Cruz Bryan, Borgonetti Vittoria, Bajo Michal, Roberto Marisa
Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA, 92073.
Neurobiol Stress. 2023 Aug 3;26:100562. doi: 10.1016/j.ynstr.2023.100562. eCollection 2023 Sep.
Excessive alcohol use disrupts neuroimmune signaling across various cell types, including neurons, microglia, and astrocytes. The present review focuses on recent, albeit limited, evidence of sex differences in biological factors that mediate neuroimmune responses to alcohol and underlying neuroimmune systems that may influence alcohol drinking behaviors. Females are more vulnerable than males to the neurotoxic and negative consequences of chronic alcohol drinking, reflected by elevations of pro-inflammatory cytokines and inflammatory mediators. Differences in cytokine, microglial, astrocytic, genomic, and transcriptomic evidence suggest females are more reactive than males to neuroinflammatory changes after chronic alcohol exposure. The growing body of evidence supports that innate immune factors modulate synaptic transmission, providing a mechanistic framework to examine sex differences across neurocircuitry. Targeting neuroimmune signaling may be a viable strategy for treating AUD, but more research is needed to understand sex-specific differences in alcohol drinking and neuroimmune mechanisms.
过度饮酒会破坏包括神经元、小胶质细胞和星形胶质细胞在内的各种细胞类型之间的神经免疫信号传导。本综述聚焦于近期虽有限但关于介导酒精神经免疫反应的生物学因素中的性别差异以及可能影响饮酒行为的潜在神经免疫系统的证据。女性比男性更容易受到慢性饮酒的神经毒性和负面后果的影响,这表现为促炎细胞因子和炎症介质水平的升高。细胞因子、小胶质细胞、星形胶质细胞、基因组和转录组学证据的差异表明,慢性酒精暴露后,女性比男性对神经炎症变化更具反应性。越来越多的证据支持先天免疫因子调节突触传递,为研究神经回路中的性别差异提供了一个机制框架。针对神经免疫信号传导可能是治疗酒精使用障碍的可行策略,但需要更多研究来了解饮酒和神经免疫机制中的性别特异性差异。