期刊
CLINICAL SCIENCE
卷 116, 期 1-2, 页码 61-70出版社
PORTLAND PRESS LTD
DOI: 10.1042/CS20080039
关键词
blood pressure; diabetes; eicosanoid; inflammation; nephropathy; soluble epoxide hydrolase
资金
- AHA (American Heart Association)
- NIH (National Institutes of Health) [HL-59699, HL-74167]
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL059699, R29HL059699, P01HL074167] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P01DK038226] Funding Source: NIH RePORTER
Hypertension and Type 2 diabetes are co-morbid diseases that lead to the development of nephropathy. sEH (soluble epoxide hydrolase) inhibitors are reported to provide protection from renal injury. We hypothesized that the sEH inhibitor AUDA [12-(3-adamantan-I-yl-ureido)-dodecanoic acid] protects the kidney from the development of nephropathy associated with hypertension and Type 2 diabetes. Hypertension was induced in spontaneously diabetic GK (Goto-Kakizaki) rats using Angll (angiotensin II) and a high-salt diet. Hypertensive GK rats were treated for 2 weeks with either AUDA or its vehicle added to drinking water. MAP (mean arterial pressure) increased from 118 +/- 2 mmHg to 182 +/- 20 and 187 +/- 6 mmHg for vehicle and AUDA-treated hypertensive GK rats respectively. AUDA treatment did not alter blood glucose. Hypertension in GK rats resulted in a 17-fold increase in urinary albumin excretion, which was decreased with AUDA treatment. Renal histological evaluation determined that AUDA treatment decreased glomerular and tubular damage. In addition, AUDA treatment attenuated macrophage infiltration and inhibited urinary excretion of MCP-I (monocyte chemoattractant protein-I) and kidney cortex MCP-I gene expression. Taken together, these results provide evidence that sEH inhibition with AUDA attenuates the progression of renal damage associated with hypertension and Type 2 diabetes.
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