Labadia A, Rivera L, Costa G, Garcia-Sacristan A
Facultad de Veterinaria, Universidad Complutense de Madrid, Spain.
Res Vet Sci. 1988 May;44(3):282-5.
alpha and beta-adrenergic receptors in detrusor muscle and bladder base of horses were investigated by in vitro responses of smooth muscle strips to exogenous agonist and antagonist drugs. Noradrenaline, isoprenaline and salbutamol induced relaxation of detrusor muscle strips which was significantly inhibited by propranolol and butoxamine suggesting that the response is mediated by beta-2 adrenergic receptors. In the urinary bladder base noradrenaline, phenylephrine and B-HT 920 induced strong contractile effects. These contractile responses were inhibited by the alpha antagonist phenoxybenzamine, the alpha-1 selective antagonist prazosin and the alpha-2 selective antagonist yohimbine. The inhibitory action of prazosin was more potent than that observed with yohimbine suggesting that the response in the bladder base of horses is mediated predominantly by alpha-1 adrenergic receptors, although alpha-2 receptors also participate.
通过平滑肌条对外源性激动剂和拮抗剂药物的体外反应,研究了马逼尿肌和膀胱底部的α和β肾上腺素能受体。去甲肾上腺素、异丙肾上腺素和沙丁胺醇可诱导逼尿肌条舒张,普萘洛尔和丁氧胺可显著抑制这种舒张,提示该反应由β-2肾上腺素能受体介导。在膀胱底部,去甲肾上腺素、苯肾上腺素和B-HT 920可诱导强烈的收缩效应。这些收缩反应可被α拮抗剂酚苄明、α-1选择性拮抗剂哌唑嗪和α-2选择性拮抗剂育亨宾抑制。哌唑嗪的抑制作用比育亨宾更强,提示马膀胱底部的反应主要由α-1肾上腺素能受体介导,尽管α-2受体也参与其中。