کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8259785 | 1534645 | 2015 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Apelin protects against acute renal injury by inhibiting TGF-β1
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کلمات کلیدی
PARP-1AKIICAM-1HDACMCP-1TGF-β1hypoxia/reperfusionHMTs2K1CATNH/R - H / RHDMs - HDM هاI/R - I / Racute kidney injury - آسیب حاد کلیهischemia/reperfusion - ایسکمی / رپرفیوژنApelin - درخواستAcute tubular necrosis - نکروز لوله ای حادHistone acetyltransferase - هیستون استیل ترانسفرازhistone deacetylase - هیستون داستیلازhistone methyltransferases - هیستون متیل ترانسفرازهاHistone methylation - هیستون متیلاسیونMonocyte chemotactic protein-1 - پروتئین chemotactic monocyte-1Poly(ADP-ribose) polymerase-1 - پلی (ADP-ribose) پلیمراز-1HAT - کلاه
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
سالمندی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Renal ischemia/reperfusion (I/R) injury is the most common cause of acute kidney injury, having a high rate of mortality and no effective therapy currently available. Apelin-13, a bioactive peptide, has been shown to inhibit the early lesions of diabetic nephropathy in several mouse models by us and others. To test whether apelin-13 protects against renal I/R induced injury, male rats were exposed to renal I/R injury with or without apelin-13 treatment for 3 days. Apelin-13 treatment markedly reduced the injury-induced tubular lesions, renal cell apoptosis, and normalized the injury induced renal dysfunction. Apelin-13 treatment inhibited the injury-induced elevation of inflammatory factors and Tgf-β1, as well as apoptosis. Apelin-13 treatment also inhibited the injury-induced elevation of histone methylation and Kmt2d, a histone methyltransferase of H3K4me2, following renal I/R injury. Furthermore, in cultured renal mesangial and tubular cells, apelin-13 suppressed the injury-induced elevation of Tgf-β1, apoptosis, H3K4me2 and Kmt2d under the in vitro hypoxia/reperfusion (H/R) conditions. Consistently, over-expression of apelin significantly inhibited H/R-induced elevation of TGF-β1, apoptosis, H3K4me2 and Kmt2d. The present study therefore suggests apelin-13 may be a therapeutic candidate for treating acute kidney injury.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1852, Issue 7, July 2015, Pages 1278-1287
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1852, Issue 7, July 2015, Pages 1278-1287
نویسندگان
Hong Chen, Danyang Wan, Lin Wang, Anlin Peng, Hongdou Xiao, Robert B. Petersen, Chengyu Liu, Ling Zheng, Kun Huang,