Kitazawa T, Kondo H, Temma K
Br J Pharmacol. 1986 Oct;89(2):259-66. doi: 10.1111/j.1476-5381.1986.tb10255.x.
The type of adrenoceptor involved in the contractile response to catecholamines in smooth muscle strips isolated from rainbow trout stomach was determined. Noradrenaline (10 nM-10 microM) and adrenaline (10 nM-3 microM) caused non-sustained contractions which were markedly decreased by phentolamine (5.4 microM) but not by carteolol (5 microM). Phenylephrine (1 microM-1 mM) was less effective in causing muscle contraction and methoxamine produced no contraction. Clonidine (100 nM-300 microM) caused no mechanical response but inhibited the contraction to noradrenaline or adrenaline but not acetylcholine or 5-hydroxytryptamine. Yohimbine (10 nM-1 microM) decreased the contraction induced by noradrenaline or adrenaline but prazosin (1 microM) did not. Tetrodotoxin (780 nM) partially reduced the contraction induced by noradrenaline or adrenaline but atropine (500 nM) did not. In the presence of atropine (1 microM), electrical transmural stimulation caused frequency-dependent, tetrodotoxin-sensitive contractions. These results suggest that the contractile response induced by noradrenaline or adrenaline is mediated by alpha 2-adrenoceptors. It is also suggested that noradrenaline and adrenaline contract the smooth muscle by direct action and by indirect action through the non-cholinergic excitatory nerve.
确定了从虹鳟鱼胃中分离出的平滑肌条对儿茶酚胺收缩反应所涉及的肾上腺素能受体类型。去甲肾上腺素(10 nM - 10 μM)和肾上腺素(10 nM - 3 μM)引起非持续性收缩,酚妥拉明(5.4 μM)可显著减弱这种收缩,但卡替洛尔(5 μM)则无此作用。苯肾上腺素(1 μM - 1 mM)引起肌肉收缩的效果较差,甲氧明则不引起收缩。可乐定(100 nM - 300 μM)不引起机械反应,但可抑制对去甲肾上腺素或肾上腺素的收缩反应,而对乙酰胆碱或5 - 羟色胺则无抑制作用。育亨宾(10 nM - 1 μM)可减弱去甲肾上腺素或肾上腺素诱导的收缩,但哌唑嗪(1 μM)则无此作用。河豚毒素(780 nM)可部分减弱去甲肾上腺素或肾上腺素诱导的收缩,但阿托品(500 nM)则无此作用。在存在阿托品(1 μM)的情况下,经壁电刺激可引起频率依赖性、对河豚毒素敏感的收缩。这些结果表明,去甲肾上腺素或肾上腺素诱导的收缩反应是由α2 - 肾上腺素能受体介导的。还表明,去甲肾上腺素和肾上腺素通过直接作用以及通过非胆碱能兴奋性神经的间接作用使平滑肌收缩。