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吲哚洛尔——一种部分激动剂的药理学

Pindolol--the pharmacology of a partial agonist.

作者信息

Clark B J, Menninger K, Bertholet A

出版信息

Br J Clin Pharmacol. 1982;13(Suppl 2):149S-158S. doi: 10.1111/j.1365-2125.1982.tb01904.x.

DOI:10.1111/j.1365-2125.1982.tb01904.x
PMID:7049208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1402130/
Abstract

1 Pindolol is a non-selective beta-adrenoceptor blocking agent; its affinity to adrenoceptors in guinea pig atria (beta 1) is not significantly different from that in guinea pig trachea (beta 1 + beta 2) and canine vascular smooth muscle (beta 2). 2 Pindolol displays a striking diversity of agonist activities in isolated tissues. Stimulant effects correspond to 40--50% of the maximum effects of isoprenaline in isolated kitten atria and guinea pig trachea and to only 10% in guinea pig atria. Effects in canine isolated mesenteric vessels are those of a full agonist, maximum responses equaling those of isoprenaline. These findings suggest that the stimulant effects of pindolol are exerted principally on beta 2-adrenoceptors. 3 Cardiac stimulation produced by pindolol in the dog is sufficient to compensate for the cardiac depression resulting from blockade of beta-adrenoceptors in the heart. Reductions in cardiac output and compensatory increases in total peripheral resistance do not occur or are much smaller than those produced by beta-adrenoceptor blocking agents lacking sympathomimetic activity. 4 Pindolol-induced relaxation of bronchial smooth muscle prevents or minimizes the bronchoconstrictor effects of injected spasmogens in the cat. 5 Pindolol has marked vasodilator activity, small doses reducing femoral and mesenteric vascular resistance by approximately 30%. Doses comparable to those used in hypertensive patients lower blood pressure by 20 mmHg in non-anaesthetized dogs.

摘要
  1. 吲哚洛尔是一种非选择性β-肾上腺素能受体阻滞剂;它对豚鼠心房(β1)肾上腺素能受体的亲和力与对豚鼠气管(β1 + β2)和犬血管平滑肌(β2)的亲和力无显著差异。2. 吲哚洛尔在离体组织中表现出显著的激动剂活性多样性。在离体小猫心房和豚鼠气管中,刺激作用相当于异丙肾上腺素最大作用的40%-50%,而在豚鼠心房中仅为10%。在犬离体肠系膜血管中的作用是完全激动剂的作用,最大反应与异丙肾上腺素的最大反应相当。这些发现表明,吲哚洛尔的刺激作用主要作用于β2-肾上腺素能受体。3. 吲哚洛尔在犬体内产生的心脏刺激足以补偿因阻断心脏β-肾上腺素能受体而导致的心脏抑制。心输出量降低和总外周阻力的代偿性增加不会出现或比缺乏拟交感活性的β-肾上腺素能受体阻滞剂所产生的要小得多。4. 吲哚洛尔诱导的支气管平滑肌舒张可预防或最小化猫体内注射致痉剂引起的支气管收缩效应。5. 吲哚洛尔具有显著的血管舒张活性,小剂量可使股动脉和肠系膜血管阻力降低约30%。在未麻醉的犬中,与用于高血压患者的剂量相当的剂量可使血压降低20 mmHg。

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1
Pindolol--the pharmacology of a partial agonist.吲哚洛尔——一种部分激动剂的药理学
Br J Clin Pharmacol. 1982;13(Suppl 2):149S-158S. doi: 10.1111/j.1365-2125.1982.tb01904.x.
2
Effects of pindolol on vascular smooth muscle.吲哚洛尔对血管平滑肌的作用。
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3
Comparative analysis of beta-1 adrenoceptor agonist and antagonist potency and selectivity of cicloprolol, xamoterol and pindolol.环丙洛尔、扎莫特罗和吲哚洛尔对β-1肾上腺素能受体激动剂及拮抗剂效能和选择性的比较分析
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4
Is the ISA of pindolol beta 2-adrenoceptor selective?吲哚洛尔对β2肾上腺素能受体有选择性吗?
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5
Pharmacological studies on the intrinsic sympathomimetic activity of the beta-adrenoceptor antagonist mepindolol.
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本文引用的文献

1
Pindolol acts as beta-adrenoceptor agonist in orthostatic hypotension: therapeutic implications.吲哚洛尔在体位性低血压中作为β-肾上腺素能受体激动剂:治疗意义。
Br Med J (Clin Res Ed). 1981 Mar 21;282(6268):929-31. doi: 10.1136/bmj.282.6268.929.
2
A study of beta-adrenoceptors in the guinea pig.豚鼠β-肾上腺素能受体的研究。
Postgrad Med J. 1981;57 Suppl 1:9-17.
3
Differential distribution of beta-1 and beta-2 adrenergic receptors in cat and guinea-pig heart.β-1和β-2肾上腺素能受体在猫和豚鼠心脏中的差异分布。
J Pharmacol Exp Ther. 1980 Mar;212(3):503-8.
4
Beta-adrenergic receptor subtypes: properties, distribution, and regulation.β-肾上腺素能受体亚型:特性、分布及调节
Annu Rev Neurosci. 1981;4:419-61. doi: 10.1146/annurev.ne.04.030181.002223.
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[Changes in hemodynamics under the effect of two beta sympathicolytics of various pharmacodynamic principle].
Arzneimittelforschung. 1974 Sep;24(9):1330-5.
6
Comparative chronotropic activity of beta-adrenoceptive antagonists.β-肾上腺素能拮抗剂的比较变时活性
Br J Pharmacol. 1970 Nov;40(3):373-81. doi: 10.1111/j.1476-5381.1970.tb10619.x.
7
Treatment of hypertension with a beta-adrenoceptor blocker. A multicentre trial with pindolol.用β-肾上腺素能受体阻滞剂治疗高血压。一项使用吲哚洛尔的多中心试验。
Br J Clin Pract. 1979 Jun;33(6):165-74, 181.
8
Nature and incidence of unwanted effects with atenolol.阿替洛尔不良反应的性质与发生率。
Postgrad Med J. 1977;53 Suppl 3:162-7.
9
pA2 values of selective beta-adrenoceptor antagonists on isolated atria demonstrate a species difference in the beta-adrenoceptor populations mediating chronotropic responses in cat and guinea-pig.选择性β-肾上腺素能受体拮抗剂对离体心房的pA2值表明,在介导猫和豚鼠变时反应的β-肾上腺素能受体群体中存在种属差异。
J Pharm Pharmacol. 1979 Oct;31(10):686-90. doi: 10.1111/j.2042-7158.1979.tb13629.x.
10
Immediate haemodynamic effects of propranolol, practolol, pindolol, atenolol and ICI 89,406 in healthy volunteers.普萘洛尔、普拉洛尔、吲哚洛尔、阿替洛尔及ICI 89,406对健康志愿者的即时血流动力学效应。
Eur J Clin Pharmacol. 1979 May 21;15(4):223-8. doi: 10.1007/BF00618509.