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Publication : Hypothalamic AgRP neurons exert top-down control on systemic TNF-α release during endotoxemia.

First Author  Boutagouga Boudjadja M Year  2022
Journal  Curr Biol Volume  32
Issue  21 Pages  4699-4706.e4
PubMed ID  36182699 Mgi Jnum  J:342741
Mgi Id  MGI:7387898 Doi  10.1016/j.cub.2022.09.017
Citation  Boutagouga Boudjadja M, et al. (2022) Hypothalamic AgRP neurons exert top-down control on systemic TNF-alpha release during endotoxemia. Curr Biol 32(21):4699-4706.e4
abstractText  Loss of appetite and negative energy balance are common features of endotoxemia in all animals and are thought to have protective roles by reducing nutrient availability to host and pathogen metabolism. Accordingly, fasting and caloric restriction have well-established anti-inflammatory properties. However, in response to reduced nutrient availability at the cellular and organ levels, negative energy balance also recruits distinct energy-sensing brain circuits, but it is not known whether these neuronal systems have a role in its anti-inflammatory effects. Here, we report that hypothalamic AgRP neurons-a critical neuronal population for the central representation of negative energy balance-have parallel immunoregulatory functions. We found that when endotoxemia occurs in fasted mice, the activity of AgRP neurons remains sustained, but this activity does not influence feeding behavior and endotoxemic anorexia. Furthermore, we found that endotoxemia acutely desensitizes AgRP neurons, which also become refractory to inhibitory signals. Mimicking this sustained AgRP neuron activity in fed mice by chemogenetic activation-a manipulation known to recapitulate core behavioral features of fasting-results in reduced acute tumor necrosis factor alpha (TNF-alpha) release during endotoxemia. Mechanistically, we found that endogenous glucocorticoids play an important role: glucocorticoid receptor deletion from AgRP neurons prevents their endotoxemia-induced desensitization, and importantly, it counteracts the fasting-induced suppression of TNF-alpha release, resulting in prolonged sickness. Together, these findings provide evidence directly linking AgRP neuron activity to the acute response during endotoxemia, suggesting that these neurons are a functional component of the immunoregulatory effects associated with negative energy balance and catabolic metabolism.
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