Blanquet F, Bouvier M, Gonella J
Br J Pharmacol. 1982 Nov;77(3):419-29. doi: 10.1111/j.1476-5381.1982.tb09314.x.
1 The effects of Leu-enkephalin, Met-enkephalin and morphine on excitatory junction potentials (e.j.ps) and inhibitory junction potentials (i.j.ps) elicited by stimulation of efferent parasympathetic nerves were studied in cats and rabbits, anaesthetized and in vitro.2 Enkephalins (0.008 mg/kg in vivo and 10(-6)M in vitro) enhanced e.j.p. amplitude in rabbit proximal colon and decreased it in rabbit distal colon and in cat colon. Enkephalins decreased i.j.p. amplitude in all the three models.3 Morphine (0.2 mg/kg in vivo and 10(-6)M in vitro) had the same effects as enkephalins on e.j.ps. In contrast, morphine decreased i.j.p. amplitude in rabbit proximal and distal colon and increased it in cat colon.4 Enkephalins and morphine induced (especially in the cat) spike activity which was potentiated by atropine (0.1 mg/kg in vivo or 10(-6)M in vitro).5 All the effects of enkephalins and morphine were antagonized by naloxone (0.2 mg/kg in vivo or 10(-6)M in vitro).6 These results suggest that the facilitatory effects of enkephalins and morphine on e.j.ps of rabbit proximal colon are due to the absence of opiate receptors on the excitatory nerve pathway and to a removal of inhibition by blockade of the non-adrenergic, non-cholinergic inhibitory pathway. Enkephalinergic intramural neurones may modulate the activation of either excitatory or inhibitory pathways in intramural reflexes.
在麻醉的猫和兔以及体外实验中,研究了亮氨酸脑啡肽、甲硫氨酸脑啡肽和吗啡对刺激传出副交感神经所诱发的兴奋性接头电位(e.j.ps)和抑制性接头电位(i.j.ps)的影响。
脑啡肽(体内0.008mg/kg,体外10⁻⁶M)增强兔近端结肠的e.j.p.幅度,而降低兔远端结肠和猫结肠的e.j.p.幅度。脑啡肽降低所有三种模型中的i.j.p.幅度。
吗啡(体内0.2mg/kg,体外10⁻⁶M)对e.j.ps的作用与脑啡肽相同。相反,吗啡降低兔近端和远端结肠的i.j.p.幅度,而增加猫结肠的i.j.p.幅度。
脑啡肽和吗啡诱导(尤其是在猫中)锋电位活动,该活动可被阿托品(体内0.1mg/kg或体外10⁻⁶M)增强。
脑啡肽和吗啡的所有作用均被纳洛酮(体内0.2mg/kg或体外10⁻⁶M)拮抗。
这些结果表明,脑啡肽和吗啡对兔近端结肠e.j.ps的促进作用是由于兴奋性神经通路上不存在阿片受体,以及通过阻断非肾上腺素能、非胆碱能抑制性通路而消除了抑制作用。含脑啡肽的壁内神经元可能调节壁内反射中兴奋性或抑制性通路的激活。