(+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats

We have previously reported that the synthetic estrogen, (+)-Z-bisdehydrodoisynolic Acid [(+)-Z-BDDA], attenuated weight gain and cardiovascular risk in obese rodents. To determine if these antiobesity effects were attributed to changes in basal metabolism, we assessed indirect calorimetry and metab...

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Main Authors: William J. Banz, April D. Strader, Kolapo M. Ajuwon, Yuqing Hou, Cal Y. Meyers, Jeremy E. Davis
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Journal of Obesity
Online Access:http://dx.doi.org/10.1155/2012/154145
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author William J. Banz
April D. Strader
Kolapo M. Ajuwon
Yuqing Hou
Cal Y. Meyers
Jeremy E. Davis
author_facet William J. Banz
April D. Strader
Kolapo M. Ajuwon
Yuqing Hou
Cal Y. Meyers
Jeremy E. Davis
author_sort William J. Banz
collection DOAJ
description We have previously reported that the synthetic estrogen, (+)-Z-bisdehydrodoisynolic Acid [(+)-Z-BDDA], attenuated weight gain and cardiovascular risk in obese rodents. To determine if these antiobesity effects were attributed to changes in basal metabolism, we assessed indirect calorimetry and metabolic profile in female obese Zucker (OZR) rats provided (+)-Z-BDDA (0.0002% food admixture) for 11 weeks. Similar to our previous findings, (+)-Z-BDDA reduced weight gain and improved lipid and glucose homeostasis in OZR rats. Furthermore, resting energy expenditure was increased by (+)-Z-BDDA, as evident by heat production and oxygen consumption. We also observed a marked reduction in respiratory quotient (RQ) along with a corresponding induction of hepatic AMPK in rodents provided (+)-Z-BDDA. Collectively, these findings indicate that (+)-Z-BDDA partially attenuated obesity and associated pathologies through increased resting energy expenditure and fatty acid utilization. Further investigation is required to fully elucidate the mechanisms involved as well as to determine the potential therapeutic implications for (+)-Z-BDDA on obesity and its related pathologies.
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institution Kabale University
issn 2090-0708
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language English
publishDate 2012-01-01
publisher Wiley
record_format Article
series Journal of Obesity
spelling doaj-art-abe2fb42c48a4328b8519cf3624f54862025-02-03T05:53:36ZengWileyJournal of Obesity2090-07082090-07162012-01-01201210.1155/2012/154145154145(+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker RatsWilliam J. Banz0April D. Strader1Kolapo M. Ajuwon2Yuqing Hou3Cal Y. Meyers4Jeremy E. Davis5Department of Animal Science, Food and Nutrition, Southern Illinois University, Carbondale, IL 62901-4317, USAPhysiology, Southern Illinois University, Carbondale, IL 62901-6512, USADepartment of Animal Sciences, Purdue University, West Lafayette, IN 47907-2054, USADepartment of Chemistry and Biochemistry, Meyers Institute for Interdisciplinary Research in Organic and Medicinal Chemistry, Southern Illinois University, Carbondale, IL 62901-4409, USADepartment of Chemistry and Biochemistry, Meyers Institute for Interdisciplinary Research in Organic and Medicinal Chemistry, Southern Illinois University, Carbondale, IL 62901-4409, USADepartment of Animal Science, Food and Nutrition, Southern Illinois University, Carbondale, IL 62901-4317, USAWe have previously reported that the synthetic estrogen, (+)-Z-bisdehydrodoisynolic Acid [(+)-Z-BDDA], attenuated weight gain and cardiovascular risk in obese rodents. To determine if these antiobesity effects were attributed to changes in basal metabolism, we assessed indirect calorimetry and metabolic profile in female obese Zucker (OZR) rats provided (+)-Z-BDDA (0.0002% food admixture) for 11 weeks. Similar to our previous findings, (+)-Z-BDDA reduced weight gain and improved lipid and glucose homeostasis in OZR rats. Furthermore, resting energy expenditure was increased by (+)-Z-BDDA, as evident by heat production and oxygen consumption. We also observed a marked reduction in respiratory quotient (RQ) along with a corresponding induction of hepatic AMPK in rodents provided (+)-Z-BDDA. Collectively, these findings indicate that (+)-Z-BDDA partially attenuated obesity and associated pathologies through increased resting energy expenditure and fatty acid utilization. Further investigation is required to fully elucidate the mechanisms involved as well as to determine the potential therapeutic implications for (+)-Z-BDDA on obesity and its related pathologies.http://dx.doi.org/10.1155/2012/154145
spellingShingle William J. Banz
April D. Strader
Kolapo M. Ajuwon
Yuqing Hou
Cal Y. Meyers
Jeremy E. Davis
(+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
Journal of Obesity
title (+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
title_full (+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
title_fullStr (+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
title_full_unstemmed (+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
title_short (+)-Z-Bisdehydrodoisynolic Acid Enhances Basal Metabolism and Fatty Acid Oxidation in Female Obese Zucker Rats
title_sort z bisdehydrodoisynolic acid enhances basal metabolism and fatty acid oxidation in female obese zucker rats
url http://dx.doi.org/10.1155/2012/154145
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