Astrocytic GABAergic Regulation in Alcohol Use and Major Depressive Disorders

Author:

Ali Dina N.1ORCID,Ali Hossam M.1ORCID,Lopez Matthew R.1ORCID,Kang Shinwoo1,Choi Doo-Sup123ORCID

Affiliation:

1. Department of Molecular Pharmacology and Experimental Therapeutics, Rochester, MN 55905, USA

2. Neuroscience Program, Rochester, MN 55905, USA

3. Department of Psychiatry and Psychology, Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA

Abstract

Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the central nervous system (CNS). Most GABAergic neurons synthesize GABA from glutamate and release it in the synaptic cleft in the CNS. However, astrocytes can also synthesize and release GABA, activating GABA receptors in the neighboring neurons in physiological and pathological conditions. As the primary homeostatic glial cells in the brain, astrocytes play a crucial role in regulating GABA homeostasis and synaptic neurotransmission. Accumulating evidence demonstrates that astrocytic GABA dysregulation is implicated in psychiatric disorders, including alcohol use disorder (AUD) and major depressive disorder (MDD), the most prevalent co-occurring psychiatric disorders. Several current medications and emerging pharmacological agents targeting GABA levels are in clinical trials for treating AUD and MDD. This review offers a concise summary of the role of astrocytic GABA regulation in AUD and MDD. We also provide an overview of the current understanding and areas of debate regarding the mechanisms by which astrocytes regulate GABA in the CNS and their potential significance in the molecular basis of AUD and MDD, paving the way toward future research directions and potential therapeutic target areas within this field.

Funder

Mayo Clinic

the Ulm Foundation

National Institute of Health

Publisher

MDPI AG

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