Exercise Improves Orofacial Pain and Modifies Neuropeptide Expression in a Rat Model of Parkinson's Disease

被引:3
|
作者
Binda, Karina Henrique [2 ,3 ,4 ]
Chacur, Marucia [2 ]
Martins, Daniel Oliveira [1 ,2 ]
机构
[1] Hosp Sirio Libanes, Lab Neurosci, Rua Daher Cutait 69, BR-05508000 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Anat, Lab Funct Neuroanat Pain, Sao Paulo, SP, Brazil
[3] Aarhus Univ, PET Ctr, Dept Nucl Med, Aarhus, Denmark
[4] Aarhus Univ, Translat Neuropsychiat Unit, Aarhus, Denmark
基金
巴西圣保罗研究基金会;
关键词
Parkinson's disease; Trigeminal pain; Treadmill exercise; Rats; 6-OHDA; GENE-RELATED PEPTIDE; ENDOCANNABINOID SYSTEM; SENSORY NEURONS; ACTIVATION; TRPV1; PATHWAY; CGRP;
D O I
10.1007/s12640-023-00651-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pain is a common non-motor symptom of Parkinson's disease (PD), which often occurs in the early disease stages. Despite the high prevalence, it remains inadequately treated. In a hemi-parkinsonian rat model, we aimed to investigate the neurochemical factors involved in orofacial pain development, with a specific focus on pain-related peptides and cannabinoid receptors. We also evaluated whether treadmill exercise could improve orofacial pain and modulate these mechanisms. Rats were unilaterally injected in the striatum with either 6-hydroxydopamine (6-OHDA) or saline. Fifteen days after stereotactic surgery, the animals were submitted to treadmill exercise (EX), or remained sedentary (SED). Pain assessment was performed before the surgical procedure and prior to each training session. Pain-related peptides, substance P (SP), calcitonin gene-related peptide (CGRP), and transient receptor potential vanilloid type 1 (TRPV1) activation and cannabinoid receptor type 1 (CB1) and type 2 (CB2) were evaluated in the trigeminal nucleus. In order to confirm the possible involvement of cannabinoid receptors, we also injected antagonists of CB1 and CB2 receptors. We confirmed the presence of orofacial pain after unilateral 6-OHDA-injection, which improved after aerobic exercise training. We also observed increased pain-related expression of SP, CGRP and TRPV1 and decreased CB1 and CB2 in the trigeminal ganglion and caudal spinal trigeminal nucleus in animals with PD, which was reversed after aerobic exercise training. In addition, we confirm the involvement of cannabinoid receptors since both antagonists decreased the nociceptive threshold of PD animals. These data suggest that aerobic exercise effectively improved the orofacial pain associated with the PD model, and may be mediated by pain-related neuropeptides and cannabinoid receptors in the trigeminal system.
引用
收藏
页码:459 / 470
页数:12
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