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Perpetuating Effects of Androgen Deficiency on Insulin-resistance

BACKGROUND/OBJECTIVES: Androgen deprivation therapy (ADT) is commonly used for treatment of prostate cancer, but is associated with side effects such as sarcopenia and insulin resistance. The role of lifestyle factors such as diet and exercise on insulin sensitivity and body composition in testoster...

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Autores principales: Cameron, Judy L., Jain, Ruhee, Rais, Maham, White, Ashley E., Beer, Tomasz M., Kievit, Paul, Winters-Stone, Kerri, Messaoudi, Ilhem, Varlamov, Oleg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140744/
https://www.ncbi.nlm.nih.gov/pubmed/27534842
http://dx.doi.org/10.1038/ijo.2016.148
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author Cameron, Judy L.
Jain, Ruhee
Rais, Maham
White, Ashley E.
Beer, Tomasz M.
Kievit, Paul
Winters-Stone, Kerri
Messaoudi, Ilhem
Varlamov, Oleg
author_facet Cameron, Judy L.
Jain, Ruhee
Rais, Maham
White, Ashley E.
Beer, Tomasz M.
Kievit, Paul
Winters-Stone, Kerri
Messaoudi, Ilhem
Varlamov, Oleg
author_sort Cameron, Judy L.
collection PubMed
description BACKGROUND/OBJECTIVES: Androgen deprivation therapy (ADT) is commonly used for treatment of prostate cancer, but is associated with side effects such as sarcopenia and insulin resistance. The role of lifestyle factors such as diet and exercise on insulin sensitivity and body composition in testosterone-deficient males is poorly understood. The aim of the present study was to examine the relationships between androgen status, diet, and insulin sensitivity. SUBJECTS/METHODS: Middle-aged (11–12-yo) intact and orchidectomized male rhesus macaques were maintained for two months on a standard chow diet, and then exposed for six months to a Western-style, high-fat/calorie-dense diet (WSD) followed by four months of caloric restriction (CR). Body composition, insulin sensitivity, physical activity, serum cytokine levels, and adipose biopsies were evaluated before and after each dietary intervention. RESULTS: Both intact and orchidectomized animals gained similar proportions of body fat, developed visceral and subcutaneous adipocyte hypertrophy, and became insulin resistant in response to the WSD. CR reduced body fat in both groups, but reversed insulin resistance only in intact animals. Orchidectomized animals displayed progressive sarcopenia, which persisted after the switch to CR. Androgen deficiency was associated with increased levels of interleukin-6 and macrophage-derived chemokine (CCL22), both of which were elevated during CR. Physical activity levels showed a negative correlation with body fat and insulin sensitivity. CONCLUSION: Androgen deficiency exacerbated the negative metabolic side effects of the WSD, such that CR alone was not sufficient to improve altered insulin sensitivity, suggesting that ADT patients will require additional interventions to reverse insulin resistance and sarcopenia.
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spelling pubmed-51407442017-02-18 Perpetuating Effects of Androgen Deficiency on Insulin-resistance Cameron, Judy L. Jain, Ruhee Rais, Maham White, Ashley E. Beer, Tomasz M. Kievit, Paul Winters-Stone, Kerri Messaoudi, Ilhem Varlamov, Oleg Int J Obes (Lond) Article BACKGROUND/OBJECTIVES: Androgen deprivation therapy (ADT) is commonly used for treatment of prostate cancer, but is associated with side effects such as sarcopenia and insulin resistance. The role of lifestyle factors such as diet and exercise on insulin sensitivity and body composition in testosterone-deficient males is poorly understood. The aim of the present study was to examine the relationships between androgen status, diet, and insulin sensitivity. SUBJECTS/METHODS: Middle-aged (11–12-yo) intact and orchidectomized male rhesus macaques were maintained for two months on a standard chow diet, and then exposed for six months to a Western-style, high-fat/calorie-dense diet (WSD) followed by four months of caloric restriction (CR). Body composition, insulin sensitivity, physical activity, serum cytokine levels, and adipose biopsies were evaluated before and after each dietary intervention. RESULTS: Both intact and orchidectomized animals gained similar proportions of body fat, developed visceral and subcutaneous adipocyte hypertrophy, and became insulin resistant in response to the WSD. CR reduced body fat in both groups, but reversed insulin resistance only in intact animals. Orchidectomized animals displayed progressive sarcopenia, which persisted after the switch to CR. Androgen deficiency was associated with increased levels of interleukin-6 and macrophage-derived chemokine (CCL22), both of which were elevated during CR. Physical activity levels showed a negative correlation with body fat and insulin sensitivity. CONCLUSION: Androgen deficiency exacerbated the negative metabolic side effects of the WSD, such that CR alone was not sufficient to improve altered insulin sensitivity, suggesting that ADT patients will require additional interventions to reverse insulin resistance and sarcopenia. 2016-08-18 2016-12 /pmc/articles/PMC5140744/ /pubmed/27534842 http://dx.doi.org/10.1038/ijo.2016.148 Text en 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
Cameron, Judy L.
Jain, Ruhee
Rais, Maham
White, Ashley E.
Beer, Tomasz M.
Kievit, Paul
Winters-Stone, Kerri
Messaoudi, Ilhem
Varlamov, Oleg
Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title_full Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title_fullStr Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title_full_unstemmed Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title_short Perpetuating Effects of Androgen Deficiency on Insulin-resistance
title_sort perpetuating effects of androgen deficiency on insulin-resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140744/
https://www.ncbi.nlm.nih.gov/pubmed/27534842
http://dx.doi.org/10.1038/ijo.2016.148
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