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Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters

OBJECTIVE: We determined the effects of fructose and glucose consumption on plasma acylation stimulating protein (ASP), adiponectin, and leptin concentrations relative to energy intake, body weight, adiposity, circulating triglycerides, and insulin sensitivity. DESIGN AND METHODS: 32 overweight/obes...

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Autores principales: Rezvani, Reza, Cianflone, Katherine, McGahan, John P., Berglund, Lars, Bremer, Andrew A., Keim, Nancy L., Griffen, Steven C., Havel, Peter J., Stanhope, Kimber L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732502/
https://www.ncbi.nlm.nih.gov/pubmed/23512943
http://dx.doi.org/10.1002/oby.20437
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author Rezvani, Reza
Cianflone, Katherine
McGahan, John P.
Berglund, Lars
Bremer, Andrew A.
Keim, Nancy L.
Griffen, Steven C.
Havel, Peter J.
Stanhope, Kimber L.
author_facet Rezvani, Reza
Cianflone, Katherine
McGahan, John P.
Berglund, Lars
Bremer, Andrew A.
Keim, Nancy L.
Griffen, Steven C.
Havel, Peter J.
Stanhope, Kimber L.
author_sort Rezvani, Reza
collection PubMed
description OBJECTIVE: We determined the effects of fructose and glucose consumption on plasma acylation stimulating protein (ASP), adiponectin, and leptin concentrations relative to energy intake, body weight, adiposity, circulating triglycerides, and insulin sensitivity. DESIGN AND METHODS: 32 overweight/obese adults consumed glucose- or fructose-sweetened beverages (25% energy requirement) with their ad libitum diets for 8 weeks, followed by sweetened beverage consumption for 2 weeks with a standardized, energy-balanced diet. Plasma variables were measured at baseline, 2, 8 and 10 weeks, and body adiposity and insulin sensitivity at baseline and 10 weeks. RESULTS: Fasting and postprandial ASP concentrations increased at 2 and/or 8 weeks. ASP increases correlated with changes in late-evening triglyceride concentrations. At 10 weeks, fasting adiponectin levels decreased in both groups, and decreases were inversely associated with baseline intra-abdominal fat volume. Sugar consumption increased fasting leptin concentrations; increases were associated with body weight changes. 24-h leptin profiles increased during glucose consumption and decreased during fructose consumption. These changes correlated with changes of 24-h insulin levels. CONCLUSIONS: The consumption of fructose and glucose beverages induced changes in plasma concentrations of ASP, adiponectin and leptin. Further study is required to determine if these changes contribute to the metabolic dysfunction observed during fructose consumption.
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spelling pubmed-37325022014-06-01 Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters Rezvani, Reza Cianflone, Katherine McGahan, John P. Berglund, Lars Bremer, Andrew A. Keim, Nancy L. Griffen, Steven C. Havel, Peter J. Stanhope, Kimber L. Obesity (Silver Spring) Article OBJECTIVE: We determined the effects of fructose and glucose consumption on plasma acylation stimulating protein (ASP), adiponectin, and leptin concentrations relative to energy intake, body weight, adiposity, circulating triglycerides, and insulin sensitivity. DESIGN AND METHODS: 32 overweight/obese adults consumed glucose- or fructose-sweetened beverages (25% energy requirement) with their ad libitum diets for 8 weeks, followed by sweetened beverage consumption for 2 weeks with a standardized, energy-balanced diet. Plasma variables were measured at baseline, 2, 8 and 10 weeks, and body adiposity and insulin sensitivity at baseline and 10 weeks. RESULTS: Fasting and postprandial ASP concentrations increased at 2 and/or 8 weeks. ASP increases correlated with changes in late-evening triglyceride concentrations. At 10 weeks, fasting adiponectin levels decreased in both groups, and decreases were inversely associated with baseline intra-abdominal fat volume. Sugar consumption increased fasting leptin concentrations; increases were associated with body weight changes. 24-h leptin profiles increased during glucose consumption and decreased during fructose consumption. These changes correlated with changes of 24-h insulin levels. CONCLUSIONS: The consumption of fructose and glucose beverages induced changes in plasma concentrations of ASP, adiponectin and leptin. Further study is required to determine if these changes contribute to the metabolic dysfunction observed during fructose consumption. 2013-06-13 2013-12 /pmc/articles/PMC3732502/ /pubmed/23512943 http://dx.doi.org/10.1002/oby.20437 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
Rezvani, Reza
Cianflone, Katherine
McGahan, John P.
Berglund, Lars
Bremer, Andrew A.
Keim, Nancy L.
Griffen, Steven C.
Havel, Peter J.
Stanhope, Kimber L.
Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title_full Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title_fullStr Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title_full_unstemmed Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title_short Effects of Sugar-sweetened Beverages on plasma Acylation Stimulating Protein, Leptin & Adiponectin and Metabolic Parameters
title_sort effects of sugar-sweetened beverages on plasma acylation stimulating protein, leptin & adiponectin and metabolic parameters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732502/
https://www.ncbi.nlm.nih.gov/pubmed/23512943
http://dx.doi.org/10.1002/oby.20437
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