Zochodne D W, Allison J A, Ho W, Ho L T, Hargreaves K, Sharkey K A
Department of Clinical Neurosciences, University of Calgary, Alberta, Canada.
Am J Physiol. 1995 Feb;268(2 Pt 2):H584-90. doi: 10.1152/ajpheart.1995.268.2.H584.
Calcitonin gene-related peptide (CGRP) is a potent vasodilator and widely distributed neuropeptide that may participate in the injury response of peripheral nerve. We examined evidence for the presence of CGRP immunoreactivity (IR) and its activity in experimental neuromas of Sprague-Dawley rats created by sectioning the midsciatic nerve with resection of 2-3 cm of its distal portion and branches. CGRP activity was evaluated by measuring local blood flow in neuromas using hydrogen polarography and laser-Doppler flowmetry. At all time points studied after nerve section (24 h, 48 h, 7 days, 14 days) there was a rise in local blood flow in the neuroma stumps. At 48 h the hyperemia was maximum but was reversed by topical application of human CGRP(8--37), a specific CGRP-receptor antagonist. CGRP presence was evaluated by immunohistochemistry and radioimmunoassay (RIA). At 24 and 48 h, CGRP IR was intense and distributed in a globular and diffuse pattern apparently not confined to discrete axonlike profiles. At 7 and 14 days, CGRP IR remained prominent and was associated with disorganized axonlike profiles, sometimes directed in a circumferential pattern around the outside of the neuroma. RIA confirmed rises in CGRP content at 24 and 48 h that accompanied the changes in local blood flow and altered distribution of CGRP IR. CGRP accumulates in a time-related fashion within experimental neuromas, where it induces among other possible actions prominent local vasodilatation. CGRP may be important in the regenerative milieu of injured nerves.
降钙素基因相关肽(CGRP)是一种强效血管舒张剂,是广泛分布的神经肽,可能参与周围神经的损伤反应。我们通过切断Sprague-Dawley大鼠坐骨神经中段并切除其2 - 3厘米远侧部分及其分支来制造实验性神经瘤,研究了CGRP免疫反应性(IR)及其活性的证据。通过使用氢极谱法和激光多普勒血流仪测量神经瘤中的局部血流来评估CGRP活性。在神经切断后的所有研究时间点(24小时、48小时、7天、14天),神经瘤残端的局部血流均增加。在48小时时充血最为明显,但局部应用人CGRP(8 - 37)(一种特异性CGRP受体拮抗剂)可使其逆转。通过免疫组织化学和放射免疫测定法(RIA)评估CGRP的存在。在24小时和48小时时,CGRP IR强烈,呈球状和弥漫性分布,显然不限于离散的轴突样结构。在7天和14天时,CGRP IR仍然突出,并与杂乱无章的轴突样结构相关,有时呈围绕神经瘤外部的圆周模式。RIA证实24小时和48小时时CGRP含量升高,这与局部血流变化和CGRP IR分布改变相伴。CGRP在实验性神经瘤内以时间相关的方式积累,在其中它除了可能的其他作用外还诱导明显的局部血管舒张。CGRP在受损神经的再生环境中可能很重要。