{"title":"简短交流:大肠能提供维生素 D 吗?","authors":"David R Fraser","doi":"10.1016/j.cbpa.2024.111784","DOIUrl":null,"url":null,"abstract":"<p><p>The discovery that vitamin D<sub>2</sub> is being generated by anaerobic microbial metabolism in the alimentary tract, raises the question whether such a source of vitamin D could contribute to vitamin D supply for the animal hosting this microbial production system. In ruminants, this microbial generation in the forestomach allows vitamin D<sub>2</sub> to be readily absorbed when it reaches the small intestine, contributing to vitamin D<sub>2</sub> and 25-hydroxyvitamin D<sub>2</sub> [25(OH)D<sub>2</sub>] found in their tissues. In monogastric animals like humans, the microbial generation of vitamin D<sub>2</sub> is occurring in the large intestine. There is evidence that vitamin D hydroxy metabolites, delivered to the lumen of the colon can be absorbed. However, the parent vitamin D is more lipophilic than its metabolites, and like lipophilic vitamin K<sub>2</sub> being produced by bacteria in the hindgut, may be poorly absorbed by the colon mucosa. It is now apparent that colon mucosal cells have the proteins megalin and cubilin in their basal membrane. These glycoproteins perform endocytosis of circulating proteins including vitamin D binding protein [DBP]. Inside the cell, DBP binds to cytoplasmic actin and thus provides an array of high affinity binding sites for vitamin D and its functional metabolites. Any traces of vitamin D<sub>2</sub> that may diffuse into the colon mucosal cells from the lumen would thus be retained and accumulate on the DBP-actin. It would then be a substrate for functional hydroxylase metabolism for local endocrine action in these cells, and subsequent delivery of 25(OH)D<sub>2</sub> by diffusion to apo-DBP in the circulation.</p>","PeriodicalId":55237,"journal":{"name":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","volume":" ","pages":"111784"},"PeriodicalIF":2.1000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Short communication: Can Vitamin D be supplied from the large intestine?\",\"authors\":\"David R Fraser\",\"doi\":\"10.1016/j.cbpa.2024.111784\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The discovery that vitamin D<sub>2</sub> is being generated by anaerobic microbial metabolism in the alimentary tract, raises the question whether such a source of vitamin D could contribute to vitamin D supply for the animal hosting this microbial production system. In ruminants, this microbial generation in the forestomach allows vitamin D<sub>2</sub> to be readily absorbed when it reaches the small intestine, contributing to vitamin D<sub>2</sub> and 25-hydroxyvitamin D<sub>2</sub> [25(OH)D<sub>2</sub>] found in their tissues. In monogastric animals like humans, the microbial generation of vitamin D<sub>2</sub> is occurring in the large intestine. There is evidence that vitamin D hydroxy metabolites, delivered to the lumen of the colon can be absorbed. However, the parent vitamin D is more lipophilic than its metabolites, and like lipophilic vitamin K<sub>2</sub> being produced by bacteria in the hindgut, may be poorly absorbed by the colon mucosa. It is now apparent that colon mucosal cells have the proteins megalin and cubilin in their basal membrane. These glycoproteins perform endocytosis of circulating proteins including vitamin D binding protein [DBP]. Inside the cell, DBP binds to cytoplasmic actin and thus provides an array of high affinity binding sites for vitamin D and its functional metabolites. Any traces of vitamin D<sub>2</sub> that may diffuse into the colon mucosal cells from the lumen would thus be retained and accumulate on the DBP-actin. 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引用次数: 0
摘要
发现维生素 D2 是由消化道中的厌氧微生物代谢产生的,这就提出了一个问题,即这种维生素 D 的来源是否有助于为寄居在这种微生物生产系统中的动物提供维生素 D。在反刍动物体内,森林胃中的这种微生物产生的维生素 D2 在到达小肠时很容易被吸收,从而有助于在其组织中发现维生素 D2 和 25-羟基维生素 D2 [25(OH)D2]。在人类等单胃动物中,维生素 D2 的微生物生成发生在大肠。有证据表明,输送到结肠腔内的维生素 D 羟基代谢物可以被吸收。然而,母体维生素 D 比其代谢物更具亲脂性,就像后肠细菌产生的亲脂性维生素 K2 一样,结肠粘膜的吸收率可能很低。现在可以明显看出,结肠粘膜细胞的基底膜上有巨球蛋白和立方蛋白。这些糖蛋白可以内吞循环蛋白,包括维生素 D 结合蛋白 [DBP]。在细胞内,DBP 与细胞质肌动蛋白结合,从而为维生素 D 及其功能代谢物提供了一系列高亲和力结合位点。因此,任何可能从管腔扩散到结肠粘膜细胞的微量维生素 D2 都会被保留并积聚在 DBP 肌动蛋白上。然后,它将成为这些细胞中局部内分泌作用的功能性羟化酶代谢的底物,随后通过扩散将 25(OH)D2 运送到血液循环中的载脂蛋白-DBP 中。
Short communication: Can Vitamin D be supplied from the large intestine?
The discovery that vitamin D2 is being generated by anaerobic microbial metabolism in the alimentary tract, raises the question whether such a source of vitamin D could contribute to vitamin D supply for the animal hosting this microbial production system. In ruminants, this microbial generation in the forestomach allows vitamin D2 to be readily absorbed when it reaches the small intestine, contributing to vitamin D2 and 25-hydroxyvitamin D2 [25(OH)D2] found in their tissues. In monogastric animals like humans, the microbial generation of vitamin D2 is occurring in the large intestine. There is evidence that vitamin D hydroxy metabolites, delivered to the lumen of the colon can be absorbed. However, the parent vitamin D is more lipophilic than its metabolites, and like lipophilic vitamin K2 being produced by bacteria in the hindgut, may be poorly absorbed by the colon mucosa. It is now apparent that colon mucosal cells have the proteins megalin and cubilin in their basal membrane. These glycoproteins perform endocytosis of circulating proteins including vitamin D binding protein [DBP]. Inside the cell, DBP binds to cytoplasmic actin and thus provides an array of high affinity binding sites for vitamin D and its functional metabolites. Any traces of vitamin D2 that may diffuse into the colon mucosal cells from the lumen would thus be retained and accumulate on the DBP-actin. It would then be a substrate for functional hydroxylase metabolism for local endocrine action in these cells, and subsequent delivery of 25(OH)D2 by diffusion to apo-DBP in the circulation.
期刊介绍:
Part A: Molecular & Integrative Physiology of Comparative Biochemistry and Physiology. This journal covers molecular, cellular, integrative, and ecological physiology. Topics include bioenergetics, circulation, development, excretion, ion regulation, endocrinology, neurobiology, nutrition, respiration, and thermal biology. Study on regulatory mechanisms at any level of organization such as signal transduction and cellular interaction and control of behavior are also published.