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[普萘洛尔和氟索洛尔对大鼠心室心肌溶酶体酶活性的影响]

[The effect of propranolol and flusoxolol on the lysosomal enzyme activity of the rat ventricular myocardium].

作者信息

Sysoliatina N A

出版信息

Eksp Klin Farmakol. 1992 Sep-Oct;55(5):33-6.

PMID:1363945
Abstract

The nonselective beta-blocker propranolol and the selective beta 1-adrenoblocker flusoxolol were tested for their effects on the activities of acid phosphatase, acid DNAase, cathepsin D, beta-glucosidase and beta-galactosidase in intact rat ventricular myocardial homogenates. The two drugs were found to have the most noticeable effect on the activity of three enzymes under study: acid phosphatase, beta-glucosidase and beta-galactosidase. They were able to stabilize lysosomal membranes during long-term homogenate preincubation at 37 degrees S. It is suggested that the mechanism of action of the drugs on intact rat ventricular myocardial lysosomes under the conditions of the study involves the binding of both propranolol and flusoxolol to beta-adrenoceptors on the lysosomes.

摘要

对非选择性β受体阻滞剂普萘洛尔和选择性β1肾上腺素能阻滞剂氟索洛尔进行了测试,观察它们对完整大鼠心室肌匀浆中酸性磷酸酶、酸性脱氧核糖核酸酶、组织蛋白酶D、β-葡萄糖苷酶和β-半乳糖苷酶活性的影响。发现这两种药物对所研究的三种酶的活性影响最为显著:酸性磷酸酶、β-葡萄糖苷酶和β-半乳糖苷酶。在37摄氏度下对匀浆进行长期预温育时,它们能够稳定溶酶体膜。提示在本研究条件下,药物对完整大鼠心室肌溶酶体的作用机制涉及普萘洛尔和氟索洛尔与溶酶体上的β肾上腺素能受体结合。

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