Pathway attenuation of fatty acid beta‐oxidation in the skeletal muscle of a type 2 diabetic mouse model. (7th August 2020)

• Record Type: Journal Article
• Authors: Zhou, Yang; Tan, Yifan; Hou, Guixue; Ren, Yan; Deng, Yamei; Yan, Keqiang; Zhang, Yue; Lin, Liang; Lou, Xiaomin; Liu, Siqi
• Is Part Of: Rapid communications in mass spectrometry. Volume 34:Number 19(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-08-07
• Subjects: Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/rcm.8869
• Languages: English
• ISSNs: 0951-4198

Abstract

Abstract : Rationale: Whether catabolic abnormalities of fatty acids exist in the skeletal muscle of type 2 diabetes mellitus (T2DM) has not been determined. In this study, we postulated that a systematic evaluation of the protein abundance and metabolic activity related to fatty acids in the skeletal muscle tissues of a T2DM mouse model was feasible to address this question. Methods: Mitochondria were extracted from wild‐type (WT) and db/db mice followed by quantitative analysis of the proteins involved in mitochondrial fatty acid oxidation (mFAO). The pathway activity of mFAO in skeletal muscle tissues was monitored in vitro using mass spectrometry, and tissue lipidomic analysis was conducted in profiling and target mode to distinguish the levels of long‐chain acylcarnitines between WT and db/db mice. Results: Two proteins related to the mFAO pathway were significantly downregulated in the skeletal muscle mitochondria of db/db mice. The measurement of mFAO pathway activity in vitro revealed that the abundance of long‐chain acylcarnitines (C14 to C18) in db/db mice was lower than that in WT mice, and the determination of acylcarnitines in skeletal muscle tissues in vivo revealed that most long‐chain acylcarnitines were decreased in db/db mice. Conclusions: The findings of lower abundance of ACAD9 and CPT1B, reduced activity of the mFAO pathway in vitro and decreased acylcarnitines in vivo firmly support that the mFAO pathway in the skeletal muscle of diabetic mice is attenuated, possibly resulting in cell/tissue dysfunction in diabetes.