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两性霉素B对大鼠心脏肌浆网膜ATP酶活性的体外抑制作用及其被1,6 - 二磷酸果糖逆转的作用

In vitro inhibition of rat heart sarcoplasmic reticular membrane ATPase activities by amphotericin B and their reversal by fructose-1,6-diphosphate.

作者信息

Rao M R, Hutcheson A E, Markov A K

机构信息

Department of Medicine, University of Mississippi Medical Center, Jackson 39216, USA.

出版信息

Biochem Mol Biol Int. 1995 Nov;37(5):821-5.

PMID:8624486
Abstract

The effect of amphotericin B on rat heart sarcoplasmic reticular membrane Na(+)-K+ and Ca2+ ATPase activities in vitro was investigated. Amphotericin B in selected concentrations of 100-1000 ng significantly inhibited the sarcoplasmic reticular membrane ATPase activities studied. Fructose-1,6-diphosphate (1000 microM concentration) completely reversed the inhibition of Ca2+ ATPase activity in particular, but failed to reverse that of Na+(-)K+ATPase activities at 1000 microM concentration. Fructose-1,6-diphosphate may afford some protection against 1000 ng amphotericin B-induced myocardial toxicity. These damages may vary depending upon the dose of amphotericin B used in experimental studies.

摘要

研究了两性霉素B对大鼠心脏肌浆网膜Na(+)-K+和Ca2+ ATP酶活性的体外作用。选定浓度为100 - 1000 ng的两性霉素B显著抑制了所研究的肌浆网膜ATP酶活性。尤其是1000微摩尔浓度的1,6-二磷酸果糖完全逆转了Ca2+ ATP酶活性的抑制作用,但在1000微摩尔浓度时未能逆转Na+(-)K+ATP酶活性的抑制作用。1,6-二磷酸果糖可能对1000 ng两性霉素B诱导的心肌毒性提供一定的保护作用。这些损伤可能因实验研究中使用的两性霉素B剂量不同而有所差异。

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In vitro induction of nitric oxide by fructose-1,6-diphosphate in the cardiovascular system of rats.1,6-二磷酸果糖在大鼠心血管系统中对一氧化氮的体外诱导作用。
Mol Cell Biochem. 1998 Aug;185(1-2):171-5. doi: 10.1023/a:1006840802595.