Alcohol dependence and withdrawal increase sensitivity of central amygdalar GABAergic synapses to the glucocorticoid receptor antagonist mifepristone in male rats

• Published in: Neurobiology of disease Vol. 164; p. 105610
• Main Authors: Khom, Sophia, Rodriguez, Larry, Gandhi, Pauravi, Kirson, Dean, Bajo, Michal, Oleata, Christopher S., Vendruscolo, Leandro F., Mason, Barbara J., Roberto, Marisa
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-03-2022; Elsevier
• Subjects: Alcohol use disorder; Alcoholism - physiopathology; Amygdala - drug effects; Amygdala - physiopathology; Animals; Central amygdala; eIPSP; Electrophysiology; GABA; GABAergic Neurons - drug effects; GABAergic Neurons - physiology; Glucocorticoid receptors; Hormone Antagonists - pharmacology; Inhibitory Postsynaptic Potentials - drug effects; Male; Mifepristone; Mifepristone - pharmacology; Rats; Rats, Sprague-Dawley; Receptors, Glucocorticoid - antagonists & inhibitors; sIPSC; Synapses - drug effects; Synapses - physiology; Synaptic transmission; Central amygdala; Alcohol use disorder; Synaptic transmission; GABA; Electrophysiology; eIPSP; Mifepristone; Glucocorticoid receptors; sIPSC
• ISSN: 0969-9961; 1095-953X
• DOI: 10.1016/j.nbd.2022.105610

Aberrant glucocorticoid signaling via glucocorticoid receptors (GR) plays a critical role in alcohol use disorder (AUD). Acute alcohol withdrawal and protracted abstinence in dependent rats are associated with increased GR signaling and changes in GR-mediated transcriptional activity in the rat central nucleus of the amygdala (CeA). The GR antagonist mifepristone decreases alcohol consumption in dependent rats during acute withdrawal and protracted abstinence. Regulation of CeA synaptic activity by GR is currently unknown. Here, we utilized mifepristone and the selective GR antagonist CORT118335 (both at 10 μM) as pharmacological tools to dissect the role of GR on GABA transmission in male, adult Sprague-Dawley rats using slice electrophysiology. We subjected rats to chronic intermittent alcohol vapor exposure for 5–7 weeks to induce alcohol dependence. A subset of dependent rats subsequently underwent protracted alcohol withdrawal for 2 weeks, and air-exposed rats served as controls. Mifepristone reduced the frequency of pharmacologically-isolated spontaneous inhibitory postsynaptic currents (sIPSC) in the CeA (medial subdivision) without affecting postsynaptic measures in all groups, suggesting decreased GABA release with the largest effect in dependent rats. CORT118335 did not significantly alter GABA transmission in naïve, but decreased sIPSC frequency in dependent rats. Similarly, mifepristone decreased amplitudes of evoked inhibitory postsynaptic potentials only in dependent rats and during protracted withdrawal. Collectively, our study provides insight into regulation of CeA GABAergic synapses by GR. Chronic ethanol enhances the efficiency of mifepristone and CORT118335, thus highlighting the potential of drugs targeting GR as a promising pharmacological avenue for the treatment of AUD.