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10.1159/000490338

http://scihub22266oqcxt.onion/10.1159/000490338
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C6065105!6065105!29870982
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suck abstract from ncbi


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pmid29870982      Kidney+Blood+Press+Res 2018 ; 43 (3): 904-13
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  • Tempol Protects Against Acute Renal Injury by Regulating PI3K/Akt/mTOR and GSK3? Signaling Cascades and Afferent Arteriolar Activity #MMPMID29870982
  • Zhang G; Wang Q; Wang W; Yu M; Zhang S; Xu N; Zhou S; Cao X; Fu X; Ma Z; Liu R; Mao J; Lai EY
  • Kidney Blood Press Res 2018[]; 43 (3): 904-13 PMID29870982show ga
  • Background/Aims:: Free radical scavenger tempol is a protective antioxidant against ischemic injury. Tubular epithelial apoptosis is one of the main changes in the renal ischemia/reperfusion (I/R) injury. Meanwhile some proteins related with apoptosis and inflammation are also involved in renal I/R injury. We tested the hypothesis that tempol protects against renal I/R injury by activating protein kinase B/mammalian target of rapamycin (PKB, Akt/mTOR) and glycogen synthase kinase 3? (GSK3?) pathways as well as the coordinating apoptosis and inflammation related proteins. Methods:: The right renal pedicle of C57Bl/6 mouse was clamped for 30 minutes and the left kidney was removed in the study. The renal injury was assessed with serum parameters by an automatic chemistry analyzer. Renal expressions of Akt/mTOR and GSK3? pathways were measured by western blot in I/R mice treated with saline or tempol (50mg/kg) and compared with sham-operated mice. Results:: The levels of blood urea nitrogen (BUN), creatinine and superoxide anion (O2.-) increased, and superoxide dismutase (SOD) and catalase (CAT) decreased significantly after renal I/R injury. However, tempol treatment prevented the changes. Besides, I/R injury reduced renal expression of p-Akt, p-GSK3?, p-mTOR, Bcl2 and increased NF-?B, p-JNK and p53 in kidney, tempol significantly normalized these changes. In addition, renal I/R injury reduced the response of afferent arteriole to Angiotensin II (Ang II), while tempol treatment improved the activity of afferent arteriole. Conclusion:: Tempol attenuates renal I/R injury. The protective mechanisms seem to relate with activation of PI3K/Akt/mTOR and GSK3? pathways, inhibition of cellular damage markers and inflammation factors, as well as improvement of afferent arteriolar activity.
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