Spinal neuronal activity and neuroinflammatory component in a mouse model of CFA-induced vestibulodynia

小胶质细胞 痛觉超敏 脊髓 神经科学 医学 加巴喷丁 慢性疼痛 神经可塑性 神经炎症 心理学 伤害 痛觉过敏 病理 炎症 内科学 受体 替代医学
作者
Serena Boccella,Michela Perrone,Antimo Fusco,Roozbe Bonsale,Rosmara Infantino,Silvia Nuzzo,Giovanni Pecoraro,Federica Ricciardi,Andrea Maria Morace,Gianluca Petrillo,Ilaria Leone,Monica Franzese,Vito de Novellis,Francesca Guida,Marco Salvatore,Sabatino Maione,Livio Luongo
出处
期刊:Brain Behavior and Immunity [Elsevier]
卷期号:119: 408-415
标识
DOI:10.1016/j.bbi.2024.04.012
摘要

Vestibulodynia is a complex pain disorder characterized by chronic discomfort in the vulvar region, often accompanied by tactile allodynia and spontaneous pain. In patients a depressive behaviour is also observed. In this study, we have used a model of vestibulodynia induced by complete Freund's adjuvant (CFA) focusing our investigation on the spinal cord neurons and microglia. We investigated tactile allodynia, spontaneous pain, and depressive-like behavior as key behavioral markers of vestibulodynia. In addition, we conducted in vivo electrophysiological recordings to provide, for the first time to our knowledge, the characterization of the spinal sacral neuronal activity in the L6-S1 dorsal horn of the spinal cord. Furthermore, we examined microglia activation in the L6-S1 dorsal horn using immunofluorescence, unveiling hypertrophic phenotypes indicative of neuroinflammation in the spinal cord. This represents a novel insight into the role of microglia in vestibulodynia pathology. To address the therapeutic aspect, we employed pharmacological interventions using GABApentin, amitriptyline, and PeaPol. Remarkably, all three drugs, also used in clinic, showed efficacy in alleviating tactile allodynia and depressive-like behavior. Concurrently, we also observed a normalization of the altered neuronal firing and a reduction of microglia hypertrophic phenotypes. In conclusion, our study provides a comprehensive understanding of the CFA-induced model of vestibulodynia, encompassing behavioral, neurophysiological and neuroinflammatory aspects. These data pave the way to investigate spinal cord first pain plasticity in vestibulodynia.
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