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己双肾上腺素:豚鼠离体组织中的β-肾上腺素能受体选择性

Hexoprenaline: beta-adrenoreceptor selectivity in isolated tissues from the guinea-pig.

作者信息

O'Donnell S R, Wanstall J C

出版信息

Clin Exp Pharmacol Physiol. 1975 Nov-Dec;2(6):541-7. doi: 10.1111/j.1440-1681.1975.tb01859.x.

Abstract
  1. A catecholamine beta-adrenoreceptor agonist, hexoprenaline, was examined in vitro on five guinea-pig tissues and its potency relative to isoprenaline (as 100) obtained. 2. Hexoprenaline clearly delineated between those tissues classified as containing beta2-adrenoreceptors (trachea, hind limb blood vessels and uterus; relative potencies 219, 110 and 76 respectively) and those classified as containing beta1-adrenoreceptors (atria and ileum; relative potencies 3.3 and 1.0 respectively). 3. Hexoprenaline differed from some previously studied noncatecholamine beta-adrenoreceptor agonists in being only two-fold less potent, relative to isoprenaline, as a vasodilator in perfused hind limb than as a tracheal relaxant.
摘要
  1. 对一种儿茶酚胺β-肾上腺素能受体激动剂海索那林进行了体外实验,实验对象为五种豚鼠组织,并得出了其相对于异丙肾上腺素(设定为100)的效价。2. 海索那林能明确区分那些被归类为含有β2-肾上腺素能受体的组织(气管、后肢血管和子宫;相对效价分别为219、110和76)和那些被归类为含有β1-肾上腺素能受体的组织(心房和回肠;相对效价分别为3.3和1.0)。3. 海索那林与一些先前研究的非儿茶酚胺β-肾上腺素能受体激动剂不同,相对于异丙肾上腺素,它作为灌注后肢血管舒张剂的效价比作为气管松弛剂的效价仅低两倍。

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