Key result
Benidipine improves renal antioxidant activity, albuminuria, and creatinine clearance in hypertensive rats.
Why the study?
The effects of benidipine hydrochloride or triple therapy on renal cortical and medullary intrinsic antioxidant enzyme activity in stroke-prone spontaneously hypertensive rats required evaluation.
Answers are grounded in this paper and cite their sources.
Suggests antioxidant renoprotection in hypertensive rat models; leaves open human translation.
Effects of benidipine hydrochloride or triple therapy (hydralazine, reserpine, and hydrochlorothiazide) on renal cortical and medullary intrinsic antioxidant enzyme (AOE) activity were evaluated in stroke-prone spontaneously hypertensive rats (SHR-SP) as an animal model for human essential hypertension with cerebral stroke. This study showed a significant decrease of renal intrinsic glutathione peroxidase (GSH-Px) activity in untreated SHR-SP. Renal GSH-Px activity in untreated SHR-SP was significantly lower than that in Wister Kyoto rats (WKY) as a normotensive reference strain. GSH-Px activity in SHR-SP was significantly improved after benidipine hydrochloride therapy. Levels of urinary albumin excretion or creatinine clearance (Ccr) in SHR-SP were also improved after the therapy. Glomerular sclerosis index was slightly improved in SHR-SP treated with benidipine hydrochloride according to light microscopic analysis. It appears that hypertension may influence the renal intrinsic GSH-Px activity, albuminuria, and Ccr in SHR-SP. Thus it is indicated that control of blood pressure may improve the GSH-Px activity in SHR-SP.
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Shou et al. (1997) studied Hypertension with cerebral stroke (stroke-prone spontaneously hypertensive rats model). Benidipine hydrochloride vs. Triple therapy (hydralazine, reserpine, and hydrochlorothiazide), untreated SHR-SP, and normotensive WKY rats was evaluated on Renal cortical and medullary intrinsic antioxidant enzyme (AOE) activity, specifically glutathione peroxidase (GSH-Px) activity. Benidipine hydrochloride significantly improved renal intrinsic glutathione peroxidase activity, urinary albumin excretion, and creatinine clearance in stroke-prone spontaneously hypertensive rats.
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