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蜂毒明肽和MCD肽中枢给药后的神经毒性

Neurotoxicity of apamin and MCD peptide upon central application.

作者信息

Habermann E

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Nov;300(2):189-91. doi: 10.1007/BF00505050.

Abstract

Besides apamin, the structurally related MCD peptide (mast cell degranulating peptide; peptide 401) is another centrally acting peptide from bee venom. In contrast to apamin, it is hardly neurotoxic upon intravenous injection in mice. Following intraventricular injection, as little as 0.3 microgram/animal produce convulsions and respiratory arrest in mice. The clinical picture differs from that elicited by apamin, and apamin is about 10 times more potent than MCD peptide when given intraventricularly. Apamin and MCD peptide injected into the spinal cord of rats in nanogram amounts, produce circumscript hyperexcitation lasting more than one day, however with complete recovery following sublethal doses. Local apamin poisoning differs from local tetanus (elicited by the same way) by its faster time course.

摘要

除了蜂毒明肽外,结构相关的MCD肽(肥大细胞脱粒肽;肽401)是蜂毒中另一种作用于中枢的肽。与蜂毒明肽不同,它静脉注射到小鼠体内时几乎没有神经毒性。脑室内注射后,每只动物仅注射0.3微克就能使小鼠发生惊厥和呼吸停止。其临床表现与蜂毒明肽引起的不同,脑室内给药时,蜂毒明肽的效力约是MCD肽的10倍。以纳克量注射到大鼠脊髓中的蜂毒明肽和MCD肽,会产生持续超过一天的局限性过度兴奋,但亚致死剂量后可完全恢复。局部蜂毒明肽中毒与局部破伤风(以相同方式引发)在时间进程上有所不同,前者更快。

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