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Low-protein diet supplemented with ketoacids reduces the severity of renal disease in 5/6 nephrectomized rats: A role for KLF15

  • Xiang Gao
  • , Lianghu Huang
  • , Fabrizio Grosjean
  • , Vittoria Esposito
  • , Jianxiang Wu
  • , Lili Fu
  • , Huimin Hu
  • , Jiangming Tan
  • , Cijian He
  • , Susan Gray
  • , Mukesh K. Jain
  • , Feng Zheng*
  • , Changlin Mei
  • *此作品的通讯作者
  • Changzheng Hospital
  • Dongfang Hospital
  • Icahn School of Medicine at Mount Sinai
  • University of Massachusetts Medical School
  • Case Western Reserve University

科研成果: 期刊稿件文章同行评审

摘要

Dietary protein restriction is an important treatment for chronic kidney disease. Herein, we tested the effect of low-protein or low-protein plus ketoacids (KA) diet in a remnant kidney model. Rats with a remnant kidney were randomized to receive normal protein diet (22%), low-protein (6%) diet (LPD), or low-protein (5%) plus KA (1%) diet for 6 months. Protein restriction prevented proteinuria, decreased blood urea nitrogen levels, and renal lesions; however, the LPD retarded growth and decreased serum albumin levels. Supplementation with KA corrected these abnormalities and provided superior renal protection compared with protein restriction alone. The levels of Kruppel-like factor-15 (KLF15), a transcription factor shown to reduce cardiac fibrosis, were decreased in remnant kidneys. Protein restriction, which increased KLF15 levels in the normal kidney, partially recovered the levels of KLF15 in remnant kidney. The expression of KLF15 in mesangial cells was repressed by oxidative stress, transforming growth factor-Β, and tumor necrosis factor (TNF)-α. The suppressive effect of TNF-α on KLF15 expression was mediated by TNF receptor-1 and nuclear factor-B. Overexpression of KLF15 in mesangial and HEK293 cells significantly decreased fibronectin and type IV collagen mRNA levels. Furthermore, KLF15 knockout mice developed glomerulosclerosis following uninephrectomy. Thus, KLF15 may be an antifibrotic factor in the kidney, and its decreased expression may contribute to the progression of kidney disease.

源语言英语
页(从-至)987-996
页数10
期刊Kidney International
79
9
DOI
出版状态已出版 - 5月 2011
已对外发布

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