Messell T, Harling H, Poulsen S S, Bersani M, Holst J J
Department of Medical Physiology, Panum Institute, Copenhagen, Denmark.
Regul Pept. 1992 Apr 9;38(3):179-98. doi: 10.1016/0167-0115(92)90101-y.
By immunohistochemistry galanin-like immunoreactivity and vasoactive intestinal polypeptide (VIP)-like immunoreactivity were found in nerve cell bodies mostly in the submucous plexus and in nerve fibres in the mucosa, submucosa and muscularis including the myenteric plexus of the porcine ileum and were found to co-exist in most of these structures. Using isolated, perfused porcine ileum we studied the release of galanin and VIP in response to electrical stimulation of the mixed periarterial nerves or to intraarterial infusions of different neuroactive agents. Nerve stimulation (4-10 Hz) inhibited the basal release of galanin and VIP from the ileum (to 69 +/- 6 and 62 +/- 6% of basal release). After infusion of the alpha-adrenergic blocker, phentolamine, (10(-6) M) electrical stimulation increased the release of both galanin and VIP (to 140 +/- 12 and 133 +/- 13% of basal output). This increase was abolished by atropine (10(-6) M) and by hexamethonium (3.10(-5) M). Infusion of norepinephrine (10(-6) M) inhibited, whereas acetylcholine (10(-6) M) stimulated the release of both peptides. The effect of the latter was abolished by atropine. The inhibitory effect of nerve stimulation was not influenced by atropine. Our results suggest that the galanin- and VIP-producing intrinsic neurons receive inhibitory signals by noradrenergic nerve fibers and stimulatory signals mediated by cholinergic nerves, possibly via a cholinergic interneuron.
通过免疫组织化学方法发现,在猪回肠的黏膜下神经丛中的神经细胞体以及黏膜、黏膜下层和肌层(包括肌间神经丛)的神经纤维中存在甘丙肽样免疫反应性和血管活性肠肽(VIP)样免疫反应性,并且在这些结构中的大多数中发现它们共存。使用离体灌注的猪回肠,我们研究了甘丙肽和VIP在混合动脉周围神经电刺激或不同神经活性药物动脉内输注后的释放情况。神经刺激(4 - 10 Hz)抑制了回肠中甘丙肽和VIP的基础释放(降至基础释放量的69±6%和62±6%)。在输注α-肾上腺素能阻滞剂酚妥拉明(10⁻⁶ M)后,电刺激增加了甘丙肽和VIP的释放(分别增至基础输出量的140±12%和133±13%)。这种增加被阿托品(10⁻⁶ M)和六甲铵(3×10⁻⁵ M)消除。去甲肾上腺素(10⁻⁶ M)输注抑制了两种肽的释放,而乙酰胆碱(10⁻⁶ M)刺激了两种肽的释放。后者的作用被阿托品消除。神经刺激的抑制作用不受阿托品影响。我们的结果表明,产生甘丙肽和VIP的内在神经元通过去甲肾上腺素能神经纤维接收抑制性信号,并通过胆碱能神经介导的刺激性信号,可能是通过胆碱能中间神经元。