Wikberg J
Acta Physiol Scand. 1977 Feb;99(2):190-207. doi: 10.1111/j.1748-1716.1977.tb10370.x.
The localization of adrenergic receptors mediating a relaxing action was investigated in innervated and denervated longitudinal muscle strips from guinea pig ileum and rabbit jejunum. Denervated preparations were contracted by drugs that had a direct effect on smooth muscle cells, such as acetylcholine and histamine, but not by stimuli acting on cholinergic neurons, such as electrical field stimulation or nicotine. After blockade of beta-adrenoceptors, norepinephrine relaxed the innervated guinea pig ileum contracted by electrical field stimulation, by stimulating alpha-adrenoceptors. Norepinephrine in low concentrations did not relax denervated preparations contracted by agents acting directly on smooth muscle. In high concentrations, it relaxed denervated preparations by a nonadrenergic mechanism, resistant to alpha- and/or beta-receptor blockade, but which was also activated by 1-(3,4-dihydroxyphenyl) ethanol. Phenylephrine only had a weak agonistic effect on the electrically stimulated innervated preparation and did not relax the denervated one. The denervated rabbit intestine contracted by acetylcholine was relaxed by norepinephrine and phenylephrine by stimulation of alpha-adrenoceptors. In the innervated preparations both drugs were more effective in inhibiting contractions induced by electrical field stimulation or eserine than those induced by exogenous acetylcholine. Both the denervated guinea pig and rabbit intestine were relaxed by stimulation of beta-adrenoceptors. It is suggested that in the guinea pig ileum alpha-adrenoceptors mediating relaxation are located only in cholinergic neurons, whereas in rabbit jejunum they are located both in these neurons and in the smooth muscle cells. Beta-adrenoceptors are located in the smooth muscle cells of both organs.
对介导舒张作用的肾上腺素能受体在豚鼠回肠和兔空肠的神经支配和去神经支配的纵行肌条中的定位进行了研究。去神经支配的标本可被对平滑肌细胞有直接作用的药物(如乙酰胆碱和组胺)收缩,但不受作用于胆碱能神经元的刺激(如电场刺激或尼古丁)收缩。β - 肾上腺素能受体被阻断后,去甲肾上腺素通过刺激α - 肾上腺素能受体使经电场刺激收缩的神经支配的豚鼠回肠舒张。低浓度的去甲肾上腺素不能使由直接作用于平滑肌的药物收缩的去神经支配的标本舒张。高浓度时,它通过一种非肾上腺素能机制使去神经支配的标本舒张,这种机制对α - 和/或β - 受体阻断有抗性,但也可被1 -(3,4 - 二羟基苯基)乙醇激活。去氧肾上腺素对经电刺激的神经支配的标本只有微弱的激动作用,且不能使去神经支配的标本舒张。由乙酰胆碱收缩的去神经支配的兔肠可被去甲肾上腺素和去氧肾上腺素通过刺激α - 肾上腺素能受体而舒张。在神经支配的标本中,这两种药物在抑制由电场刺激或毒扁豆碱诱导的收缩方面比抑制由外源性乙酰胆碱诱导的收缩更有效。刺激β - 肾上腺素能受体可使去神经支配的豚鼠和兔肠舒张。提示在豚鼠回肠中,介导舒张的α - 肾上腺素能受体仅位于胆碱能神经元中,而在兔空肠中,它们既位于这些神经元中,也位于平滑肌细胞中。β - 肾上腺素能受体位于这两个器官的平滑肌细胞中。