Smet P J, Moore K H, Jonavicius J
Division of Surgery, Repatriation General Hospital, Daw Park, Australia.
Lab Invest. 1997 Jul;77(1):37-49.
The distribution of nerves containing calcitonin gene-related peptide (CGRP), substance P (SP), neurokinin A (NKA), and vasoactive intestinal peptide (VIP) was examined in the human urinary bladder, using both single- and double-label immunohistochemistry. Nerves containing CGRP and tachykinins were typically present within the subepithelial region, encircling intramural ganglia and around blood vessels. These nerves were sparsely distributed, and only very rarely projected to the smooth muscle bundles of the detrusor. In contrast, VIP-containing nerves formed a dense subepithelial plexus and also projected to the detrusor muscle bundles. The double-label studies revealed that approximately 26% +/- 10% of CGRP-immunoreactive nerves also contained SP and NKA, but that no CGRP fibers coexpressed VIP. Conversely, all SP-immunoreactive fibers also contained CGRP, and many coexpressed NKA. At least three neurochemically distinct populations of nerves can therefore be discerned in the human bladder: VIP/-, CGRP/-, and CGRP/SP/ +/- NKA. The density of CGRP and SP-immunoreactive nerves within the subepithelium of 14 women with urodynamically-proven idiopathic detrusor instability was increased by 82% (p = 0.003) and 94% (p = 0.036), respectively, relative to that of 14 control women with no symptoms of frequency or urgency. This effect was not due to an increase in overall nerve density, because immunoreactivity for the general nerve marker, protein gene product, was not significantly different between the two groups (p = 0.21). The results indicate that at least some patients with detrusor instability demonstrate increases in a specific class of nerve fibers containing CGRP and SP. These peptides are characteristic of sensory neurons in a number of species, suggesting that abnormalities in the afferent arm of the micturition reflex may be associated with detrusor instability.
运用单标记和双标记免疫组织化学方法,对人膀胱中含降钙素基因相关肽(CGRP)、P物质(SP)、神经激肽A(NKA)和血管活性肠肽(VIP)的神经分布进行了研究。含CGRP和速激肽的神经通常位于上皮下区域,环绕壁内神经节和血管周围。这些神经分布稀疏,极少投射至逼尿肌的平滑肌束。相比之下,含VIP的神经形成密集的上皮下神经丛,也投射至逼尿肌束。双标记研究显示,约26%±10%的CGRP免疫反应性神经也含SP和NKA,但无CGRP纤维共表达VIP。相反,所有SP免疫反应性纤维也含CGRP,且许多共表达NKA。因此,在人膀胱中可辨别出至少三种神经化学性质不同的神经群体:VIP/-、CGRP/-和CGRP/SP/+/-NKA。与14名无尿频或尿急症状的对照女性相比,14名经尿动力学证实为特发性逼尿肌不稳定的女性上皮下CGRP和SP免疫反应性神经密度分别增加了82%(p = 0.003)和94%(p = 0.036)。这种效应并非由于总神经密度增加,因为两组间一般神经标志物蛋白基因产物的免疫反应性无显著差异(p = 0.21)。结果表明,至少部分逼尿肌不稳定患者特定类型的含CGRP和SP的神经纤维增加。这些肽是许多物种感觉神经元的特征,提示排尿反射传入支异常可能与逼尿肌不稳定有关。