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The GLP-1 Receptor Agonist Exendin-4 and Diazepam Differentially Regulate GABAA Receptor-Mediated Tonic Currents in Rat Hippocampal CA3 Pyramidal Neurons.

PLoS One · 2015

Last updated 2026-05-28

In a study on rat brain cells, the GLP-1 drug exendin-4 (10 nM) and the anti-anxiety drug diazepam (1 μM) both increased certain brain cell activity linked to calming signals. When used together, exendin-4 only further increased a specific type of signal (tonic current) by doubling it, while diazepam alone had already increased both tonic and synaptic signals by factors of 1.3 to 1.6.

AI summary of the abstract below.

JournalPLoS One, 2015
Citations25
Relative citation ratio1.01
NIH percentile51
Molecules
Conditions studied Alzheimers, Anxiety, Depression

Abstract

Glucagon-like peptide-1 (GLP-1) is a metabolic hormone that is secreted in a glucose-dependent manner and enhances insulin secretion. GLP-1 receptors are also found in the brain where their signalling affects neuronal activity. We have previously shown that the GLP-1 receptor agonists, GLP-1 and exendin-4 enhanced GABA-activated synaptic and tonic currents in rat hippocampal CA3 pyramidal neurons. The hippocampus is the centre for memory and learning and is important for cognition. Here we examined if exendin-4 similarly enhanced the GABA-activated currents in the presence of the benzodiazepine diazepam. In whole-cell recordings in rat brain slices, diazepam (1 μM), an allosteric positive modulator of GABAA receptors, alone enhanced the spontaneous inhibitory postsynaptic current (sIPSC) amplitude and frequency by a factor of 1.3 and 1.6, respectively, and doubled the tonic GABAA current normally recorded in the CA3 pyramidal cells. Importantly, in the presence of exendin-4 (10 nM) plus diazepam (1 μM), only the tonic but not the sIPSC currents transiently increased as compared to currents recorded in the presence of diazepam alone. The results suggest that exendin-4 potentiates a subpopulation of extrasynaptic GABAA receptors in the CA3 pyramidal neurons.

Verbatim abstract via PubMed 25927918 ↗