Conjugated linoleic acid rat pretreatment reduces renal damage in ischemia/reperfusion injury: Unraveling antiapoptotic mechanisms and regulation of phosphorylated mammalian target of rapamycin

Javedan, Gholamali; Shidfar, Farzad; Davoodi, Sayed Hossein; Ajami, Marjan; Gorjipour, Fazel; Sureda, Antoni; Nabavi, Seyed Mohammad; Daglia, Maria; Pazoki-Toroudi, Hamidreza

Abstract

Scope: Conjugated linoleic acids (CLAs) are dietary components with beneficial effects on human health. The aim of this study was to evaluate the potential benefits of CLA pretreatment in a rat model of renal ischemia/reperfusion injury (IRI). Methods and results: Animals were treated with CLAs (200 mg/kg/day) or water for two weeks prior to sham surgery or to surgery to induce IRI. Renal function, oxidative stress, apoptosis, and cell proliferation markers, were evaluated. Moreover, kidney sections were submitted to histological evaluation. IRI induced increased serum creatinine, blood urea nitrogen, fractional sodium excretion, malondialdehyde, Bax, and phosphorylated mammalian target of rapamycin (P-mTOR), and decreased clearance of creatine, superoxide dismutase and catalase activities, and Bax in comparison with control groups. CLA prefeeding restored, at least in part, the above reported markers to normal levels, increased the anti-apoptotic protein, B-cell lymphoma 2 (Bcl-2), and reduce the histological damage. Conclusion: The results suggest that the decreased renal tissue damage and improved renal function and oxidative stress, in rats pretreated with CLAs before renal IRI induction, could be associated with downregulation of Bax and P-mTOR, and upregulation of Bcl-2. CLAs pretreatment resulted to protect against IRI through the regulation of signaling pathways involved in apoptosis.

Más información

Título según WOS: ID WOS:000393156600013 Not found in local WOS DB
Título de la Revista: MOLECULAR NUTRITION & FOOD RESEARCH
Volumen: 60
Número: 12
Editorial: Wiley
Fecha de publicación: 2016
Página de inicio: 2665
Página final: 2677
DOI:

10.1002/mnfr.201600112

Notas: ISI