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Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet

Diabetes and the related disease metabolic syndrome are epidemic in the United States, in part due to a shift in diet and decrease in physical exercise. PAS kinase is a sensory protein kinase associated with many of the phenotypes of these diseases, including hepatic triglyceride accumulation and me...

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Autores principales: Pape, Jenny A., Newey, Colleen R., Burrell, Haley R., Workman, Audrey, Perry, Katelyn, Bikman, Benjamin T., Bridgewater, Laura C., Grose, Julianne H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316003/
https://www.ncbi.nlm.nih.gov/pubmed/30558306
http://dx.doi.org/10.3390/nu10121990
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author Pape, Jenny A.
Newey, Colleen R.
Burrell, Haley R.
Workman, Audrey
Perry, Katelyn
Bikman, Benjamin T.
Bridgewater, Laura C.
Grose, Julianne H.
author_facet Pape, Jenny A.
Newey, Colleen R.
Burrell, Haley R.
Workman, Audrey
Perry, Katelyn
Bikman, Benjamin T.
Bridgewater, Laura C.
Grose, Julianne H.
author_sort Pape, Jenny A.
collection PubMed
description Diabetes and the related disease metabolic syndrome are epidemic in the United States, in part due to a shift in diet and decrease in physical exercise. PAS kinase is a sensory protein kinase associated with many of the phenotypes of these diseases, including hepatic triglyceride accumulation and metabolic dysregulation in male mice placed on a high-fat diet. Herein we provide the first characterization of the effects of western diet (high-fat high-sugar, HFHS) on Per-Arnt-Sim kinase mice (PASK(−/−)) and the first characterization of both male and female PASK(−/−) mice. Soleus muscle from the PASK(−/−) male mice displayed a 2-fold higher oxidative phosphorylation capacity than wild type (WT) on the normal chow diet. PASK(−/−) male mice were also resistant to hepatic triglyceride accumulation on the HFHS diet, displaying a 2.7-fold reduction in hepatic triglycerides compared to WT mice on the HFHS diet. These effects on male hepatic triglyceride were further explored through mass spectrometry-based lipidomics. The absence of PAS kinase was found to affect many of the 44 triglycerides analyzed, preventing hepatic triglyceride accumulation in response to the HFHS diet. In contrast, the female mice showed resistance to hepatic triglyceride accumulation on the HFHS diet regardless of genotype, suggesting the effects of PAS kinase may be masked.
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spelling pubmed-63160032019-01-08 Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet Pape, Jenny A. Newey, Colleen R. Burrell, Haley R. Workman, Audrey Perry, Katelyn Bikman, Benjamin T. Bridgewater, Laura C. Grose, Julianne H. Nutrients Article Diabetes and the related disease metabolic syndrome are epidemic in the United States, in part due to a shift in diet and decrease in physical exercise. PAS kinase is a sensory protein kinase associated with many of the phenotypes of these diseases, including hepatic triglyceride accumulation and metabolic dysregulation in male mice placed on a high-fat diet. Herein we provide the first characterization of the effects of western diet (high-fat high-sugar, HFHS) on Per-Arnt-Sim kinase mice (PASK(−/−)) and the first characterization of both male and female PASK(−/−) mice. Soleus muscle from the PASK(−/−) male mice displayed a 2-fold higher oxidative phosphorylation capacity than wild type (WT) on the normal chow diet. PASK(−/−) male mice were also resistant to hepatic triglyceride accumulation on the HFHS diet, displaying a 2.7-fold reduction in hepatic triglycerides compared to WT mice on the HFHS diet. These effects on male hepatic triglyceride were further explored through mass spectrometry-based lipidomics. The absence of PAS kinase was found to affect many of the 44 triglycerides analyzed, preventing hepatic triglyceride accumulation in response to the HFHS diet. In contrast, the female mice showed resistance to hepatic triglyceride accumulation on the HFHS diet regardless of genotype, suggesting the effects of PAS kinase may be masked. MDPI 2018-12-15 /pmc/articles/PMC6316003/ /pubmed/30558306 http://dx.doi.org/10.3390/nu10121990 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pape, Jenny A.
Newey, Colleen R.
Burrell, Haley R.
Workman, Audrey
Perry, Katelyn
Bikman, Benjamin T.
Bridgewater, Laura C.
Grose, Julianne H.
Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title_full Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title_fullStr Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title_full_unstemmed Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title_short Per-Arnt-Sim Kinase (PASK) Deficiency Increases Cellular Respiration on a Standard Diet and Decreases Liver Triglyceride Accumulation on a Western High-Fat High-Sugar Diet
title_sort per-arnt-sim kinase (pask) deficiency increases cellular respiration on a standard diet and decreases liver triglyceride accumulation on a western high-fat high-sugar diet
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316003/
https://www.ncbi.nlm.nih.gov/pubmed/30558306
http://dx.doi.org/10.3390/nu10121990
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