Life and Health Sciences Research Institute (ICVS), School of Medicine, Campus of Gualtar, University of Minho, 4710-057 Braga, Portugal; ICVS/3B's, PT Government Associate Laboratory, Braga, Guimarães, Portugal.
Life and Health Sciences Research Institute (ICVS), School of Medicine, Campus of Gualtar, University of Minho, 4710-057 Braga, Portugal; ICVS/3B's, PT Government Associate Laboratory, Braga, Guimarães, Portugal; Polytechnic Institute of Viana do Castelo, Viana do Castelo, Portugal.
Brain Res Bull. 2021 Feb;167:56-70. doi: 10.1016/j.brainresbull.2020.11.018. Epub 2020 Nov 26.
Chronic neuropathic pain affects 7-10 % of the population and is often accompanied by comorbid emotional disorders, which greatly reduce the quality of life of the patients, impairing physical, cognitive, emotional, and social functioning. Despite the higher prevalence and severity of chronic pain in women, the number of publications using female animals remains scarce. While in the chronic constriction injury (CCI) model the development of mechanical/thermal hyperalgesia, allodynia and spontaneous pain has been shown in both sexes, little is known on CCI-induced emotional impairments and sciatic nerve histopathology in female rats, as well as on the contributions of ovarian hormones to peripheral nerve injury. In this work, young adult rats (Wistar Han) were assigned to one of five groups: gonadally intact females (SHAM/SHAM), ovariectomized females (SHAM/OVX), gonadally intact females with CCI (CCI/SHAM); ovariectomized females with CCI (CCI/OVX) and males with CCI (CCI). In the postoperative period, CCI animals, both females and males, displayed visible gait abnormalities, limping and guarding the affected hind paw although locomotion was not affected. Neuropathic females developed sustained mechanical allodynia, with CCI/OVX animals displaying symptoms two weeks before CCI/SHAM females. Interestingly, regarding mechanical and cold allodynia, CCI males slowly recovered from week 3 onwards. While CCI induced neither anxiety- nor depressive-like behaviour in females, ovariectomy per se induced anhedonic-like behaviour, regardless of CCI surgery. Histopathological analysis of the sciatic nerve showed CCI induced nerve damage, fibrosis, myelin sheath degradation and inflammation. Single-cell electrophysiological data from the rostral ventromedial medulla (RVM) suggests this area is partly involved in descending facilitation associated with experimental neuropathic pain. Altogether, our findings demonstrate CCI females display distinct sensory, emotional, electrophysiological, and histopathological impairments from males, and that ovariectomy aggravates females' responses to peripheral nerve injury.
慢性神经性疼痛影响了 7-10%的人群,常伴有合并的情绪障碍,极大地降低了患者的生活质量,损害了身体、认知、情感和社交功能。尽管女性慢性疼痛的患病率和严重程度更高,但使用雌性动物的出版物数量仍然很少。虽然在慢性缩窄性损伤 (CCI) 模型中,两性都表现出机械/热痛觉过敏、痛觉过敏和自发性疼痛,但对于雌性大鼠 CCI 引起的情绪障碍和坐骨神经组织病理学以及卵巢激素对周围神经损伤的影响知之甚少。在这项工作中,年轻成年大鼠(Wistar Han)被分为五组之一:性腺完整的雌性(SHAM/SHAM)、卵巢切除的雌性(SHAM/OVX)、CCI 后的性腺完整雌性(CCI/SHAM);CCI 后的卵巢切除雌性(CCI/OVX)和 CCI 的雄性。在术后期间,CCI 动物,无论是雌性还是雄性,都表现出明显的步态异常,跛行和保护受影响的后脚,尽管运动不受影响。神经性雌性动物发展出持续的机械痛觉过敏,CCI/OVX 动物在 CCI/SHAM 雌性动物之前两周出现症状。有趣的是,关于机械和冷痛觉过敏,CCI 雄性动物从第 3 周开始缓慢恢复。虽然 CCI 没有引起雌性动物出现焦虑或抑郁样行为,但卵巢切除本身会引起快感缺失样行为,而与 CCI 手术无关。坐骨神经的组织病理学分析显示 CCI 引起了神经损伤、纤维化、髓鞘降解和炎症。来自吻侧腹内侧髓质 (RVM) 的单细胞电生理数据表明,该区域部分参与与实验性神经性疼痛相关的下行易化。总的来说,我们的研究结果表明,CCI 雌性动物表现出与雄性动物不同的感觉、情绪、电生理和组织病理学损伤,并且卵巢切除加重了雌性动物对周围神经损伤的反应。