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肠道吸收的生理学与病理生理学

Physiology and pathophysiology of intestinal absorption.

作者信息

Caspary W F

机构信息

Department of Medicine, Johann-Wolfgang-Goethe University, Frankfurt, Germany.

出版信息

Am J Clin Nutr. 1992 Jan;55(1 Suppl):299S-308S. doi: 10.1093/ajcn/55.1.299s.

Abstract

Final digestion and absorption of carbohydrates (CHO) occur after intraluminal hydrolysis by pancreatic alpha-amylase at the surface of the mucosal membrane in close relationship between disaccharide hydrolysis and the glucalogue carrier system. In general, Na(+)-dependent transport is the rate-limiting step of CHO absorption. The rate of absorption is determined by mode of ingestion, chemical composition of the meal, gastric emptying, pancreatic digestion, intestinal digestion and absorption, and intestinal motility. A delay of absorption of CHO may be achieved by dietary fibers, alpha-amylase inhibitors, or alpha-glucosidase inhibitors. Final protein digestion is achieved by a dual mechanism: intact peptide absorption with subsequent intracellular hydrolysis to free amino acids (AA) and membrane hydrolysis of peptides followed by absorption of free AA. More complex is the mechanism of lipid absorption: emulsification, lipolysis, micellar formation, membrane translocation, intracellular resynthesis, chylomicron formation, and lymphatic drainage. The most critical steps in lipid digestion are lipolysis and micellar formation.

摘要

碳水化合物(CHO)的最终消化和吸收发生在胰α-淀粉酶在粘膜表面进行腔内水解之后,此时二糖水解与葡萄糖载体系统密切相关。一般来说,钠依赖性转运是CHO吸收的限速步骤。吸收速率由摄入方式、膳食的化学成分、胃排空、胰腺消化、肠道消化与吸收以及肠道蠕动决定。膳食纤维、α-淀粉酶抑制剂或α-葡萄糖苷酶抑制剂可能会导致CHO吸收延迟。蛋白质的最终消化通过双重机制实现:完整肽的吸收以及随后细胞内水解为游离氨基酸(AA),还有肽的膜水解,随后游离AA被吸收。脂质吸收的机制更为复杂:乳化、脂解、微胶粒形成、膜转运、细胞内再合成、乳糜微粒形成以及淋巴引流。脂质消化中最关键的步骤是脂解和微胶粒形成。

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