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Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate

Vitamin E nicotinate (tocopherol nicotinate, tocopheryl nicotinate; TN) is an ester of two vitamins, tocopherol (vitamin E) and niacin (vitamin B3), in which niacin is linked to the hydroxyl group of active vitamin E. This vitamin E ester can be chemically synthesized and is used for supplementation...

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Autores principales: Marcocci, Lucia, Suzuki, Yuichiro J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562962/
https://www.ncbi.nlm.nih.gov/pubmed/31083512
http://dx.doi.org/10.3390/antiox8050127
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author Marcocci, Lucia
Suzuki, Yuichiro J.
author_facet Marcocci, Lucia
Suzuki, Yuichiro J.
author_sort Marcocci, Lucia
collection PubMed
description Vitamin E nicotinate (tocopherol nicotinate, tocopheryl nicotinate; TN) is an ester of two vitamins, tocopherol (vitamin E) and niacin (vitamin B3), in which niacin is linked to the hydroxyl group of active vitamin E. This vitamin E ester can be chemically synthesized and is used for supplementation. However, whether TN is formed in the biological system was unclear. Our laboratory previously detected TN in rat heart tissues, and its level was 30-fold lower in a failing heart (Wang et al., PLoS ONE 2017, 12, e0176887). The rat diet used in these experiments contained vitamin E acetate (tocopherol acetate; TA) and niacin separately, but not in the form of TN. Since only TN, but not other forms of vitamin E, was decreased in heart failure, the TN structure may elicit biologic functions independent of serving as a source of active vitamin E antioxidant. To test this hypothesis, the present study performed metabolomics to compare effects of TN on cultured cells to those of TA plus niacin added separately (TA + N). Human vascular smooth muscle cells were treated with TN or with TA + N (100 μM) for 10 min. Metabolite profiles showed that TN and TA + N influenced the cells differentially. TN effectively upregulated various primary fatty acid amides including arachidonoylethanoamine (anandamide/virodhamine) and palmitamide. TN also activated mitogen-activated protein kinases. These results suggest a new biological function of TN to elicit cell signaling.
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spelling pubmed-65629622019-06-17 Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate Marcocci, Lucia Suzuki, Yuichiro J. Antioxidants (Basel) Article Vitamin E nicotinate (tocopherol nicotinate, tocopheryl nicotinate; TN) is an ester of two vitamins, tocopherol (vitamin E) and niacin (vitamin B3), in which niacin is linked to the hydroxyl group of active vitamin E. This vitamin E ester can be chemically synthesized and is used for supplementation. However, whether TN is formed in the biological system was unclear. Our laboratory previously detected TN in rat heart tissues, and its level was 30-fold lower in a failing heart (Wang et al., PLoS ONE 2017, 12, e0176887). The rat diet used in these experiments contained vitamin E acetate (tocopherol acetate; TA) and niacin separately, but not in the form of TN. Since only TN, but not other forms of vitamin E, was decreased in heart failure, the TN structure may elicit biologic functions independent of serving as a source of active vitamin E antioxidant. To test this hypothesis, the present study performed metabolomics to compare effects of TN on cultured cells to those of TA plus niacin added separately (TA + N). Human vascular smooth muscle cells were treated with TN or with TA + N (100 μM) for 10 min. Metabolite profiles showed that TN and TA + N influenced the cells differentially. TN effectively upregulated various primary fatty acid amides including arachidonoylethanoamine (anandamide/virodhamine) and palmitamide. TN also activated mitogen-activated protein kinases. These results suggest a new biological function of TN to elicit cell signaling. MDPI 2019-05-11 /pmc/articles/PMC6562962/ /pubmed/31083512 http://dx.doi.org/10.3390/antiox8050127 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marcocci, Lucia
Suzuki, Yuichiro J.
Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title_full Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title_fullStr Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title_full_unstemmed Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title_short Metabolomics Studies to Assess Biological Functions of Vitamin E Nicotinate
title_sort metabolomics studies to assess biological functions of vitamin e nicotinate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562962/
https://www.ncbi.nlm.nih.gov/pubmed/31083512
http://dx.doi.org/10.3390/antiox8050127
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