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蜂毒肽对豚鼠子宫前列腺素生成的影响。

Effect of melittin on prostaglandin production by guinea-pig uterus.

作者信息

Johnson F A, Poyser N L

机构信息

Department of Pharmacology, University of Edinburgh Medical School, UK.

出版信息

J Reprod Fertil. 1991 Nov;93(2):577-83. doi: 10.1530/jrf.0.0930577.

DOI:10.1530/jrf.0.0930577
PMID:1787478
Abstract

Melittin, an activator of phospholipase (PL) A-2, increased the outputs of prostaglandin (PG) F-2 alpha and 6-keto-PGF-1 alpha, but not of PGE-2, from Day-7 guinea-pig uterus superfused in vitro. Reducing the extracellular calcium concentration (by omitting calcium chloride from the superfusing fluid) partially inhibited the stimulatory effect of melittin on uterine PG production. TMB-8 (an intracellular calcium antagonist) completely prevented the stimulation of PGF-2 alpha and 6-keto-PGF-1 alpha output by melittin, although the production of both PGs tended to increase after stopping the melittin and TMB-8 treatments. TMB-8 also inhibited the increases in outputs of PGF-2 alpha, 6-keto-PGF-1 alpha and PGE-2 and prevented contraction of the uterus induced by exogenous PLA-2. Trifluoperazine (a calmodulin antagonist) had no inhibitory effect on the increases in outputs of PGF-2 alpha and 6-keto-PGF-1 alpha produced by melittin; it potentiated the stimulatory effect of melittin on 6-keto-PGF-1 alpha output and allowed melittin to increase PGE-2 output. When melittin was applied twice to the superfused uterus with an interval of 1 h between each treatment, partial refractoriness of the responses to melittin was seen: the magnitudes of the increases in PGF-2 alpha and 6-keto-PGF-1 alpha outputs were 40-50% less after the second treatment than after the first treatment. These results show that melittin stimulates the synthesis of PGF-2 alpha and PGI-2 (measured as 6-keto-PGF-1 alpha) in guinea-pig uterus by mechanisms which are calcium dependent.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

蜂毒肽是磷脂酶(PL)A - 2的激活剂,可增加体外灌流的孕7天豚鼠子宫中前列腺素(PG)F - 2α和6 - 酮 - PGF - 1α的释放量,但不增加PGE - 2的释放量。降低细胞外钙浓度(通过从灌流液中省略氯化钙)可部分抑制蜂毒肽对子宫PG生成的刺激作用。TMB - 8(一种细胞内钙拮抗剂)完全阻止了蜂毒肽对PGF - 2α和6 - 酮 - PGF - 1α释放的刺激,尽管在停止蜂毒肽和TMB - 8处理后,两种PG的生成量仍有增加的趋势。TMB - 8还抑制了PGF - 2α、6 - 酮 - PGF - 1α和PGE - 2释放量的增加,并阻止了外源性PLA - 2诱导的子宫收缩。三氟拉嗪(一种钙调蛋白拮抗剂)对蜂毒肽引起的PGF - 2α和6 - 酮 - PGF - 1α释放量增加没有抑制作用;它增强了蜂毒肽对6 - 酮 - PGF - 1α释放的刺激作用,并使蜂毒肽增加了PGE - 2的释放量。当对灌流的子宫两次应用蜂毒肽,每次处理间隔1小时时,可观察到对蜂毒肽反应的部分不应性:第二次处理后PGF - 2α和6 - 酮 - PGF - 1α释放量增加的幅度比第一次处理后少40 - 50%。这些结果表明,蜂毒肽通过钙依赖性机制刺激豚鼠子宫中PGF - 2α和PGI - 2(以6 - 酮 - PGF - 1α衡量)的合成。(摘要截短于250字)

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引用本文的文献

1
The effect of caffeine on prostaglandin output from the guinea-pig uterus.咖啡因对豚鼠子宫前列腺素分泌的影响。
Br J Pharmacol. 1994 Sep;113(1):103-10. doi: 10.1111/j.1476-5381.1994.tb16180.x.