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Lowering increased glucose uptake in diabetics by inhibiting the intestinal glucose transporter, sodium-glucose linked transporter 1 (SLGT1) through bioactive compounds represents a promising target for novel drug development (164)

Pastural et al., 2009)

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SCFA metabolites, such as acetate, propionate, and butyrate, can act on fatty acid receptors in epithelial, enteroendocrine, and neuronal cells, and they could affect the central nervous system in experimental model organisms (53, 54)