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妊娠大鼠及经雌激素预处理大鼠胃中前列腺素E2的失活

Inactivation of prostaglandin E2 in the stomach of pregnant and oestrogen pretreated rats.

作者信息

Elegbe R A

出版信息

Biochem Exp Biol. 1978;14(1):69-76.

PMID:743485
Abstract

The stomach of pregnant and oestrogen pretreated female rats were found to inactivate significantly exogenous PGE2 when administered orally. The mean basal acid output of pregnant and oestrogen pretreated female rats were also diminished by oral infusion of PGE2. Though the exact mechanism for these phenomena cannot be readily seen from this work, it is suggested that metabolites of PGE2 may be responsible for the acid lowering and ulcer ameliorating effects of PGE2.

摘要

研究发现,怀孕及经雌激素预处理的雌性大鼠口服外源性前列腺素E2(PGE2)时,胃会使其显著失活。口服输注PGE2也会使怀孕及经雌激素预处理的雌性大鼠的基础胃酸分泌量减少。尽管从这项研究中无法直接看出这些现象的确切机制,但有人认为PGE2的代谢产物可能是PGE2降低胃酸及改善溃疡作用的原因。

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