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大鼠离体胃底中儿茶酚胺介导的舒张作用的特征:非典型β-肾上腺素能受体的证据

Characterization of catecholamine-mediated relaxations in rat isolated gastric fundus: evidence for an atypical beta-adrenoceptor.

作者信息

McLaughlin D P, MacDonald A

机构信息

Department of Biological Sciences, Glasgow College.

出版信息

Br J Pharmacol. 1991 Jun;103(2):1351-6. doi: 10.1111/j.1476-5381.1991.tb09792.x.

Abstract
  1. Experiments were carried out in order to characterize the receptors mediating relaxant responses to catecholamines in the rat gastric fundus. The effects of noradrenaline, isoprenaline and the 'atypical' or beta 3-adrenoceptor agonist, BRL 37344, on methacholine-induced tone were measured. Prazosin, propranolol and cyanopindolol were used as antagonists. 2. Relaxant responses to noradrenaline, in the presence of propranolol (1 microM) were antagonized in a concentration-dependent manner by prazosin (0.01 to 1 microM), although this antagonism was weak and non-competitive in nature. Relaxant responses to isoprenaline, in the presence of prazosin (0.1 microM), were antagonized only by the highest concentration of propranolol (1 microM) giving a pKB of 6.3 BRL 37344 also relaxed the rat gastric fundus in the presence of prazosin (0.1 microM), and the responses to BRL 37344 were unaffected by propranolol (1 microM). 3. Tachyphylaxis to BRL 37344 was observed, a second concentration-response curve being significantly shifted to the right. Exposure of tissues to BRL 37344 (1 microM) between concentration-response curves also caused an 11 fold rightward shift in the response to isoprenaline. 4. In the presence of prazosin (0.1 microM) and propranolol (1 microM), the rank order of potency of the agonists was: (-)-isoprenaline (1.0) greater than (-)-noradrenaline (0.39) greater than BRL 37344 (0.10). 5. Responses to BRL 37344 in the presence of prazosin (0.1 microM) and propranolol (1 microM) were antagonized by (+/-)-cyanopindolol (1 microM), with a pKB of 6.56. Responses to isoprenaline, under the same conditions, were antagonized in a competitive manner by (+/-)-cyanopindolol (0.1-1 microM), with the slope of a Schild plot close to unity and a pA2 value of 7.44. 6. The resistance to blockade by prazosin and propranolol and the antagonism by cyanopindolol of the responses mediated by isoprenaline and BRL 37344 suggest that atypical beta-adrenoceptors similar to 'atypical',beta-adrenoceptors in rat adipocytes and other tissues are present in the rat gastric fundus.
摘要
  1. 开展实验以表征介导大鼠胃底对儿茶酚胺舒张反应的受体。测定了去甲肾上腺素、异丙肾上腺素以及“非典型”或β3 - 肾上腺素能受体激动剂BRL 37344对乙酰甲胆碱诱导的张力的影响。哌唑嗪、普萘洛尔和氰吲哚洛尔用作拮抗剂。2. 在普萘洛尔(1微摩尔)存在的情况下,对去甲肾上腺素的舒张反应被哌唑嗪(0.01至1微摩尔)以浓度依赖性方式拮抗,尽管这种拮抗作用较弱且本质上是非竞争性的。在哌唑嗪(0.1微摩尔)存在的情况下,对异丙肾上腺素的舒张反应仅被最高浓度的普萘洛尔(1微摩尔)拮抗,pKB为6.3。在哌唑嗪(0.1微摩尔)存在的情况下,BRL 37344也使大鼠胃底舒张,并且对BRL 37344的反应不受普萘洛尔(1微摩尔)影响。3. 观察到对BRL 37344的快速耐受性,第二条浓度 - 反应曲线明显右移。在浓度 - 反应曲线之间将组织暴露于BRL 37344(1微摩尔)也导致对异丙肾上腺素的反应向右移动11倍。4. 在哌唑嗪(0.1微摩尔)和普萘洛尔(1微摩尔)存在的情况下,激动剂的效价顺序为:(-)-异丙肾上腺素(1.0)>(-)-去甲肾上腺素(0.39)>BRL 37344(0.10)。5. 在哌唑嗪(0.1微摩尔)和普萘洛尔(1微摩尔)存在的情况下,对BRL 37344的反应被(±)-氰吲哚洛尔(1微摩尔)拮抗,pKB为6.56。在相同条件下,对异丙肾上腺素的反应被(±)-氰吲哚洛尔(0.1 - 1微摩尔)以竞争性方式拮抗,Schild图的斜率接近1,pA2值为7.44。6. 对哌唑嗪和普萘洛尔阻断的抗性以及氰吲哚洛尔对异丙肾上腺素和BRL 37344介导的反应的拮抗作用表明,大鼠胃底中存在与大鼠脂肪细胞和其他组织中的“非典型”β - 肾上腺素能受体类似的非典型β - 肾上腺素能受体。

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