Renal Protective Effect of Sirtuin 1

نویسندگان

  • Yi-jun Dong
  • Nian Liu
  • Zhi Xiao
  • Tao Sun
  • Shu-hui Wu
  • Wei-xia Sun
  • Zhong-gao Xu
  • Hang Yuan
چکیده

Silent information regulator 2 (Sir2) is a nicotinamide adenine dinucleotide- (NAD(+)-) dependent deacetylase. The homology of SIRT1 and Sir2 has been extensively studied. SIRT1 deacetylates target proteins using the coenzyme NAD(+) and is therefore linked to cellular energy metabolism and the redox state through multiple signalling and survival pathways. During the past decade, investigators have reported that SIRT1 activity is essential in cancer, neurodegenerative diseases, diabetes, cardiovascular disease, and other age-related diseases. In the kidneys, SIRT1 may inhibit renal cell apoptosis, inflammation, and fibrosis. Therefore its activation may also become a new therapeutic target in the patients with chronic kidney disease including diabetic nephropathy. In this paper, we would like to review the protective functions of sirtuins and the role of SIRT1 in the onset of kidney disease based on previous studies, including diabetic nephropathy, acute renal injury, chronic kidney disease as well as lupus nephritis.

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Sirtuin is a nicotinamide adenine dinucleotide-dependent deacetylase. One of its isoforms, Sirt1, is a key molecule in glucose, lipid, and energy metabolism. The renal protective effects of Sirt1 are found in various models of renal disorders with metabolic impairment, such as diabetic nephropathy. Protective effects include the maintenance of glomerular barrier function, anti-fibrosis effects,...

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Comment on “Renal Protective Effect of Sirtuin 1”

I read the review article written by Dong et al. [1] regarding the renal effects of sirtuin 1 with great interest. The authors described the harmful effects of advanced glycation endproducts on podocyte apoptosis via increasing Bcl-2 protein secondary to forkhead box O4 (FOXO4) acetylation in diabetes mellitus according toChung et al.’ findings.However, Chuang et al. [2] demonstrated that the a...

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عنوان ژورنال:

دوره 2014  شماره 

صفحات  -

تاریخ انتشار 2014