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β-肾上腺素能受体拮抗剂的内在拟交感活性对麻醉犬血流动力学效应的影响。

The influence of the intrinsic sympathomimetic activity of beta-adrenoceptor antagonists on haemodynamic effects in anaesthetized dogs.

作者信息

Wale J L, Austin M, Conway J, Reeves M

出版信息

Clin Exp Pharmacol Physiol. 1979 Jan-Feb;6(1):11-9. doi: 10.1111/j.1440-1681.1979.tb00002.x.

Abstract
  1. The effects of propranolol, atenolol (ICI 66,082), practolol and pindolol on heart rate and maximal left ventricular dp/dt, atrioventricular conduction time, mean aortic flow and diastolic blood pressure during cardiac pacing were investigated over a wide dose range (0.025-4.0 mg/kg, i.v.) in dogs anaesthetized with pentobarbitone.2. Propranolol and atenolol produced similar reductions in haemodynamic parameters. Propranolol had no further effect in dogs pretreated with atenolol. 3. Practolol tended to cause smaller reductions in the haemodynamic parameters than either propranolol or atenolol. Subsequent administration of propranolol still had some depressant activity. 4. Pindolol produced a biphasic response, with depression of cardiac function at the low doses (0.025 and 0.1 mg/kg), but a reversal of effect as the dose was increased. 5. It is therefore concluded that, in anaesthetized dogs, the intrinsic activity of practolol and pindolol limits the fall in heart rate, cardiac conduction, aortic flow and maximal dp/dt observed with beta-adrenoceptor blockade. With pindolol, however, the influence of intrinsic activity is observed only in high doses related to beta-adrenoceptor blockade.
摘要
  1. 在戊巴比妥麻醉的犬中,研究了普萘洛尔、阿替洛尔(ICI 66,082)、普拉洛尔和吲哚洛尔在较宽剂量范围(静脉注射0.025 - 4.0 mg/kg)内对心脏起搏期间心率、左心室最大dp/dt、房室传导时间、平均主动脉血流量和舒张压的影响。

  2. 普萘洛尔和阿替洛尔对血流动力学参数产生了相似的降低作用。在用阿替洛尔预处理的犬中,普萘洛尔没有进一步的作用。

  3. 普拉洛尔导致的血流动力学参数降低往往比普萘洛尔或阿替洛尔小。随后给予普萘洛尔仍有一些抑制活性。

  4. 吲哚洛尔产生双相反应,低剂量(0.025和0.1 mg/kg)时心脏功能受到抑制,但随着剂量增加作用逆转。

  5. 因此得出结论,在麻醉犬中,普拉洛尔和吲哚洛尔的内在活性限制了β - 肾上腺素能受体阻断时观察到的心率、心脏传导、主动脉血流量和最大dp/dt的下降。然而,对于吲哚洛尔,内在活性的影响仅在与β - 肾上腺素能受体阻断相关的高剂量时观察到。

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