Suppr超能文献

OPC - 2009对豚鼠离体气管、右心房和左心房标本的β - 肾上腺素能受体刺激特性。

The beta-adrenoceptor stimulant properties of OPC-2009 on guinea-pig isolated tracheal, right atrial and left atrial preparations.

作者信息

Yabuuchi Y

出版信息

Br J Pharmacol. 1977 Dec;61(4):513-21. doi: 10.1111/j.1476-5381.1977.tb07543.x.

Abstract
  1. The beta-adrenoceptor stimulant properties of 5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxy-carbostyril hydrochloride hemihydrate (OPC-2009) were compared with those of isoprenaline and salbutamol on guinea-pig isolated tissues. 2. In producing tracheal relaxation, OPC-2009 was approximately 7 times more potent and salbutamol 5 times less potent than isoprenaline. Both compounds were less potent than isoprenaline in increasing either the rate of beating of isolated right atria or the contractile force of left atria, OPC-2009 being 4 and 127 times and salbutamol being 100 and 700 times less potent on the respective preparations. 3. Selectivity calculated from EC50 ratio indicates that OPC-2009 was approximately 26 times and salbutamol approximately 21 times more selective than isoprenaline for tracheal smooth muscle as compared to right atrial muscle, whereas OPC-2009 was approximately 850 times and salbutamol 140 times more selective than isoprenaline for tracheal smooth muscle as compared to left atria. 4. The responses to OPC-2009 on trachea and right atria were not altered by treatment of animals with reserpine 24 h previously. Propranolol was a competitive antagonist of OPC-2009 on these tissues. 5. OPC-2009 at high concentrations competitively antagonized the positive chronotropic and inotropic responses to isoprenaline, indicating that OPC-2009 like salbutamol, may be classified as a partial agonist. 6. The results indicate that the action of OPC-2009 is more selective for tracheal smooth muscle than cardiac muscle and are interpreted in the light of subdivisions of beta-adrenoceptors.
摘要
  1. 在豚鼠离体组织上,比较了盐酸半水合5-(1-羟基-2-异丙氨基丁基)-8-羟基-卡巴唑(OPC-2009)与异丙肾上腺素和沙丁胺醇的β-肾上腺素受体激动特性。2. 在产生气管松弛方面,OPC-2009的效力约为异丙肾上腺素的7倍,沙丁胺醇的效力比异丙肾上腺素低5倍。在增加离体右心房的跳动速率或左心房的收缩力方面,这两种化合物的效力均低于异丙肾上腺素,在各自的制剂上,OPC-2009的效力分别低4倍和127倍,沙丁胺醇的效力分别低100倍和700倍。3. 根据EC50比值计算的选择性表明,与右心房肌相比,OPC-2009对气管平滑肌的选择性约为异丙肾上腺素的26倍,沙丁胺醇约为21倍;而与左心房相比,OPC-2009对气管平滑肌的选择性约为异丙肾上腺素的850倍,沙丁胺醇为140倍。4. 预先用利血平处理动物24小时,对OPC-2009在气管和右心房上的反应无影响。普萘洛尔是OPC-2009在这些组织上的竞争性拮抗剂。5. 高浓度的OPC-2009竞争性拮抗异丙肾上腺素的正性变时和变力反应,表明OPC-2009与沙丁胺醇一样,可归类为部分激动剂。6. 结果表明,OPC-2009对气管平滑肌的作用比对心肌更具选择性,并根据β-肾上腺素受体的细分进行了解释。

相似文献

8
Beta-adrenoceptor profile of ractopamine HCl in isolated smooth and cardiac muscle tissues of rat and guinea-pig.
J Pharm Pharmacol. 1991 Dec;43(12):844-7. doi: 10.1111/j.2042-7158.1991.tb03192.x.

引用本文的文献

1
Asthma and COPD: A Focus on β-Agonists - Past, Present and Future.
Handb Exp Pharmacol. 2024;285:369-451. doi: 10.1007/164_2023_679.
6
Pharmacological characterization and anatomical localization of prejunctional beta-adrenoceptors in the rat kidney.
Br J Pharmacol. 1994 Apr;111(4):1296-308. doi: 10.1111/j.1476-5381.1994.tb14886.x.

本文引用的文献

1
THE SPIRALLY CUT TRACHEAL STRIP PREPARATION.
J Pharm Pharmacol. 1965 Jun;17:384-5. doi: 10.1111/j.2042-7158.1965.tb07688.x.
2
A COMPARISON OF THE CARDIAC STIMULATING AND BRONCHODILATOR ACTIONS OF SELECTED SYMPATHOMIMETIC AMINES.
Proc Soc Exp Biol Med. 1964 Jun;116:331-3. doi: 10.3181/00379727-116-29239.
3
IN VIVO INACTIVATION OF CATECHOLAMINES IN MICE.
Acta Pharmacol Toxicol (Copenh). 1963;20:267-73. doi: 10.1111/j.1600-0773.1963.tb01744.x.
5
Some quantitative uses of drug antagonists.
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
6
Differentiation of receptors responsive to isoproterenol.
Life Sci. 1967 Nov 1;6(21):2241-9. doi: 10.1016/0024-3205(67)90031-8.
7
Differentiation of receptor systems activated by sympathomimetic amines.
Nature. 1967 May 6;214(5088):597-8. doi: 10.1038/214597a0.
9
Salbutamol: a new, selective beta-adrenoceptive receptor stimulant.
Br J Pharmacol. 1969 Jan;35(1):141-51. doi: 10.1111/j.1476-5381.1969.tb07975.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验