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μ-阿片受体调节豚鼠气道中的非胆碱能收缩神经。

Mu-opioid receptors modulate non-cholinergic constrictor nerves in guinea-pig airways.

作者信息

Frossard N, Barnes P J

机构信息

Department of Clinical Pharmacology, Brompton Hospital, London, U.K.

出版信息

Eur J Pharmacol. 1987 Sep 23;141(3):519-22. doi: 10.1016/0014-2999(87)90578-4.

Abstract

A role of opioids as inhibitors of the non-adrenergic non-cholinergic (NANC) excitatory nerves has been studied in the guinea-pig bronchi using electrical field stimulation. Morphine and DAGO gave dose-dependent inhibition of NANC contraction, which was reversed by naloxone, whereas the cholinergic nerve and substance P responses were unaffected. [Met5]enkephalin and [Leu5]enkephalin weakly inhibited NANC contraction, whereas dynorphin-(1-13) had no effect. These results suggest that opiates inhibit NANC bronchoconstriction via mu-opioid receptors.

摘要

利用电场刺激,在豚鼠支气管中研究了阿片类药物作为非肾上腺素能非胆碱能(NANC)兴奋性神经抑制剂的作用。吗啡和DAGO对NANC收缩产生剂量依赖性抑制,这种抑制可被纳洛酮逆转,而胆碱能神经和P物质反应不受影响。[Met5]脑啡肽和[Leu5]脑啡肽对NANC收缩有微弱抑制作用,而强啡肽-(1-13)则无作用。这些结果表明,阿片类药物通过μ-阿片受体抑制NANC支气管收缩。

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