Abnormal lipid profile of dystrophic cardiac tissue as demonstrated by one- and two-dimensional magic-angle spinning 1H NMR spectroscopy

被引:82
作者
Griffin, JL
Williams, HJ
Sang, E
Nicholson, JK
机构
[1] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
[2] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
关键词
dystrophin; Duchenne muscular dystrophy; mdx; diffusion-weighted spectroscopy; H-1 MAS NMR spectroscopy; pattern recognition;
D O I
10.1002/mrm.1185
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
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 (similar to 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) H-1 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, T-2- and diffusion-weighted H-1 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 T-2 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. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:249 / 255
页数:7
相关论文
共 37 条
  • [1] THE STRUCTURAL AND FUNCTIONAL DIVERSITY OF DYSTROPHIN
    AHN, AH
    KUNKEL, LM
    [J]. NATURE GENETICS, 1993, 3 (04) : 283 - 291
  • [2] ANTHONY ML, 1994, MOL PHARMACOL, V46, P199
  • [3] 2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE
    AUE, WP
    BARTHOLDI, E
    ERNST, RR
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) : 2229 - 2246
  • [4] Nuclear magnetic resonance spectroscopic and principal components analysis investigations into biochemical effects of three model hepatotoxins
    Beckwith-Hall, BM
    Nicholson, JK
    Nicholls, AW
    Foxall, PJD
    Lindon, JC
    Connor, SC
    Abdi, M
    Connelly, J
    Holmes, E
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (04) : 260 - 272
  • [5] Bollard ME, 2000, MAGNET RESON MED, V44, P201, DOI 10.1002/1522-2594(200008)44:2<201::AID-MRM6>3.0.CO
  • [6] 2-5
  • [7] BULLFIELD G, 1984, P NATL ACAD SCI USA, V81, P1189
  • [8] 3 MUSCULAR-DYSTROPHIES - LOSS OF CYTOSKELETON EXTRACELLULAR-MATRIX LINKAGE
    CAMPBELL, KP
    [J]. CELL, 1995, 80 (05) : 675 - 679
  • [9] Quantitative neuropathology by high resolution magic angle spinning proton magnetic resonance spectroscopy
    Cheng, LL
    Ma, MJ
    Becerra, L
    Ptak, T
    Tracey, I
    Lackner, A
    Gonzalez, RG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) : 6408 - 6413
  • [10] ENERGY STATUS OF CELLS LACKING DYSTROPHIN - AN INVIVO INVITRO STUDY OF MDX MOUSE SKELETAL-MUSCLE
    DUNN, JF
    FROSTICK, S
    BROWN, G
    RADDA, GK
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1096 (02) : 115 - 120