Wu Jianfei, Liu Yu, Wang Binglong, Wang Yilin, Liu Bo, Tan Youguo, Cai Duanfang, Liu Kezhi, Wei Daixu
Zigong Institute of Brain Science, Zigong Psychiatric Research Center, Zigong Affiliated Hospital of Southwest Medical University, Zigong, China.
Department of Psychiatry, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Animal Model Exp Med. 2025 Jul 23. doi: 10.1002/ame2.70059.
Maternal viral infection during pregnancy can lead to maternal immune activation (MIA), increasing the risk of neurodevelopmental disorders in offspring. Amantadine (AMA) exhibits antiviral activity and is widely employed in the management of neurologic conditions. Nevertheless, the efficacy of AMA in treating MIA is currently not established.
MIA was induced by polyinosinic acid-polycytidylic acid (poly(I:C)); AMA was administered from embryonic (E) day 11.5 for 3 days. BV-2 cells were stimulated using poly(I:C) and treated with AMA. Behavior was assessed via open field test, elevated plus maze test, three-chamber sociability test, and marble burying test. Neuronal morphology was vizualized using Nissl stain; apoptosis via TUNEL (terminal deoxynucleotidyl transferase dUTP nick-end labeling) stain; protein expression (Iba1, NeuN, CD68, TNF-α [tumor necrosis factor-alpha], IL-1β [interleukin-1β]) using immunofluorescence (IF); interleukin-6 (IL-6) levels using enzyme-linked immunosorbent assay; reactive oxygen species using staining; Iba1, NeuN, Bcl-2, Bax, and cleaved caspase 3 using Western blot; and gene expression changes using RNA-seq.
AMA treatment reduced the levels of IL-6 in maternal blood, improved autism-like behaviors in MIA offspring, and effectively prevented neuronal damage and neuroinflammation. In vitro cellular studies have demonstrated that AMA effectively downregulates the expression levels of pro-inflammatory cytokines, including IL-6, TNF-α, and IL-1β. RNA-seq analysis indicated that AMA mitigates abnormal activation of microglia by modulating inflammatory pathways associated with IL-6.
AMA can prevent the development of neuropsychiatric disorders in MIA offspring. This effect may be related to its ability to attenuate neuronal damage, reduce neuronal apoptosis, and inhibit neuroinflammation, indicating that the antiviral drug AMA may be a potential treatment for MIA.
孕期母体病毒感染可导致母体免疫激活(MIA),增加后代神经发育障碍的风险。金刚烷胺(AMA)具有抗病毒活性,广泛用于神经系统疾病的治疗。然而,AMA治疗MIA的疗效目前尚未确定。
通过聚肌苷酸-聚胞苷酸(poly(I:C))诱导MIA;从胚胎(E)第11.5天开始给予AMA,持续3天。用poly(I:C)刺激BV-2细胞并用AMA处理。通过旷场试验、高架十字迷宫试验、三室社交试验和埋珠试验评估行为。用尼氏染色观察神经元形态;用TUNEL(末端脱氧核苷酸转移酶dUTP缺口末端标记)染色观察细胞凋亡;用免疫荧光(IF)检测蛋白表达(Iba1、NeuN、CD68、TNF-α[肿瘤坏死因子-α]、IL-1β[白细胞介素-1β]);用酶联免疫吸附测定法检测白细胞介素-6(IL-6)水平;用染色法检测活性氧;用蛋白质印迹法检测Iba1、NeuN、Bcl-2、Bax和裂解的半胱天冬酶3;用RNA测序检测基因表达变化。
AMA治疗降低了母体血液中IL-6的水平,改善了MIA后代的自闭症样行为,并有效预防了神经元损伤和神经炎症。体外细胞研究表明,AMA有效下调了包括IL-6、TNF-α和IL-1β在内的促炎细胞因子的表达水平。RNA测序分析表明,AMA通过调节与IL-6相关的炎症途径减轻小胶质细胞的异常激活。
AMA可预防MIA后代神经精神疾病的发生。这种作用可能与其减轻神经元损伤、减少神经元凋亡和抑制神经炎症的能力有关,表明抗病毒药物AMA可能是治疗MIA的潜在药物。