Excitatory/inhibitory imbalance in autism spectrum disorder: Implications for interventions and therapeutics
Gaining deeper insight into the excitation–inhibition imbalance is crucial for advancing more effective pharmacological and behavioural interventions in autism spectrum disorders, encompassing approaches such as transcranial magnetic stimulation (TMS), novel drug development, biomarker discovery and patient stratification.
Objectives: Imbalance between excitation and inhibition and increased excitatory-inhibitory (E-I) ratio is a common mechanism in autism spectrum disorders (ASD) that is responsible for the learning and memory, cognitive, sensory, motor deficits, and seizures occurring in these disorders. ASD are very heterogeneous and better understanding of E-I imbalance in brain will lead to better diagnosis and treatments.
Methods: We perform a critical literature review of the causes and presentations of E-I imbalance in ASD.
Results: E-I imbalance in ASD is due primarily to abnormal glutamatergic and GABAergic neurotransmission in key brain regions such as neocortex, hippocampus, amygdala, and cerebellum. Other causes are due to dysfunction of neuropeptides (oxytocin), synaptic proteins (neuroligins), and immune system molecules (cytokines). At the neuropathological level E-I imbalance in ASD is presented as a "minicolumnopathy". E-I imbalance alters the manner by which the brain processes information and regulates behaviour. New developments for investigating E-I imbalance such as optogenetics and transcranial magnetic stimulation (TMS) are presented. Non-invasive brain stimulation methods such as TMS for treatment of the core symptoms of ASD are discussed.
Conclusions: Understanding E-I imbalance has important implications for developing better pharmacological and behavioural treatments for ASD, including TMS, new drugs, biomarkers and patient stratification.
Keywords: Autistic disorder; biomarkers; electroencephalography; transcranial magnetic stimulation; translational medical research.
Read the article: https://pubmed.ncbi.nlm.nih.gov/26469219/