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膀胱平滑肌中β-肾上腺素能受体亚型分布的种属差异。

Species differences in the distribution of beta-adrenoceptor subtypes in bladder smooth muscle.

作者信息

Yamazaki Y, Takeda H, Akahane M, Igawa Y, Nishizawa O, Ajisawa Y

机构信息

Division of Discovery Research, Kissei Pharmaceutical Co., Ltd., Hotaka, Nagano, Japan.

出版信息

Br J Pharmacol. 1998 Jun;124(3):593-9. doi: 10.1038/sj.bjp.0701870.

Abstract
  1. The beta-adrenoceptor (beta-AR) subtypes mediating relaxation of the rabbit, rat and canine detrusors were subjected to functional investigation using selective beta-AR agonists and antagonists. 2. In all three species, isoprenaline, noradrenaline and adrenaline each produced a concentration-dependent relaxation of the detrusor. The rank order for their relaxing potency was isoprenaline>adrenaline>noradrenaline in rabbits and rats, but isoprenaline>noradrenaline>adrenaline in dogs. 3. Dobutamine did not produce relaxation of the detrusors at concentrations that are selective for beta1-AR. The selective beta2-AR agonist, procaterol, had a more potent relaxing effect on rabbit and rat detrusors than on the canine detrusor. CGP-12177A, a selective beta3-AR agonist, was more effective in the rabbit than in the other two species. On the other hand, the relaxing effect of another beta3-AR agonist, CL316243, was more pronounced in dogs and rats than in rabbits. 4. CGP-20712A (10(-9) to 10(-7) M), a selective beta1-AR antagonist, caused a slight rightward shift of the concentration-relaxation response curve for isoprenaline in the canine detrusor (pA2 9.41), but not in the rabbit and rat detrusors. ICI-118,551, a selective beta2-AR antagonist, antagonized the isoprenaline-induced relaxation in rabbits (pA2 9.45) and rats (pA2 9.05), but not in dogs. Bupranolol, a non-selective beta-AR antagonist, caused a rightward shift of the concentration-relaxation curve for isoprenaline in the rabbit (pA2 9.32) and rat (pA2 8.98). However, higher concentrations (3 x 10(-8) to 10(-5) M) were needed to induce a rightward shift of the curve for isoprenaline in the dog (pA2 8.19) than in the other two species. 5. We have confirmed that the distribution of beta-AR subtypes in the detrusor muscle varies significantly from species to species and we provide here the first evidence of the presence of beta3-AR in the detrusor. It is suggested that the relaxation induced by adrenoceptor agonists in urinary bladder smooth muscle may be mediated mainly via beta2-AR in rabbits, via both beta2- and beta3-AR in rats, but mainly via beta3-AR in dogs.
摘要
  1. 使用选择性β-肾上腺素能受体(β-AR)激动剂和拮抗剂对介导兔、大鼠和犬逼尿肌舒张的β-AR亚型进行功能研究。2. 在所有这三个物种中,异丙肾上腺素、去甲肾上腺素和肾上腺素均可使逼尿肌产生浓度依赖性舒张。在兔和大鼠中,它们的舒张效力顺序为异丙肾上腺素>肾上腺素>去甲肾上腺素,但在犬中为异丙肾上腺素>去甲肾上腺素>肾上腺素。3. 多巴酚丁胺在对β1-AR有选择性的浓度下不会使逼尿肌舒张。选择性β2-AR激动剂丙卡特罗对兔和大鼠逼尿肌的舒张作用比对犬逼尿肌更强。选择性β3-AR激动剂CGP-12177A在兔中的效果比在其他两个物种中更明显。另一方面,另一种β3-AR激动剂CL316243的舒张作用在犬和大鼠中比在兔中更显著。4. 选择性β1-AR拮抗剂CGP-20712A(10⁻⁹至10⁻⁷M)使犬逼尿肌中异丙肾上腺素的浓度-舒张反应曲线轻微右移(pA2 9.41),但在兔和大鼠逼尿肌中未出现这种情况。选择性β2-AR拮抗剂ICI-118,551拮抗异丙肾上腺素在兔(pA2 9.45)和大鼠(pA2 9.05)中诱导的舒张,但在犬中无此作用。非选择性β-AR拮抗剂布普洛尔使兔(pA2 9.32)和大鼠(pA2 8.98)中异丙肾上腺素的浓度-舒张曲线右移。然而,与其他两个物种相比,需要更高浓度(3×10⁻⁸至10⁻⁵M)才能使犬中异丙肾上腺素的曲线右移(pA2 8.19)。5. 我们已经证实,逼尿肌中β-AR亚型的分布在不同物种之间有显著差异,并且我们在此提供了逼尿肌中存在β3-AR的首个证据。提示肾上腺素能受体激动剂在膀胱平滑肌中诱导的舒张可能主要通过兔中的β2-AR、大鼠中的β2-和β3-AR以及犬中的β3-AR介导。

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