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肺中的β-肾上腺素能受体介导对抗原诱导的组胺释放的抑制作用。

The beta-adrenoceptors of the lung mediating inhibition of antigen-induced histamine release.

作者信息

Sörenby L

出版信息

Eur J Pharmacol. 1975 Feb;30(2):140-7. doi: 10.1016/0014-2999(75)90092-8.

Abstract

The beta-adrenoceptor stimulants, isoprenaline (IPR), orciprenaline (OPR), terbutaline (TRB), and ITP were studied for effects on antigen-induced release of histamine from guinea-pig lung tissue and for effects on guinea-pig isolated trachea and heart. The order of potency for the agents in the four funct-ons studied were: (a) inhibition of histamine release, IPR greater than OPR approximately equal to TRB greater than ITP equal 0; (b) heart stimulation, chronotropic effect, IPR greater than OPR greater than ITP approximately equal to TRB; (c) heart stimulation, inotropic effect, IPR greater than OPR greater than ITP greater than TRB; (d) trachea relaxation: IPR greater than TRB greater than OPR greater than ITP. These findings suggest that the beta-adrenoceptors mediating inhibition of antigen-induced release of histamine are more related to those mediating trachea relaxation (beta2) than those mediating cardiac stimulation (beta1).

摘要

研究了β-肾上腺素受体激动剂异丙肾上腺素(IPR)、奥西那林(OPR)、特布他林(TRB)和ITP对豚鼠肺组织抗原诱导的组胺释放的影响,以及对豚鼠离体气管和心脏的影响。在所研究的四种功能中,这些药物的效力顺序为:(a)抑制组胺释放,IPR>OPR≈TRB>ITP=0;(b)心脏刺激,变时作用,IPR>OPR>ITP≈TRB;(c)心脏刺激,变力作用,IPR>OPR>ITP>TRB;(d)气管舒张:IPR>TRB>OPR>ITP。这些发现表明,介导抑制抗原诱导的组胺释放的β-肾上腺素受体与介导气管舒张(β2)的受体比与介导心脏刺激(β1)的受体更相关。

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