Gao R, Penzes P
Department of Physiology, Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA.
Curr Mol Med. 2015;15(2):146-67. doi: 10.2174/1566524015666150303003028.
Autism Spectrum Disorders (ASD) and Schizophrenia (SCZ) are cognitive disorders with complex genetic architectures but overlapping behavioral phenotypes, which suggests common pathway perturbations. Multiple lines of evidence implicate imbalances in excitatory and inhibitory activity (E/I imbalance) as a shared pathophysiological mechanism. Thus, understanding the molecular underpinnings of E/I imbalance may provide essential insight into the etiology of these disorders and may uncover novel targets for future drug discovery. Here, we review key genetic, physiological, neuropathological, functional, and pathway studies that suggest alterations to excitatory/inhibitory circuits are keys to ASD and SCZ pathogenesis.
自闭症谱系障碍(ASD)和精神分裂症(SCZ)是具有复杂遗传结构但行为表型重叠的认知障碍,这表明存在共同的通路扰动。多条证据表明兴奋性和抑制性活动失衡(E/I失衡)是一种共同的病理生理机制。因此,了解E/I失衡的分子基础可能为这些疾病的病因提供重要见解,并可能发现未来药物研发的新靶点。在这里,我们综述了关键的遗传、生理、神经病理学、功能和通路研究,这些研究表明兴奋性/抑制性回路的改变是ASD和SCZ发病机制的关键。