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非甾体抗炎药芬司匹利对雪貂气管体外神经源性黏液分泌的影响。

Effect of fenspiride, a non-steroidal antiinflammatory agent, on neurogenic mucus secretion in ferret trachea in vitro.

作者信息

Khawaja A M, Liu Y C, Rogers D F

机构信息

Thoracic Medicine, National Heart & Lung Institute (Imperial College), Dovehouse Street, London, UK.

出版信息

Pulm Pharmacol Ther. 1999;12(6):363-8. doi: 10.1006/pupt.1999.0221.

Abstract

Neural mechanisms contribute to control of mucus secretion in the airways. Fenspiride is a non-steroidal antiinflammatory agent which has a variety of actions, including inhibition of neurogenic bronchoconstriction. The effect of fenspiride on neurally-mediated mucus secretion was investigated in vitro in electrically-stimulated ferret trachea, using(35)SO(4)as a mucus marker. Cholinergic secretory responses were isolated using adrenoceptor and tachykinin receptor antagonists. Tachykinin responses were isolated using cholinoceptor and adrenoceptor antagonists. Electrical stimulation increased cholinergic secretion by;90% and tachykininergic secretion by;40%. Fenspiride (1 microM-1 mM) tended to inhibit cholinergic secretion in a concentration-dependent manner, although only at 1 mM was inhibition (by 87%) significant. Inhibition by fenspiride of tachykininergic secretion was not concentration-dependent, and again significant inhibition (by 85%) was only at 1 mM. Inhibition was not due to loss of tissue viability, as assessed by restitution of secretory response after washout. Fenspiride also inhibited secretion induced by acetylcholine, but did not inhibit substance P-induced secretion. Histamine receptor antagonists increased basal secretion by 164%, whereas fenspiride did not affect basal secretion. We conclude that, in ferret trachea in vitro, fenspiride inhibits neurally-mediated mucus secretion, with antimuscarinic action the most plausible mechanism of action, but not necessarily the only mechanism.

摘要

神经机制有助于控制气道中的黏液分泌。芬司匹利是一种具有多种作用的非甾体抗炎药,包括抑制神经源性支气管收缩。在体外,以(35)SO(4)作为黏液标记物,研究了芬司匹利对电刺激雪貂气管中神经介导的黏液分泌的影响。使用肾上腺素能受体和速激肽受体拮抗剂分离胆碱能分泌反应。使用胆碱能受体和肾上腺素能受体拮抗剂分离速激肽反应。电刺激使胆碱能分泌增加90%,速激肽能分泌增加40%。芬司匹利(1微摩尔/升-1毫摩尔/升)倾向于以浓度依赖的方式抑制胆碱能分泌,尽管只有在1毫摩尔/升时抑制作用(87%)才显著。芬司匹利对速激肽能分泌的抑制作用不依赖于浓度,同样只有在1毫摩尔/升时才有显著抑制作用(85%)。通过冲洗后分泌反应的恢复评估,抑制作用不是由于组织活力丧失。芬司匹利还抑制乙酰胆碱诱导的分泌,但不抑制P物质诱导的分泌。组胺受体拮抗剂使基础分泌增加164%,而芬司匹利不影响基础分泌。我们得出结论,在体外雪貂气管中,芬司匹利抑制神经介导的黏液分泌,抗毒蕈碱作用是最合理的作用机制,但不一定是唯一的机制。

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