Department of Cardiovascular Ultrasound, The People's Hospital of China Medical University & The People's Hospital of Liaoning Province, Shenyang, China.
Department of Psychiatry, The First Hospital of China Medical University, Shenyang, China.
Transl Psychiatry. 2021 Sep 27;11(1):495. doi: 10.1038/s41398-021-01617-y.
Schizophrenia (SZ) is a neurodevelopmental disorder. There remain significant gaps in understanding the neural trajectory across development in SZ. A major research focus is to clarify the developmental functional changes of SZ and to identify the specific timing, the specific brain regions, and the underlying mechanisms of brain alterations during SZ development. Regional homogeneity (ReHo) characterizing brain function was collected and analyzed on humans with SZ (hSZ) and healthy controls (HC) cross-sectionally, and methylazoxymethanol acetate (MAM) rats, a neurodevelopmental model of SZ, and vehicle rats longitudinally from adolescence to adulthood. Metabolomic and proteomic profiling in adult MAM rats and vehicle rats was examined and bioanalyzed. Compared to HC or adult vehicle rats, similar ReHo alterations were observed in hSZ and adult MAM rats, characterized by increased frontal (medial prefrontal and orbitofrontal cortices) and decreased posterior (visual and associated cortices) ReHo. Longitudinal analysis of MAM rats showed aberrant ReHo patterns as decreased posterior ReHo in adolescence and increased frontal and decreased posterior ReHo in adulthood. Accordingly, it was suggested that the visual cortex was a critical locus and adolescence was a sensitive window in SZ development. In addition, metabolic and proteomic alterations in adult MAM rats suggested that central carbon metabolism disturbance and mitochondrial dysfunction were the potential mechanisms underlying the ReHo alterations. This study proposed frontal-posterior functional imbalance and aberrant function developmental patterns in SZ, suggesting that the adolescent visual cortex was a critical locus and a sensitive window in SZ development. These findings from linking data between hSZ and MAM rats may have a significant translational contribution to the development of effective therapies in SZ.
精神分裂症(SZ)是一种神经发育障碍。目前,对于 SZ 患者在整个发育过程中的神经轨迹仍存在很大的理解差距。一个主要的研究重点是阐明 SZ 的发育功能变化,并确定 SZ 发育过程中大脑改变的特定时间、特定脑区和潜在机制。本研究通过对横断面 SZ 患者(hSZ)和健康对照(HC)以及纵向从青春期到成年的亚氨基二乙酸(MAM)大鼠和载体大鼠进行脑功能区域一致性(ReHo)特征分析,研究了 SZ 发育过程中的脑功能变化。并对成年 MAM 大鼠和载体大鼠进行了代谢组学和蛋白质组学分析。与 HC 或成年载体大鼠相比,hSZ 和成年 MAM 大鼠均表现出类似的 ReHo 改变,特征为额部(内侧前额叶和眶额皮质)增加和后部(视觉和相关皮质)减少。MAM 大鼠的纵向分析显示,青春期时后部 ReHo 减少,成年时额叶和后部 ReHo 增加,存在异常的 ReHo 模式。因此,认为视觉皮层是 SZ 发育的关键部位,青春期是 SZ 发育的敏感窗口。此外,成年 MAM 大鼠的代谢和蛋白质组学改变表明,中枢碳代谢紊乱和线粒体功能障碍可能是 ReHo 改变的潜在机制。本研究提出了 SZ 中的额-后功能失衡和异常功能发育模式,提示青春期视觉皮层是 SZ 发育的关键部位和敏感窗口。这些将 hSZ 和 MAM 大鼠的数据进行关联的发现,可能对 SZ 有效治疗方法的开发具有重要的转化意义。