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血管紧张素转换酶抑制剂和钙拮抗剂对右心室肥厚大鼠蛋白质代谢的不同影响。

Different effects of an angiotensin converting enzyme inhibitor and a calcium antagonist on protein metabolism in rats with right ventricular hypertrophy.

作者信息

Tanaka K, Honda M, Kuramochi T, Hashimoto M, Masumura S, Mansoor A M, Ishikawa S, Morioka S

机构信息

4th Department of Internal Medicine, Shimane Medical University, Izumo, Japan.

出版信息

J Hypertens. 1994 Oct;12(10):1147-54.

PMID:7836730
Abstract

OBJECTIVE

We examined the effects of a calcium antagonist and an angiotensin converting enzyme (ACE) inhibitor on contractile and non-contractile protein metabolism and cardiac function in a monocrotaline-induced right ventricular hypertrophy model, in order to define the effects of these drugs on cardiac hypertrophy.

METHODS

One week after monocrotaline injection, male Sprague-Dawley rats were given either a calcium antagonist (nilvadipine; 3 mg/kg per day) or an ACE inhibitor (delapril-HCl; 30 mg/kg per day) for 2 weeks. Right ventricular pressure, the right ventricle: (left ventricle + interventricular septum) ratio, myosin isoenzymes, collagen concentration, collagen types and contractility of right ventricular free wall were examined.

RESULTS

In untreated rats significant monocrotaline-induced right ventricular hypertrophy with an increase in the proportion of collagen types III and V was observed. There were no significant changes in collagen concentration. Both drugs reduced right ventricular pressure to the same degree and decreased right ventricular hypertrophy. However, the inhibitory effect of delapril on right ventricular hypertrophy was stronger than that of nilvadipine. Nilvadipine reduced the collagen concentration and reversed changes in collagen types, whereas delapril did not have any significant effect on collagen concentration or collagen types. Cardiac contractility was improved by delapril, but not by nilvadipine.

CONCLUSIONS

The results show that a calcium antagonist disproportionately inhibited contractile and non-contractile protein metabolism, whereas an ACE inhibitor proportionally inhibited them and improved cardiac function in a model of right ventricular hypertrophy. The improvement in cardiac function may be due partly to the proportional inhibition of contractile and non-contractile proteins elicited by an ACE inhibitor.

摘要

目的

我们在一种由野百合碱诱导的右心室肥大模型中,研究了一种钙拮抗剂和一种血管紧张素转换酶(ACE)抑制剂对收缩和非收缩蛋白代谢以及心脏功能的影响,以明确这些药物对心脏肥大的作用。

方法

在注射野百合碱一周后,给雄性斯普拉格 - 道利大鼠给予钙拮抗剂(尼伐地平;每天3毫克/千克)或ACE抑制剂(盐酸地拉普利;每天30毫克/千克),持续2周。检测右心室压力、右心室:(左心室 + 室间隔)比值、肌球蛋白同工酶、胶原蛋白浓度、胶原蛋白类型以及右心室游离壁的收缩性。

结果

在未治疗的大鼠中,观察到显著的野百合碱诱导的右心室肥大,且III型和V型胶原蛋白的比例增加。胶原蛋白浓度无显著变化。两种药物均使右心室压力降低至相同程度,并减轻了右心室肥大。然而,地拉普利对右心室肥大的抑制作用强于尼伐地平。尼伐地平降低了胶原蛋白浓度并逆转了胶原蛋白类型的变化,而地拉普利对胶原蛋白浓度或胶原蛋白类型没有任何显著影响。地拉普利改善了心脏收缩性,但尼伐地平没有。

结论

结果表明,在右心室肥大模型中,钙拮抗剂对收缩和非收缩蛋白代谢的抑制不成比例,而ACE抑制剂则成比例地抑制它们并改善了心脏功能。心脏功能的改善可能部分归因于ACE抑制剂对收缩和非收缩蛋白的成比例抑制。

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