Lidberg P, Dahlström A, Lundberg J M, Ahlman H
Regul Pept. 1983 Sep;7(1):41-52. doi: 10.1016/0167-0115(83)90280-x.
In an experimental in vivo model to study gastropyloric motility in the cat a contraction of the stomach and the pyloric sphincter was regularly obtained in animals subjected to electrical vagal nerve stimulation or local intraarterial (i.a.) injection of substance P (SP). Much more infrequently contractile motor responses were recorded at splanchnic nerve stimulation. The contractile effects of SP were sensitive to atropine or local infusion of a SP analogue, (D-Pro2,D-Trp7,9)-SP, indicating that SP activated a final common cholinergic neuron in both stomach and pylorus. However, there seemed to be separate transmission mechanisms in these two regions based on the results of the physiological studies. The vagally induced pyloric contraction was noncholinergic, nonadrenergic, but sensitive to ganglionic blockade (hexamethonium) or the SP analogue, indicating involvement of SP in a peptidergic pathway to the sphincter. The infrequent splanchnically induced pyloric contraction was sensitive to atropine, the SP analogue or ganglionic blockade (hexamethonium) in favour of SP acting on a final cholinergic neuron in this system. On the other hand the gastric contraction, obtained at either extrinsic nerve stimulations or local i.a. injection of SP, was sensitive to atropine or the SP analogue but hexamethonium resistant. These findings suggest antidromic activation of SP-containing axon collaterals of the extrinsic nerves terminating on cholinergic neurons of the gastric wall. When afferent C-fibres of the vagal nerve were selectively activated by local heating, pyloric contraction and gastric relaxation were obtained via vago-vagal reflexes. After cervical vagotomy heating of the distal end of the vagal nerve elicited a gastric contraction, previously demonstrated to be atropine sensitive and hexamethonium resistant, but no pyloric motor response. This suggests that the antidromic activation mechanism was present only in the stomach, not in the pylorus.
在一项研究猫胃幽门运动的体内实验模型中,对接受电迷走神经刺激或局部动脉内(i.a.)注射P物质(SP)的动物,胃和幽门括约肌会规律性地出现收缩。在内脏神经刺激时,收缩性运动反应的记录则少得多。SP的收缩作用对阿托品或局部输注SP类似物(D-脯氨酸2,D-色氨酸7,9)-SP敏感,表明SP激活了胃和幽门中最终的共同胆碱能神经元。然而,根据生理学研究结果,这两个区域似乎存在不同的传递机制。迷走神经诱导的幽门收缩是非胆碱能、非肾上腺素能的,但对神经节阻断(六甲铵)或SP类似物敏感,表明SP参与了通向括约肌的肽能途径。不常见的内脏神经诱导的幽门收缩对阿托品、SP类似物或神经节阻断(六甲铵)敏感,这有利于SP作用于该系统中的最终胆碱能神经元。另一方面,无论是外在神经刺激还是局部动脉内注射SP所获得的胃收缩,对阿托品或SP类似物敏感,但对六甲铵有抗性。这些发现提示终止于胃壁胆碱能神经元的外在神经含SP轴突侧支的逆向激活。当通过局部加热选择性激活迷走神经的传入C纤维时,通过迷走-迷走反射可获得幽门收缩和胃舒张。颈迷走神经切断后,加热迷走神经远端可引起胃收缩,先前已证明该收缩对阿托品敏感且对六甲铵有抗性,但无幽门运动反应。这表明逆向激活机制仅存在于胃中,而不存在于幽门中。