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卡托普利对大鼠慢性嘌呤霉素氨基核苷肾病的影响。

Effect of captopril on chronic puromycin aminonucleoside nephrosis in rats.

作者信息

Radin M J, Wilke W L, Fettman M J

出版信息

Res Commun Chem Pathol Pharmacol. 1986 Nov;54(2):279-82.

PMID:3538253
Abstract

The effect of captopril, an angiotensin converting enzyme inhibitor, on the progression of chronic puromycin aminonucleoside (PAN) nephrosis was examined. Rats were injected with 15 mg/100 gm body weight PAN and 5 mg/100 gm body weight, on weeks - 1 and 5, respectively. A third group was injected with an equivalent volume of 0.9% saline, intraperitoneally (Group III) on week - 1 and 5. Beginning week 0, group I received 50 mg/kg captopril daily in the drinking water for 12 weeks. Group II received no treatment. Captopril failed to attenuate the peak level of proteinuria induced by the first injection of PAN or to alter the rate of decline of proteinuria when begun 1 week after the PAN injection. However, captopril did blunt the increase in urinary protein excretion following the second injection of PAN (p less than 0.05). Group II became hypertensive compared to Group I on week 8 and 12 and Group III on week 12 (p less than 0.05). Group I and II could not be distinguished on the basis of renal histologic rank (p = 0.80). We conclude that captopril affords some protection against the development of PAN-induced proteinuria, but it does not accelerate the recovery phase when glomerular permselectivity is being regained.

摘要

研究了血管紧张素转换酶抑制剂卡托普利对慢性嘌呤霉素氨基核苷(PAN)肾病进展的影响。大鼠分别在第-1周和第5周腹腔注射15mg/100g体重的PAN和5mg/100g体重的PAN。第三组在第-1周和第5周腹腔注射等量的0.9%生理盐水(第三组)。从第0周开始,第一组大鼠在饮水中每日给予50mg/kg卡托普利,持续12周。第二组未接受治疗。卡托普利未能减轻首次注射PAN诱导的蛋白尿峰值水平,也未能改变在PAN注射1周后开始给药时蛋白尿的下降速率。然而,卡托普利确实抑制了第二次注射PAN后尿蛋白排泄的增加(p<0.05)。与第一组相比,第二组在第8周和第12周以及与第三组在第12周时出现高血压(p<0.05)。根据肾脏组织学分级,第一组和第二组无法区分(p=0.80)。我们得出结论,卡托普利对PAN诱导的蛋白尿的发生有一定的保护作用,但在肾小球滤过选择性恢复时,它不会加速恢复阶段。

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