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Effects of losartan on D-galactose on the protective effect of kidney
PAGE \* MERGEFORMAT 11
Effects of losartan on D-galactose on the protective effect of kidney
[Abstract] Objective To investigate the angiotensin receptor antagonist losartan on D-galactose on rat renal protective effect and possible mechanisms. Methods 36 rats were randomly divided into 3 groups: normal control group, aged model group and the losartan treatment group, 12 in each group. D-galactose preparation of continuous intraperitoneal injection of subacute aging rats. histologic examination of renal pathological changes detected by immunohistochemistry in renal tissue connective tissue growth factor ( CTGF), plasminogen activator inhibitor -1 (PAI-1) levels. Results Histological examination revealed glomerular volume increased in model group, sparse, varying degrees of focal segmental glomerulosclerosis tubular lumen to expand the kitchen shaped tubular atrophy, interstitial fibrosis; treatment changes in renal tissue compared with model group, eased. semiquantitative immunohistochemical analysis showed that the treatment group CTGF, PAI-1 levels compared with model group was significantly lower (P lt;0.05). Conclusion Losartan inhibits CTGF, PAI-1 expression and inhibit the accumulation of extracellular matrix to reduce the renal interstitial fibrosis, and thus reduce the aging, play renal protective effects.
[Keywords:] losartan; aging; connective tissue growth factor; plasminogen activator inhibitor -1
Kidney most important organ of the body, the aging effects on the body is important. At present the mechanisms of aging lead to kidney is not completely clear (1), a number of regulatory factors in the renin - angiotensin system (RAS) plays an important role . senescence and renal pathological changes are likely to increase urine protein and kidney-related increase in local angiotensin. losartan angiotensin (Ang ) receptor antagonist, could block Ang and its receptor combination of receptor antagonist from its biological effects, thereby red
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