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Increased fat synthesis based on enhanced glycolytic activity (pklr1, sterol regulatory element-binding protein-1 [SREBP1c], fas, and liver X receptor a [lxra]) in aged mice partly accounted for hepatic steatosis (increased leukocytic infiltration) and necrosis (increased plasma aspartate aminotransferase [AST] activity), compared with reduced srebp1c and fas mRNA levels in young mice

The whole difference is that glucagon receptor, which layers energy burning on top of the appetite-and-insulin effects of the older molecule

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MitoTam-01 trial: mitochondrial targeting as plausible approach to cancer therapy