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Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources

The quantitative role of different segments of the gastrointestinal tract for Ca absorption, the respective mechanisms, and their regulation are not fully identified for ruminants, that is, cattle. In different in vitro experiments the forestomach wall has been demonstrated to be a major site for ac...

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Autores principales: Schröder, Bernd, Wilkens, Mirja R, Ricken, Gundula E, Leonhard-Marek, Sabine, Fraser, David R, Breves, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673643/
https://www.ncbi.nlm.nih.gov/pubmed/26564067
http://dx.doi.org/10.14814/phy2.12615
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author Schröder, Bernd
Wilkens, Mirja R
Ricken, Gundula E
Leonhard-Marek, Sabine
Fraser, David R
Breves, Gerhard
author_facet Schröder, Bernd
Wilkens, Mirja R
Ricken, Gundula E
Leonhard-Marek, Sabine
Fraser, David R
Breves, Gerhard
author_sort Schröder, Bernd
collection PubMed
description The quantitative role of different segments of the gastrointestinal tract for Ca absorption, the respective mechanisms, and their regulation are not fully identified for ruminants, that is, cattle. In different in vitro experiments the forestomach wall has been demonstrated to be a major site for active Ca absorption in sheep and goats. In order to further clarify the role of the bovine rumen for Ca transport with special attention to luminal Ca concentrations, its ionic form, and pH, electrophysiological and unidirectional flux rate measurements were performed with isolated bovine rumen epithelial tissues. For Ca flux studies (J(ms), J(sm)) in vitro Ussing chamber technique was applied. Standard RT-PCR method was used to characterize TRPV6 and PMCA1 as potential contributors to transepithelial active Ca transport. At Ca concentrations of 1.2 mmol L(−1) on both sides of the tissues, J(ms) were higher than J(sm) resulting under some conditions in significant Ca net flux rates (J(net)), indicating the presence of active Ca transport. In the absence of an electrical gradient, J(net) could significantly be stimulated in the presence of luminal short-chain fatty acids (SCFAs). Increasing the luminal Ca concentrations up to 11.2 mmol L(−1) resulted in significant increases in J(ms) without influencing J(sm). Providing Ca in its form as respective chloride, formate, or propionate salts there was no significant effect on J(ms). No transcripts specific for Ca channel TRPV6 could be demonstrated. Our results indicate different mechanisms for Ca absorption in bovine rumen as compared with those usually described for the small intestines.
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spelling pubmed-46736432015-12-15 Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources Schröder, Bernd Wilkens, Mirja R Ricken, Gundula E Leonhard-Marek, Sabine Fraser, David R Breves, Gerhard Physiol Rep Original Research The quantitative role of different segments of the gastrointestinal tract for Ca absorption, the respective mechanisms, and their regulation are not fully identified for ruminants, that is, cattle. In different in vitro experiments the forestomach wall has been demonstrated to be a major site for active Ca absorption in sheep and goats. In order to further clarify the role of the bovine rumen for Ca transport with special attention to luminal Ca concentrations, its ionic form, and pH, electrophysiological and unidirectional flux rate measurements were performed with isolated bovine rumen epithelial tissues. For Ca flux studies (J(ms), J(sm)) in vitro Ussing chamber technique was applied. Standard RT-PCR method was used to characterize TRPV6 and PMCA1 as potential contributors to transepithelial active Ca transport. At Ca concentrations of 1.2 mmol L(−1) on both sides of the tissues, J(ms) were higher than J(sm) resulting under some conditions in significant Ca net flux rates (J(net)), indicating the presence of active Ca transport. In the absence of an electrical gradient, J(net) could significantly be stimulated in the presence of luminal short-chain fatty acids (SCFAs). Increasing the luminal Ca concentrations up to 11.2 mmol L(−1) resulted in significant increases in J(ms) without influencing J(sm). Providing Ca in its form as respective chloride, formate, or propionate salts there was no significant effect on J(ms). No transcripts specific for Ca channel TRPV6 could be demonstrated. Our results indicate different mechanisms for Ca absorption in bovine rumen as compared with those usually described for the small intestines. John Wiley & Sons, Ltd 2015-11-12 /pmc/articles/PMC4673643/ /pubmed/26564067 http://dx.doi.org/10.14814/phy2.12615 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Incsn behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Schröder, Bernd
Wilkens, Mirja R
Ricken, Gundula E
Leonhard-Marek, Sabine
Fraser, David R
Breves, Gerhard
Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title_full Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title_fullStr Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title_full_unstemmed Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title_short Calcium transport in bovine rumen epithelium as affected by luminal Ca concentrations and Ca sources
title_sort calcium transport in bovine rumen epithelium as affected by luminal ca concentrations and ca sources
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673643/
https://www.ncbi.nlm.nih.gov/pubmed/26564067
http://dx.doi.org/10.14814/phy2.12615
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