MacDonald A, Watt K
School of Biological and Biomedical Sciences, Glasgow Caledonian University, UK.
J Auton Pharmacol. 1999 Apr;19(2):91-5. doi: 10.1046/j.1365-2680.1999.00121.x.
The present study was carried out to further investigate the nature of the beta-adrenoceptor in rabbit jejunum using BRL 37344, a selective beta3-adrenoceptor agonist, cyanopindolol, a beta-adrenoceptor antagonist with blocking activity at beta3-adrenoceptors and SR 59230A, a new selective beta3-adrenoceptor antagonist. Isoprenaline produced a concentration-dependent inhibition of the spontaneous contractions of rabbit jejunum with a pD2 of 7.14. Propranolol (1 microM) shifted the isoprenaline concentration-response curve (CRC) to the right with a concentration-ratio of 5.85, considerably less than would be expected for an action at classical beta-adrenoceptors (estimated pA2 6.66). BRL 37344 also produced a concentration-dependent inhibition of spontaneous contractions with a pD2 of 7.41. The BRL 37344 CRC was unaffected by propranolol (1 microM). In the presence of propranolol (1 microM), cyanopindolol (1 microM) shifted the isoprenaline CRC to the right (concentration-ratio of 21). Cyanopindolol also shifted the BRL 37344 CRC to the right (concentration-ratio of 38). These shifts are consistent with the affinity of cyanopindolol for beta3-adrenoceptors (estimated pA2 values of 7.27 and 7.38 against isoprenaline and BRL 37344, respectively). In the presence of propranolol (1 microM), SR 59230A produced a concentration-dependent rightward shift of the isoprenaline CRC. The Schild plot gave a pA2 value of 7.16, although the slope of the regression line was significantly different from unity (0.65). SR 59230A also produced a concentration-dependent shift of the BRL 37344 CRC. The Schild plot gave a pA2 of 7.58 with the slope of the regression line not significantly different from unity (0.81). The presence of beta3-adrenoceptors mediating relaxation of spontaneous contractions in rabbit jejunum is supported by the relatively poor antagonism of isoprenaline by propranolol, the relaxant effect of BRL 37344 and the antagonism of isoprenaline and BRL 37344 by cyanopindolol and SR 59230A. The lack of simple competitive antagonism of isoprenaline, but not BRL 37344, by SR 59230A may suggest more than one population of atypical beta-adrenoceptor.
本研究旨在使用选择性β3肾上腺素能受体激动剂BRL 37344、对β3肾上腺素能受体具有阻断活性的β肾上腺素能受体拮抗剂氰吲哚洛尔以及新型选择性β3肾上腺素能受体拮抗剂SR 59230A,进一步研究兔空肠中β肾上腺素能受体的性质。异丙肾上腺素对兔空肠的自发收缩产生浓度依赖性抑制,pD2为7.14。普萘洛尔(1微摩尔)使异丙肾上腺素浓度-反应曲线(CRC)右移,浓度比为5.85,远低于经典β肾上腺素能受体作用预期值(估计pA2为6.66)。BRL 37344也对自发收缩产生浓度依赖性抑制,pD2为7.41。BRL 37344的CRC不受普萘洛尔(1微摩尔)影响。在普萘洛尔(1微摩尔)存在下,氰吲哚洛尔(1微摩尔)使异丙肾上腺素CRC右移(浓度比为21)。氰吲哚洛尔也使BRL 37344的CRC右移(浓度比为38)。这些右移与氰吲哚洛尔对β3肾上腺素能受体的亲和力一致(针对异丙肾上腺素和BRL 37344的估计pA2值分别为7.27和7.38)。在普萘洛尔(1微摩尔)存在下,SR 59230A使异丙肾上腺素CRC产生浓度依赖性右移。Schild图给出的pA2值为7.16,尽管回归线斜率显著不同于1(0.65)。SR 59230A也使BRL 37344的CRC产生浓度依赖性右移。Schild图给出的pA2为7.58,回归线斜率与1无显著差异(0.81)。普萘洛尔对异丙肾上腺素的拮抗作用相对较弱、BRL 37344的舒张作用以及氰吲哚洛尔和SR 59230A对异丙肾上腺素和BRL 37344的拮抗作用,均支持兔空肠中存在介导自发收缩舒张的β3肾上腺素能受体。SR 59230A对异丙肾上腺素(而非BRL 37344)缺乏简单竞争性拮抗作用,可能提示存在不止一种非典型β肾上腺素能受体群体。