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黄嘌呤氧化酶抑制剂别嘌醇对高胆固醇血症诱导的高血压大鼠肾损伤的影响。

Effects of allopurinol, a xanthine oxidase inhibitor, on renal injury in hypercholesterolemia-induced hypertensive rats.

作者信息

Minami Mayumi, Ishiyama Akihiro, Takagi Masao, Omata Masao, Atarashi Keiichiro

机构信息

Department of Nephrology and Endocrinology, The University of Tokyo, Tokyo Metropolitan Police Hospital, Tokyo, Japan. mayuminami@ aol.com

出版信息

Blood Press. 2005;14(2):120-5. doi: 10.1080/08037050510008878.

Abstract

To investigate if increased lipid peroxidation is involved in hypercholesterolemia-induced hypertension and renal injury, we examined the effects of allopurinol, a xanthine oxidase inhibitor, on these conditions. Groups of male Sprague--Dawley rats were fed for 8 weeks with a high-cholesterol diet (4% cholesterol), a high-cholesterol plus allopurinol (10 mg/kgBW/day) diet or a normal diet. Systolic blood pressure (SBP), serum lipids, uric acid (UA) and malondialdehyde (MDA) as a measure of lipid peroxides, and urinary excretion of protein (UP) were measured after 0, 4 and 8 weeks. Urinary excretion of nitrite plus nitrate (UNOx) and iron (UFe), and MDA in the kidney were measured after 8 weeks. The renal injury was evaluated by the glomerular sclerosis score (SS). The high-cholesterol diet increased SBP, serum total cholesterol and UA, MDA in the serum and kidney, UP, UNOx, UFe and SS. Allopurinol ameliorated cholesterol-induced elevation in serum UA, MDA in the serum and kidney, UP, UNOx, UFe and SS, but did not affect SBP. Hence, our results suggest that lipid peroxidation may be involved in hypercholesterolemia-induced renal injury, and that suppression of lipid peroxidation can reduce such injury.

摘要

为了研究脂质过氧化增加是否参与高胆固醇血症诱导的高血压和肾损伤,我们检测了黄嘌呤氧化酶抑制剂别嘌呤醇对这些情况的影响。将雄性斯普拉格-道利大鼠分为几组,分别用高胆固醇饮食(4%胆固醇)、高胆固醇加别嘌呤醇(10毫克/千克体重/天)饮食或正常饮食喂养8周。在0、4和8周后测量收缩压(SBP)、血脂、尿酸(UA)和作为脂质过氧化物指标的丙二醛(MDA),以及尿蛋白排泄量(UP)。在8周后测量尿中亚硝酸盐加硝酸盐排泄量(UNOx)和铁排泄量(UFe)以及肾脏中的MDA。通过肾小球硬化评分(SS)评估肾损伤。高胆固醇饮食使SBP、血清总胆固醇和UA、血清和肾脏中的MDA、UP、UNOx、UFe和SS升高。别嘌呤醇改善了胆固醇诱导的血清UA、血清和肾脏中的MDA、UP、UNOx、UFe和SS升高,但不影响SBP。因此,我们的结果表明脂质过氧化可能参与高胆固醇血症诱导的肾损伤,并且抑制脂质过氧化可以减轻这种损伤。

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