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Vitamin D-Mediated Regulation of Intestinal Calcium Absorption

Vitamin D is a critical regulator of calcium and bone homeostasis. While vitamin D has multiple effects on bone and calcium metabolism, the regulation of intestinal calcium (Ca) absorption efficiency is a critical function for vitamin D. This is necessary for optimal bone mineralization during growt...

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Detalles Bibliográficos
Autor principal: Fleet, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416674/
https://www.ncbi.nlm.nih.gov/pubmed/36014856
http://dx.doi.org/10.3390/nu14163351
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author Fleet, James C.
author_facet Fleet, James C.
author_sort Fleet, James C.
collection PubMed
description Vitamin D is a critical regulator of calcium and bone homeostasis. While vitamin D has multiple effects on bone and calcium metabolism, the regulation of intestinal calcium (Ca) absorption efficiency is a critical function for vitamin D. This is necessary for optimal bone mineralization during growth, the protection of bone in adults, and the prevention of osteoporosis. Intestinal Ca absorption is regulated by 1,25 dihydroxyvitamin D (1,25(OH)(2) D), a hormone that activates gene transcription following binding to the intestinal vitamin D receptor (VDR). When dietary Ca intake is low, Ca absorption follows a vitamin-D-regulated, saturable pathway, but when dietary Ca intake is high, Ca absorption is predominately through a paracellular diffusion pathway. Deletion of genes that mediate vitamin D action (i.e., VDR) or production (CYP27B1) eliminates basal Ca absorption and prevents the adaptation of mice to low-Ca diets. Various physiologic or disease states modify vitamin-D-regulated intestinal absorption of Ca (enhanced during late pregnancy, reduced due to menopause and aging).
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spelling pubmed-94166742022-08-27 Vitamin D-Mediated Regulation of Intestinal Calcium Absorption Fleet, James C. Nutrients Review Vitamin D is a critical regulator of calcium and bone homeostasis. While vitamin D has multiple effects on bone and calcium metabolism, the regulation of intestinal calcium (Ca) absorption efficiency is a critical function for vitamin D. This is necessary for optimal bone mineralization during growth, the protection of bone in adults, and the prevention of osteoporosis. Intestinal Ca absorption is regulated by 1,25 dihydroxyvitamin D (1,25(OH)(2) D), a hormone that activates gene transcription following binding to the intestinal vitamin D receptor (VDR). When dietary Ca intake is low, Ca absorption follows a vitamin-D-regulated, saturable pathway, but when dietary Ca intake is high, Ca absorption is predominately through a paracellular diffusion pathway. Deletion of genes that mediate vitamin D action (i.e., VDR) or production (CYP27B1) eliminates basal Ca absorption and prevents the adaptation of mice to low-Ca diets. Various physiologic or disease states modify vitamin-D-regulated intestinal absorption of Ca (enhanced during late pregnancy, reduced due to menopause and aging). MDPI 2022-08-16 /pmc/articles/PMC9416674/ /pubmed/36014856 http://dx.doi.org/10.3390/nu14163351 Text en © 2022 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fleet, James C.
Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title_full Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title_fullStr Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title_full_unstemmed Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title_short Vitamin D-Mediated Regulation of Intestinal Calcium Absorption
title_sort vitamin d-mediated regulation of intestinal calcium absorption
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416674/
https://www.ncbi.nlm.nih.gov/pubmed/36014856
http://dx.doi.org/10.3390/nu14163351
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