Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.
J Neurochem. 2013 Jul;126(2):165-82. doi: 10.1111/jnc.12261. Epub 2013 May 22.
Psychiatric and neurodegenerative disorders, including intellectual disability, autism spectrum disorders (ASD), schizophrenia (SZ), and Alzheimer's disease, pose an immense burden to society. Symptoms of these disorders become manifest at different stages of life: early childhood, adolescence, and late adulthood, respectively. Progress has been made in recent years toward understanding the genetic substrates, cellular mechanisms, brain circuits, and endophenotypes of these disorders. Multiple lines of evidence implicate excitatory and inhibitory synaptic circuits in the cortex and hippocampus as key cellular substrates of pathogenesis in these disorders. Excitatory/inhibitory balance--modulated largely by dopamine--critically regulates cortical network function, neural network activity (i.e. gamma oscillations) and behaviors associated with psychiatric disorders. Understanding the molecular underpinnings of synaptic pathology and neuronal network activity may thus provide essential insight into the pathogenesis of these disorders and can reveal novel drug targets to treat them. Here, we discuss recent genetic, neuropathological, and molecular studies that implicate alterations in excitatory and inhibitory synaptic circuits in the pathogenesis of psychiatric disorders across the lifespan.
精神神经疾病,包括智力障碍、自闭症谱系障碍(ASD)、精神分裂症(SZ)和阿尔茨海默病,给社会带来了巨大的负担。这些疾病的症状分别在生命的不同阶段表现出来:儿童早期、青少年和晚年。近年来,人们在理解这些疾病的遗传基础、细胞机制、大脑回路和内表型方面取得了进展。多种证据表明,皮质和海马中的兴奋性和抑制性突触回路是这些疾病发病机制的关键细胞基础。兴奋性/抑制性平衡——主要受多巴胺调节——对皮质网络功能、神经网络活动(即伽马振荡)和与精神疾病相关的行为具有关键调节作用。因此,了解突触病理学和神经元网络活动的分子基础可能为这些疾病的发病机制提供重要的见解,并揭示治疗这些疾病的新药物靶点。在这里,我们讨论了最近的遗传、神经病理学和分子研究,这些研究表明,兴奋性和抑制性突触回路的改变与整个生命周期的精神疾病的发病机制有关。