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类固醇对猪支气管β-肾上腺素能受体介导的舒张作用。

Effect of steroids on beta-adrenoceptor-mediated relaxation of pig bronchus.

作者信息

Foster P S, Goldie R G, Paterson J W

出版信息

Br J Pharmacol. 1983 Feb;78(2):441-5. doi: 10.1111/j.1476-5381.1983.tb09409.x.

Abstract

1--Progesterone, testosterone (40 microM), cortisol and cortisol hemisuccinate (80 microM) caused 6-8 fold potentiations of (+/-)-isoprenaline (Iso)-induced relaxations of pig bronchus while several other steroids caused smaller potentiations or had no effect. 2--17 beta-Oestradiol (40 microM) increased the potency of Iso, (-)-adrenaline (Adr) and (-)-noradrenaline (NA) by 10.6, 2.3 and 2.6 fold respectively but had no significant effect on the potency of fenoterol (Fen). 3--Inhibition of catechol-O-methyl transferase (COMT) with U-0521 (30 microM) caused a 6 fold increase in the potency of Iso but failed to alter the potency of Adr, NA or Fen. The extraneuronal uptake inhibitor normetanephrine (50 microM) caused significant 2 fold increases in the potency of Iso and Adr but did not potentiate the responses to NA or Fen. 4--In preparations where the potency of Iso had already been increased by U-0521 (30 microM) or by normetanephrine, 17 beta-oestradiol produced no significant further increase in potency. These results indicate that steroid-induced increases in the potency of catecholamines in pig bronchus can be explained in terms of inhibition of COMT or extraneuronal uptake or both.

摘要
  1. 孕酮、睾酮(40微摩尔)、皮质醇和半琥珀酸皮质醇(80微摩尔)使(±)-异丙肾上腺素(Iso)诱导的猪支气管舒张增强了6至8倍,而其他几种类固醇则使舒张增强较小或无作用。2. 17β-雌二醇(40微摩尔)分别使Iso、(-)-肾上腺素(Adr)和(-)-去甲肾上腺素(NA)的效力提高了10.6倍、2.3倍和2.6倍,但对非诺特罗(Fen)的效力无显著影响。3. 用U-0521(30微摩尔)抑制儿茶酚-O-甲基转移酶(COMT)使Iso的效力增加了6倍,但未能改变Adr、NA或Fen的效力。神经外摄取抑制剂去甲间肾上腺素(50微摩尔)使Iso和Adr的效力显著增加了2倍,但未增强对NA或Fen的反应。4. 在Iso的效力已因U-0521(30微摩尔)或去甲间肾上腺素而增加的制剂中,17β-雌二醇未使效力进一步显著增加。这些结果表明,类固醇诱导的猪支气管中儿茶酚胺效力增加可通过抑制COMT或神经外摄取或两者来解释。

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