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内源性类洋地黄钠钾ATP酶抑制剂与脑功能

Endogenous digitalis-like Na+, K+-ATPase inhibitors, and brain function.

作者信息

Lichtstein D, Rosen H

机构信息

Department of Physiology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Neurochem Res. 2001 Sep;26(8-9):971-8. doi: 10.1023/a:1012340702763.

Abstract

Digitalis-like compounds are recently identified steroids synthesized by the adrenal gland, which resemble the structure of plant cardiac glycosides. These compounds, like the plant steroids, bind to and inhibit the activity of the Na+, K+-ATPase. The possible function of the endogenous digitalis-like compounds has to be evaluated in view of the presence of different isoforms of the Na+, K+-ATPase, which differ in their sensitivity to digitalis. This review focuses on recent published data on the Na+, K+-ATPase inhibitors, the digitalis-like compounds, regarding their structure, biosynthesis and secretion from the adrenal gland, physiological role and pathological implications in diseases such as hypertension and depression. Emphasis is given to studies describing the involvement of these compounds in brain function.

摘要

洋地黄样化合物是最近发现的由肾上腺合成的类固醇,其结构类似于植物强心苷。这些化合物与植物类固醇一样,能结合并抑制Na +,K + -ATP酶的活性。鉴于存在对洋地黄敏感性不同的Na +,K + -ATP酶的不同同工型,必须对内源性洋地黄样化合物的可能功能进行评估。本综述重点关注最近发表的关于Na +,K + -ATP酶抑制剂(洋地黄样化合物)的结构、生物合成、从肾上腺的分泌、生理作用以及在高血压和抑郁症等疾病中的病理意义的数据。重点是描述这些化合物参与脑功能的研究。

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