1. Hypothalamic astrocyte NAD+ salvage pathway mediates the coupling of dietary fat overconsumption in a mouse model of obesity.
- Author
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Park, Jae Woo, Park, Se Eun, Koh, Wuhyun, Jang, Won Hee, Choi, Jong Han, Roh, Eun, Kang, Gil Myoung, Kim, Seong Jun, Lim, Hyo Sun, Park, Chae Beom, Jeong, So Yeon, Moon, Sang Yun, Lee, Chan Hee, Kim, Sang Yeob, Choi, Hyung Jin, Min, Se Hee, Lee, C. Justin, and Kim, Min-Seon
- Abstract
Nicotinamide adenine dinucleotide (NAD)
+ serves as a crucial coenzyme in numerous essential biological reactions, and its cellular availability relies on the activity of the nicotinamide phosphoribosyltransferase (NAMPT)-catalyzed salvage pathway. Here we show that treatment with saturated fatty acids activates the NAD+ salvage pathway in hypothalamic astrocytes. Furthermore, inhibition of this pathway mitigates hypothalamic inflammation and attenuates the development of obesity in male mice fed a high-fat diet (HFD). Mechanistically, CD38 functions downstream of the NAD+ salvage pathway in hypothalamic astrocytes burdened with excess fat. The activation of the astrocytic NAMPT–NAD+ –CD38 axis in response to fat overload induces proinflammatory responses in the hypothalamus. It also leads to aberrantly activated basal Ca2+ signals and compromised Ca2+ responses to metabolic hormones such as insulin, leptin, and glucagon-like peptide 1, ultimately resulting in dysfunctional hypothalamic astrocytes. Our findings highlight the significant contribution of the hypothalamic astrocytic NAD+ salvage pathway, along with its downstream CD38, to HFD-induced obesity.The cellular levels of the critical coenzyme nicotinamide adenine dinucleotide (NAD)+ depend on its salvage pathway. Here, the authors show that the NAD+ salvage pathway in hypothalamic astrocytes is activated to promote obesity in high fat diet-fed mice. [ABSTRACT FROM AUTHOR]- Published
- 2024
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