College of Life Science, Henan Normal University, Xinxiang, 453007, Henan, China.
Department of Neurology, Xinxiang City First People's Hospital, Xinxiang, 453000, Henan, China.
J Neuroinflammation. 2024 Jun 19;21(1):159. doi: 10.1186/s12974-024-03152-1.
A significant decrease in estrogen levels puts menopausal women at high risk for major depression, which remains difficult to cure despite its relatively clear etiology. With the discovery of abnormally elevated inflammation in menopausal depressed women, immune imbalance has become a novel focus in the study of menopausal depression. In this paper, we examined the characteristics and possible mechanisms of immune imbalance caused by decreased estrogen levels during menopause and found that estrogen deficiency disrupted immune homeostasis, especially the levels of inflammatory cytokines through the ERα/ERβ/GPER-associated NLRP3/NF-κB signaling pathways. We also analyzed the destruction of the blood-brain barrier, dysfunction of neurotransmitters, blockade of BDNF synthesis, and attenuation of neuroplasticity caused by inflammatory cytokine activity, and investigated estrogen-immuno-neuromodulation disorders in menopausal depression. Current research suggests that drugs targeting inflammatory cytokines and NLRP3/NF-κB signaling molecules are promising for restoring homeostasis of the estrogen-immuno-neuromodulation system and may play a positive role in the intervention and treatment of menopausal depression.
雌激素水平显著下降使绝经后妇女面临重度抑郁症的高风险,尽管其病因相对明确,但这种疾病仍难以治愈。随着绝经后抑郁女性炎症异常升高的发现,免疫失衡已成为绝经后抑郁症研究的一个新焦点。在本文中,我们研究了绝经期间雌激素水平下降引起的免疫失衡的特征和可能机制,发现雌激素缺乏破坏了免疫稳态,特别是通过 ERα/ERβ/GPER 相关 NLRP3/NF-κB 信号通路影响炎症细胞因子水平。我们还分析了炎症细胞因子活性引起的血脑屏障破坏、神经递质功能障碍、BDNF 合成受阻以及神经可塑性减弱,并研究了绝经后抑郁症中的雌激素免疫神经调节紊乱。目前的研究表明,针对炎症细胞因子和 NLRP3/NF-κB 信号分子的药物有望恢复雌激素免疫神经调节系统的稳态,可能在绝经后抑郁症的干预和治疗中发挥积极作用。