BULBRING E, CREMA A
Br J Pharmacol Chemother. 1958 Dec;13(4):444-57. doi: 10.1111/j.1476-5381.1958.tb00236.x.
In isolated guinea-pig intestine 5-hydroxytryptamine increased the longitudinal muscle contractions in response to acetylcholine while the ganglionic action of nicotine was first facilitated and then blocked. Phenyldiguanide, veratrine, veratridine and protoveratrine, like 5-hydroxytryptamine, depressed the response to nicotine, leaving that to acetylcholine unaffected.The sensory stimulants, like 5-hydroxytryptamine, facilitated the peristaltic reflex when applied to the mucosa, and abolished it when applied to the serosa. Preceding the block, the initial effect of low concentrations of 5-hydroxytryptamine applied to the serosa was a short stimulation of peristalsis.Concentrations of 5-hydroxytryptamine which had an approximately equal stimulant action (mucosal 1 to 4 x 10(-6), serosal 2 to 8 x 10(-8)) were tested when various parts of the reflex arc were blocked. During block by procaine introduced into the lumen, mucosal application of 5-hydroxytryptamine re-established peristalsis, but serosal application of 5-hydroxytryptamine had no effect. During block by hexamethonium or atropine present in the bath, 5-hydroxytryptamine restored peristalsis more effectively by serosal application than by mucosal application. During block by serosal application of 5-hydroxytryptamine, morphine, phenoxybenzamine or dihydroergotamine, mucosal application of 5-hydroxytryptamine restored the peristaltic reflex while serosal application had no effect. During block by 2-bromo-lysergic acid diethylamide or lysergic acid diethylamide acting from the serosal surface, 5-hydroxytryptamine had no effect whether acting on the mucosal or on the serosal surface.It is concluded that 5-hydroxytryptamine facilitates the peristaltic reflex at two sites: when introduced into the lumen it stimulates mucosal sensory receptors; when acting from the serosal surface it sensitizes the muscle to the transmitter acetylcholine. There is also a transient stimulant action on the ganglia which is soon followed by inhibition; this indicates that 5-hydroxytryptamine applied to the serosa abolishes peristalsis by ganglion block.
在离体豚鼠肠中,5-羟色胺可增强乙酰胆碱引起的纵肌收缩,而尼古丁的神经节作用先是增强,随后被阻断。苯二胍、藜芦碱、藜芦定和原藜芦碱与5-羟色胺一样,可抑制对尼古丁的反应,而对乙酰胆碱的反应无影响。感觉刺激剂与5-羟色胺一样,作用于黏膜时可促进蠕动反射,作用于浆膜时则可消除该反射。在阻断之前,低浓度5-羟色胺作用于浆膜的初始效应是短暂刺激蠕动。当反射弧的不同部位被阻断时,测试了具有大致相同刺激作用的5-羟色胺浓度(黏膜1至4×10⁻⁶,浆膜2至8×10⁻⁸)。在通过向肠腔内注入普鲁卡因进行阻断期间,黏膜应用5-羟色胺可恢复蠕动,但浆膜应用5-羟色胺则无作用。在浴液中存在六甲铵或阿托品进行阻断期间,5-羟色胺通过浆膜应用比通过黏膜应用更有效地恢复蠕动。在通过浆膜应用5-羟色胺、吗啡、酚苄明或二氢麦角胺进行阻断期间,黏膜应用5-羟色胺可恢复蠕动反射,而浆膜应用则无作用。在通过2-溴麦角酰二乙胺或麦角酰二乙胺从浆膜表面起作用进行阻断期间,5-羟色胺无论作用于黏膜还是浆膜表面均无作用。结论是,5-羟色胺在两个部位促进蠕动反射:当注入肠腔时,它刺激黏膜感觉受体;当从浆膜表面起作用时,它使肌肉对递质乙酰胆碱敏感。对神经节也有短暂的刺激作用,随后很快出现抑制作用;这表明应用于浆膜的5-羟色胺通过神经节阻断消除蠕动。