Voss H P, Shukrula S, Wu T S, Donnell D, Bast A
Department of Pharmacochemistry, Leiden/Amsterdam Center for Drug Research, The Netherlands.
J Pharmacol Exp Ther. 1994 Oct;271(1):386-9.
Responses were measured of the highly potent beta-2 adrenoceptor agonist TA 2005, a new bronchodilator, on isolated guinea pig right and left atria and papillary muscle. The main objectives of the study were to investigate the selectivity of the compound and to determine whether guinea pig isolated heart tissues could be used as a model for investigating mechanisms of clinical cardiac side effects. It was found that the inotropic responses in all tissues were mediated by the beta-1 adrenoceptor only. TA 2005 was a partial agonist for the inotropic response compared with I-isoprenaline. For the right atrial chronotropic response, however, TA 2005 exerted a biphasic effect and reached 84% of the I-isoprenaline response. The first phase was mediated by the beta-2 adrenoceptor, whereas the second phase was beta-1 adrenoceptor mediated. Approximately 64% of the TA 2005 chronotropic response was exerted via the beta-2 adrenoceptor. Addition of the beta-2-selective antagonist ICI 188.551 blocked the beta-2 adrenoceptor-mediated response, providing only a monophasic response. Addition of the beta-1-selective antagonist ICI 89.406 resulted in further separation of the phases. The finding that a beta-2-mediated chronotropic response exists on the right atrium of the guinea pig sheds new light on selectivity studies. It is suggested that quantification of beta-1/beta-2 selectivity of beta adrenoceptor agonists be performed not on the basis of measurement of guinea pig right atrial chronotropism but rather on the basis of measurement of guinea pig left atrial inotropism.(ABSTRACT TRUNCATED AT 250 WORDS)
对新型支气管扩张剂、高效β2肾上腺素能受体激动剂TA 2005作用于豚鼠离体左右心房及乳头肌的反应进行了测定。本研究的主要目的是调查该化合物的选择性,并确定豚鼠离体心脏组织是否可作为研究临床心脏副作用机制的模型。结果发现,所有组织中的变力反应仅由β1肾上腺素能受体介导。与异丙肾上腺素相比,TA 2005是变力反应的部分激动剂。然而,对于右心房变时反应,TA 2005发挥双相作用,达到异丙肾上腺素反应的84%。第一相由β2肾上腺素能受体介导,而第二相由β1肾上腺素能受体介导。TA 2005变时反应中约64%是通过β2肾上腺素能受体发挥作用的。添加β2选择性拮抗剂ICI 188.551可阻断β2肾上腺素能受体介导的反应,仅产生单相反应。添加β1选择性拮抗剂ICI 89.406可使各相进一步分离。豚鼠右心房存在β2介导的变时反应这一发现为选择性研究提供了新的线索。建议对β肾上腺素能受体激动剂β1/β2选择性的量化不应基于豚鼠右心房变时性的测量,而应基于豚鼠左心房变力性的测量。(摘要截短于250字)