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猫胆总管十二指肠连接处肾上腺素能受体的原位研究。

Adrenoceptors in the cat choledochoduodenal junction studied in situ.

作者信息

Liedberg G, Persson C G

出版信息

Br J Pharmacol. 1970 Jul;39(3):619-26. doi: 10.1111/j.1476-5381.1970.tb10369.x.

Abstract
  1. The effects of adrenaline, noradrenaline, isoprenaline and terbutaline (PINN), 1-(3,5-dihydroxyphenyl)-2(t-butylamino)-ethanol, on the sphincter of Oddi were studied in anaesthetized cats. Both adrenaline and noradrenaline (1-4 mug/kg) increased resistance to flow through the sphincter. This effect was blocked by dibenamine (0.5-2.5 mg/kg) and by phenoxybenzamine (0.5-1.0 mg/kg).2. Isoprenaline (0.5-5.0 mug/kg) as well as terbutaline (0.5-10.0 mug/kg) inhibited the spontaneous sphincter activity and decreased flow resistance. In these doses, isoprenaline provoked marked tachycardia and relaxation of the duodenum, whereas the cardial and intestinal effects of terbutaline were minimal. The effects were blocked by propranolol (0.5-1.0 mg/kg).3. The results confirm earlier observations of the presence of alpha-adrenoceptors active in contraction of the sphincter musculature and of beta-adrenoceptors active in its relaxation. It is suggested that the beta-adrenoceptors belong to the beta(2) type according to Lands' classification.
摘要
  1. 在麻醉猫身上研究了肾上腺素、去甲肾上腺素、异丙肾上腺素和特布他林(PINN,即1-(3,5-二羟基苯基)-2-(叔丁氨基)-乙醇)对Oddi括约肌的作用。肾上腺素和去甲肾上腺素(1 - 4微克/千克)均增加了通过括约肌的血流阻力。这种作用被酚苄明(0.5 - 2.5毫克/千克)和苯氧苄胺(0.5 - 1.0毫克/千克)阻断。

  2. 异丙肾上腺素(0.5 - 5.0微克/千克)以及特布他林(0.5 - 10.0微克/千克)抑制了括约肌的自发活动并降低了血流阻力。在这些剂量下,异丙肾上腺素引起明显的心动过速和十二指肠松弛,而特布他林对心脏和肠道的作用最小。这些作用被普萘洛尔(0.5 - 1.0毫克/千克)阻断。

  3. 结果证实了早期的观察结果,即存在对括约肌肌肉收缩起作用的α - 肾上腺素能受体以及对其松弛起作用的β - 肾上腺素能受体。根据Lands的分类,提示β - 肾上腺素能受体属于β(2)型。

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[Spasmolytic effects on Oddi's sphincter].[对奥迪括约肌的解痉作用]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1953;218(6):462-78.

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