Differential Roles of Each Orexin Receptor Signaling in Obesity

Orexins are hypothalamic neuropeptides that regulate feeding, energy expenditure, and sleep. Although orexin-deficient mice are susceptible to obesity, little is known about the roles of the orexin receptors in long-term energy metabolism. Here, we performed the metabolic characterization of orexin...

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Veröffentlicht in:iScience 2019-10, Vol.20, p.1-13
Hauptverfasser: Kakizaki, Miyo, Tsuneoka, Yousuke, Takase, Kenkichi, Kim, Staci J., Choi, Jinhwan, Ikkyu, Aya, Abe, Manabu, Sakimura, Kenji, Yanagisawa, Masashi, Funato, Hiromasa
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Sprache:eng
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Zusammenfassung:Orexins are hypothalamic neuropeptides that regulate feeding, energy expenditure, and sleep. Although orexin-deficient mice are susceptible to obesity, little is known about the roles of the orexin receptors in long-term energy metabolism. Here, we performed the metabolic characterization of orexin receptor-deficient mice. Ox1r-deficient mice were resistant to diet-induced obesity, and their food intake was similar between chow and high-fat food. Ox2r-deficient mice exhibited less energy expenditure than wild-type mice when fed a high-fat diet. Neither Ox1r-deficient nor Ox2r-deficient mice showed body weight gain similar to orexin-deficient mice. Although the presence of a running wheel suppressed diet-induced obesity in wild-type mice, the effect was weaker in orexin neuron-ablated mice. Finally, we did not detect abnormalities in brown adipose tissues of orexin-deficient mice. Thus, each orexin receptor signaling has a unique role in energy metabolism, and orexin neurons are involved in the interactive effect of diet and exercise on body weight gain. [Display omitted] •Food intakes of Ox1r-deficient mice are similar between chow and high-fat food•Ox2r-deficient mice exhibit less energy expenditure when fed a high-fat diet•Orexin neurons are involved in the interactive effect of diet and exercise•Orexin-deficient mice have normal brown adipose tissue Physiology; Cellular Physiology; Endocrinology; Diabetology
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2019.09.003