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Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate

BACKGROUND: Micronutrient inadequate intake is responsible of pathological deficiencies and there is a need of assessing the effectiveness of metal supplementation, frequently proposed to rebalance poor diets. Manganese (Mn) is present in many enzymatic intracellular systems crucial for the regulati...

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Autores principales: Foglieni, Chiara, Cavarelli, Mariangela, Piscopiello, Mariarosaria, Fulgenzi, Alessandro, Ferrero, Maria Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171306/
https://www.ncbi.nlm.nih.gov/pubmed/21781350
http://dx.doi.org/10.1186/1475-2891-10-77
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author Foglieni, Chiara
Cavarelli, Mariangela
Piscopiello, Mariarosaria
Fulgenzi, Alessandro
Ferrero, Maria Elena
author_facet Foglieni, Chiara
Cavarelli, Mariangela
Piscopiello, Mariarosaria
Fulgenzi, Alessandro
Ferrero, Maria Elena
author_sort Foglieni, Chiara
collection PubMed
description BACKGROUND: Micronutrient inadequate intake is responsible of pathological deficiencies and there is a need of assessing the effectiveness of metal supplementation, frequently proposed to rebalance poor diets. Manganese (Mn) is present in many enzymatic intracellular systems crucial for the regulation of cell metabolism, and is contained in commercially available metal supplements. METHODS: We compared the effects of two different commercial Mn forms, gluconate (MnGluc) and oxyprolinate (MnOxP). For this purpose we used the polarized Caco-2 cells cultured on transwell filters, an established in vitro model of intestinal epithelium. Since micronutrient deficiency may accelerate mitochondrial efficiency, the mitochondrial response of these cells, in the presence of MnGluc and MnOxP, by microscopy methods and by ATP luminescence assay was used. RESULTS: In the presence of both MnOxP and MnGluc a sustained mitochondrial activity was shown by mitoTraker labeling (indicative of mitochondrial respiration), but ATP intracellular content remained comparable to untreated cells only in the presence of MnOxP. In addition MnOxP transiently up-regulated the antioxidant enzyme Mn superoxide dismutase more efficiently than MnGluc. Both metal treatments preserved NADH and βNADPH diaphorase oxidative activity, avoided mitochondrial dysfunction, as assessed by the absence of a sustained phosphoERK activation, and were able to maintain cell viability. CONCLUSIONS: Collectively, our data indicate that MnOxP and MnGluc, and primarily the former, produce a moderate and safe modification of Caco-2 cell metabolism, by activating positive enzymatic mechanisms, thus could contribute to long-term maintenance of cell homeostasis.
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spelling pubmed-31713062011-09-13 Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate Foglieni, Chiara Cavarelli, Mariangela Piscopiello, Mariarosaria Fulgenzi, Alessandro Ferrero, Maria Elena Nutr J Research BACKGROUND: Micronutrient inadequate intake is responsible of pathological deficiencies and there is a need of assessing the effectiveness of metal supplementation, frequently proposed to rebalance poor diets. Manganese (Mn) is present in many enzymatic intracellular systems crucial for the regulation of cell metabolism, and is contained in commercially available metal supplements. METHODS: We compared the effects of two different commercial Mn forms, gluconate (MnGluc) and oxyprolinate (MnOxP). For this purpose we used the polarized Caco-2 cells cultured on transwell filters, an established in vitro model of intestinal epithelium. Since micronutrient deficiency may accelerate mitochondrial efficiency, the mitochondrial response of these cells, in the presence of MnGluc and MnOxP, by microscopy methods and by ATP luminescence assay was used. RESULTS: In the presence of both MnOxP and MnGluc a sustained mitochondrial activity was shown by mitoTraker labeling (indicative of mitochondrial respiration), but ATP intracellular content remained comparable to untreated cells only in the presence of MnOxP. In addition MnOxP transiently up-regulated the antioxidant enzyme Mn superoxide dismutase more efficiently than MnGluc. Both metal treatments preserved NADH and βNADPH diaphorase oxidative activity, avoided mitochondrial dysfunction, as assessed by the absence of a sustained phosphoERK activation, and were able to maintain cell viability. CONCLUSIONS: Collectively, our data indicate that MnOxP and MnGluc, and primarily the former, produce a moderate and safe modification of Caco-2 cell metabolism, by activating positive enzymatic mechanisms, thus could contribute to long-term maintenance of cell homeostasis. BioMed Central 2011-07-25 /pmc/articles/PMC3171306/ /pubmed/21781350 http://dx.doi.org/10.1186/1475-2891-10-77 Text en Copyright ©2011 Foglieni et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Foglieni, Chiara
Cavarelli, Mariangela
Piscopiello, Mariarosaria
Fulgenzi, Alessandro
Ferrero, Maria Elena
Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title_full Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title_fullStr Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title_full_unstemmed Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title_short Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate
title_sort mn bioavailability by polarized caco-2 cells: comparison between mn gluconate and mn oxyprolinate
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171306/
https://www.ncbi.nlm.nih.gov/pubmed/21781350
http://dx.doi.org/10.1186/1475-2891-10-77
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