21. Holzenberger, M.; Dupont, J.; Ducos, B.; Leneuve, P.; Géloën, A.; Even, P.; Cervera, P.; Bouc, Y. IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice. Nature 2003, 421, 182–187. [Google Scholar] [CrossRef]
  22. Xu, J.; Gontier, G.; Chaker, Z.; Lacube, P.; Dupont, J.; Holzenberger, M. Longevity effect of IGF-1R(+/-) mutation depends on genetic background-specific receptor activation. Aging Cell 2014, 13, 19–28. [Google Scholar] [CrossRef] [Green Version]
  23. Suh, Y.; Atzmon, G.; Cho, M.; Hwang, D.; Liu, B.; Leahy, D.; Barzilai, N.; Cohen, P. Functionally significant insulin-like growth factor I receptor mutations in centenarians. Proc. Natl. Acad. Sci. USA 2008, 105, 3438–3442. [Google Scholar] [CrossRef] [Green Version]
  24. Milman, S.; Atzmon, G.; Huffman, D.; Wan, J.; Crandall, J.; Cohen, P.; Barzilai, N. Low insulin-like growth factor-1 level predicts survival in humans with exceptional longevity. Aging Cell 2014, 13, 769–771. [Google Scholar] [CrossRef] [PubMed]
  25. van Heemst, D.; Beekman, M.; Mooijaart, S.; Heijmans, B.; Brandt, B.; Zwaan, B.; Slagboom, P.; Westendorp, R. Reduced insulin/IGF-1 signalling and human longevity. Aging Cell 2005, 4, 79–85. [Google Scholar] [CrossRef] [PubMed]
  26. Franceschi, C.; Zaikin, A.; Gordleeva, S.; Ivanchenko, M.; Bonifazi, F.; Storci, G.; Bonafè, M. Inflammaging 2018: An update and a model. Semin. Immunol. 2018, 40, 1–5. [Google Scholar] [CrossRef] [PubMed]
  27. Coppé, J.-P.; Patil, C.K.; Rodier, F.; Sun, Y.; Muñoz, D.P.; Goldstein, J.; Nelson, P.S.; Desprez, P.-Y.; Campisi, J. Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor. PLoS Biol. 2008, 6, 2853–2868. [Google Scholar] [CrossRef] [PubMed]
  28. Baker, D.J.; Childs, B.G.; Durik, M.; Wijers, M.E.; Sieben, C.J.; Zhong, J.; Saltness, R.A.; Jeganathan, K.B.; Verzosa, G.C.; Pezeshki, A.; et al. Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan. Nature 2016, 530, 184–189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. De Cecco, M.; Ito, T.; Petrashen, A.P.; Elias, A.E.; Skvir, N.J.; Criscione, S.W.; Caligiana, A.; Brocculi, G.; Adney, E.M.; Boeke, J.D.; et al. L1 drives IFN in senescent cells and promotes age-associated inflammation. Nature 2019, 566, 73–78. [Google Scholar] [CrossRef]
  30. Huang, J.; Xie, Y.; Sun, X.; Zeh, H.J., 3rd; Kang, R.; Lotze, M.T.; Tang, D. DAMPs, ageing, and cancer: The ‘DAMP Hypothesis’. Ageing Res. Rev. 2015, 24, 3–16. [Google Scholar] [CrossRef] [Green Version]
  31. Spadaro, O.; Goldberg, E.L.; Camell, C.D.; Youm, Y.-H.; Kopchick, J.J.; Nguyen, K.Y.; Bartke, A.; Sun, L.Y.; Dixit, V.D. Growth Hormone Receptor Deficiency Protects against Age-Related NLRP3 Inflammasome Activation and Immune Senescence. Cell Rep. 2016, 14, 1571–1580. [Google Scholar] [CrossRef] [Green Version]
  32. Greer, E.L.; Brunet, A. FOXO transcription factors at the interface between longevity and tumor suppression. Oncogene 2005, 24, 7410–7425. [Google Scholar] [CrossRef] [Green Version]
  33. Furuyama, T.; Kitayama, K.; Shimoda, Y.; Ogawa, M.; Sone, K.; Yoshida-Araki, K.; Hisatsune, H.; Nishikawa, S.-I.; Nakayama, K.; Nakayama, K.; et al. Abnormal angiogenesis in Foxo1 (Fkhr)-deficient mice. J. Biol. Chem. 2004, 279, 34741–34749. [Google Scholar] [CrossRef] [Green Version]
  34. Yamaza, H.; Komatsu, T.; Wakita, S.; Kijogi, C.; Park, S.; Hayashi, H.; Chiba, T.; Mori, R.; Furuyama, T.; Mori, N.; et al. FoxO1 is involved in the antineoplastic effect of calorie restriction. Aging Cell 2010, 9, 372–382. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Shimokawa, I.; Komatsu, T.; Hayashi, N.; Kim, S.E.; Kawata, T.; Park, S.; Hayashi, H.; Yamaza, H.; Chiba, T.; Mori, R. The life-extending effect of dietary restriction requires Foxo3 in mice. Aging Cell 2015, 14, 707–709. [Google Scholar] [CrossRef] [PubMed]
  36. Paik, J.-H.; Kollipara, R.; Chu, G.; Ji, H.; Xiao, Y.; Ding, Z.; Miao, L.; Tothova, Z.; Horner, J.W.; Carrasco, D.R.; et al. FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis. Cell 2007, 128, 309–323. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Lin, K.; Dorman, J.B.; Rodan, A.; Kenyon, C. daf-16: An HNF-3/forkhead family member that can function to double the life-span of Caenorhabditis elegans. Science 1997, 278, 1319–1322. [Google Scholar] [CrossRef] [Green Version]
  38. Ogg, S.; Paradis, S.; Gottlieb, S.; Patterson, G.I.; Lee, L.; Tissenbaum, H.A.; Ruvkun, G. The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans. Nature 1997, 389, 994–999. [Google Scholar] [CrossRef]
  39. Kwon, E.-S.; Narasimhan, S.D.; Yen, K.; Tissenbaum, H.A. A new DAF-16 isoform regulates longevity. Nature 2010, 466, 498–502. [Google Scholar] [CrossRef] [Green Version]
  40. Lin, K.; Hsin, H.; Libina, N.; Kenyon, C. Regulation of the Caenorhabditis elegans longevity protein DAF-16 by insulin/IGF-1 and germline signaling. Nat. Genet. 2001, 28, 139–145. [Google Scholar] [CrossRef]
  41. Willcox, B.J.; Donlon, T.A.; He, Q.; Chen, R.; Grove, J.S.; Yano, K.; Masaki, K.H.; Willcox, D.C.; Rodriguez, B.; Curb, J.D. FOXO3A genotype is strongly associated with human longevity. Proc. Natl. Acad. Sci. USA 2008, 105, 13987–13992. [Google Scholar] [CrossRef] [Green Version]
  42. Teumer, A.; Qi, Q.; Nethander, M.; Aschard, H.; Bandinelli, S.; Beekman, M.; Berndt, S.I.; Bidlingmaier, M.; Broer, L. CHARGE Longevity Working Group. Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. Aging Cell 2016, 15, 811–824. [Google Scholar] [CrossRef] [Green Version]
  43. Kim, D.H.; Lee, B.G.; Lee, J.W.; Kim, M.E.; Lee, J.S.; Chung, J.H.; Yu, B.P.; Dong, H.H.; Chung, H.Y. FoxO6-mediated IL-1β induces hepatic insulin resistance and age-related inflammation via the TF/PAR2 pathway in aging and diabetic mice. Redox Biol. 2019, 24, 101184. [Google Scholar] [CrossRef]
  44. Litvak, V.; Ratushny, A.V.; Lampano, A.E.; Schmitz, F.; Huang, A.C.; Raman, A.; Rust, A.G.; Bergthaler, A.; Aitchison, J.D.; Aderem, A. A FOXO3–IRF7 gene regulatory circuit limits inflammatory sequelae of antiviral responses. Nature 2012, 490, 421–425. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Pearson, K.J.; Lewis, K.N.; Price, N.L.; Chang, J.W.; Perez, E.; Cascajo, M.V.; Tamashiro, K.L.; Poosala, S.; Csiszar, A.; Ungvari, Z.; et al. Nrf2 mediates cancer protection but not prolongevity induced by caloric restriction. Proc. Natl. Acad. Sci. USA 2008, 105, 2325–2330. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Sykiotis, G.P.; Bohmann, D. Stress-activated cap“n”collar transcription factors in aging and human disease. Sci. Signal. 2010, 3, re3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Schwarz, M.; Münzel, P.A.; Braeuning, A. Non-melanoma skin cancer in mouse and man. Arch. Toxicol 2013, 87, 783–798. [Google Scholar] [CrossRef] [PubMed]
  48. Passos, G.F.; Medeiros, R.; Marcon, R.; Nascimento, A.F.G.; Calixto, J.B.; Pianowski, L.F. The role of PKC/ERK1/2 signaling in the anti-inflammatory effect of tetracyclic triterpene euphol on TPA-induced skin inflammation in mice. Eur. J. Pharm. 2013, 698, 413–420. [Google Scholar] [CrossRef] [Green Version]
  49. Przybysz, A.J.; Choe, K.P.; Roberts, L.J.; Strange, K. Increased age reduces DAF-16 and SKN-1 signaling and the hormetic response of Caenorhabditis elegans to the xenobiotic juglone. Mech. Ageing Dev. 2009, 130, 357–369. [Google Scholar] [CrossRef] [Green Version]
  50. Mori, R.; Tanaka, K.; de Kerckhove, M.; Okamoto, M.; Kashiyama, K.; Tanaka, K.; Kim, S.; Kawata, T.; Komatsu, T.; Park, S.; et al. Reduced FOXO1 Accelerates Skin Wound Healing and Attenuates Scarring. Am. J. Pathol. 2014, 184, 2465–2467. [Google Scholar] [CrossRef] [Green Version]
  51. Nakae, J.; Oki, M.; Cao, Y. The FoxO transcription factors and metabolic regulation. FEBS Lett. 2008, 582, 54–67. [Google Scholar] [CrossRef] [Green Version]
  52. Kamohara, R.; Yamaza, H.; Tsuchiya, T.; Komatsu, T.; Park, S.; Hayashi, H.; Chiba, T.; Mori, R.; Otabe, S.; Yamada, K.; et al. Overexpression of the adiponectin gene mimics the metabolic and stress resistance effects of calorie restriction, but not the anti-tumor effect. Exp. Gerontol. 2015, 64, 46–54. [Google Scholar] [CrossRef] [Green Version]
  53. Kitamura, M.; Hiramatsu, N. Real-time monitoring of ER stress in living cells and animals using ESTRAP assay. Method. Enzymol. 2011, 490, 93–106. [Google Scholar]
  54. Chalkiadaki, A.; Guarente, L. Sirtuins mediate mammalian metabolic responses to nutrient availability. Nat. Rev. Endocrinol. 2012, 8, 287–296. [Google Scholar] [CrossRef] [PubMed]
  55. Guarente, L. SIRT1 and other sirtuins in metabolism. Genes. Dev. 2014, 25, 138–145. [Google Scholar]
  56. Banerjee, K.K.; Ayyub, C.; Zeeshan, A.S.; Mandot, V.; Prasad, G. dSir2 in the adult fat body, but not in muscles, regulates life span in a diet-dependent manner. Cell Rep. 2012, 2, 1485–1491. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Hirschey, M.D.; Shimazu, T.; Jing, E.; Grueter, C.A.; Collins, A.M.; Aouizerat, B.; Stančáková, A.; Goetzman, E.; Lam, M.M.; Schwer, B.; et al. SIRT3 deficiency and mitochondrial protein hyperacetylation accelerate the development of the metabolic syndrome. Mol. Cell 2011, 44, 177–190. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Kume, S.; Uzu, T.; Horiike, K.; Chin-Kanasaki, M.; Isshiki, K.; Araki, S.-I.; Sugimoto, T.; Haneda, M.; Kashiwagi, A.; Koya, D. Calorie restriction enhances cell adaptation to hypoxia through Sirt1-dependent mitochondrial autophagy in mouse aged kidney. J. Clin. Investig. 2010, 120, 1043–1055. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Mercken, E.M.; Hu, J.; Krzysik-Walker, S.; Wei, M.; Li, Y.; McBurney, M.W.; de Cabo, R.; Longo, V.D. SIRT1 but not its increased expression is essential for lifespan extension in caloric-restricted mice. Aging Cell 2014, 13, 193–196. [Google Scholar] [CrossRef] [Green Version]
  60. Holliday, R. Food, reproduction and longevity: Is the extended lifespan of calorie-restricted animals an evolutionary adaptation? Bioessays 1989, 10, 125–127. [Google Scholar] [CrossRef]
  61. Bishop, N.A.; Guarente, L. Two neurons mediate diet-restriction-induced longevity in C. elegans. Nature 2007, 447, 545–549. [Google Scholar] [CrossRef]
  62. Bargmann, C.I.; Horvitz, H.R. Chemosensory neurons with overlapping functions direct chemotaxis to multiple chemicals in C. elegans. Neuron 1991, 7, 729–742. [Google Scholar] [CrossRef]
  63. Shimokawa, I.; Higami, Y. Leptin signaling and aging: Insight from caloric restriction. Mech. Ageing Dev. 2001, 122, 1511–1519. [Google Scholar] [CrossRef]
  64. Sainsbury, A.; Zhang, L. Role of the hypothalamus in the neuroendocrine regulation of body weight and composition during energy deficit. Obes. Rev. 2011, 13, 234–257. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Michalkiewicz, M.; Knestaut, K.M.; Bytchkova, E.Y.; Michalkiewicz, T. Hypotension and reduced catecholamines in neuropeptide Y transgenic rats. Hypertension 2003, 41, 1056–1062. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Smiałowska, M.; Domin, H.; Zieba, B.; Koźniewska, E.; Michalik, R.; Piotrowski, P.; Kajta, M. Neuroprotective effects of neuropeptide Y-Y2 and Y5 receptor agonists in vitro and in vivo. Neuropeptides 2009, 43, 235–249. [Google Scholar] [CrossRef] [PubMed]
  67. Shimokawa, I.; Fukuyama, T.; Yanagihara-Outa, K.; Tomita, M.; Komatsu, T.; Higami, Y.; Tuchiya, T.; Chiba, T.; Yamaza, Y. Effects of caloric restriction on gene expression in the arcuate nucleus. Neurobiol. Aging 2003, 24, 117–123. [Google Scholar] [CrossRef]
  68. Chiba, T.; Tamashiro, Y.; Park, D.; Kusudo, T.; Fujie, R.; Komatsu, T.; Kim, S.E.; Park, S.; Hayashi, H.; Mori, R.; et al. A key role for neuropeptide Y in lifespan extension and cancer suppression via dietary restriction. Sci. Rep. 2014, 4, 4517. [Google Scholar] [CrossRef] [Green Version]
  69. Luque, R.M.; Park, S.; Kineman, R.D. Severity of the catabolic condition differentially modulates hypothalamic expression of growth hormone-releasing hormone in the fasted mouse: Potential role of neuropeptide Y and corticotropin-releasing hormone. Endocrinology 2007, 148, 300–309. [Google Scholar] [CrossRef] [Green Version]
  70. Park, S.; Fujishita, C.; Komatsu, T.; Kim, S.E.; Chiba, T.; Mori, R.; Shimokawa, I. NPY antagonism reduces adiposity and attenuates age-related imbalance of adipose tissue metabolism. FASEB J. 2014, 28, 5337–5348. [Google Scholar] [CrossRef] [Green Version]
  71. Park, S.; Komatsu, T.; Kim, S.E.; Tanaka, K.; Hayashi, H.; Mori, R.; Shimokawa, I. Neuropeptide Y resists excess loss of fat by lipolysis in calorie-restricted mice: A trait potential for the life-extending effect of calorie restriction. Aging Cell 2017, 16, 339–348. [Google Scholar] [CrossRef] [Green Version]
  72. Liao, C.-Y.; Rikke, B.A.; Johnson, T.E.; Gelfond, J.A.L.; Diaz, V.; Nelson, J.F. Fat maintenance is a predictor of the murine lifespan response to dietary restriction. Aging Cell 2011, 10, 629–639. [Google Scholar] [CrossRef] [Green Version]
  73. Minor, R.K.; López, M.; Younts, C.M.; Jones, B.; Pearson, K.J.; Anson, M.R.; Dieguez, C.; de Cabo, R. The arcuate nucleus and neuropeptide Y contribute to the antitumorigenic effect of calorie restriction. Aging Cell 2011, 10, 483–492. [Google Scholar] [CrossRef] [Green Version]
  74. Farzi, A.; Reichmann, F.; Holzer, P. The homeostatic role of neuropeptide Y in immune function and its impact on mood and behaviour. Acta Physiol. (Oxf.) 2015, 213, 603–627. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Chida, Y.; Sudo, N.; Kubo, C. Does stress exacerbate liver diseases? J. Gastroenterol. Hepatol. 2006, 21, 202–208. [Google Scholar] [CrossRef] [PubMed]
  76. Sigala, B.; McKee, C.; Soeda, J.; Pazienza, V.; Morgan, M.; Lin, C.I.; Selden, C.; Vander Borght, S.; Mazzoccoli, G.; Roskams, T.; et al. Sympathetic nervous system catecholamines and neuropeptide Y neurotransmitters are upregulated in human NAFLD and modulate the fibrogenic function of hepatic stellate cells. PLoS ONE 2013, 8, e72928. [Google Scholar] [CrossRef] [PubMed]
  77. Huan, H.-B.; Wen, X.-D.; Chen, X.-J.; Wu, L.; Wu, L.L.; Zhang, L.; Yang, D.P.; Zhang, X.; Bie, P.; Qian, C.; et al. Sympathetic nervous system promotes hepatocarcinogenesis by modulating inflammation through activation of alpha1-adrenergic receptors of Kupffer cells. Brain Behav. Immun. 2016, 59, 118–134. [Google Scholar] [CrossRef] [PubMed]
  78. Kinoshita, A.; Hayashi, H.; Kusano, N.; Inoue, S.; Komatsu, T.; Mori, R.; Park, S.; Takatsuki, M.; Eguchi, S.; Shimokawa, I. Neuropeptide Y inhibits hepatocarcinogenesis in overnutrition in mice. Acta Medica Nagasakiensia 2019, 41, 711–722. [Google Scholar]
  79. Baldock, P.A.; Lin, S.; Zhang, L.; Karl, T.; Shi, Y.; Driessler, F.; Zengin, A.; Hörmer, B.; Lee, N.J.; Wong, I.P.; et al. Neuropeptide y attenuates stress-induced bone loss through suppression of noradrenaline circuits. J. Bone Miner. Res. 2014, 29, 2238–2249. [Google Scholar] [CrossRef]
Nutrients 11 03068 g001 550
Figure 1. Mechanisms underlying the life-extending and tumor-inhibiting effects of calorie restriction in mammals. Inhibition of the growth hormone (GH)-insulin-like growth factor-1 (IGF-1) signal promotes activation of FoxO1, FoxO3, and Nrf2 transcription factors, resulting in activated target genes and inhibition of cancer and aging, and thus counteracting “inflammaging.” By contrast, attenuation of the GH-IGF-1 signal reduces activity of mechanistic target of rapamycin (Mtor). In C. elegans, the Daf-2 pathway regulates skn-1 (mammalian Nrf2), although no evidence for this regulation is shown in mammals. Sirtuins (Sirts) modulate activities of key molecules mediating calorie restriction (CR) effects by epigenetic mechanisms, mostly deacetylation. Dotted and straight lines represent attenuated and strengthened signals, respectively. Arrows and bars represent activation and inhibition of target molecules, respectively.
Figure 1. Mechanisms underlying the life-extending and tumor-inhibiting effects of calorie restriction in mammals. Inhibition of the growth hormone (GH)-insulin-like growth factor-1 (IGF-1) signal promotes activation of FoxO1, FoxO3, and Nrf2 transcription factors, resulting in activated target genes and inhibition of cancer and aging, and thus counteracting “inflammaging.” By contrast, attenuation of the GH-IGF-1 signal reduces activity of mechanistic target of rapamycin (Mtor). In C. elegans, the Daf-2 pathway regulates skn-1 (mammalian Nrf2), although no evidence for this regulation is shown in mammals. Sirtuins (Sirts) modulate activities of key molecules mediating calorie restriction (CR) effects by epigenetic mechanisms, mostly deacetylation. Dotted and straight lines represent attenuated and strengthened signals, respectively. Arrows and bars represent activation and inhibition of target molecules, respectively.
Nutrients 11 03068 g001
Nutrients 11 03068 g002 550
Figure 2. The inhibiting effects of CR on skin tumorigenesis are diminished in Foxo1+/− mice. (A) The fraction of mice bearing papilloma (diameter ≤ 1 mm) increased over time more rapidly in Foxo1 +/− CR mice compared with wild-type (WT) CR mice (p = 0.0103 by Log-rank test); WT- ad libitum (AL) mice versus vs. Foxo1+/− AL mice, p = 0.0663. DMBA, 7,12-dimethyl-benz (a) anthracene. (B) Epidermal thickness during TPA (12-O-tetradecanoyl phorbol 13-acetate) treatment. Statistics: genotype, p = 0.0331; diet, p = 0.2993; time; p < 0.0001 by 3-f ANOVA. (C) Epidermal cell proliferation in response to TPA treatment. PCNA, proliferating cell nuclear antigen. Statistics: genotype, p = 0.0193; genotype x diet, p = 0.0401 by 3-f ANOVA. (D) The number of dermal macrophages immunohistochemically stained with F4/80 antibody. Statistics: diet; p = 0.0001; genotype; p = 0.1374; time, p = 0.0152 by 3-f ANOVA. (E) Cox2 mRNA expression levels in response to TPA treatment (normalized by Atp5f1 mRNA levels). Statistics: diet; p = 0.0123; genotype x diet; p = 0.0399 by 3f-ANOVA). **p < 0.01 by Tukey’s honestly significant difference (HSD) test. (F) Gclc mRNA expression levels in response to TPA treatment (normalized by Atp5f1 mRNA levels). Statistics: genotype; p = 0.0207; diet; p = 0.0175.
Figure 2. The inhibiting effects of CR on skin tumorigenesis are diminished in Foxo1+/− mice. (A) The fraction of mice bearing papilloma (diameter ≤ 1 mm) increased over time more rapidly in Foxo1 +/− CR mice compared with wild-type (WT) CR mice (p = 0.0103 by Log-rank test); WT- ad libitum (AL) mice versus vs. Foxo1+/− AL mice, p = 0.0663. DMBA, 7,12-dimethyl-benz (a) anthracene. (B) Epidermal thickness during TPA (12-O-tetradecanoyl phorbol 13-acetate) treatment. Statistics: genotype, p = 0.0331; diet, p = 0.2993; time; p < 0.0001 by 3-f ANOVA. (C) Epidermal cell proliferation in response to TPA treatment. PCNA, proliferating cell nuclear antigen. Statistics: genotype, p = 0.0193; genotype x diet, p = 0.0401 by 3-f ANOVA. (D) The number of dermal macrophages immunohistochemically stained with F4/80 antibody. Statistics: diet; p = 0.0001; genotype; p = 0.1374; time, p = 0.0152 by 3-f ANOVA. (E) Cox2 mRNA expression levels in response to TPA treatment (normalized by Atp5f1 mRNA levels). Statistics: diet; p = 0.0123; genotype x diet; p = 0.0399 by 3f-ANOVA). **p < 0.01 by Tukey’s honestly significant difference (HSD) test. (F) Gclc mRNA expression levels in response to TPA treatment (normalized by Atp5f1 mRNA levels). Statistics: genotype; p = 0.0207; diet; p = 0.0175.
Nutrients 11 03068 g002
Nutrients 11 03068 g003 550
Figure 3. Foxo1+/− mice become tolerant to endotoxin, particularly in CR conditions. (A) Survival rates after LPS injection. Initial numbers of mice in each group, n = 9–12. Statistics: diet, p = 0.0263; genotype x diet, p = 0.0498 by likelihood ratio test. (B) Reduction of the rate of secreted alkaline phosphatase (SEAP) activity (ratios relative to the values at 0 h in respective groups) in the blood after intraperitoneal injection of lipopolysaccharide (LPS). The data represent means ± SE (n = 9−12). No error bars were added in Foxo1+/− AL and Ctrl AL groups to avoid overlapping. Statistics (when data between 2 and 8 h were analyzed): genotype, p = 0.0093; diet, p < 0.0001 by 3-f ANOVA).
Figure 3. Foxo1+/− mice become tolerant to endotoxin, particularly in CR conditions. (A) Survival rates after LPS injection. Initial numbers of mice in each group, n = 9–12. Statistics: diet, p = 0.0263; genotype x diet, p = 0.0498 by likelihood ratio test. (B) Reduction of the rate of secreted alkaline phosphatase (SEAP) activity (ratios relative to the values at 0 h in respective groups) in the blood after intraperitoneal injection of lipopolysaccharide (LPS). The data represent means ± SE (n = 9−12). No error bars were added in Foxo1+/− AL and Ctrl AL groups to avoid overlapping. Statistics (when data between 2 and 8 h were analyzed): genotype, p = 0.0093; diet, p < 0.0001 by 3-f ANOVA).
Nutrients 11 03068 g003
Nutrients 11 03068 g004a 550Nutrients 11 03068 g004b 550
Figure 4. Effects of Npy deficiency in the occurrence and growth of hepatocellular carcinoma (HCC) and steatohepatitis. Ctrl and −/− represent male control (Npy+/−) mice and Npy−/− mice, respectively. Figure 4A–C were modified from original data published by Kinoshita, A., et al. [78]. (A) The proportion of mice bearing microscopic HCC (diameter < 1 mm) at 28 weeks. n = 12 in each group. Statistics: diet, p = 0.0195 by logistic regression; CR vs. AL, p = 0.0192, CR vs. HFD, p = 0.0310. (B) Growth of HCC. Liver weights were normalized to body weights (g/g) in mice sacrificed at 28 and 48 weeks of age. n = 12 in each group at 28 weeks; at 48 weeks, n = 9–12. Closed circles: blue, liver bearing macroscopic HCC (diameter ≥ 1 mm); red, liver bearing microscopic (diameter < 1 mm) HCC; green, liver bearing no HCC. Statistics: genotype x age, p < 0.0001 by 3-f ANOVA; Npy−/− (48) vs. Ctrl (48), p < 0.0001 by Tukey’s HSD test); **p < 0.001. ***p < 0.0001 by Tukey’s HSD test. (C) The degree of steatohepatitis (the number of inflammatory foci/mm2 in the liver). Bars represent means ± SE (n = 8~12 in each group). Statistics: age, p = 0.0117; diet, p < 0.0001; genotype, p = 0.0069 by 3-f ANOVA; *p < 0.05 by Tukey’s HSD test. (D) A schematic model for the antagonizing role of Npy over norepinephrine (NE)-adrenergic receptor (Adr) signaling in the sympathetic nervous system (SNS) under CR conditions. CR promotes lipolysis, whereas CR inhibits an excess loss of fat via the action of Npy in the SNS. This trait is necessary for the life-extending effect of CR. CR inhibits steatohepatitis and HCC without Npy.
Figure 4. Effects of Npy deficiency in the occurrence and growth of hepatocellular carcinoma (HCC) and steatohepatitis. Ctrl and −/− represent male control (Npy+/−) mice and Npy−/− mice, respectively. Figure 4A–C were modified from original data published by Kinoshita, A., et al. [78]. (A) The proportion of mice bearing microscopic HCC (diameter < 1 mm) at 28 weeks. n = 12 in each group. Statistics: diet, p = 0.0195 by logistic regression; CR vs. AL, p = 0.0192, CR vs. HFD, p = 0.0310. (B) Growth of HCC. Liver weights were normalized to body weights (g/g) in mice sacrificed at 28 and 48 weeks of age. n = 12 in each group at 28 weeks; at 48 weeks, n = 9–12. Closed circles: blue, liver bearing macroscopic HCC (diameter ≥ 1 mm); red, liver bearing microscopic (diameter < 1 mm) HCC; green, liver bearing no HCC. Statistics: genotype x age, p < 0.0001 by 3-f ANOVA; Npy−/− (48) vs. Ctrl (48), p < 0.0001 by Tukey’s HSD test); **p < 0.001. ***p < 0.0001 by Tukey’s HSD test. (C) The degree of steatohepatitis (the number of inflammatory foci/mm2 in the liver). Bars represent means ± SE (n = 8~12 in each group). Statistics: age, p = 0.0117; diet, p < 0.0001; genotype, p = 0.0069 by 3-f ANOVA; *p < 0.05 by Tukey’s HSD test. (D) A schematic model for the antagonizing role of Npy over norepinephrine (NE)-adrenergic receptor (Adr) signaling in the sympathetic nervous system (SNS) under CR conditions. CR promotes lipolysis, whereas CR inhibits an excess loss of fat via the action of Npy in the SNS. This trait is necessary for the life-extending effect of CR. CR inhibits steatohepatitis and HCC without Npy.
Nutrients 11 03068 g004aNutrients 11 03068 g004b

Share and Cite

MDPI and ACS Style

Komatsu, T.; Park, S.; Hayashi, H.; Mori, R.; Yamaza, H.; Shimokawa, I. Mechanisms of Calorie Restriction: A Review of Genes Required for the Life-Extending and Tumor-Inhibiting Effects of Calorie Restriction. Nutrients 2019, 11, 3068. https://0-doi-org.brum.beds.ac.uk/10.3390/nu11123068

AMA Style

Komatsu T, Park S, Hayashi H, Mori R, Yamaza H, Shimokawa I. Mechanisms of Calorie Restriction: A Review of Genes Required for the Life-Extending and Tumor-Inhibiting Effects of Calorie Restriction. Nutrients. 2019; 11(12):3068. https://0-doi-org.brum.beds.ac.uk/10.3390/nu11123068

Chicago/Turabian Style

Komatsu, Toshimitsu, Seongjoon Park, Hiroko Hayashi, Ryoichi Mori, Haruyoshi Yamaza, and Isao Shimokawa. 2019. "Mechanisms of Calorie Restriction: A Review of Genes Required for the Life-Extending and Tumor-Inhibiting Effects of Calorie Restriction" Nutrients 11, no. 12: 3068. https://0-doi-org.brum.beds.ac.uk/10.3390/nu11123068

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop