Department of Preventive Medicine and Institute of Nutrition and Diseases, School of Public Health, Wenzhou Medical University, Wenzhou, Zhejiang, China; Department of Neurology and Institute of Geriatric Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Department of Neurology and Institute of Geriatric Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Int Immunopharmacol. 2024 Sep 30;139:112715. doi: 10.1016/j.intimp.2024.112715. Epub 2024 Jul 19.
Citalopram and escitalopram are structurally close-related antidepressants and both forms are widely used in the world. We aimed to comparatively evaluate the anti-neuroinflammatory and neuroprotective effects of escitalopram and citalopram in Parkinson's disease (PD) mouse model. Mice were randomly divided into six groups and received 6-hydroxydopamine (6-OHDA) or vehicle administration. The mice were then treated with escitalopram, citalopram or saline for consecutive 7 days. Behaviors, neuroinflammation, neurotransmitters, and neurotoxicity were assessed. Results showed that citalopram but not escitalopram worsened body weight loss and increased freezing time in the PD mice. Both drugs had no impact on the anxiety-like behaviors but ameliorated the depressive-like behaviors as in elevated plus maze and sucrose splash tests. Escitalopram but not citalopram ameliorated motor discoordination in the PD mice as in rotarod test. In accordance, escitalopram but not citalopram attenuated the 6-OHDA-induced nigrostriatal dopaminergic loss. Further mechanistic investigations showed that both drugs mitigated activations of microglia and astrocytes and/or levels of pro-inflammatory cytokines in the PD mice, but escitalopram showed appreciably better effects in the substantia nigra. Neurotransmitter examination in the prefrontal cortex suggested that the two drugs had comparable effects on the disturbed neurotransmitters in the PD mice, but citalopram was prone to disrupt certain normal homeostasis. In conclusion, escitalopram is moderately superior than citalopram to suppress neuroinflammation and to protect against dopaminergic neuronal death and motor discoordination in the 6-OHDA-induced PD mice. Our findings imply that escitalopram shall be prescribed with priority over citalopram to treat PD patients with depression as escitalopram may meanwhile provide greater additional benefits to the patients.
西酞普兰和艾司西酞普兰是结构上密切相关的抗抑郁药,两种形式在世界范围内广泛使用。我们旨在比较评估艾司西酞普兰和西酞普兰在帕金森病(PD)小鼠模型中的抗神经炎症和神经保护作用。小鼠被随机分为六组,接受 6-羟多巴胺(6-OHDA)或载体给药。然后,小鼠连续 7 天用艾司西酞普兰、西酞普兰或生理盐水治疗。评估行为、神经炎症、神经递质和神经毒性。结果表明,西酞普兰而非艾司西酞普兰加重 PD 小鼠体重减轻和增加冻结时间。两种药物对焦虑样行为没有影响,但在高架十字迷宫和蔗糖飞溅试验中改善了抑郁样行为。艾司西酞普兰而非西酞普兰改善了 PD 小鼠的运动协调障碍,如在旋转棒试验中。相应地,艾司西酞普兰而非西酞普兰减轻了 6-OHDA 诱导的黑质纹状体多巴胺能神经元丧失。进一步的机制研究表明,两种药物均减轻了 PD 小鼠小胶质细胞和星形胶质细胞的激活和/或促炎细胞因子的水平,但艾司西酞普兰在黑质中表现出更好的效果。前额叶皮层中的神经递质检查表明,两种药物对 PD 小鼠中受干扰的神经递质具有相当的作用,但西酞普兰更容易破坏某些正常的体内平衡。总之,艾司西酞普兰比西酞普兰更能适度抑制神经炎症,保护多巴胺能神经元死亡和 6-OHDA 诱导的 PD 小鼠运动协调障碍。我们的发现表明,在治疗伴有抑郁的 PD 患者时,应优先开处方艾司西酞普兰,而不是西酞普兰,因为艾司西酞普兰可能会给患者带来更大的额外益处。