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The results indicate that Gipr -expressing cells in the AP underlie the ability of GIPR agonists to reduce food intake in lean and DIO mice and, taken together with the previous report that GABAergic Gipr KO mice do not exhibit reduced food intake in response to acyl-GIP, suggest that subpopulations of GABAergic Gipr -expressing neurones located in the AP mediate both the appetite-suppressing and anti-aversive effects of exogenous GIPR agonists 6

Under hypoxia, the mitochondrial ETC is inhibited, and energy synthesis and Asp synthesis are limited, which leads to the dependence of tumor cells on the environmental uptake of Asp

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