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Nature Communications · 2017 ·Vol. 8 ·期 1 ·1-15 · IF 12.124

Caffeine inhibits hypothalamic A1R to excite oxytocin neuron and ameliorate dietary obesity in mice

Wu Liufeng,Meng Jia,Shen Qing,Zhang Yi,Pan Susu,Chen Zhuo,Zhu Ling-Qiang,Lu Youming,Huang Yuan,Zhang Guo

Caffeine, an antagonist of the adenosine receptor A 1 R, is used as a dietary supplement to reduce body weight, although the underlying mechanism is unclear. Here, we report that adenosine level in the cerebrospinal fluid, and hypothalamic expression of A 1 R, are increased in the diet-induced obesity (DIO) mouse. We find that mice with overexpression of A 1 R in the neurons of paraventricular nucleus (PVN) of the hypothalamus are hyperphagic, have glucose intolerance and high body weight. Central or peripheral administration of caffeine reduces the body weight of DIO mice by the suppression of appetite and increasing of energy expenditure. We also show that caffeine excites oxytocin expressing neurons, and blockade of the action of oxytocin significantly attenuates the effect of caffeine on energy balance. These data suggest that caffeine inhibits A 1 Rs expressed on PVN oxytocin neurons to negatively regulate energy balance in DIO mice.

CAS / MDL: 58-61-7
研究领域: 药理学 · 神经科学 · 肥胖研究
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