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非甾体抗炎药对豚鼠离体回肠胆碱能和组胺诱导收缩的影响。

The effects of non-steroidal anti-inflammatory drugs on cholinergic and histamine-induced contractions of guinea-pig isolated ileum.

作者信息

Famaey J P, Fontaine J, Reuse J

出版信息

Br J Pharmacol. 1977 Jun;60(2):165-71. doi: 10.1111/j.1476-5381.1977.tb07737.x.

Abstract

1 Eleven non-steroidal anti-inflammatory drugs (NSAID) reversibly inhibited contractions of the longitudinal muscle of the guinea pig isolated ileum induced by acetylcholine, histamine, electrical transmural stimulation and nicotine in this order of increasing potency. 2. After the addition of prostaglandins E1, E2 or F2alpha, with partially effective concentrations of NSAID (but not with higher concentrations which almost totally prevented the responses) the inhibitory effects of NSAID were reversibly lost, except for electrically induced contractions and prostaglandin F2alpha. 3 The effects of NSAID may be due to actions on biological membranes or on distribution of ions in addition to their inhibitory effect on prostaglandin synthesis. Prostaglandins may reverse the inhibition by non-selective sensitization of smooth muscle to various agonists.

摘要
  1. 11种非甾体抗炎药(NSAID)可依次以递增的效力可逆性抑制豚鼠离体回肠纵肌由乙酰胆碱、组胺、电透壁刺激和尼古丁诱导的收缩。2. 在加入前列腺素E1、E2或F2α后,对于部分有效浓度的NSAID(但不是几乎完全阻止反应的较高浓度),除电诱导收缩和前列腺素F2α外,NSAID的抑制作用可逆性丧失。3. NSAID的作用可能除了对前列腺素合成有抑制作用外,还归因于对生物膜的作用或离子分布的影响。前列腺素可能通过使平滑肌对各种激动剂非选择性敏感来逆转这种抑制作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61d0/1667402/d60b8bd25428/brjpharm00445-0009-a.jpg

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