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doi: 10.1016/j.neuropharm.2013.08.005 [DOI] [PubMed] [Google Scholar] 70.McClean PL, Parthsarathy V, Faivre E, Holscher C

The effect builds up slowly

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[5] [6] The GIP receptor component is thought to contribute to metabolic and appetite-related effects, whilst glucagon receptor activation may increase energy expenditure and promote fat breakdown (lipolysis) in the liver and adipose tissue
GIPRs are abundantly expressed on -cells, and their activation induces a rise in cAMP and intracellular calcium levels, facilitating glucose-dependent insulin release from pancreatic -cells (118)