Disruption of circadian timing increases synaptic inhibition and reduces cholinergic responsiveness in the dentate gyrus

• Published in: Hippocampus Vol. 31; no. 4; pp. 422 - 434
• Main Authors: McMartin, Laura, Kiraly, Marianna, Heller, H. Craig, Madison, Daniel V., Ruby, Norman F.
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.04.2021; Wiley Subscription Services, Inc
• Subjects: acetylcholine; Acetylcholine receptors (muscarinic); Animals; Arrhythmia; Carbachol; Cell activation; Cholinergic Agents - pharmacology; Circadian rhythms; Cricetinae; dentate; Dentate gyrus; Dentate Gyrus - physiology; Excitatory Postsynaptic Potentials - physiology; Genomes; Granule cells; Hippocampus; Hippocampus - physiology; Inhibitory postsynaptic potentials; Membrane potential; Mice; Neurons - physiology; Potentiation; Rats; Receptor mechanisms; sex differences; Siberian hamster; Spatial memory; Synaptic Transmission - physiology; carbachol; acetylcholine; hippocampus; sex differences; dentate; Siberian hamster
• ISSN: 1050-9631; 1098-1063
• DOI: 10.1002/hipo.23301

We investigated synaptic mechanisms in the hippocampus that could explain how loss of circadian timing leads to impairments in spatial and recognition memory. Experiments were performed in hippocampal slices from Siberian hamsters (Phodopus sungorus) because, unlike mice and rats, their circadian rhythms are easily eliminated without modifications to their genome and without surgical manipulations, thereby leaving neuronal circuits intact. Recordings of excitatory postsynaptic field potentials and population spikes in area CA1 and dentate gyrus granule cells revealed no effect of circadian arrhythmia on basic functions of synaptic circuitry, including long‐term potentiation. However, dentate granule cells from circadian‐arrhythmic animals maintained a more depolarized resting membrane potential than cells from circadian‐intact animals; a significantly greater proportion of these cells depolarized in response to the cholinergic agonist carbachol (10 μM), and did so by increasing their membrane potential three‐fold greater than cells from the control (entrained) group. Dentate granule cells from arrhythmic animals also exhibited higher levels of tonic inhibition, as measured by the frequency of spontaneous inhibitory postsynaptic potentials. Carbachol also decreased stimulus‐evoked synaptic excitation in dentate granule cells from both intact and arrhythmic animals as expected, but reduced stimulus‐evoked synaptic inhibition only in cells from control hamsters. These findings show that loss of circadian timing is accompanied by greater tonic inhibition, and increased synaptic inhibition in response to muscarinic receptor activation in dentate granule cells. Increased inhibition would likely attenuate excitation in dentate‐CA3 microcircuits, which in turn might explain the spatial memory deficits previously observed in circadian‐arrhythmic hamsters.