Mild metabolic stress is sufficient to disturb the formation of pyramidal cell ensembles during gamma oscillations. Issue 12 (December 2020)

• Record Type: Journal Article
• Authors: Elzoheiry, Shehabeldin; Lewen, Andrea; Schneider, Justus; Both, Martin; Hefter, Dimitri; Boffi, Juan Carlos; Hollnagel, Jan-Oliver; Kann, Oliver
• Is Part Of: Journal of cerebral blood flow & metabolism. Volume 40:Issue 12(2020)
• Page Start: 2401
• Page End: 2415
• Publication Date: 2020-12
• Subjects: Brain slice -- cognition -- electrophysiology -- energy metabolism -- widefield microscopy; Cerebral circulation -- Periodicals; Brain -- Metabolism -- Periodicals; Brain -- Blood-vessels -- Periodicals; Cerebrovascular disease -- Periodicals; 612.824
• DOI: 10.1177/0271678X19892657
• Languages: English
• ISSNs: 0271-678X

Abstract

Disturbances of cognitive functions occur rapidly during acute metabolic stress. However, the underlying mechanisms are not fully understood. Cortical gamma oscillations (30–100 Hz) emerging from precise synaptic transmission between excitatory principal neurons and inhibitory interneurons, such as fast-spiking GABAergic basket cells, are associated with higher brain functions, like sensory perception, selective attention and memory formation. We investigated the alterations of cholinergic gamma oscillations at the level of neuronal ensembles in the CA3 region of rat hippocampal slice cultures. We combined electrophysiology, calcium imaging (CamKII.GCaMP6f) and mild metabolic stress that was induced by rotenone, a lipophilic and highly selective inhibitor of complex I in the respiratory chain of mitochondria. The detected pyramidal cell ensembles showing repetitive patterns of activity were highly sensitive to mild metabolic stress. Whereas such synchronised multicellular activity diminished, the overall activity of individual pyramidal cells was unaffected. Additionally, mild metabolic stress had no effect on the rate of action potential generation in fast-spiking neural units. However, the partial disinhibition of slow-spiking neural units suggests that disturbances of ensemble formation likely result from alterations in synaptic inhibition. Our study bridges disturbances on the (multi-)cellular and network level to putative cognitive impairment on the system level.