Department of Pharmacology, Xuanwu Hospital of Capital Medical University, Beijing Institute for Brain Disorders, Beijing Engineering Research Center for Nerve System Drugs, Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing 100053, China.
Department of Psychiatry, University of Alberta, Edmonton, Alberta, Canada T6G 2R3.
Psychiatry Res. 2017 Nov;257:249-259. doi: 10.1016/j.psychres.2017.07.075. Epub 2017 Jul 31.
Recent studies have shown that white matter lesions play an important role in the pathogenesis of schizophrenia. DHF-6 is a novel flavanone derivative synthesized in our laboratory. The purpose of the present study was to investigate the effects of DHF-6 on behavioral changes and white matter pathology in a 0.2% cuprizone-fed C57BL/6 mice model. The results showed that cuprizone induced a decrease in spontaneous alternations in the Y-maze test, an increase in locomotor activity in the open field test, demyelination determined by electron microscopy, a decline in the expression of myelin basic protein (MBP), a decrease in the differentiation of oligodendrocyte precursor cells (OPCs) into mature oligodendrocytes (OLs), and an activation of microglia and astrocytes in the corpus callosum measured by western blot and/or immunocytochemical analyses. Intragastric administration of DHF-6 (25 and 50mg/kg) for 5-weeks increased the spontaneous alternations, reduced locomotor activity, reversed demyelination and MBP decrease, promoted OPCs differentiation into mature OLs, and inhibited the activation of microglia and astrocytes. These results suggest that DHF-6 may improve cognitive impairment and the positive symptoms of schizophrenia by alleviating white matter lesions via facilitating remyelination and inhibiting neuroinflammation, thus may be beneficial in the treatment of schizophrenia.
最近的研究表明,脑白质病变在精神分裂症的发病机制中起着重要作用。DHF-6 是我们实验室合成的一种新型黄烷酮衍生物。本研究旨在探讨 DHF-6 对 0.2% 双硫仑喂养 C57BL/6 小鼠模型行为改变和脑白质病理学的影响。结果表明,双硫仑诱导 Y 迷宫试验自发交替减少,旷场试验运动活性增加,电镜下脱髓鞘,髓鞘碱性蛋白(MBP)表达下降,少突胶质细胞前体细胞(OPCs)分化为成熟少突胶质细胞(OLs)减少,以及通过western blot 和/或免疫细胞化学分析测量的胼胝体中小胶质细胞和星形胶质细胞的激活。连续 5 周灌胃给予 DHF-6(25 和 50mg/kg)可增加自发交替,减少运动活性,逆转脱髓鞘和 MBP 减少,促进 OPCs 分化为成熟 OLs,并抑制小胶质细胞和星形胶质细胞的激活。这些结果表明,DHF-6 可能通过促进髓鞘再生和抑制神经炎症来改善认知障碍和精神分裂症的阳性症状,从而有益于精神分裂症的治疗。