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...

Full description

Bibliographic Details
Main Authors: Nicholas A. Hulett, Leslie A. Knaub, Sara E. Hull, Gregory B. Pott, Rick Peelor, Benjamin F. Miller, Kartik Shankar, Michael C. Rudolph, Jane E. B. Reusch, Rebecca L. Scalzo
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/15/20/4438
Description
Summary: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 (<i>p</i> < 0.0001). Blood glucose and insulin resistance were greater in males (<i>p</i> = 0.01) and HFHS-fed rats (<i>p</i> < 0.001). HFHS-fed males had higher mitochondrial respiration compared with females (<i>p</i> < 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.
ISSN:2072-6643