Ekblad E, Arnbjörnsson E, Ekman R, Håkanson R, Sundler F
Department of Medical Cell Research, Lund, Sweden.
Dig Dis Sci. 1989 Aug;34(8):1217-30. doi: 10.1007/BF01537270.
At present our knowledge of enteric peptide-containing neurons in man is limited. In this study we have used human appendices removed at surgery to examine the peptidergic innervation by immunocytochemistry, immunochemistry, and pharmacological in vitro experiments. Immunocytochemistry revealed a variety of peptide-containing nerve fiber populations in the human appendix. VIP/PHI-, VIP/PHI/NPY-, SP/NKA-, galanin-, and enkephalin-containing nerve fibers were numerous; CGRP- and GRP-containing nerve fibers were moderate in number, while only scattered NPY-, enkephalin/BAM-, and somatostatin-containing nerve fibers could be found. No CCK-, dynorphin A-, or dynorphin B-immunoreactive nerve fibers could be detected. The coexistence of VIP/PHI, SP/NKA, and enkaphalin/BAM can be anticipated from the known sequence of their respective precursors. However, the coexistence of VIP/PHI and NPY was unexpected but corroborates previous observations in other species. Interestingly, SP and CGRP did not seem to coexist in nerve fibers of the human appendix. Immunochemistry (RIA and HPLC) confirmed the presence of VIP, NPY, SP, galanin, CGRP, GRP, enkephalin, and somatostatin. Motor activity studies suggest that acetylcholine plays a major role in the electrically evoked contractions, since atropine suppressed these contractions. Galanin (10(-8)-10(-6) M) and GRP (10(-9)-10(-7) M) caused concentration-dependent contractions that were unaffected by tetrodotoxin and thus probably reflect a direct action on smooth muscle receptors. GRP (10(-9) M) enhanced the electrically induced cholinergic contraction (to 193 +/- 24%), while met-enkephalin (10(-6) M) reduced it (to 54 +/- 6%). Both peptides failed to affect the contractile response to exogenous acetylcholine and probably act to modulate the release of acetylcholine. NPY, VIP, CGRP, SP, and somatostatin failed to induce contraction or to affect the electrically evoked contractions.
目前,我们对人类肠道含肽神经元的了解有限。在本研究中,我们利用手术切除的人体阑尾,通过免疫细胞化学、免疫化学和体外药理学实验来检测肽能神经支配。免疫细胞化学显示,人体阑尾中存在多种含肽神经纤维群体。含血管活性肠肽/肽组氨酸异亮氨酸、血管活性肠肽/肽组氨酸异亮氨酸/神经肽Y、速激肽/神经激肽A、甘丙肽和脑啡肽的神经纤维数量众多;含降钙素基因相关肽和胃泌素释放肽的神经纤维数量中等,而仅能发现散在的含神经肽Y、脑啡肽/铃蟾肽和生长抑素的神经纤维。未检测到含胆囊收缩素、强啡肽A或强啡肽B的免疫反应性神经纤维。血管活性肠肽/肽组氨酸异亮氨酸、速激肽/神经激肽A和脑啡肽/铃蟾肽的共存可根据其各自前体的已知序列推测得出。然而,血管活性肠肽/肽组氨酸异亮氨酸和神经肽Y的共存出乎意料,但证实了先前在其他物种中的观察结果。有趣的是,速激肽和降钙素基因相关肽似乎不在人体阑尾的神经纤维中共存。免疫化学(放射免疫分析和高效液相色谱法)证实了血管活性肠肽、神经肽Y、速激肽、甘丙肽、降钙素基因相关肽、胃泌素释放肽、脑啡肽和生长抑素的存在。运动活性研究表明,乙酰胆碱在电诱发的收缩中起主要作用,因为阿托品可抑制这些收缩。甘丙肽(10⁻⁸ - 10⁻⁶ M)和胃泌素释放肽(10⁻⁹ - 10⁻⁷ M)引起浓度依赖性收缩,且不受河豚毒素影响,因此可能反映了对平滑肌受体的直接作用。胃泌素释放肽(10⁻⁹ M)增强了电诱发的胆碱能收缩(至193±24%),而甲硫氨酸脑啡肽(10⁻⁶ M)则使其减弱(至54±6%)。这两种肽均未影响对外源性乙酰胆碱的收缩反应,可能作用于调节乙酰胆碱的释放。神经肽Y、血管活性肠肽、降钙素基因相关肽、速激肽和生长抑素未能诱导收缩或影响电诱发的收缩。