Wu Hangfei, Dong Zhao, Liu Yinglu, Zhang Qing, Zhang Mingjie, Hu Guanqun, Yu Shengyuan, Han Xun
Department of Neurology, 12520Shanghai Changhai Hospital, Shanghai, China.
Department of Neurology, The First Medical Center, 104607Chinese PLA General Hospital, Beijing, China.
Mol Pain. 2023 Jan-Dec;19:17448069231152129. doi: 10.1177/17448069231152129.
: Migraine is a common type of primary headache with disabling brain dysfunction. It has been found that pituitary adenylate cyclase activating polypeptide (PACAP) is involved in the pathogenesis of migraine, however, the role of PACAP and its receptors in chronic migraine remains unclear. Therefore, the present study aimed to explore the changes of PACAP and its receptors in different duration after recurrent dural inflammation soup stimulations and to investigate the co-expression between PACAP and calcitonin gene-related peptide (CGRP). : Adult male rats were implanted with cannula surrounding superior sagittal sinus, which was followed by dural infusion of inflammatory soup (IS) or normal saline (NS). The rats were randomly divided into 4 groups ( = 8 for each group): IS stimulation for seven days (IS-7 group), IS stimulation for 14 days (IS-14 group), IS stimulation for 21 days (IS-21 group), and NS control for 21 days (CON group). The facial mechanical withdrawal threshold was daily measured during the whole experiment. The behavioral changes (ipsilateral and bilateral face grooming behavior) in a plastic cage of rats were observed and recorded. The expression of PACAP, its receptors (PAC1, VPAC1, VPAC2), and CGRP in the trigeminal ganglia (TG) and the trigeminal nucleus caudalis (TNC) was examined by immunohistochemistry. Immunofluorescence was used to explore the co-expression of PACAP, PAC1 receptor, and CGRP after repeated IS administration in the TG. : The ipsilateral facial grooming time of IS-21 group displayed an apparent increase than CON group after repeated stimulation on day 2, while significant differences were observed on day 14. No differences were found between the IS-21 and CON group in bilateral facial grooming. Dural IS stimulation induced a significantly decrease in facial mechanical withdrawal thresholds. PACAP positive cells in the regions of TNC were gradually decreased with the IS days increasing. PACAP and PAC1 receptor expression in the TG had a trend of increasing first and then decreasing. There was no significant difference in expression of VPAC1 and VPAC2 in the TG and the TNC. Immunofluorescence showed that PACAP was mainly expressed in TG neurons. PACAP and PAC1 receptor co-expression decreased gradually after repetitive IS stimulation. While the co-expression between PACAP and CGRP reached the peak in IS-7 group after repetitive IS stimulation, and then decreased. : This study demonstrated that repetitive chemical stimulations induced a gradual decrease of PACAP in the TNC, while the PACAP and PAC1 receptor expression in TG showed dynamical changes of increasing first and then decreasing after repeated IS administration. These results suggested exhaustion of PACAP could be involved in the duration of chronic migraine and implied PACAP may contribute to the pathology of migraine through the PAC1 receptor, which was associated with CGRP.
偏头痛是一种常见的原发性头痛,伴有使人丧失能力的脑功能障碍。现已发现垂体腺苷酸环化酶激活多肽(PACAP)参与偏头痛的发病机制,然而,PACAP及其受体在慢性偏头痛中的作用仍不清楚。因此,本研究旨在探讨反复硬脑膜炎症汤刺激后不同时间段PACAP及其受体的变化,并研究PACAP与降钙素基因相关肽(CGRP)之间的共表达情况。:成年雄性大鼠在矢状窦上植入套管,随后向硬脑膜内注入炎症汤(IS)或生理盐水(NS)。大鼠被随机分为4组(每组n = 8):IS刺激7天(IS - 7组)、IS刺激14天(IS - 14组)、IS刺激21天(IS - 21组)和NS对照21天(CON组)。在整个实验过程中每天测量面部机械性退缩阈值。观察并记录大鼠在塑料笼中的行为变化(同侧和双侧面部梳理行为)。通过免疫组织化学检测三叉神经节(TG)和三叉神经尾核(TNC)中PACAP及其受体(PAC1、VPAC1、VPAC2)和CGRP的表达。采用免疫荧光法探讨反复给予IS后TG中PACAP、PAC1受体和CGRP的共表达情况。:反复刺激第2天后,IS - 21组同侧面部梳理时间比CON组明显增加,而在第14天观察到显著差异。IS - 21组和CON组在双侧面部梳理方面未发现差异。硬脑膜IS刺激导致面部机械性退缩阈值显著降低。随着IS刺激天数增加,TNC区域的PACAP阳性细胞逐渐减少。TG中PACAP和PAC1受体表达呈先升高后降低的趋势。TG和TNC中VPAC1和VPAC2的表达无显著差异。免疫荧光显示,PACAP主要在TG神经元中表达。反复给予IS刺激后,PACAP与PAC1受体的共表达逐渐降低。而反复给予IS刺激后,PACAP与CGRP的共表达在IS - 7组达到峰值,然后降低。:本研究表明,反复化学刺激导致TNC中PACAP逐渐减少,而反复给予IS后TG中PACAP和PAC1受体表达呈先升高后降低的动态变化。这些结果提示PACAP耗竭可能参与慢性偏头痛的病程,并暗示PACAP可能通过与CGRP相关的PAC1受体促成偏头痛的病理过程。