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三种β-肾上腺素能受体拮抗剂对麻醉犬外周血管对异丙肾上腺素反应的阻断作用。

Blockade of peripheral vascular responses to isoprenaline by three beta-adrenoceptor antagonists in the anaesthetized dog.

作者信息

Hainsworth R, Karim F, Stoker J B

出版信息

Br J Pharmacol. 1974 Jun;51(2):161-8. doi: 10.1111/j.1476-5381.1974.tb09643.x.

Abstract

1 A dog's hind limb was vascularly isolated by strong nylon snares and its sympathetic nerve supply interrupted. Blood was perfused at constant flow into the femoral artery and drained from the femoral vein. In some dogs the cardiac nerves were cut.2 Isoprenaline infused intravenously caused an increase in heart rate and a decrease in arterial resistance.3 Practolol (2 mg/kg) effectively blocked heart rate responses to isoprenaline infused at up to 10 mug/min but was relatively ineffective in blocking arterial responses. ICI 66082 (2 mg/kg) reduced vasomotor responses and propranolol (0.5 mg/kg) abolished vasomotor responses.4 Small cumulative doses of beta-adrenoceptor antagonists were given to some dogs. Practolol blocked heart rate responses in lower doses than were required to block vasomotor responses. Propranolol preferentially blocked vasomotor responses and ICI 66082 was intermediate between the other two in its effects.

摘要
  1. 用结实的尼龙圈套器对一只狗的后肢进行血管隔离,并切断其交感神经供应。血液以恒定流量灌注到股动脉中,并从股静脉引流出来。在一些狗中,切断了心脏神经。

  2. 静脉注射异丙肾上腺素导致心率增加和动脉阻力降低。

  3. 心得宁(2毫克/千克)有效地阻断了对以高达10微克/分钟的速度静脉注射异丙肾上腺素的心率反应,但在阻断动脉反应方面相对无效。ICI 66082(2毫克/千克)降低了血管运动反应,而普萘洛尔(0.5毫克/千克)消除了血管运动反应。

  4. 给一些狗给予小剂量累积的β-肾上腺素能拮抗剂。心得宁阻断心率反应所需的剂量低于阻断血管运动反应所需的剂量。普萘洛尔优先阻断血管运动反应,ICI 66082的作用介于其他两者之间。

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1
The physiology of the veins.静脉的生理学。
J Physiol. 1921 Aug 3;55(3-4):226-45. doi: 10.1113/jphysiol.1921.sp001964.
4
Response of large hindlimb veins of the dog to sympathetic nerve stimulation.
Am J Physiol. 1968 Aug;215(2):299-307. doi: 10.1152/ajplegacy.1968.215.2.299.
5
Action of propranolol on the dog heart.普萘洛尔对犬心脏的作用。
Cardiovasc Res. 1973 Nov;7(6):729-39. doi: 10.1093/cvr/7.6.729.
7
Selective blockade of adrenoceptive beta receptors in the heart.心脏中肾上腺素能β受体的选择性阻断。
Br J Pharmacol Chemother. 1968 Jan;32(1):201-18. doi: 10.1111/j.1476-5381.1968.tb00444.x.

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