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Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics
OBJECTIVE: Salsalate treatment has well-known effects on improving glycemia and the objective of this study was to examine whether the mechanism of this effect is related to changes in adipose tissue. METHODS: We conducted a randomized double-blind and placebo-controlled trial in obese Hispanics (18...
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/PMC4340767/ https://www.ncbi.nlm.nih.gov/pubmed/25644856 http://dx.doi.org/10.1002/oby.20991 |
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author | Alderete, Tanya L. Sattler, Fred R Richey, Joyce M. Allayee, Hooman Mittelman, Steven D. Sheng, Xia Tucci, Jonathan Gyllenhammer, Lauren E. Grant, Edward G. Goran, Michael I. |
author_facet | Alderete, Tanya L. Sattler, Fred R Richey, Joyce M. Allayee, Hooman Mittelman, Steven D. Sheng, Xia Tucci, Jonathan Gyllenhammer, Lauren E. Grant, Edward G. Goran, Michael I. |
author_sort | Alderete, Tanya L. |
collection | PubMed |
description | OBJECTIVE: Salsalate treatment has well-known effects on improving glycemia and the objective of this study was to examine whether the mechanism of this effect is related to changes in adipose tissue. METHODS: We conducted a randomized double-blind and placebo-controlled trial in obese Hispanics (18-35 years). The intervention consisted of 4 g/day of salsalate (n=11) versus placebo (n=13) for 4 weeks. Outcome measures included glycemia, adiposity, ectopic fat, and adipose tissue gene expression and inflammation. RESULTS: In those receiving salsalate, plasma fasting glucose decreased by 3.4% (P<0.01), free fatty acids decreased by 42.5% (P=0.06) and adiponectin increased by 27.7% (P<0.01). Salsalate increased insulin AUC by 38% (P=0.01) and HOMA-B by 47.2% (P<0.01) while estimates of insulin sensitivity/resistance were unaffected. These metabolic improvements occurred without changes in total, abdominal, visceral, or liver fat. Plasma markers of inflammation/immune activation were unchanged following salsalate. Salsalate had no effects on adipose tissue including adipocyte size, presence of crown-like structures, or gene expression of adipokines, immune cell markers, or cytokines downstream of NF-κB with the exception of downregulation of IL-1β (P<0.01). CONCLUSIONS: Our findings suggest that metabolic improvements in response to salsalate occurred without alterations in adiposity, ectopic fat, or adipose tissue gene expression and inflammation. |
format | Online Article Text |
id | pubmed-4340767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43407672016-03-01 Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics Alderete, Tanya L. Sattler, Fred R Richey, Joyce M. Allayee, Hooman Mittelman, Steven D. Sheng, Xia Tucci, Jonathan Gyllenhammer, Lauren E. Grant, Edward G. Goran, Michael I. Obesity (Silver Spring) Article OBJECTIVE: Salsalate treatment has well-known effects on improving glycemia and the objective of this study was to examine whether the mechanism of this effect is related to changes in adipose tissue. METHODS: We conducted a randomized double-blind and placebo-controlled trial in obese Hispanics (18-35 years). The intervention consisted of 4 g/day of salsalate (n=11) versus placebo (n=13) for 4 weeks. Outcome measures included glycemia, adiposity, ectopic fat, and adipose tissue gene expression and inflammation. RESULTS: In those receiving salsalate, plasma fasting glucose decreased by 3.4% (P<0.01), free fatty acids decreased by 42.5% (P=0.06) and adiponectin increased by 27.7% (P<0.01). Salsalate increased insulin AUC by 38% (P=0.01) and HOMA-B by 47.2% (P<0.01) while estimates of insulin sensitivity/resistance were unaffected. These metabolic improvements occurred without changes in total, abdominal, visceral, or liver fat. Plasma markers of inflammation/immune activation were unchanged following salsalate. Salsalate had no effects on adipose tissue including adipocyte size, presence of crown-like structures, or gene expression of adipokines, immune cell markers, or cytokines downstream of NF-κB with the exception of downregulation of IL-1β (P<0.01). CONCLUSIONS: Our findings suggest that metabolic improvements in response to salsalate occurred without alterations in adiposity, ectopic fat, or adipose tissue gene expression and inflammation. 2015-02-03 2015-03 /pmc/articles/PMC4340767/ /pubmed/25644856 http://dx.doi.org/10.1002/oby.20991 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 Alderete, Tanya L. Sattler, Fred R Richey, Joyce M. Allayee, Hooman Mittelman, Steven D. Sheng, Xia Tucci, Jonathan Gyllenhammer, Lauren E. Grant, Edward G. Goran, Michael I. Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title | Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title_full | Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title_fullStr | Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title_full_unstemmed | Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title_short | Salsalate Treatment Improves Glycemia Without Altering Adipose Tissue in Non-Diabetic Obese Hispanics |
title_sort | salsalate treatment improves glycemia without altering adipose tissue in non-diabetic obese hispanics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340767/ https://www.ncbi.nlm.nih.gov/pubmed/25644856 http://dx.doi.org/10.1002/oby.20991 |
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