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Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization
Nicotinamide N-methyltransferase (Nnmt) methylates nicotinamide, a form of vitamin B3, to produce N1-methylnicotinamide (MNAM). Nnmt is an emerging metabolic regulator in adipocytes but its role in the liver, a tissue with the strongest Nnmt expression, is not known. In spite of its overall high exp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529375/ https://www.ncbi.nlm.nih.gov/pubmed/26168293 http://dx.doi.org/10.1038/nm.3882 |
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author | Hong, Shangyu Moreno-Navarrete, Jose M Wei, Xiaojing Kikukawa, Yusuke Tzameli, Iphigenia Prasad, Deepthi Lee, Yoonjin Asara, John M Fernandez-Real, Jose Manuel Maratos-Flier, Eleftheria Pissios, Pavlos |
author_facet | Hong, Shangyu Moreno-Navarrete, Jose M Wei, Xiaojing Kikukawa, Yusuke Tzameli, Iphigenia Prasad, Deepthi Lee, Yoonjin Asara, John M Fernandez-Real, Jose Manuel Maratos-Flier, Eleftheria Pissios, Pavlos |
author_sort | Hong, Shangyu |
collection | PubMed |
description | Nicotinamide N-methyltransferase (Nnmt) methylates nicotinamide, a form of vitamin B3, to produce N1-methylnicotinamide (MNAM). Nnmt is an emerging metabolic regulator in adipocytes but its role in the liver, a tissue with the strongest Nnmt expression, is not known. In spite of its overall high expression, here we find that hepatic expression of Nnmt is highly variable and correlates with multiple metabolic parameters in mice and in humans. Further, we find that suppression of hepatic Nnmt expression in vivo alters glucose and cholesterol metabolism and that the metabolic effects of Nnmt in the liver are mediated by its product MNAM. Supplementation of high fat diet with MNAM decreases serum and liver cholesterol and liver triglycerides levels in mice. Mechanistically, increasing Nnmt expression or MNAM levels stabilizes sirtuin 1 protein, an effect, which is required for their metabolic benefits. In summary, we describe a novel regulatory pathway for vitamin B3 that could provide a new opportunity for metabolic disease therapy. |
format | Online Article Text |
id | pubmed-4529375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-45293752016-01-31 Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization Hong, Shangyu Moreno-Navarrete, Jose M Wei, Xiaojing Kikukawa, Yusuke Tzameli, Iphigenia Prasad, Deepthi Lee, Yoonjin Asara, John M Fernandez-Real, Jose Manuel Maratos-Flier, Eleftheria Pissios, Pavlos Nat Med Article Nicotinamide N-methyltransferase (Nnmt) methylates nicotinamide, a form of vitamin B3, to produce N1-methylnicotinamide (MNAM). Nnmt is an emerging metabolic regulator in adipocytes but its role in the liver, a tissue with the strongest Nnmt expression, is not known. In spite of its overall high expression, here we find that hepatic expression of Nnmt is highly variable and correlates with multiple metabolic parameters in mice and in humans. Further, we find that suppression of hepatic Nnmt expression in vivo alters glucose and cholesterol metabolism and that the metabolic effects of Nnmt in the liver are mediated by its product MNAM. Supplementation of high fat diet with MNAM decreases serum and liver cholesterol and liver triglycerides levels in mice. Mechanistically, increasing Nnmt expression or MNAM levels stabilizes sirtuin 1 protein, an effect, which is required for their metabolic benefits. In summary, we describe a novel regulatory pathway for vitamin B3 that could provide a new opportunity for metabolic disease therapy. 2015-07-13 2015-08 /pmc/articles/PMC4529375/ /pubmed/26168293 http://dx.doi.org/10.1038/nm.3882 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Hong, Shangyu Moreno-Navarrete, Jose M Wei, Xiaojing Kikukawa, Yusuke Tzameli, Iphigenia Prasad, Deepthi Lee, Yoonjin Asara, John M Fernandez-Real, Jose Manuel Maratos-Flier, Eleftheria Pissios, Pavlos Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title | Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title_full | Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title_fullStr | Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title_full_unstemmed | Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title_short | Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization |
title_sort | nicotinamide n-methyltransferase regulates hepatic nutrient metabolism through sirt1 protein stabilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529375/ https://www.ncbi.nlm.nih.gov/pubmed/26168293 http://dx.doi.org/10.1038/nm.3882 |
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