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Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats
Men are diagnosed with type 2 diabetes at lower body mass indexes than women; the role of skeletal muscle in this sex difference is poorly understood. Type 2 diabetes impacts skeletal muscle, particularly in females who demonstrate a lower oxidative capacity compared to males. To address mechanistic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610114/ https://www.ncbi.nlm.nih.gov/pubmed/37892512 http://dx.doi.org/10.3390/nu15204438 |
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author | Hulett, Nicholas A. Knaub, Leslie A. Hull, Sara E. Pott, Gregory B. Peelor, Rick Miller, Benjamin F. Shankar, Kartik Rudolph, Michael C. Reusch, Jane E. B. Scalzo, Rebecca L. |
author_facet | Hulett, Nicholas A. Knaub, Leslie A. Hull, Sara E. Pott, Gregory B. Peelor, Rick Miller, Benjamin F. Shankar, Kartik Rudolph, Michael C. Reusch, Jane E. B. Scalzo, Rebecca L. |
author_sort | Hulett, Nicholas A. |
collection | PubMed |
description | Men are diagnosed with type 2 diabetes at lower body mass indexes than women; the role of skeletal muscle in this sex difference is poorly understood. Type 2 diabetes impacts skeletal muscle, particularly in females who demonstrate a lower oxidative capacity compared to males. To address mechanistic differences underlying this sex disparity, we investigated skeletal muscle mitochondrial respiration in female and male rats in response to chronic high-fat, high-sugar (HFHS) diet consumption. Four-week-old Wistar Rats were fed a standard chow or HFHS diet for 14 weeks to identify sex-specific adaptations in mitochondrial respirometry and characteristics, transcriptional patterns, and protein profiles. Fat mass was greater with the HFHS diet in both sexes when controlled for body mass (p < 0.0001). Blood glucose and insulin resistance were greater in males (p = 0.01) and HFHS-fed rats (p < 0.001). HFHS-fed males had higher mitochondrial respiration compared with females (p < 0.01 sex/diet interaction). No evidence of a difference by sex or diet was found for mitochondrial synthesis, dynamics, or quality to support the mitochondrial respiration sex/diet interaction. However, transcriptomic analyses indicate sex differences in nutrient handling. Sex-specific differences occurred in PI3K/AKT signaling, PPARα/RXRα, and triacylglycerol degradation. These findings may provide insight into the clinical sex differences in body mass index threshold for diabetes development and tissue-specific progression of insulin resistance. |
format | Online Article Text |
id | pubmed-10610114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106101142023-10-28 Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats Hulett, Nicholas A. Knaub, Leslie A. Hull, Sara E. Pott, Gregory B. Peelor, Rick Miller, Benjamin F. Shankar, Kartik Rudolph, Michael C. Reusch, Jane E. B. Scalzo, Rebecca L. Nutrients Article Men are diagnosed with type 2 diabetes at lower body mass indexes than women; the role of skeletal muscle in this sex difference is poorly understood. Type 2 diabetes impacts skeletal muscle, particularly in females who demonstrate a lower oxidative capacity compared to males. To address mechanistic differences underlying this sex disparity, we investigated skeletal muscle mitochondrial respiration in female and male rats in response to chronic high-fat, high-sugar (HFHS) diet consumption. Four-week-old Wistar Rats were fed a standard chow or HFHS diet for 14 weeks to identify sex-specific adaptations in mitochondrial respirometry and characteristics, transcriptional patterns, and protein profiles. Fat mass was greater with the HFHS diet in both sexes when controlled for body mass (p < 0.0001). Blood glucose and insulin resistance were greater in males (p = 0.01) and HFHS-fed rats (p < 0.001). HFHS-fed males had higher mitochondrial respiration compared with females (p < 0.01 sex/diet interaction). No evidence of a difference by sex or diet was found for mitochondrial synthesis, dynamics, or quality to support the mitochondrial respiration sex/diet interaction. However, transcriptomic analyses indicate sex differences in nutrient handling. Sex-specific differences occurred in PI3K/AKT signaling, PPARα/RXRα, and triacylglycerol degradation. These findings may provide insight into the clinical sex differences in body mass index threshold for diabetes development and tissue-specific progression of insulin resistance. MDPI 2023-10-19 /pmc/articles/PMC10610114/ /pubmed/37892512 http://dx.doi.org/10.3390/nu15204438 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hulett, Nicholas A. Knaub, Leslie A. Hull, Sara E. Pott, Gregory B. Peelor, Rick Miller, Benjamin F. Shankar, Kartik Rudolph, Michael C. Reusch, Jane E. B. Scalzo, Rebecca L. Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title | Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title_full | Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title_fullStr | Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title_full_unstemmed | Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title_short | Sex Differences in the Skeletal Muscle Response to a High Fat, High Sucrose Diet in Rats |
title_sort | sex differences in the skeletal muscle response to a high fat, high sucrose diet in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610114/ https://www.ncbi.nlm.nih.gov/pubmed/37892512 http://dx.doi.org/10.3390/nu15204438 |
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