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SR 58611A对犬结肠运动的抑制作用:β3肾上腺素能受体作用的证据

Inhibitory effects of SR 58611A on canine colonic motility: evidence for a role of beta 3-adrenoceptors.

作者信息

De Ponti F, Cosentino M, Costa A, Girani M, Gibelli G, D'Angelo L, Frigo G, Crema A

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, Italy.

出版信息

Br J Pharmacol. 1995 Apr;114(7):1447-53. doi: 10.1111/j.1476-5381.1995.tb13368.x.

Abstract
  1. In order to clarify whether atypical or beta 3-adrenoceptors can modulate canine colonic motility in vivo, we studied the effects of SR 58611A (a selective agonist for atypical beta-adrenoceptors) alone and after pretreatment with beta-adrenoceptor antagonists on colonic motility in the conscious dog. The gastrocolonic response (postprandial increase in motility) was monitored by means of electrodes and strain-gauge force transducers chronically implanted along the distal colon. In some experiments, heart rate was also measured. The possible role of beta 3-adrenoceptors in mediating the effects of SR 58611A was also tested in vitro in circular muscle strips taken from the canine distal colon. 2. Intravenous infusion of SR 58611A, ritodrine or isoprenaline at doses inducing the same degree of tachycardia inhibited the gastrocolonic response to a different extent, with SR 58611A and ritodrine being more effective than isoprenaline. 3. In a dose-response study, SR 58611A was more potent in inhibiting colonic motility than in inducing tachycardia: the ED35 values for inhibition of colonic motility and induction of tachycardia were 23 and 156 micrograms kg-1, i.v., respectively. 4. The inhibitory effect of SR 58611A 100 micrograms kg-1, i.v., on the gastrocolonic response was reversed by alprenolol (non-selective beta-adrenoceptor antagonist), but resistant to CGP 20712A (beta 1-adrenoceptor antagonist) or ICI 118551 (beta 2-adrenoceptor antagonist). 5. In vitro, SR 58611A concentration-dependently relaxed circular muscle strips, an effect that was competitively antagonized by alprenolol with a pA2 value of 7.1, but resistant to CGP 20712A (100 nM), ICI 118551 (100 nM) or tetrodotoxin (1 microM). 6. The present study provides strong functional evidence for a role of atypical or beta 3-adrenoceptors in the modulation of canine colonic motility both in vivo and in vitro by an inhibitory effect most likely at the smooth muscle level.
摘要
  1. 为了阐明非典型或β3 - 肾上腺素能受体是否能在体内调节犬结肠运动,我们研究了SR 58611A(一种非典型β - 肾上腺素能受体的选择性激动剂)单独使用时以及在用β - 肾上腺素能拮抗剂预处理后对清醒犬结肠运动的影响。通过沿远端结肠长期植入的电极和应变片式力传感器监测胃结肠反射(餐后运动增加)。在一些实验中,还测量了心率。在取自犬远端结肠的环形肌条中进行体外实验,以测试β3 - 肾上腺素能受体在介导SR 58611A作用中的可能作用。2. 静脉输注能引起相同程度心动过速的剂量的SR 58611A、利托君或异丙肾上腺素,对胃结肠反射的抑制程度不同,SR 58611A和利托君比异丙肾上腺素更有效。3. 在剂量 - 反应研究中,SR 58611A抑制结肠运动比引起心动过速更有效:静脉注射时,抑制结肠运动和引起心动过速的ED35值分别为23和156微克/千克。4. 静脉注射100微克/千克的SR 58611A对胃结肠反射的抑制作用可被阿普洛尔(非选择性β - 肾上腺素能拮抗剂)逆转,但对CGP 20712A(β1 - 肾上腺素能拮抗剂)或ICI 118551(β2 - 肾上腺素能拮抗剂)有抗性。5. 在体外,SR 58611A浓度依赖性地使环形肌条松弛,阿普洛尔能竞争性拮抗该作用,pA2值为7.1,但对CGP 20712A(100 nM)、ICI 118551(100 nM)或河豚毒素(1 microM)有抗性。6. 本研究提供了有力的功能证据,证明非典型或β3 - 肾上腺素能受体通过最可能在平滑肌水平的抑制作用,在体内和体外调节犬结肠运动中发挥作用。

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