Short communication: Can Vitamin D be supplied from the large intestine?

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.

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Publication Details

Journal
Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology
Published
2024-11-23
DOI
https://doi.org/10.1016/j.cbpa.2024.111784
Citations
1
Primary Topic
Intestinal and Peritoneal Adhesions
Type
article
Field-Weighted Citation Impact
0.57
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article

Short communication: Can Vitamin D be supplied from the large intestine?

David R. Fraser
1 citations
Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology
Intestinal and Peritoneal Adhesions
0.57
article

Short communication: Can Vitamin D be supplied from the large intestine?

David R. Fraser
article en
1 citations

Abstract

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.

Comparative Biochemistry and Physiology Part A Molecular & Integrative PhysiologyVol. 300
The University of Sydney (AU)
Zero hunger
Openalex Percentile: Top 27%
Intestinal and Peritoneal Adhesions
0.57
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