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Age‐dependent changes in metabolite profile and lipid saturation in dystrophic mice
Author(s) -
LeeMcMullen Brittany,
Chrzanowski Stephen M.,
Vohra Ravneet,
Forbes Sean C.,
Vandenborne Krista,
Edison Arthur S.,
Walter Glenn A.
Publication year - 2019
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.4075
Subject(s) - metabolite , saturation (graph theory) , chemistry , biophysics , biology , biochemistry , mathematics , combinatorics
Duchenne Muscular Dystrophy (DMD) is a fatal X‐linked genetic disorder. In DMD, the absence of the dystrophin protein causes decreased sarcolemmal integrity resulting in progressive replacement of muscle with fibrofatty tissue. The effects of lacking dystrophin on muscle and systemic metabolism are still unclear. Therefore, to determine the impact of the absence of dystrophin on metabolism, we investigated the metabolic and lipid profile at two different, well‐defined stages of muscle damage and stabilization in mdx mice. We measured NMR‐detectable metabolite and lipid profiles in the serum and muscles of mdx mice at 6 and 24 weeks of age. Metabolites were determined in muscle in vivo using 1 H MRI/MRS, in isolated muscles using 1 H‐HR‐MAS NMR, and in serum using high resolution 1 H/ 13 C NMR. Dystrophic mice were found to have a unique lipid saturation profile compared with control mice, revealing an age‐related metabolic change. In the 6‐week‐old mdx mice, serum lipids were increased and the degree of lipid saturation changed between 6 and 24 weeks. The serum taurine‐creatine ratio increased over the life span of mdx, but not in control mice. Furthermore, the saturation index of lipids increased in the serum but decreased in the tissue over time. Finally, we demonstrated associations between MRI‐T 2 , a strong indicator of inflammation/edema, with tissue and serum lipid profiles. These results indicate the complex temporal changes of metabolites in the tissue and serum during repetitive bouts of muscle damage and regeneration that occur in dystrophic muscle.