Abnormal lipid profile of dystrophic cardiac tissue as demonstrated by one‐ and two‐dimensional magic‐angle spinning 1H NMR spectroscopy
Open Access
- 24 July 2001
- journal article
- research article
- Published by Wiley in Magnetic Resonance in Medicine
- Vol. 46 (2) , 249-255
- https://doi.org/10.1002/mrm.1185
Abstract
Dystrophin, a protein associated with sarcolemma and cell membranes, is not expressed in sufferers of Duchenne muscular dystrophy (DMD), or in the mdx mouse. DMD is a fatal disorder, with a significant proportion of fatalities associated with cardiac failure (∼40% having dilated cardiomyopathy and >90% clinically significant cardiac defects at death). In this study, the metabolic composition of intact dystrophic cardiac tissue was investigated using high‐resolution magic‐angle spinning (HRMAS) 1H NMR spectroscopy with both 1‐ and 2D pulse sequences coupled with pattern recognition (PR). While conventional solvent presaturation spectra indicated increases in CH2 chain length in lipids, PR analysis of correlation spectroscopy (COSY) spectra demonstrated that this was also accompanied by an increase in concentration of lactate or threonine along with a relative decrease in CH = CHCH2CO groups in these lipids. To investigate the physical environment of these lipids, T2‐ and diffusion‐weighted 1H MAS NMR spectra were acquired on whole‐tissue samples. The relatively increased lipid signal intensity in dystrophic tissue was due to an increase in molecules with long T2 and short diffusion rates. The use of a range of pulse programs allowed the direct probing of the biochemical environment in which the lipid infiltration occurred, and by coupling the experiments to PR the significance of lipid infiltration and accumulation was also assessed. Magn Reson Med 46:249–255, 2001.Keywords
This publication has 29 references indexed in Scilit:
- Regeneration and myogenic cell proliferation correlate with taurine levels in dystrophin- and MyoD-Deficient musclesThe Anatomical Record, 1998
- Magnetic resonance imaging of regenerating and dystrophic mouse muscleBiochemistry and Cell Biology, 1998
- Quantitative neuropathology by high resolution magic angle spinning proton magnetic resonance spectroscopyProceedings of the National Academy of Sciences, 1997
- Components of energy expenditure in themdx mouse model of Duchenne muscular dystrophyPflügers Archiv - European Journal of Physiology, 1996
- Defective regulation of energy metabolism in mdx-mouse skeletal musclesBiochemical Journal, 1994
- In vivo 2D 1H NMR of mdx mouse muscle and myoblast cells during fusion: Evidence for a characteristic signal of long chain fatty acidsNeuromuscular Disorders, 1993
- Cellular energetics of dystrophic muscleJournal of the Neurological Sciences, 1993
- The structural and functional diversity of dystrophinNature Genetics, 1993
- Dystrophin: The protein product of the duchenne muscular dystrophy locusCell, 1987
- X chromosome-linked muscular dystrophy (mdx) in the mouse.Proceedings of the National Academy of Sciences, 1984