Remodeling of the arcuate nucleus energy-balance circuit is inhibited in obese mice

David E G McNay, Nadege Briançon, Maia V Kokoeva, Eleftheria Maratos-Flier, Jeffrey S Flier

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188 Citations (Scopus)

Abstract

In the CNS, the hypothalamic arcuate nucleus (ARN) energy-balance circuit plays a key role in regulating body weight. Recent studies have shown that neurogenesis occurs in the adult hypothalamus, revealing that the ARN energy-balance circuit is more plastic than originally believed. Changes in diet result in altered gene expression and neuronal activity in the ARN, some of which may reflect hypothalamic plasticity. To explore this possibility, we examined the turnover of hypothalamic neurons in mice with obesity secondary to either high-fat diet (HFD) consumption or leptin deficiency. We found substantial turnover of neurons in the ARN that resulted in ongoing cellular remodeling. Feeding mice HFD suppressed neurogenesis, as demonstrated by the observation that these mice both generated fewer new neurons and retained more old neurons. This suppression of neuronal turnover was associated with increased apoptosis of newborn neurons. Leptin-deficient mice also generated fewer new neurons, an observation that was explained in part by a loss of hypothalamic neural stem cells. These data demonstrate that there is substantial postnatal turnover of the arcuate neuronal circuitry in the mouse and reveal the unexpected capacity of diet and leptin deficiency to inhibit this neuronal remodeling. This insight has important implications for our understanding of nutritional regulation of energy balance and brain function.
Original languageEnglish
Pages (from-to)142-152
Number of pages11
JournalThe Journal of Clinical Investigation
Volume122
Issue number1
Early online date27 Dec 2011
DOIs
Publication statusPublished - 3 Jan 2012

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    McNay, D. E. G., Briançon, N., Kokoeva, M. V., Maratos-Flier, E., & Flier, J. S. (2012). Remodeling of the arcuate nucleus energy-balance circuit is inhibited in obese mice. The Journal of Clinical Investigation, 122(1), 142-152. https://doi.org/10.1172/JCI43134