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Down syndrome is a metabolic disease: altered insulin signaling mediates peripheral and brain dysfunctions
For example, SCFA receptors such as GPCR41 and GPCR43, medium and long-chain fatty acid receptors GPCR40 and GPCR120, and the chenodeoxycholic acid receptor farnesoid X receptor (FXR) expressed in intestinal cells and other tissues have been associated with the modulation of various host-specific metabolic processes, including the inhibition of insulin secretion, reduction of non-esterified fatty acid release, suppression of bile acid synthesis, and regulation of fatty acid metabolism 5
Ylitalo K, Vanttinen T, Halmesmaki E, Tyni T
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