Santamaria L, Terenghi G, Curtis J, de Blaquière G E, Pereira J H, Turk J L, Polak J M
Department of Histochemistry, Royal Postgraduate Medical School, Hammersmith Hospital, London, U.K.
Int J Lepr Other Mycobact Dis. 1994 Mar;62(1):64-74.
A marked depletion of neuropeptide-immunoreactive nerves, a consequence of the nerve damage which is commonly found in leprosy, has been reported in peripheral tissues of leprosy patients and of a leprosy animal model. The aim of this study was to investigate peripheral reinnervation following a denatured autologous muscle graft in an animal model of leprosy nerve damage. Possible reinnervation of the foot-pad skin was studied by immunohistochemistry using antisera to the neuronal marker protein gene product 9.5 (PGP), the neuropeptides calcitonin gene-related peptide (CGRP), substance P (SP), vasoactive intestinal peptide (VIP), and the C-flanking peptide of neuropeptide Y (CPON). The extent of the reinnervation process was assessed by image analysis quantification at different time points. At 8 weeks after muscle grafting, there were small numbers of immunoreactive nerves (p < 0.05). At 12, 16, and 20 weeks postoperatively there was a gradual increase in all immunostaining. At 20 weeks, no significant difference was found for PGP-, CGRP-, and SP-immunoreactive nerves in the epidermal and subepidermal layers compared to control (contralateral) tissue. In experimental tissue the recovery of immunoreactive nerves around sweat glands took longer (up to 12 weeks) than in other skin compartments, but after that time the recovery was rapid and at 20 weeks no difference was measured for VIP-immunoreactive nerves in comparison with controls. Around blood vessels, the recovery of CGRP- and CPON-immunoreactive fibers was slow, and at 20 weeks a difference with control samples (p < 0.01) was noted. In the same area, there was no significant difference for PGP immunoreactivity between controls and tissues at 20 weeks. In contrast, the immunoreactive nerve bundles in the dermis showed a faster recovery than nerves in other skin areas, with amounts similar to controls at 20 weeks. The significant recovery of immunoreactive nerves, in particular of those containing sensory neuropeptide, is consistent with the described functional recovery.
在麻风病患者和麻风病动物模型的外周组织中,已报道了神经肽免疫反应性神经的显著减少,这是麻风病中常见的神经损伤的结果。本研究的目的是在麻风病神经损伤动物模型中,研究变性自体肌肉移植后的外周神经再支配情况。通过使用针对神经元标记蛋白基因产物9.5(PGP)、神经肽降钙素基因相关肽(CGRP)、P物质(SP)、血管活性肠肽(VIP)和神经肽Y的C端侧翼肽(CPON)的抗血清进行免疫组织化学研究足底皮肤的可能神经再支配。通过在不同时间点进行图像分析定量来评估神经再支配过程的程度。肌肉移植后8周,有少量免疫反应性神经(p<0.05)。术后12周、16周和20周,所有免疫染色逐渐增加。在20周时,与对照(对侧)组织相比,表皮和表皮下层中PGP、CGRP和SP免疫反应性神经没有显著差异。在实验组织中,汗腺周围免疫反应性神经的恢复比其他皮肤区域需要更长时间(长达12周),但在那之后恢复迅速,在20周时,与对照相比,VIP免疫反应性神经没有差异测量。在血管周围,CGRP和CPON免疫反应性纤维的恢复缓慢,在20周时与对照样品有差异(p<;0.01)。在同一区域,20周时对照和组织之间PGP免疫反应性没有显著差异。相比之下,真皮中的免疫反应性神经束比其他皮肤区域的神经恢复更快,在20周时数量与对照相似。免疫反应性神经,特别是那些含有感觉神经肽的神经的显著恢复与所描述的功能恢复一致。