Antiretroviral therapy potentiates high-fat diet induced obesity and glucose intolerance

Objective: Breakthroughs in HIV treatment, especially combination antiretroviral therapy (ART), have massively reduced AIDS-associated mortality. However, ART administration amplifies the risk of non-AIDS defining illnesses including obesity, diabetes, and cardiovascular disease, collectively known...

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Main Authors: Mark E. Pepin (Author), Lindsey E. Padgett (Author), Ruth E. McDowell (Author), Ashley R. Burg (Author), Manoja K. Brahma (Author), Cassie Holleman (Author), Teayoun Kim (Author), David Crossman (Author), Olaf Kutsch (Author), Hubert M. Tse (Author), Adam R. Wende (Author), Kirk M. Habegger (Author)
Format: Book
Published: Elsevier, 2018-06-01T00:00:00Z.
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001 doaj_fedf00fc7bf543b3ab7496c3a6c6834c
042 |a dc 
100 1 0 |a Mark E. Pepin  |e author 
700 1 0 |a Lindsey E. Padgett  |e author 
700 1 0 |a Ruth E. McDowell  |e author 
700 1 0 |a Ashley R. Burg  |e author 
700 1 0 |a Manoja K. Brahma  |e author 
700 1 0 |a Cassie Holleman  |e author 
700 1 0 |a Teayoun Kim  |e author 
700 1 0 |a David Crossman  |e author 
700 1 0 |a Olaf Kutsch  |e author 
700 1 0 |a Hubert M. Tse  |e author 
700 1 0 |a Adam R. Wende  |e author 
700 1 0 |a Kirk M. Habegger  |e author 
245 0 0 |a Antiretroviral therapy potentiates high-fat diet induced obesity and glucose intolerance 
260 |b Elsevier,   |c 2018-06-01T00:00:00Z. 
500 |a 2212-8778 
500 |a 10.1016/j.molmet.2018.04.006 
520 |a Objective: Breakthroughs in HIV treatment, especially combination antiretroviral therapy (ART), have massively reduced AIDS-associated mortality. However, ART administration amplifies the risk of non-AIDS defining illnesses including obesity, diabetes, and cardiovascular disease, collectively known as metabolic syndrome. Initial reports suggest that ART-associated risk of metabolic syndrome correlates with socioeconomic status, a multifaceted finding that encompasses income, race, education, and diet. Therefore, determination of causal relationships is extremely challenging due to the complex interplay between viral infection, ART, and the many environmental factors. Methods: In the current study, we employed a mouse model to specifically examine interactions between ART and diet that impacts energy balance and glucose metabolism. Previous studies have shown that high-fat feeding induces persistent low-grade systemic and adipose tissue inflammation contributing to insulin resistance and metabolic dysregulation via adipose-infiltrating macrophages. Studies herein test the hypothesis that ART potentiates the inflammatory effects of a high-fat diet (HFD). C57Bl/6J mice on a HFD or standard chow containing ART or vehicle, were subjected to functional metabolic testing, RNA-sequencing of epididymal white adipose tissue (eWAT), and array-based kinomic analysis of eWAT-infiltrating macrophages. Results: ART-treated mice on a HFD displayed increased fat mass accumulation, impaired glucose tolerance, and potentiated insulin resistance. Gene set enrichment and kinomic array analyses revealed a pro-inflammatory transcriptional signature depicting granulocyte migration and activation. Conclusion: The current study reveals a HFD-ART interaction that increases inflammatory transcriptional pathways and impairs glucose metabolism, energy balance, and metabolic dysfunction. Keywords: Antiretroviral therapy, Obesity, Glucose intolerance, Adipose tissue inflammation, Insulin resistance, Macrophage activation 
546 |a EN 
690 |a Internal medicine 
690 |a RC31-1245 
655 7 |a article  |2 local 
786 0 |n Molecular Metabolism, Vol 12, Iss , Pp 48-61 (2018) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2212877818302321 
787 0 |n https://doaj.org/toc/2212-8778 
856 4 1 |u https://doaj.org/article/fedf00fc7bf543b3ab7496c3a6c6834c  |z Connect to this object online.