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      The cannabinoid 1-receptor silent antagonist O-2050 attenuates preference for high-fat diet and activated astrocytes in mice.

      Journal of pharmacological sciences
      Animals, Astrocytes, drug effects, metabolism, Dietary Fats, administration & dosage, Dronabinol, analogs & derivatives, pharmacology, Feeding Behavior, physiology, psychology, Food Preferences, Hypothalamus, cytology, Male, Mice, Mice, Inbred ICR, Pyrans, Receptor, Cannabinoid, CB1, antagonists & inhibitors

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          Abstract

          Endocannabinoids have been shown to activate reward-related feeding and to promote astrocytic differentiation. We investigated whether high-fat diet (HFD) intake produced a preference for HFD via an endocannabinoid-dependent mechanism. In the conditioned place preference test, the 2-week HFD-intake group showed preference for HFD and had increased expression of a marker for reactive astrocytes, glial fibrillary acid protein (GFAP), in the hypothalamus. The cannabinoid CB(1)-receptor antagonist O-2050 reduced the preference for HFD and expression of GFAP in the hypothalamus. These results suggested that HFD intake led to the development of a preference for HFD via astrocytic CB(1) receptors in the hypothalamus.

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