Age-associated changes to neuronal dynamics involve a disruption of excitatory/inhibitory balance in C. elegans

Author:

Wirak Gregory S1ORCID,Florman Jeremy2ORCID,Alkema Mark J3ORCID,Connor Christopher W45,Gabel Christopher V6ORCID

Affiliation:

1. Graduate Program for Neuroscience, Department of Physiology and Biophysics, Boston University

2. Department of Neurobiology, University of Massachusetts Medical School

3. University of Massachusetts Medical School

4. Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital

5. Research Associate Professor of Physiology and Biophysics, Boston University School of Medicine

6. Department of Physiology and Biophysics, Neurophotonics Center, Boston University School of Medicine

Abstract

In the aging brain, many of the alterations underlying cognitive and behavioral decline remain opaque. Caenorhabditis elegans offers a powerful model for aging research, with a simple, well-studied nervous system to further our understanding of the cellular modifications and functional alterations accompanying senescence. We perform multi-neuronal functional imaging across the aged C. elegans nervous system, measuring an age-associated breakdown in system-wide functional organization. At single-cell resolution, we detect shifts in activity dynamics toward higher frequencies. In addition, we measure a specific loss of inhibitory signaling that occurs early in the aging process and alters the systems’ critical excitatory/inhibitory balance. These effects are recapitulated with mutation of the calcium channel subunit UNC-2/CaV2α. We find that manipulation of inhibitory GABA signaling can partially ameliorate or accelerate the effects of aging. The effects of aging are also partially mitigated by disruption of the insulin signaling pathway, known to increase longevity, or by a reduction of caspase activation. Data from mammals are consistent with our findings, suggesting a conserved shift in the balance of excitatory/inhibitory signaling with age that leads to breakdown in global neuronal dynamics and functional decline.

Funder

National Institutes of Health

Boston University School of Medicine

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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