Next Article in Journal
A Randomized, Double-Blind, Placebo Controlled Trial to Determine the Effectiveness a Polyphenolic Extract (Hibiscus sabdariffa and Lippia citriodora) in the Reduction of Body Fat Mass in Healthy Subjects
Next Article in Special Issue
The Pharmacological Effects and Health Benefits of Platycodon grandiflorus—A Medicine Food Homology Species
Previous Article in Journal
Banana Powder as an Additive to Common Wheat Pasta
Previous Article in Special Issue
Ginger Water Reduces Body Weight Gain and Improves Energy Expenditure in Rats
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Phytochemicals and Traditional Use of Two Southernmost Chilean Berry Fruits: Murta (Ugni molinae Turcz) and Calafate (Berberis buxifolia Lam.)

1
Departamento Ciencias de la Salud, Carrera de Nutrición y Dietética, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile
2
Instituto Forestal, Sede Coyhaique, Coyhaique 5951840, Chile
3
Departamento Ciencia de los Alimentos y Tecnología Química, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago 8380492, Chile
*
Author to whom correspondence should be addressed.
Submission received: 30 November 2019 / Revised: 28 December 2019 / Accepted: 30 December 2019 / Published: 6 January 2020
(This article belongs to the Special Issue Nutraceuticals in Human Health)

Abstract

:
Murta and calafate have been traditionally used by indigenous and rural peoples of Chile. Research on murta and calafate has gained interest due to their attractive sensory properties as well as a global trend in finding new fruits with potential health benefits. The objective of this review was to summarize the potential use of murta and calafate as sources of nutraceuticals regarding both the traditional and the up-to-date scientific knowledge. A search of historical documents recorded in the Digital National Library as well as scientific articles in the Web of Science database were performed using combinations of keywords with the botanical nomenclature. Peer-reviewed scientific articles did meet the inclusion criteria (n = 38) were classified in phytochemicals (21 papers) and biological activity (17 papers). Murta and calafate are high oxygen radical absorbance capacity (ORAC)-value fruits and promising sources of natural antioxidants, antimicrobial, and vasodilator compounds with nutraceutical potential. The bioactivity of anthocyanin metabolites in murta and calafate must continue to be studied in order to achieve adequate information on the biological activity and health-promoting effects derived for the consumption of murta and calafate fruit.

1. Introduction

Historically, indigenous peoples of Chile have had a deep relationship with nature; flora native to their territories has been used for various purposes, such as food, fuel, religious ceremonies, decoration, dyeing, and medicine [1]. In this context, the Mapuche (“people of the earth” in the Mapuzugun language) hold a vast, rich body of knowledge about flora that has been learned and transmitted within the culture throughout space and time [2,3]. Moreover, southernmost communities, such as the Aónikenk (“people of the south” in the Aónikoaish language) and the Yámana (“human being” in the Yahgan language), collected several edible plant roots, wild fruits, and seeds to survive in extremally harsh conditions [4]. In these particular areas, two small berry-type fruits known as murta, murtilla, or uñi (Ugni molinae Turcz, Myrtaceae) and calafate (Berberis buxifolia Lam., Berberidaceae) grow in the wild of the Patagonia. Murta is an evergreen bush that naturally grows in Chile from south of Talca (35° SL) to the Palena River (44° SL) (Figure 1), forming part of the deciduous forests of Nothofagus as well as the southern evergreen forests [5]. In these habitats, murta grows alongside other edible Chilean fruit plants such as peumo (Cryptocarya alba), boldo (Peumus boldus), keule (Gomortega queule), avellano or gevuin (Gevuina avellana), diverse michay species (Berberis darwinii, B. serrata, B. dentata), litre (Lithraea caustica), pitra (Myrceugenia planipes), and luma (Amomyrtus luma) [1]. Calafate is an evergreen spiny bush which naturally grows in Chile from Curicó (35° SL) to the Cape Horn Archipelago (56° SL) [6]. Nevertheless, it is most abundant from Valdivia (40° SL) to the Strait of Magellan (54° SL) (Figure 1).
During the last decade, interest in studying these berry-type fruits has increased, due to their attractive sensory properties as well as a global trend in finding new fruits with potential health benefits. Berry-type fruits are well known for their high polyphenol, and especially anthocyanin content [7]. Specifically, wild berry-type fruits stand out over their cultivated counterparts in terms of polyphenol content [8]. Furthermore, the extreme weather conditions that predominate during southern Chilean summers (a high-temperature oscillation) may favor the plant biosynthesis of anthocyanins [9]. Both murta and calafate fruits can be sources of anthocyanins with nutraceutical potential. Lee [10] defined Nutraceuticals as foods or part of foods that provide both health benefits to reduce the risk of chronic diseases and basic nutrition. Therefore, this review summarizes the potential use of murta and calafate as sources of nutraceuticals regarding both the traditional and the up-to-date scientific knowledge. This review would like to contribute to the development of both new research and indigenous peoples, in line with the 2030 agenda for sustainable development goals of the United Nations with its promise to “leave no one behind”.

2. Traditional Knowledge around Murta and Calafate

The search strategy of historical documents was focused in revising manuscripts written by recognized naturalists of the Chilean flora such as Juan Ignacio Molina (1740–1829) [11], Claude Gay (1800–1873) [12,13], Charles Darwin (1809–1882) [4], and Ernesto Wilhelm de Mosbach (1882–1963) [1] available in Digital National Library database (www.memoriachilena.cl). At the same time, ethnobotany and ethnopharmacology books were also suitable publications that were extensively reviewed.

2.1. Murta and Calafate in the Mapuche and Rural Culture

The Mapuche are the most prominent indigenous peoples in Chile, due to both their social and demographic weight and cultural identity. Mapuche have historically settled between the Itata (36° SL) and Toltén (38° SL) Rivers (Figure 1) in Chile [2]. In this sense, Figure 1 contrasts the wild distribution of murta and calafate and the historically territory occupied by the Mapuche people.
The first records regarding the traditional uses of murta fruit (Figure 2a) by the Mapuche indicate the preparation of a sweet stomach wine that was an appetite stimulant, and “whose aroma was appreciated as the most delicate Muscat” [11]. In this sense, the aromatic properties of murta fruits were early recognized; Gay [13] indicated that country people eat murta fruits with a great pleasure and prepared pleasant and aromatic confections. Nowadays people from the countryside consume murta as dried fruits and in the preparation of jams [14].
Mapuche used the word maki to name black fruits [1]. In this sense, calafate (Figure 2b) were appreciated as fruit rich in pigments where the root and bark of calafate were also used to obtain purple and yellow dyes [14].
The Mapuche tradition of using plants for medicinal purposes was recorded in the archives of the several settlers and naturalists who, in turn, enriched them with the contribution of medicinal plants from Europe and other regions [15]. Since 2008, the traditional use of medicinal plants has been recognized by the Chilean Health Ministry [16]. The traditional use of murta includes making a leaf infusion to treat urinary and throat infections, while the fruit is known for its astringent power [14,17]. In the case of calafate, traditional uses include using its roots to control fevers, as an anti-inflammatory, and to ease stomach pains, indigestion, and colitis [14,17].

2.2. Calafate in the Extreme South Communities of Chile

Historical records on the use of native flora as food and medicine by extreme south communities are more limited than the information available about the indigenous peoples of the central and southern zone of Chile. Among the communities of the extreme south Chile, the Aónikenk were an exclusively cultural entity defined by a particular tradition, language, and lifestyle [18], who occupied the territory located between the Santa Cruz River (50° SL) and the Strait of Magellan (54° SL) (Figure 1). The Aónikenk had a significant collecting tradition in which not only women participated but also involved men, children, and occasionally elderly people [18]. Calafate as well as other native fruits like zarzaparrilla (Ribes magellanicum), chaura (Pernettya mucronata), murtilla (Empetrum rubrum), and strawberry (Rubus geoides) were consumed mainly as fresh fruits during the harvest season (November to March) [4]. Furthermore, Aónikenk women occasionally painted their faces with calafate juice, believing it would whiten the skin tone [18].
The Yámana were the southernmost ethnic group in the world who lived in the territory of the Cape Horn Archipelago (56° SL) in the south of Tierra del Fuego Island and the Beagle Channel (Figure 1) [18]. Yámana were maritime hunter-gatherers who spent much of their lives in their anan (tree bark canoe). Men collected firewood, fruits, and vegetables [19]. A Yámana legend says that whoever tastes the bittersweet flavor of calafate will return to the extreme south territory [20].

3. Scientific Knowledge around Murta and Calafate

The search strategy of scientific literature is detailed in the flow diagram of Figure 3.
Relevant publications were identified through an initial search in Web of Science database using the current botanical nomenclature in the title. The time interval for obtaining the records was between 1975 and 2020. Since 1994, the search results identified a higher number of documents on murta (58 records) than on calafate (31 records). Each abstract was revised and publications associated to plant sciences, environmental sciences and ecology that did not report any information about nutritional and phytochemical composition of murta and calafate (36 records) were excluded. At the same time, publications that did not contain original data (four records) were also excluded. Suitable publications were extensively reviewed and scientific articles contained the same data as other studies (11 papers) were excluded. Papers did meet the inclusion criteria were classified in phytochemicals (21 papers) and biological activity (17 papers) in terms to analize the the up-to-date scientific evidence of murta and calafate as sources of nutraceuticals.

3.1. Nutritional Content of Murta and Calafate Fruits

Murta fruit has a soluble solid content (SS) around 19 °Brix, a titratable acid around 8 meq Na OH/100 g, and a pH around 4.3 [21]. The sensory properties of murta fruit include the sweetness of a strawberry, the pungency of a guava, and the texture of a dried blueberry [22]. Furthermore, volatile compounds identified in murta fruit aroma have been described as fruity, sweet, and floral; ethyl hexanoate and 4-methoxy-2,5-dimethyl-furan-3-one are the most potent compounds found in murta [23]. The proximate analysis of murta fruit shows a content in moisture of 76.9%, protein of 1.2 g/100 g, fat of 0.9 g/100 g, crude fibre of 2.5 g/100 g, ash of 0.5 g/100 g and carbohydrates (by difference) of 18.5 g/100g expressed on fresh weight (FW) [24]. Furthermore, murta has a content in ascorbic acid of 210 mg/100 g [25].
Calafate fruit has a SS content between 25–31 °Brix and a titratable acid around 2 g malic acid/100 g (15 meq NaOH/100 g) [26]. Calafate fruit has a higher SS content than murta, and the highest SS content in comparison to other berries such as maqui (19 °Brix), pomegranate (15 °Brix), blueberry (14 °Brix), blackberry (13 °Brix), red raspberry (11 °Brix), and strawberry (9 °Brix) [27]. The proximate composition, sugars, and ascorbic acid of calafate fruit shows a content in moisture of 75%, protein of 2.6 g/100 g, ether extract of 0.18 g/100 g, crude fibre of 7.0 g/100 g, ash of 0.9 g/100 g, glucose of 3.0 g/100 g, fructose of 0.8 g/100 g and ascorbic acid of 74.0 mg/100 g expressed on FW [28].

3.2. Phytochemicals in Murta and Calafate Fruits

Phytochemicals (i.e., phenolic compounds, terpenoids, alkaloids, and nitrogen-containing compounds) can be defined as non-nutrient chemicals found in plants that demonstrate biological activity against chronic diseases [29,30]. Furthermore, several phytochemicals such as phenolic compounds and terpenoids have been used throughout human history as condiments and pigments [31].

3.2.1. Anthocyanins in Murta and Calafate Fruit

Anthocyanins are the common coloring compounds found in a large number of plants and are responsible for the purple, red, blue, and orange colors of berry-type fruits [32]. Chemically, anthocyanins are phenolic compounds belonging to the flavonoid class, with two benzene rings joined by a linear three-carbon chain, possessing the C6–C3–C6 basic skeleton [33]. Anthocyanins are formed by the modification of anthocyanidins by glycosyl and aromatic or aliphatic acyl moieties [34]. The basic structure of an anthocyanidin is a flavonoid ion (2-phenylbenzopyrilium) that can vary based on the different positions of hydroxyl groups (OH) or methoxyls (OCH3) (Figure 4a). Six anthocyanidins (cyanidin, delphinidin, pelargonidin, peonidin, malvidin, and petunidin) are the most common in plants [33,35] and are present in berry-type fruits [32,36].
The use of LC-MS as an analytical chemistry technique has allowed for the identification and/or tentative identification of the anthocyanin profile of murta and calafate. In a first report, two anthocyanins (cyanidin-3-O-glucoside and peonidin-3-O-glucoside) were identified in murta whereas 18 anthocyanins (3-O-monoglycosylated and 3,5-O-diglycosylated delphinidins, cyanidins, petunidins, peonidins, and malvidins) were most abundant in calafate [28,37,38]. As can be expected by the wide variability of colors observed in murta ecotypes, subsequent studies [39] have described a greater number of anthocyanins where 3-O-glucosides of delphinidin, petunidin, and malvidin have been also identified in murta fruit. Based on these findings, murta (Figure 4a) and calafate (Figure 4b) could be used as promising sources of a wide variety of anthocyanins.

3.2.2. Phenolic Acids and Other Flavonoids in Murta and Calafate Fruit

The identification of other phenolic compounds in murta and calafate indicate the presence of phenolic acids (gallic acid, benzoic acid, p-coumaric acid, and hydrocaffeic acid), flavan-3-ols (epicatechin) and flavonols (quercetin, rutin, luteolin, kaempferol, and myricetin) in murta fruits [39,40]. On the other hand, 20 hydroxycinnamic acids and flavonols such as hyperoside, isoquercitrin, quercetin, rutin, myricetin, and isorhamnetin are more abundant in calafate fruits [39,41,42]. Furthermore, among flavonoid subclasses, murta shows higher flavonol and flava-3-ols content (0.29 and 0.27 µmoL/g FW respectively) than calafate (0.16 and 0.24 µmoL/g FW respectively) whereas calafate has a higher anthocyanin content (17.8 µmoL/g FW) than murta (0.21 µmoL/g FW) associated with the deep-blue color of the calafate fruit [28].
The existing research on murta and calafate show that phenolic compounds are the main phytochemicals studied in these berry-type fruits.

3.3. Phytochemical Changes in Murta and Calafate

The main factors that affect the polyphenol content in plants are genotype, environment, stage at fruit harvest, and storage and processing [15]. When wild plants are studied, domestication emerges as a key factor affecting polyphenol content due to changes in the allocation of nutrients within the plant (domestication syndrome) that occur during the continuous process of selection [43].

3.3.1. Genotype vs. Environment

Phytochemical changes in murta have been studied in its leaves and stems and its fruits. The total amount of flavonols (rutin, kaempferol, and quercetin) in wild murta plant (leaves) is significantly higher (~20%) than in cultivated murta plants, showing the domestication effect [44]. Results on the flavonol content in murta fruit have been inconsistent. In one study, no significant differences between wild and cultivated murta fruits were found [44,45]. Conversely, in another study by Augusto [40], the total phenolic compounds in the fruits of wild and selected murta (14-4) genotype were 19.4 and 40.3 mg GAE/g in dry weight, respectively. Consistent with the results of phenolic compound content, the antioxidant capacity (AC) of the wild murta genotype was lower than the selected murta (14-4) genotype for both DPPH (76.5 and 134.4 mu moL TEAC/g) and ABTS (157.0 and 294.0 mu moL TEAC/g) tests [40]. These results show that phenolic content and AC in murta fruits did not decrease as a result of the domestication process.
In addition to differences in polyphenol content among different murta genotypes, the effect of the environment may cause the same variety to present differences depending on the harvest year. In this context, Alfaro et al. [46] indicate that genotype and growing season have a significant effect on the polyphenol content and AC of murta fruits; the lowest polyphenol content (283 ± 72 mg GAE/100 g DW) was obtained for the 14-4 genotype in 2008, and the highest value (2152 ± 290 mg GAE/100 g DW) was observed for the variety South Pearl-INIA in 2007. Furthermore, a canonical discriminant analysis of seasonal differences showed that the South Pearl-INIA variety had the greatest variation in polyphenol content in relation to the other genotypes studied [46]. The same authors indicate that rainfall and frosts were the most relevant climate factors that may explain the seasonal variation of total polyphenol content of murta fruits [46].
In the case of calafate, the effect of genotype and environment on phytochemical changes is scarce. Mariangel et al. [47] indicated that the phenolic composition of calafate fruit can vary according to the geographical area of fruit collection. However, it is difficult to determine if these differences are attributed to the different genotypes evaluated and/or to the effect of the environment. On the other hand, Arena et al. [48] demonstrated that calafate fruits from field conditions with different light intensities (i.e., 100%, 57%, 24% of natural irradiance) show significant differences in anthocyanin content. Fruits grown under high light intensity (299.7 mg/100 g FW) had an anthocyanin content 2.9 times higher than fruits grown under medium light intensity (103.8 mg/100 g FW) [48]. The authors associated a higher anthocyanin content with a higher photosynthetic rate and a concomitant increase in SS and sugar content measured under the same conditions [48].

3.3.2. Stage at Fruit Harvest

Berry-type fruits harvested at different maturity stages present different chemical characteristics as well as phenolic compound profiles; in immature fruits proanthocyanidins are predominant while in mature fruits anthocyanins predominate [49,50,51]. From an ecological point of view, plants with immature fruits—without viable seeds—have high phenolic and proanthocyanidin contents that act as deterrent compounds to prevent their consumption by insects and herbivores [52]. In contrast, ripe fruits have attractive colors (anthocyanins and other pigments) and a sweet taste to stimulate their consumption by herbivores and the consequent dispersion of seeds [52].
Phytochemical changes during fruit development and ripening have been studied in calafate fruits as well as other berry-type fruits [49,50,51,53]. Early studies attempted to understand the main changes in phenolic compounds and AC during the process of fruit maturation and ripening in order to establish the best maturity index for calafate fruit according to phenolic compound content [26,54]. According to this study, for calafate fruits collected in March, the maximum anthocyanin content (761 mg/100 g FW) coincided with the highest accumulation of SS (25 °Brix) 126 days after flowering [54].

3.3.3. Storage and Fruit Processing

In fruits, anthocyanins are mainly found in the epicarp (peel) [55] where they are stored in the cell vacuole and remain stable in intact fruits [56]. During fruit processing, the plant cell loses its compartmentalization and anthocyanins are exposed to the action of enzymes (polyphenol oxidase), other fruit components, and environmental conditions that favor their degradation [57]. Several factors such as temperature, pH, light, oxygen, ascorbic acid, metal ions, sugars, and enzymes may affect the stability of anthocyanins during processing and storage [58]. The mechanism of anthocyanin degradation has been studied in some plant species such as roselle (Hibiscus sabdariffa); a metal-catalyzed oxidation followed by condensation (brown polymer) and a deglycosylation followed by scission (phloroglucinaldehyde and phenolic acids) were identified as two pathways of anthocyanin degradation [59].
Fleshy fruits have high moisture content, thereby they are classified as highly perishable commodities [60]. The dehydration of murta and calafate fruits emerges as an attractive conservation alternative given also the high seasonality of their production, allowing for the commercialization of value-added dehydrated fruit products throughout the year. Different drying processes for murta, such as freeze-drying [61,62], convective drying, combined infrared-convective drying [63], vacuum drying [62,64,65], atmospheric drying [62,64], infrared-radiation [62], and sun-drying [62] have been evaluated in order to preserve the polyphenols, the AC, and/or the microstructure of fresh murta fruit. Lopez et al. [62] reported that freeze-drying showed the highest retention of total flavonoids as well as anthocyanins and the least damage of murta microstructure. No studies on the drying of calafate fruit have been published.
The understanding of the phytochemical changes in murta and calafate facilitates the design and development of formulations and the evaluation of the efficacy of new nutraceutical products.

3.4. Validation of Traditional Use and New Insights in the Research of Murta and Calafate

Different methods of biological activity have been used to validate the traditional uses of murta and calafate as well as to examine some potential uses of calafate shoots and fruits (Table 1).
Some studies identified phytochemicals such as triterpenoids, phenolic compounds, and isoquinoline alkaloids. However, in many cases it is difficult to correlate a specific compound to a specific biological effect. In addition, some studies lacked detailed information about the genotype and time of harvest of raw materials. This information is particularly important because, as was discussed previously, genotype, environment, and time of harvest have been shown to affect the phytochemistry of murta and calafate.

3.4.1. Antioxidant Capacity

Based on a traditional use of murta leaf that suggests antioxidant, anti-inflammatory, and antimicrobial activity, an early study of murta leaf AC (ORAC method) in vivo was evaluated in the plasma of healthy volunteers before and after the ingestion of a murta leaf infusion (1%) twice a day for three days [66]. The results indicated a significant increase (from 2.258 to 3.108 μM TE/L) in the AC of the volunteers’ plasma. Later, murta leaf AC was attributed to the presence of polyphenols such as phenolic acids, hydrolyzable tannins, flavanols (epicatechin), and flavonols (myricetin, quercetin) [67]. In another study, Albrecht et al. [82] examined the beneficial effect of calafate fruit on oxidative stress induced by chloramphenicol. Calafate-fruit aqueous extracts were shown to reduce oxidative stress caused by chloramphenicol in human blood cells by significantly diminishing reactive oxygen species (ROS). In parallel with the decrease of ROS, the fruit extract protected the viability of leukocytes [82].

3.4.2. Anti-Inflammatory Activity

To study the biological activity of murta-leaf triterpenoids, the topical anti-inflammatory activity of alphitolic, asiatic, and corosolic acids isolated from murta leaf were evaluated in vivo in a mouse ear model; inflammation was induced with either arachidonic acid or 12-O-tetradecanoylphorbol-13 acetate [69]. Only corosolic acid was active in the arachidonic acid-induced inflammation assay, with similar potency to nimesulide, while the three triterpene acids together inhibited 12-O-tetradecanoylphorbol-13 acetate-induced inflammation with potencies comparable to that of indomethacin [69]. Furthermore, Goity et al. [70] and Arancibia-Radich et al. [71] indicated that the differences in the anti-inflammatory activity of murta leaf is associated to the different quantitative composition of phenolic compounds and triterpenoids.
The anti-inflammatory potential of calafate fruit has been studied by Reyes-Farias et al. [83] where aqueous extracts were able to modulate the proinflammatory state generated by the interaction between adipocytes and macrophages in vitro.

3.4.3. Antimicrobial Activity

The antimicrobial activity of murta leaf extract against clinically important microorganisms with antibiotic resistance (Staphylococcus aureus, Enterobacter aerogenes, Pseudomonas aeruginosa, and Candida albicans) in vitro has been shown by Avello et al. [72] and Shen et al. [73]. Furthermore, Shene et al. [74] described the antimicrobial activity of murta leaf in human gut bacteria and Di Castillo et al. [75] showed the antimicrobial activity of murta leaf against Escherichia coli and Listeria monocytogenes.
Junqueira-Gonzalves et al. [39] studied the antibacterial activity (E. coli (ATCC 25922) and Salmonella typhi (ATCC 14028)) of ethanolic and acidic methanolic extracts. A methanolic murta fruit extract (100 μL) was equivalent to the activity of all of the antibiotics (tetracycline, clotrimazole, gentamicin, amikacin, ceftriaxone, cefuroxim, cefotaxim, ampicillin, ciprofloxacin, and ampicillin/sulbactam) tested in the case of S. typhi. However, in the case of E. coli, 100 μL of the extract was equivalent to the activity of tetracycline, amikacin, cefuroxim, cefotaxim, ampicillin, and ciprofloxacin.
The antimicrobial activity of calafate roots and shoots (stem and leaves) against Gram-positive bacteria (Staphylococcus aureus, Bacillus cereus, Staphylococcus epidermidis, and Bacillus subtilis) has been associated with the presence of isoquinoline alkaloids [78,81]. Calafate root had the highest alkaloid yield and berberine was the main alkaloid identified [79].

3.4.4. Analgesic Activity

Delporte et al. [68] studied the analgesic activity of dichloromethane, ethyl acetate, and methanol extracts from murta leaves on acute pain in mice. Murta-leaf extracts produced antinociception in chemical and thermal pain models through a mechanism partially linked to either lipooxygenase and/or cyclooxygenase via the arachidonic acid cascade and/or opioid receptors. Flavonoids and triterpenoids were associated with the antinociceptive activity [68].

3.4.5. New Insights in the Research of Murta and Calafate

In order to explore in the potential beneficial effect of murta and calafate fruit on the management of cardiovascular disease, Jofre et al. [76] and Calfío and Huidobro-Toro [77] studied the antioxidant and vasodilator activity of murta and calafate fruit in rat models. Dose-dependent vasodilator activity in the presence of endothelium was shown in aortic rings. Its hypotensive mechanism is partially mediated by nitric oxide synthase/guanylate cyclase and large-conductance calcium-dependent potassium channels [76]. Similarly, vascular responses of main glycosylated anthocyanins found in calafate fruit were endothelium-dependent and mediated by NO production [77]. Nevertheless, the authors propose that the anthocyanin-induced vasodilation is not due to an antioxidant mechanism [77]. Furthermore, Furrianca et al. [80] showed that a calafate-root ethanolic extract had hypoglycemic effects, stimulating glucose uptake in non-resistant and insulin-resistant liver (HepG2) cells by activating AMPK protein.

3.5. Potential Health Benefits Associated with Murta and Calafate Fruit Consumption

The high consumption of anthocyanin-rich foods has been associated with several health benefits in humans [84,85,86,87]. Internationally, these potential anti-inflammatory, antioxidant, hypoglycaemic, and cardioprotective health benefits found in berry-type fruits are used as a strategy to promote consumption. Antioxidant capacity measured in vitro is commonly determined in studies of phenolic profiling [9,88] however the in vitro method of measuring total antioxidant capacity is questionable due to it having almost zero relevance for human (animal) physiology. Nevertheless, the ORAC value as a way to determine AC in vitro is considered a quality parameter in the international market of berry-type agri-foods [88]. Speisky et al. [89] reported 27 fruit species grown in Chile, where the total phenolic content of murta (863 mg GAE/100g FW) and calafate (1201 mg GAE/100g FW) were higher than well-known polyphenol-rich fruits such as blackberry (671 mg GAE/100g FW) and blueberry (529 mg GAE/100g FW). Murta and calafate were grouped among the highest ORAC (10,000–25,000 µmoL TE/100 g FW) fruits where calafate had the highest ORAC (25,662 µmoL TE/100 g FW) value; 2.8-fold higher than blackberry and 2.9-fold higher than blueberry [89].
As was mentioned previously, polyphenols are susceptible to degradation by heat, oxygen, and changes in pH, among others that may occur not only during product storage, but also into the gastrointestinal (GI) tract [57]. For example, it is well known that anthocyanins are unstable at high pH, and the shift from the acidic pH (pH 2) of the stomach to the almost neutral pH of the duodenum (pH 6) may be responsible for their specific hydrolysis and/or degradation [90,91,92]. Bioaccessibility, defined as the amount of compounds that are released from the food matrix after digestion [90] is measured to determine the impact of the food matrix on the protection and/or release of bioactive compounds as well as the stability of bioactive compounds during GI digestion. Ah-Hen et al. [93] compared the bioaccessibility of murta fruit and juice during an in vitro GI digestion process showing that juice as food matrix released bioactive compounds earlier in the gastric stage, while murta fruit released bioactive compounds in the small intestine. However, both murta fruit and juice achieved a high bioaccessibility index of polyphenols (70%) after being digested by the small intestine [93].
According to anthocyanin metabolism, its degradation is a result of chemical instability and the impact of bacterial catabolism, resulting in a number of circulating phenolic metabolites [94]. Along this line, Bustamante et al. [95] performed a pharmacokinetic study of phenolic compounds in gerbil plasma after the consumption of calafate, where the amount of 16 phenolic acids increased 4–8 h post-intake. Although all catabolites were found in concentration peaks between 0.1 and 1 mu M, no parental anthocyanins were detected [95]. Currently, it is postulated that anthocyanin bioactivity in vivo results from lesser studied, though more bioavailable, phenolic metabolites [96,97] and some authors have demonstrated that these phenolic metabolites are more active on inflammatory biomarkers than their precursor structures (parent anthocyanins) [97,98]. In this sense, the bioactivity of anthocyanin metabolites in murta and calafate must continue to be studied in order to achieve adequate information on the biological activity and health-promoting effects derived for the consumption of murta and calafate fruit.

4. Conclusions and Future Perspectives

This review, for the first time, approximates the traditional knowledge of murta and calafate with the scientific research on both species. Scientific knowledge of murta and calafate is much more limited compared to other South American fruits such as maqui (Aristotelia chilensis (Mol.) Stuntz) and acai (Euterpe oleracea Mart.) for which there are 96 and 232 records (article, proceedings paper, book chapter, and review) available in the Web of Science database, respectively. Advances in the study of the nutritional composition of fruits, the identification of phytochemicals, the validation of traditional use, and the biological activity of certain phytochemicals indicate that murta and calafate are promising sources of natural antioxidants, antimicrobial, and vasodilator compounds with nutraceutical potential. Like international studies on nutraceuticals in other berry-type fruits such as blueberries [95,96,97] future studies are needed to establish the mechanisms of action of both murta and calafate anthocyanins (and their metabolites) in antioxidant and anti-inflammatory activity. These studies are needed in order to further the study of the potential health benefits associated with the consumption of these berry-type fruits. From the nutritional point of view, murta appears to be a good source of ascorbic acid, similar to other fruits in the Myrtaceae family such as camu camu (Myrciaria dubia (Kunth) McVaugh, 397 mg/100 g FW) and white guava (Psidium guajava L., 142 mg/100 g FW), which are internationally recognized as good sources of vitamin C [99].
Plant domestication is a necessary strategy to guarantee the sustainable use of Chilean botanical resources and to standardize the quality of the raw materials derived from murta and calafate. Murta domestication programs are around 20 years old, while calafate has only very recently been domesticated. At the same time, sustainable harvesting of wild murta and calafate performed by several indigenous and rural communities can be an alternative for supplying raw materials for future research. This review will be a useful reference for new research on murta and calafate, respecting and recognizing the traditional knowledge in the hands of indigenous and rural peoples from south and extreme south of Chile.

Author Contributions

C.F. performed the historical and scientific search of literature; C.F. and P.R. structured the review and analyzed the main papers; A.P. provided the review on nutritional composition; J.S. provided the review on botany and distribution. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

We are sincerely grateful to the Biblioteca Nacional of Chile for granting us access to and permission to use images of Abate José Ignacio Molina, Claudio Gay, and Charles Darwin, and to Carlos Aldunate, Director of the Museo Chileno de Arte Precolombino for the permission to use the picture of Father Ernesto Wilhem de Mösbach.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wilhem De Mösbach, E. Botánica Indígena; Editorial Andrés Bello: Santiago, Chile, 1992; pp. 26–33. [Google Scholar]
  2. Estomba, D.; Ladio, A.; Lozada, M. Medicinal wild plant knowledge and gathering patterns in a Mapuche community from North-western Patagonia. J. Ethnopharmacol. 2006, 103, 109–119. [Google Scholar] [CrossRef]
  3. Lozada, M.; Ladio, A.; Weigandt, M. Cultural transmission of ethnobotanical knowledge in a rural community of northwestern Patagonia, Argentina. Econ. Bot. 2006, 60, 374–385. [Google Scholar] [CrossRef]
  4. Darwin, C. Viaje de un Naturalista Alrededor del Mundo; Joaquín Gil: Buenos Aires, Argentina, 1945; p. 618. [Google Scholar]
  5. Seguel, I.; Torralbo, L. Murtilla: El berry nativo del Sur de Chile. Rev. Tierra Adentro 2004, 57, 20–25. [Google Scholar]
  6. Hoffmann, A. Flora Silvestre de Chile. Zona Araucana. Árboles, Arbustos y Enredaderas Leñosas; Fundación Claudio Gay: Santiago, Chile, 1982; p. 258. [Google Scholar]
  7. Seeram, N.P. Berry fruits: Compositional elements, biochemical activities, and the impact of their intake on human health, performance, and disease. J. Agric. Food Chem. 2008, 56, 627–629. [Google Scholar] [CrossRef] [PubMed]
  8. Halvorsen, B.L.; Holte, K.; Myhrstad, M.C.W.; Barikmo, I.; Hvattum, E.; Remberg, S.F.; Wold, A.-B.; Haffner, K.; Baugerod, H.; Andersen, L.F.; et al. A systematic screening of total antioxidants in dietary plants. J. Nutr. 2002, 132, 461–471. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Fredes, C.; Yousef, G.G.; Robert, P.; Grace, M.H.; Lila, M.A.; Gómez, M.; Gebauer, M.; Montenegro, G. Anthocyanin profiling of wild maqui berries (Aristotelia chilensis [Mol.] Stuntz) from different geographical regions in Chile. J. Sci. Food Agric. 2014, 94, 2639–2648. [Google Scholar] [CrossRef] [PubMed]
  10. Lee, S. Strategic design of delivery systems for nutraceuticals. In Nanotechnology Applications in Food: Flavor, Stability, Nutrition, and Safety; Oprea, O.E., Grumezescu, A.M., Eds.; Academic Press, Elsevier Inc.: London, UK, 2017; pp. 65–86. [Google Scholar]
  11. Molina, J.I. Compendio de la Historia Geográfica, Natural y Civil del Reyno de Chile; Don Antonio de Sancha: Madrid, España, 1788; p. 418. [Google Scholar]
  12. Gay, C. Historia Física y Política de Chile. Botánica. Tomo Primero; Museo de Historia Natural de Santiago: Santiago, Chile, 1845; p. 535. [Google Scholar]
  13. Gay, C. Historia Física y Política de Chile. Botánica. Tomo Segundo; Museo de Historia Natural de Santiago: Santiago, Chile, 1846; p. 372. [Google Scholar]
  14. Montenegro, G. Chile Nuestra Flora Útil; Universidad Católica de Chile: Santiago, Chile, 2002; p. 267. [Google Scholar]
  15. Fredes, C.; Montenegro, G. Chilean plants as a source of polyphenols. In Natural Antioxidants and Biocides from Wild Medicinal Plants; Céspedes, C., Sampietro, D., Seigler, D., Rai, M., Eds.; CAB International: Wallingford, UK, 2013; pp. 116–136. [Google Scholar]
  16. Minsal-Ministerio de Salud. Medicamentos Herbarios Tradicionales. 2009. Available online: https://www.minsal.cl/wp-content/uploads/2018/02/Libro-MHT-2010.pdf (accessed on 10 April 2018).
  17. Muñoz, O.; Montes, M.; Wilkomirsky, T. Plantas Medicinales de Uso en Chile. Química y Farmacología; Editorial Universitaria: Santiago, Chile, 2001; p. 330. [Google Scholar]
  18. Martinic, M. Los Aónikenk: Historia y Cultura; Universidad de Magallanes: Punta Arenas, Chile, 1995; p. 387. [Google Scholar]
  19. Barros, A. Aborígenes Australes de América; Editorial Lord Cochrane: Santiago, Chile, 1975; pp. 15–25. [Google Scholar]
  20. Cárdenas, R. Poemas Migratorios; Armando Menedin: Santiago, Chile, 1974; pp. 29–30. [Google Scholar]
  21. Torres, A.; Seguel, I.; Contreras, G.; Castro, M. Physico-chemical characterization of murta (murtilla) fruits Ugni molinae Turcz. Agric. Técnica 1999, 59, 260–270. [Google Scholar]
  22. Schreckinger, M.E.; Lotton, J.; Lila, M.A.; De Mejia, E.G. Berries from South America: A comprehensive review on chemistry, health potential, and commercialization. J. Med. Food 2010, 13, 233–246. [Google Scholar] [CrossRef]
  23. Scheuermann, E.; Seguel, I.; Montenegro, A.; Bustos, R.; Hormazabal, E.; Quiroz, A. Evolution of aroma compounds of murtilla fruits (Ugni molinae Turcz) during storage. J. Sci. Food Agric. 2008, 88, 485–492. [Google Scholar] [CrossRef]
  24. Ah-Hen, K.S.; Vega-Gálvez, A.; Moraga, N.O.; Lemus-Mondaca, R. Modelling of rheological behaviour of pulps and purées from fresh and frozen-thawed murta (Ugni molinae Turcz) berries. Int. J. Food Eng. 2012, 8. [Google Scholar] [CrossRef]
  25. Arancibia-Avila, P.; Namiesnik, J.; Toledo, F.; Werner, E.; Martinez-Ayala, A.M.; Rocha-Guzmán, N.E.; Gallegos-Infante, J.A.; Gorinstein, S. The influence of different time durations of thermal processing on berries quality. Food Control 2012, 26, 587–593. [Google Scholar] [CrossRef]
  26. Arena, M.E.; Zuleta, A.; Dyner, L.; Constenla, D.; Ceci, L.; Curvetto, N. Berberis buxifolia fruit growth and ripening: Evolution in carbohydrate and organic acid contents. Sci. Hortic. 2013, 158, 52–58. [Google Scholar] [CrossRef]
  27. Fredes, C.; Montenegro, G.; Zoffoli, J.; Santander, F.; Robert, P. Comparison of total phenolic, total anthocyanin and antioxidant activity of polyphenol-rich fruits grown in Chile. Cienc. Investig. Agrar. 2014, 41, 49–60. [Google Scholar] [CrossRef] [Green Version]
  28. Ruiz, A.; Hermosin-Gutierrez, I.; Mardones, C.; Vergara, C.; Herlitz, E.; Vega, M.; Dorau, C.; Winterhalter, P.; Von Baer, D. Polyphenols and antioxidant activity of calafate (Berberis microphylla) fruits and other native berries from southern Chile. J. Agric. Food Chem. 2010, 58, 6081–6089. [Google Scholar] [CrossRef] [PubMed]
  29. Liu, R.H. Potential synergy of phytochemicals in cancer prevention: Mechanism of action. J. Nutr. 2004, 134, 3479S–3485S. [Google Scholar] [CrossRef] [Green Version]
  30. Reilly, K. On-farm and fresh produce management. In Handbook of Plant Food Phytochemicals: Sources Stability and Extraction; Tiwari, B.K., Brunton, N., Brennan, C., Eds.; Wiley-Blackwell Publishing Co.: Hoboken, NJ, USA, 2013; pp. 201–235. [Google Scholar]
  31. Springob, K.; Kutchan, T.M. Introduction to the different classes of natural products. In Plant-Derived Natural Products; Osbourn, A.E., Lanzotti, V., Eds.; Springer: New York, NY, USA, 2009; pp. 1–50. [Google Scholar]
  32. Robert, P.; Fredes, C. The encapsulation of anthocyanins from berry-type fruits: Trends in foods. Molecules 2015, 20, 5875–5888. [Google Scholar] [CrossRef]
  33. Manach, C.; Scalbert, A.; Morand, C.; Rémésy, C.; Jiménez, L. Polyphenols: Food sources and bioavailability. Am. J. Clin. Nutr. 2004, 79, 727–747. [Google Scholar] [CrossRef] [Green Version]
  34. Castañeda-Ovando, A.; Pacheco-Hernández, M.L.; Páez-Hernández, M.A.; Rodríguez, J.A.; Galán-Vidal, C.A. Chemical studies of anthocyanins: A review. Food Chem. 2009, 113, 859–871. [Google Scholar] [CrossRef]
  35. Khoo, H.E.; Azlan, A.; Tang, S.T.; Lim, S.M. Anthocyanindins and anthocyanins: Colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr. Res. 2017, 61, 1361779. [Google Scholar] [CrossRef] [Green Version]
  36. Robert, P.; García, P.; Fredes, C. Drying and preservation of polyphenols. In Advances in Technologies for Producing Food-Relevant Polyphenols; Cuevas-Valenzuela, J., Vergara Salinas, J.R., Pérez-Correa, J.R., Eds.; CRC Press, Taylor and Francis Group: Boca Raton, FL, USA, 2017; pp. 281–302. [Google Scholar]
  37. Brito, A.; Areche, C.; Sepulveda, B.; Kennelly, E.J.; Simirgiotis, M.J. Anthocyanin characterization, total phenolic quantification and antioxidant features of some Chilean edible berry extracts. Molecules 2014, 19, 10936–10955. [Google Scholar] [CrossRef] [Green Version]
  38. Ramirez, J.E.; Zambrano, R.; Sepulveda, B.; Kennelly, E.J.; Simirgiotis, M.J. Anthocyanins and antioxidant capacities of six Chilean berries by HPLC-HR-ESI-ToF-MS. Food Chem. 2015, 176, 106–114. [Google Scholar] [CrossRef] [PubMed]
  39. Junqueira-Goncalves, M.P.; Yanez, L.; Morales, C.; Navarro, M.; Contreras, R.A.; Zuniga, G.E. Isolation and characterization of phenolic compounds and anthocyanins from murta (Ugni molinae Turcz) fruits. Assessment of antioxidant and antibacterial activity. Molecules 2015, 20, 5698–5713. [Google Scholar] [CrossRef] [PubMed]
  40. Augusto, T.R.; Scheuerman, E.S.; Alencar, S.M.; D’Arce, M.A.; Costa De Camargo, A.; Vieira, T.M. Phenolic compounds and antioxidant activity of hydroalcoholic extracts of wild and cultivated murtilla (Ugni molinae Turcz). Food Sci. Technol. 2014, 34, 667–673. [Google Scholar] [CrossRef] [Green Version]
  41. Ruiz, A.; Mardones, C.; Vergara, C.; Hermosin-Gutierrez, I.; Von Baer, D.; Hinrichsen, P.; Rodriguez, R.; Arribillaga, D.; Dominguez, E. Analysis of hydroxycinnamic acids derivatives in calafate (Berberis microphylla G. Forst) berries by liquid chromatography with photodiode array and mass spectrometry detection. J. Chromatogr. A 2013, 1281, 38–45. [Google Scholar] [CrossRef] [PubMed]
  42. Ruiz, A.; Mardones, C.; Vergara, C.; Von Baer, D.; Gomez-Alonso, S.; Gomez, M.V.; Hermosin-Gutierrez, I. Isolation and structural elucidation of anthocyanidin 3,7-beta-o-diglucosides and caffeoyl-glucaric acids from calafate berries. J. Agric. Food Chem. 2014, 62, 6918–6925. [Google Scholar] [CrossRef] [PubMed]
  43. Meyer, R.S.; DuVal, A.E.; Jensen, H.R. Patterns and processes in crop domestication: An historical review and quantitative analysis of 203 global food crops. New Phytol. 2012, 196, 29–48. [Google Scholar] [CrossRef] [PubMed]
  44. Chacon-Fuentes, M.; Parra, L.; Rodriguez-Saona, C.; Seguel, I.; Ceballos, R.; Quiroz, A. Domestication in murtilla (Ugni molinae) reduced defensive flavonol levels but increased resistance against a native herbivorous insect. Environ. Entomol. 2015, 44, 627–637. [Google Scholar] [CrossRef]
  45. Chacon-Fuentes, M.; Parra, L.; Lizama, M.; Seguel, I.; Urzua, A.; Quiroz, A. Plant flavonoid content modified by domestication. Environ. Entomol. 2017, 46, 1080–1089. [Google Scholar] [CrossRef]
  46. Alfaro, S.; Mutis, A.; Palma, R.; Quiroz, A.; Seguel, I.; Scheuermann, E. Influence of genotype and harvest year on polyphenol content and antioxidant activity in murtilla (Ugni molinae Turcz) fruit. J. Soil Sci. Plant Nutr. 2013, 13, 67–78. [Google Scholar] [CrossRef] [Green Version]
  47. Mariangel, E.; Reyes-Diaz, M.; Lobos, W.; Bensch, E.; Schalchli, H.; Ibarra, P. The antioxidant properties of calafate (Berberis microphylla) fruits from four different locations in southern Chile. Cienc. Investig. Agrar. 2013, 40, 161–170. [Google Scholar] [CrossRef] [Green Version]
  48. Arena, M.E.; Postemsky, P.D.; Curvetto, N.R. Changes in the phenolic compounds and antioxidant capacity of Berberis microphylla G. Forst berries in relation to light intensity and fertilization. Sci. Hortic. 2017, 218, 63–71. [Google Scholar] [CrossRef]
  49. Vvedenskaya, I.O.; Vorsa, N. Flavonoid composition over fruit development and maturation in American cranberry, Vaccinium macrocarpon Ait. Plant Sci. 2004, 167, 1043–1054. [Google Scholar] [CrossRef]
  50. Kulkarni, A.P.; Aradhya, S.M. Chemical changes and antioxidant activity in pomegranate arils during fruit development. Food Chem. 2005, 93, 319–324. [Google Scholar] [CrossRef]
  51. Wang, S.Y.; Chen, C.-T.; Wang, C.Y. The influence of light and maturity on fruit quality and flavonoid content of red raspberries. Food Chem. 2009, 112, 676–684. [Google Scholar] [CrossRef]
  52. Parr, A.J.; Bolwell, G.P. Phenols in the plant and in man. The potential for possible nutritional enhancement of the diet by modifying the phenols content or profile. J. Sci. Food Agric. 2000, 80, 985–1012. [Google Scholar] [CrossRef]
  53. Fredes, C.; Montenegro, G.; Zoffoli, J.P.; Gómez, M.; Robert, P. Polyphenol content and antioxidant activity of maqui (Aristotelia chilensis [Mol.] Stuntz) during fruit development and maturation in Central Chile. Chil. J. Agric. Res. 2012, 72, 582–589. [Google Scholar] [CrossRef] [Green Version]
  54. Arena, M.; Curvetto, N. Berberis buxifolia fruiting: Kinetic growth behavior and evolution of chemical properties during the fruiting period and different growing seasons. Sci. Hortic. 2008, 118, 120–127. [Google Scholar] [CrossRef]
  55. Wang, S.Y.; Chen, H.; Camp, M.J.; Ehlenfeldt, M.K. Genotype and growing season influence blueberry antioxidant capacity and other quality attributes. Int. J. Food Sci. Technol. 2012, 47, 1540–1549. [Google Scholar] [CrossRef]
  56. Patras, A.; Brunton, N.P.; O’Donnell, C.; Tiwari, B.K. Effect of thermal processing on anthocyanin stability in foods; mechanisms and kinetics of degradation. Trends Food Sci. Technol. 2010, 21, 3–11. [Google Scholar] [CrossRef]
  57. De Pascual-Teresa, S.; Sanchez-Ballesta, M.T. Anthocyanins: From plant to health. Phytochem. Rev. 2008, 7, 281–299. [Google Scholar] [CrossRef]
  58. Rhim, J.-W. Kinetics of thermal degradation of anthocyanin pigment solutions driven from red flower cabbage. Food Sci. Biotech. 2002, 11, 361–364. [Google Scholar]
  59. Mundombe Sinela, A.; Mertz, C.; Achir, N.; Rawat, N.; Vidot, K.; Fulcrand, H.; Dornier, M. Exploration of reaction mechanisms of anthocyanin degradation in a roselle extract through kinetic studies on formulated model media. Food Chem. 2017, 235, 67–75. [Google Scholar] [CrossRef] [PubMed]
  60. Sharma, H.P.; Sugandha, P.H. Enzymatic added extraction and clarification of fruit juices-A review. Crit. Rev. Food Sci. Nutr. 2017, 57, 1215–1227. [Google Scholar] [CrossRef] [PubMed]
  61. Reyes, A.; Bubnovich, V.; Bustos, R.; Vásquez, M.; Vega, R.; Scheuermann, E. Comparative study of different process conditions of freeze drying of ‘Murtilla’ berry. Dry. Technol. 2010, 28, 1416–1425. [Google Scholar] [CrossRef]
  62. López, J.; Ah-Hen, K.S.; Vega-Gálvez, A.; Morales, A.; García-Segovia, P.; Uribe, E. Effects of drying methods on quality attributes of murta (Ugni molinae Turcz) berries: Bioactivity, nutritional aspects, texture profile, microstructure and functional properties. J. Food Process Eng. 2017, 40, e12511. [Google Scholar] [CrossRef]
  63. Puente-Díaz, L.; Ah-Hen, K.; Vega-Gálvez, A.; Lemus-Mondaca, R.; Di Scala, K. Combined infrared-convective drying of murta (Ugni molinae Turcz) berries: Kinetic modeling and quality assessment. Dry. Technol. 2013, 31, 329–338. [Google Scholar] [CrossRef]
  64. Ah-Hen, K.; Zambra, C.E.; Aguëro, J.E.; Vega-Gálvez, A.; Lemus-Mondaca, R. Moisture diffusivity coefficient and convective drying modelling of murta (Ugni molinae Turcz): Influence of temperature and vacuum on drying kinetics. Food Bioprocess Technol. 2013, 6, 919–930. [Google Scholar] [CrossRef]
  65. López, J.; Vega-Gálvez, A.; Bilbao-Sainz, C.; Chiou, B.-S.; Uribe, E.; Quispe-Fuentes, I. Influence of vacuum drying temperature on: Physico-chemical composition and antioxidant properties of murta berries. J. Food Process Eng. 2017, 40, e12569. [Google Scholar]
  66. Avello, M.; Pastene, E. Actividad antioxidante de infusos de Ugni molinae Turcz (“Murtilla”). Bol. Latinoam. Caribe Plantas Med. Aromat. 2005, 4, 33–39. [Google Scholar]
  67. Rubilar, M.; Pinelo, M.; Ihl, M.; Scheuermann, E.; Sineiro, J.; Nuñez, M.J. Murta leaves (Ugni molinae Turcz) as a source of antioxidant polyphenols. J. Agric. Food Chem. 2006, 54, 59–64. [Google Scholar] [CrossRef]
  68. Delporte, C.; Backhouse, N.; Inostroza, V.; Aguirre, M.C.; Peredo, N.; Silva, X.; Negrete, R.; Miranda, H.F. Analgesic activity of Ugni molinae (murtilla) in mice models of acute pain. J. Ethnopharmacol. 2007, 112, 162–165. [Google Scholar] [CrossRef] [PubMed]
  69. Aguirre, M.C.; Delporte, C.; Backhouse, N.; Erazo, S.; Letelier, M.E.; Cassels, B.K.; Silva, X.; Alegría, S.; Negrete, R. Topical anti-inflammatory activity of 2α-hydroxy pentacyclic triterpene acids from the leaves of Ugni molinae. Bioorg. Med. Chem. 2006, 14, 5673–5677. [Google Scholar] [CrossRef] [PubMed]
  70. Goity, L.E.; Queupil, M.J.; Jara, D.; Alegria, S.E.; Pena, M.; Barriga, A.; Aguirre, M.C.; Delporte, C. An HPLC-UV and HPLC-ESI-MS based method for identification of anti-inflammatory triterpenoids from the extracts of Ugni molinae. Bol. Latinoam. Caribe Plantas Med. Aromat. 2013, 12, 108–116. [Google Scholar]
  71. Arancibia-Radich, J.; Pena-Cerda, M.; Jara, D.; Valenzuela-Bustamante, P.; Goity, L.; Valenzuela-Barra, G.; Silva, X.; Garrido, G.; Delporte, C.; Seguel, I. Comparative study of anti-inflammatory activity and qualitative-quantitative composition of triterpenoids from ten genotypes of Ugni molinae. Bol. Latinoam. Caribe Plantas Med. Aromat. 2016, 15, 274–287. [Google Scholar]
  72. Avello, M.; Valdivia, R.; Mondaca, M.A.; Ordoñez, J.L.; Bittner, M.; Becerra, J. Activity of Ugni molinae Turcz against microorganisms with clinical importance. Bol. Latinoam. Caribe Plantas Med. Aromat. 2009, 8, 141–144. [Google Scholar]
  73. Shene, C.; Reyes, A.K.; Villarroel, M.; Sineiro, J.; Pinelo, M.; Rubilar, M. Plant location and extraction procedure strongly alter the antimicrobial activity of murta extracts. Eur. Food Res. Technol. 2009, 228, 467–475. [Google Scholar] [CrossRef]
  74. Shene, C.; Canquil, N.; Jorquera, M.; Pinelo, M.; Rubilar, M.; Acevedo, F.; Vergara, C.; Von Baer, D.; Mardones, C. In vitro activity on human gut bacteria of murta leaf extracts (Ugni molinae Turcz), a native plant from Southern Chile. J. Food Sci. 2012, 77, M323–M329. [Google Scholar] [CrossRef]
  75. De Dicastillo, C.L.; Bustos, F.; Valenzuela, X.; Lopez-Carballo, G.; Vilarino, J.M.; Galotto, M.J. Chilean berry Ugni molinae Turcz fruit and leaves extracts with interesting antioxidant, antimicrobial and tyrosinase inhibitory properties. Food Res. Int. 2017, 102, 119–128. [Google Scholar] [CrossRef]
  76. Jofre, I.; Pezoa, C.; Cuevas, M.; Scheuermann, E.; Freires, I.A.; Rosalen, P.L.; De Alencar, S.M.; Romero, F. Antioxidant and vasodilator activity of Ugni molinae Turcz. (murtilla) and its modulatory mechanism in hypotensive response. Oxid. Med. Cell. Longev. 2016, 6513416. [Google Scholar] [CrossRef] [Green Version]
  77. Calfío, C.; Huidobro-Toro, J.P. Potent vasodilator and cellular antioxidant activity of endemic patagonian calafate berries (Berberis microphylla) with nutraceutical potential. Molecules 2019, 24, 2700. [Google Scholar] [CrossRef] [Green Version]
  78. Manosalva, L.; Mutis, A.; Urzua, A.; Fajardo, V.; Quiroz, A. Antibacterial activity of alkaloid fractions from Berberis microphylla G. Forst and study of synergism with ampicillin and cephalothin. Molecules 2016, 21, 76. [Google Scholar] [CrossRef] [Green Version]
  79. Manosalva, L.; Mutis, A.; Diaz, J.; Urzua, A.; Fajardo, V.; Quiroz, A. Identification of isoquinoline alkaloids from Berberis microphylla by HPLC ESI-MS/MS. Bol. Latinoam. Caribe Plantas Med. Aromat. 2014, 13, 324–335. [Google Scholar]
  80. Furrianca, M.C.; Alvear, M.; Zambrano, T.; Fajardo, V.; Salazar, L.A. Hypoglycemic effect of Berberis microphylla G. Forst root extract. Trop. J. Pharm. Res. 2017, 16, 2179–2184. [Google Scholar] [CrossRef] [Green Version]
  81. Pitta-Alvarez, S.I.; Medina-Bolivar, F.; Alvarez, M.A.; Scambatto, A.A.; Marconi, P.L. In vitro shoot culture and antimicrobial activity of Berberis buxifolia Lam. Vitr. Cell. Dev. Biol. Plant 2008, 44, 502–507. [Google Scholar] [CrossRef]
  82. Albrecht, C.; Pellarin, G.; Rojas, M.J.; Albesa, I.; Eraso, A.J. Beneficial effect of Berberis buxifolia Lam, Zizyphus mistol Griseb and Prosopis alba extracts on oxidative stress induced by chloramphenicol. Medicina (Buenos Aires) 2010, 70, 65–70. [Google Scholar]
  83. Reyes-Farias, M.; Vasquez, K.; Ovalle-Marin, A.; Fuentes, F.; Parra, C.; Quitral, V.; Jimenez, P.; Garcia-Diaz, D.F. Chilean native fruit extracts inhibit inflammation linked to the pathogenic interaction between adipocytes and macrophages. J. Med. Food. 2015, 18, 601–608. [Google Scholar] [CrossRef] [Green Version]
  84. Chang, H.C.; Peng, C.H.; Yeh, D.M.; Kao, E.S.; Wang, C.J. Hibiscus sabdariffa extract inhibits obesity and fat accumulation, and improves liver steatosis in humans. Food Funct. 2014, 5, 734–739. [Google Scholar] [CrossRef]
  85. De Ferrars, R.M.; Czank, C.; Zhang, Q. The pharmacokinetics of anthocyanins and their metabolites in humans. Br. J. Pharmacol. 2014, 171, 3268–3282. [Google Scholar] [CrossRef] [Green Version]
  86. Zhang, X.; Huang, H.; Zhao, X. Effects of flavonoids-rich Chinese bayberry (Myrica rubra Sieb. et Zucc.) pulp extracts on glucose consumption in human HepG2 cells. J. Funct. Foods 2015, 14, 144–153. [Google Scholar] [CrossRef]
  87. Pavlidou, E.; Giaginis, C.; Fasoulas, A.; Petridis, D. Evaluation of the effect of blueberries consumption on chronic diseases, illness prevention and health promotion. Nat. Prod. J. 2018, 8, 45–53. [Google Scholar] [CrossRef]
  88. Siddiq, M.; Dolan, K.D.; Perkins-Veazie, O.; Collins, J.K. Effect of pectinolytic and cellulytic enzymes on the physical, chemical, and antioxidant properties of blueberry (Vaccinium corymbosum L.) juice. LWT-Food Sci. Technol. 2018, 92, 127–132. [Google Scholar] [CrossRef]
  89. Speisky, H.; López-Alarcón, C.; Gómez, M.; Fuentes, J.; Sandoval-Vicuña, C. First web-based database on total phenolics and oxygen radical absorbance capacity (ORAC) of fruits produced and consumed within the South Andes Region of South America. J. Agric. Food Chem. 2012, 60, 8851–8859. [Google Scholar] [CrossRef]
  90. Lila, M.; Ribnicky, D.; Rojo, L.; Rojas-Silva, P.; Oren, A.; Havenaar, R.; Janle, E.; Raskin, I.; Yousef, G.; Grace, M. Complementary approaches to gauge the bioavailability and distribution of ingested berry polyphenolics. J. Agric. Food Chem. 2012, 60, 5763–5771. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Flores, F.; Singh, R.; Kerr, W.; Pegg, R.; Kong, F. Total phenolics content and antioxidant capacities of microencapsulated blueberry anthocyanins during in vitro digestion. Food Chem. 2014, 153, 272–278. [Google Scholar] [CrossRef] [PubMed]
  92. Mosele, J.I.; Macià, A.; Romero, M.P.; Motilva, M.J. Stability and metabolism of Arbutus unedo bioactive compounds (phenolics and antioxidants) under in vitro digestion and colonic fermentation. Food Chem. 2016, 201, 120–130. [Google Scholar] [CrossRef] [PubMed]
  93. Ah-Hen, K.S.; Mathias-Rettig, K.; Gomez-Perez, L.S.; Riquelme-Asenjo, G.; Lemus-Mondaca, R.; Munoz-Farina, O. Bioaccessibility of bioactive compounds and antioxidant activity in murta (Ugni molinae T.) berries juices. J. Food Meas. Charact. 2018, 12, 602–615. [Google Scholar] [CrossRef]
  94. Kay, C.D.; Mazza, G.J.; Holub, B.J. Anthocyanins exist in the circulation primarily as metabolites in adult men. J. Nutr. 2005, 135, 2582–2588. [Google Scholar] [CrossRef] [Green Version]
  95. Bustamante, L.; Pastene, E.; Duran-Sandoval, D.; Vergara, C.; Von Baer, D.; Mardones, C. Pharmacokinetics of low molecular weight phenolic compounds in gerbil plasma after the consumption of calafate berry (Berberis microphylla) extract. Food Chem. 2018, 268, 347–354. [Google Scholar] [CrossRef]
  96. Amin, H.P.; Czank, C.; Raheem, S.; Zhang, Q.; Botting, N.P.; Cassidy, A.; Kay, C.D. Anthocyanins and their physiologically relevant metabolites alter the expression of IL-6 and VCAM-1 in CD40L and oxidized LDL challenged vascular endothelial cells. Mol. Nutr. Food Res. 2015, 59, 1095–1106. [Google Scholar] [CrossRef] [Green Version]
  97. Warner, E.F.; Zhang, Q.; Raheem, Q.S.; O’Hagan, D.; O’Connell, M.A.; Kay, C.D. Common phenolic metabolites of flavonoids, but not their unmetabolized precursors, reduce the secretion of vascular cellular adhesion molecules by human endothelial cells. J. Nutr. 2016, 146, 465–473. [Google Scholar] [CrossRef] [Green Version]
  98. Warner, E.F.; Smith, M.J.; Zhang, Q.; Raheem, K.S.; O’Hagan, D.; O’Connell, M.A.; Kay, C.D. Signatures of anthocyanin metabolites identified in humans inhibit biomarkers of vascular inflammation in human endothelial cells. Mol. Nutr. Food Res. 2017, 61. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  99. Abe, L.T.; Lajolo, F.M.; Genovese, M.I. Potential dietary sources of ellagic acid and other antioxidants among fruits consumed in Brazil: Jabuticaba (Myrciaria jaboticaba (Vell.) Berg). J. Sci. Food Agric. 2012, 92, 1679–1687. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Distribution of murta (red) and calafate (blue) in a Chilean map, and the territory of Mapuche (winter white), Aónikenk (soft blue) and Yámana (brown).
Figure 1. Distribution of murta (red) and calafate (blue) in a Chilean map, and the territory of Mapuche (winter white), Aónikenk (soft blue) and Yámana (brown).
Foods 09 00054 g001
Figure 2. Murta (a) and calafate (b) fruits.
Figure 2. Murta (a) and calafate (b) fruits.
Foods 09 00054 g002
Figure 3. Summary of the search and selection protocols used to identify scientific articles included in the review.
Figure 3. Summary of the search and selection protocols used to identify scientific articles included in the review.
Foods 09 00054 g003
Figure 4. Anthocyanidin basic chemical structure (a), anthocyanins in murta (b) and calafate (c), and their different glycosylation patters.
Figure 4. Anthocyanidin basic chemical structure (a), anthocyanins in murta (b) and calafate (c), and their different glycosylation patters.
Foods 09 00054 g004
Table 1. Traditional medicinal use, biological activity, and phytochemicals reported for murta and calafate.
Table 1. Traditional medicinal use, biological activity, and phytochemicals reported for murta and calafate.
Plant OrganTraditional UseBiological ActivityPhytochemicalsReference
Murta leafUrinary and throat infectionAntioxidantNR[66]
AntioxidantPhenolic acids, hydrolyzable tannins, epicatechin, myricetin, quercetin[67]
AnalgesicFlavonoids and triterpenoids[68]
Anti-inflammatoryTriterpenoids[69]
Anti-inflammatoryTriterpenoids and phenolic compounds[70,71]
AntimicrobialCatechin, rutin, isoquercitrin, ellagic acid, quercitrin, narcissin, isorhamnetin-3-O-glucoside[72,73,74,75]
Murta fruitAstringentAntimicrobialIsoquinoline alkaloids[39]
VasodilatorGallic acid, catechin, quercetin-3-β-D-glucoside, myricetin, quercetin, and kaempferol[76,77]
Calafate rootControl fever, anti-inflammatory, stomach pain, indigestion, colitisAntimicrobialIsoquinoline alkaloids[78,79]
HypoglycaemicNR[80]
Calafate shootNRAntimicrobialIsoquinoline alkaloids[78,79,81]
Calafate fruitNRAntioxidantNR[82]
Anti-inflammatoryPhenolic compounds[83]
NR: Not reported.

Share and Cite

MDPI and ACS Style

Fredes, C.; Parada, A.; Salinas, J.; Robert, P. Phytochemicals and Traditional Use of Two Southernmost Chilean Berry Fruits: Murta (Ugni molinae Turcz) and Calafate (Berberis buxifolia Lam.). Foods 2020, 9, 54. https://0-doi-org.brum.beds.ac.uk/10.3390/foods9010054

AMA Style

Fredes C, Parada A, Salinas J, Robert P. Phytochemicals and Traditional Use of Two Southernmost Chilean Berry Fruits: Murta (Ugni molinae Turcz) and Calafate (Berberis buxifolia Lam.). Foods. 2020; 9(1):54. https://0-doi-org.brum.beds.ac.uk/10.3390/foods9010054

Chicago/Turabian Style

Fredes, Carolina, Alejandra Parada, Jaime Salinas, and Paz Robert. 2020. "Phytochemicals and Traditional Use of Two Southernmost Chilean Berry Fruits: Murta (Ugni molinae Turcz) and Calafate (Berberis buxifolia Lam.)" Foods 9, no. 1: 54. https://0-doi-org.brum.beds.ac.uk/10.3390/foods9010054

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