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大鼠脑中前列腺素合成的抑制

Inhibition of prostaglandin synthesis in rat brain.

作者信息

Abdel-Halim M S, Sjöquist B, Anggård E

出版信息

Acta Pharmacol Toxicol (Copenh). 1978 Oct;43(4):266-72. doi: 10.1111/j.1600-0773.1978.tb02264.x.

Abstract

Rats were injected with one of five drugs alleged to inhibit brain prostaglandin (PG) synthesis: indomethacin, diclofenac, naproxen, aspiring and paracetamol. Animals were killed after 30 min. and the endogenous formation of PGF2alpha and PGE2 in brain homogenates was measured by mass fragmentography using deuterium labelled PGF2alpha and PGE2 as internal standards. Diclofenac, indomethacin, and naproxen inhibited dose dependently, the synthesis of PGF2alpha. The ED50 for diclofenac was 0.4 mg/kg, for indomethacin 1 mg/kg and for naproxen 2 mg/kg. In equieffective doses indomethacin had the longest duration. The time taken for the inhibition to decline to half its maximal value was 32 hrs for indomethacin and about 15 hrs for diclofenac and naproxen. Under the present conditions aspirin and paracetamol failed to produce significant reduction of PG synthesis in the rat brain homogenates in doses up to 100 mg/kg.

摘要

给大鼠注射五种据称能抑制脑前列腺素(PG)合成的药物之一:吲哚美辛、双氯芬酸、萘普生、阿司匹林和对乙酰氨基酚。30分钟后处死动物,以氘标记的PGF2α和PGE2作为内标,采用质量碎片分析法测定脑匀浆中PGF2α和PGE2的内源性生成。双氯芬酸、吲哚美辛和萘普生剂量依赖性地抑制PGF2α的合成。双氯芬酸的半数有效剂量(ED50)为0.4毫克/千克,吲哚美辛为1毫克/千克,萘普生为2毫克/千克。在等效剂量下,吲哚美辛的作用持续时间最长。吲哚美辛抑制作用降至最大值一半所需的时间为32小时,双氯芬酸和萘普生约为15小时。在目前条件下,剂量高达100毫克/千克时,阿司匹林和对乙酰氨基酚未能使大鼠脑匀浆中的PG合成显著减少。

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