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Article

The Beneficial Effects of Allicin in Chronic Kidney Disease Are Comparable to Losartan

1
Renal Physiopathology Laboratory, Depterment of Nephrology, Instituto Nacional de Cardiología “Ignacio Chávez”, Mexico City 14080, Mexico
2
Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados-IPN, Mexico City 07360, Mexico
3
Histopathology Laboratory, Research Subdivision, School of Medicine, Universidad Panamericana, Donatello 43, Mexico City 03910, Mexico
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(9), 1980; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18091980
Received: 20 July 2017 / Revised: 24 August 2017 / Accepted: 13 September 2017 / Published: 16 September 2017
(This article belongs to the Special Issue Nutraceuticals in Human Health and Disease)
Recent studies suggest that allicin may play a role in chronic kidney disease (CKD), reducing hypertension and oxidative stress and improving renal dysfunction. In the present study, CKD was induced by 5/6 nephrectomy and the animals were divided into four treatment groups as follows: control (C), CKD, CKD+allicin (40 mg/kg pathway oral) (CKDA), and CKD+Losartan (20 mg/kg) (CKDL). After CKD induction, the rats developed hypertension from week 3 to the end of the study. This was associated with increased creatinine and blood urea nitrogen (BUN) levels in serum, increased albuminuria, increased urinary excretion of N-acetyl-β-d-glucosaminidase (NAG), increased nephrin expression, and incrased histological alterations in the cortex. The levels of angiotensin receptors and endothelial nitric oxide synthase (eNOS) were decreased in the renal cortex from the CKD group. Otherwise, lipid and protein oxidation were higher in the CKD group than in the control group. A disturbance was observed in the expression levels of the nuclear factor erythroid 2-related factor 2/Kelch ECH associating protein 1 system (Nrf2/keap1) and the antioxidant enzymes catalase, superoxide dismutase, and heme oxygenase-1. Allicin or losartan treatments relieved renal dysfunction, hypertension, and oxidative stress. In addition, both treatments showed the same efficacy on the expression of angiotensin receptors, the nephrin, Nrf2/keap1 pathway, and eNOS. Further in silico analyses suggest that allicin and losartan could have a common mechanism involving interaction with AT1 receptors. Allicin showed antihypertensive, antioxidant, and nephroprotective effects. The beneficial effects showed by allicin are similar, or even better, than those of losartan. In fact, the effect of allicin on blood pressure and renal function is comparable to reductions seen with losartan, a prescription drug commonly used as a first-line therapy. View Full-Text
Keywords: allicin; hypertension; chronic kidney disease; oxidative stress; losartan allicin; hypertension; chronic kidney disease; oxidative stress; losartan
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MDPI and ACS Style

García Trejo, E.M.Á.; Arellano Buendía, A.S.; Sánchez Reyes, O.; García Arroyo, F.E.; Arguello García, R.; Loredo Mendoza, M.L.; Tapia, E.; Sánchez Lozada, L.G.; Osorio Alonso, H. The Beneficial Effects of Allicin in Chronic Kidney Disease Are Comparable to Losartan. Int. J. Mol. Sci. 2017, 18, 1980. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18091980

AMA Style

García Trejo EMÁ, Arellano Buendía AS, Sánchez Reyes O, García Arroyo FE, Arguello García R, Loredo Mendoza ML, Tapia E, Sánchez Lozada LG, Osorio Alonso H. The Beneficial Effects of Allicin in Chronic Kidney Disease Are Comparable to Losartan. International Journal of Molecular Sciences. 2017; 18(9):1980. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18091980

Chicago/Turabian Style

García Trejo, Ehécatl M.Á., Abraham S. Arellano Buendía, Omegar Sánchez Reyes, Fernando E. García Arroyo, Raúl Arguello García, María L. Loredo Mendoza, Edilia Tapia, Laura G. Sánchez Lozada, and Horacio Osorio Alonso. 2017. "The Beneficial Effects of Allicin in Chronic Kidney Disease Are Comparable to Losartan" International Journal of Molecular Sciences 18, no. 9: 1980. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18091980

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