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Gastrointestinal carbohydrate and fat absorption processes represent the physiological pathways for the breakdown and uptake of dietary nutrients in the small intestine. Carbohydrate digestion is primarily facilitated by alpha-glucosidase enzymes in the brush border, which convert complex sugars into monosaccharides for transport via proteins such as Sodium/glucose cotransporter 1 (SGLT1) and GLUT2 (StatPearls, 2023; PubMed, 2004). Fat absorption requires emulsification by bile salts and hydrolysis by pancreatic lipase, followed by the uptake of lipids and cholesterol through transporters such as Niemann-Pick C1-Like 1 (NPC1L1) and CD36 (PubMed, 2021; NIH, 2022). These processes are major therapeutic targets for metabolic conditions; alpha-glucosidase inhibitors like acarbose are used to control postprandial hyperglycemia in type 2 diabetes, while lipase inhibitors like orlistat and cholesterol absorption inhibitors like ezetimibe are used to manage obesity and hyperlipidemia (StatPearls, 2023; PubMed, 2017). Because these interventions result in undigested nutrients reaching the large intestine, they are commonly associated with gastrointestinal side effects, including flatulence, diarrhea, and malabsorption of fat-soluble vitamins (StatPearls, 2023).
Inhibition of intestinal enzymes (e.g., alpha-glucosidase, pancreatic lipase) and transport proteins (e.g., NPC1L1) to reduce the systemic uptake of glucose and lipids.
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