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氯霉素的肌肉松弛特性。

Muscle relaxant properties of chloramphenicol.

作者信息

Banerjee S, Mitra C

出版信息

J Pharm Sci. 1976 May;65(5):704-8. doi: 10.1002/jps.2600650519.

Abstract

Experiments with the guinea pig ileum, guinea pig trachea, rat fundal strip, rat colon, rat vas deferens, and toad heart indicated that chloramphenicol inhibited smooth muscles, decreasing both the height and frequency of spontaneous contraction. Chloramphenicol-induced relaxation was not mediated through adrenergic, cholinergic, or histaminergic mechanisms. The degree of muscle relaxation was related to the concentration of chloramphenicol, and the relaxant effect could be reversed by removing chloramphenicol from site of action by washing. Its action appears to be direct on the muscle, possibly by interfering with the energy-generating mechanism.

摘要

对豚鼠回肠、豚鼠气管、大鼠胃底条、大鼠结肠、大鼠输精管和蟾蜍心脏进行的实验表明,氯霉素可抑制平滑肌,降低自发收缩的高度和频率。氯霉素诱导的松弛不是通过肾上腺素能、胆碱能或组胺能机制介导的。肌肉松弛程度与氯霉素浓度有关,通过冲洗从作用部位去除氯霉素可逆转松弛作用。其作用似乎是直接作用于肌肉,可能是通过干扰能量产生机制。

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