Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophy

Neuromuscular Disorders

Volumn 7, Issue 6-7, 1997, Pages 379-386

  Ragusa, Robert J ^a   Chow, Ching K ^b   Porter, John D ^a,c  

^a UNIVERSITY OF KENTUCKY   (United States)

^b UNIVERSITY OF KENTUCKY   (United States)

^c UNIVERSITY OF KENTUCKY MEDICAL CENTER   (United States)

Author keywords

Extraocular muscle; mdx mouse; Muscular dystrophy; Oxidative stress

Indexed keywords

ANTIOXIDANT; CATALASE; DYSTROPHIN; FREE RADICAL; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE PEROXIDASE; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; ENZYME ACTIVITY; EXTRAOCULAR MUSCLE; HYPEROXIA; LIMB; LIPID PEROXIDATION; MOUSE; MUSCLE ATROPHY; MUSCLE DISEASE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN DEFICIENCY; SKELETAL MUSCLE;

ANIMALS; CATALASE; DYSTROPHIN; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; HYPEROXIA; LIPID PEROXIDATION; MICE; MICE, INBRED MDX; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, ANIMAL; OXIDATIVE STRESS; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCES;

EID: 0030861564     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(97)00096-5     Document Type: Article

References (51)

1. Partridge T. Pathophysiology of muscular dystrophy. Br J Hosp Med 1993;49:26-36.
2. 2+-ATPase activity in avian dystrophic muscle. Biochem Biophys Res Commun 1988;151:1434-1440.
3. Sunada Y, Bernier SM, Kozak CA, Yamada Y. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain to dy locus. J Biol Chem 1994;269:13729-13732.
4. Watanabe K, Yamada K, Mizutani T, Totsuka T. Elevation of the level of thiobarbituric acid reactive products in hindleg skeletal muscle of dystrophic mice, but non-elevation in tongue muscle. Free Radic Res Commun 1993;19:93-100.
5. Ohta K, Mizuno Y. Pathogenesis of progressive muscular dystrophy: studies on free radical metabolism in an animal model. Acta Neurol Scand 1988;77:108-114.
6. Murphy ME, Kehrer JP. Activities of antioxidant enzymes in muscle, liver and lung of chickens with inherited muscular dystrophy. Biochem Biophys Res Commun 1986;134:550-556.
7. Omaye ST, Tappel AL. Glutathione peroxidase, glutathione reductase and thiobarbituric acid reactive products in muscles of chickens and mice with genetic muscular dystrophy. Life Sci 1974;15:137-145.
8. McCaman MW. Enzyme studies of skeletal muscle in mice with heredity muscular dystrophy. Am J Physiol 1963;205:897-901.
9. Austin LM, DeNiese M, McGregor A, Arthur W, Guru Sihghe A, Gould MK. Potential oxyradical damage and energy states in individual muscle fibers from degenerating muscle diseases. Neuromusc Disord 1992;2:27-33.
10. Burr IM, Asayama K, Fenichel GF. Superoxide dismutase, glutathione peroxidase and catalase in neuromuscular disease. Muscle Nerve 1987;10:150-154.
11. Vradkar AM, Tanksdale KG, Desai AD. Superoxide dismutase, alpha galactosidase, and plasminogen activator activity in normal and Duchenne dystrophic muscle. Can J Clin Biochem 1986;2:5-8.
12. Mechler F, Imre S, Dioszeghy P. Lipid peroxidation and superoxide dismutase activity in muscle and erythrocytes in Duchenne muscular dystrophy. J Neurol Sci 1984;63:279-283.
13. Ragusa RJ, Chow CK, St Clair DK, Porter JD. Extraocular, limb and diaphragm muscle group-specific antioxidant enzyme activity patterns in control and mdx mice. J Neurol Sci 1996;139:180-186.
14. Hauser E, Hoger H, Bittner R, Widhalm K, Herkner K, Lubec G. Oxyradical damage and mitochondrial enzyme activities in the mdx mouse. Neuropediatrics 1995;26:260-262.
15. Foxley A, Edwards RHT, Jackson MJ. Enhanced lipid peroxidation in Duchenne dystrophy muscle may be secondary to muscle damage. Biochem Soc Trans 1991;19:180S.
16. Rando TA, Dhawan J, Whirl M, Franco AA. Muscle cells from mdx (muscular dystrophy) mice have an increased susceptibility to free radical induced injury. Soc Neurosci Abstr 1996;22:1942.
17. Rando TA, Dziesietnik M-H, Dhawan J, Yu Y, Whirl M. Oxidative injury precedes muscle necrosis in dystrophin-deficient (mdx) mice. Neurology 1997;48:A442-A443.
18. Smith PK, Krohn RI, Hermanson GT, Mallia AK, Gartner FH, Provenzano MD, Fujimoto EK, Goeke NM, Olson BJ, Clenk DC. Measurement of protein using bicinchoninic acid. Anal Biochem 1985;150:76-85.
19. McCord JM, Fridovich I. Superoxide dismutase: an enzymatic function for erythrocuprein (hemocuprein). J Biol Chem 1969;244:6049-6055.
20. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967;70:158-169.
21. Carlberg I, Mannervik B. Glutathione reductase. Methods Enzymol 1985;113:484-490.
22. Langdon RG. Glucose-6-phosphate dehydrogenase from erythrocytes. Methods Enzymol 1966;9:126-131.
23. Beers RF, Sizer IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 1952;195:133-140.
24. Li X-Y, Chow CK. An improved method for measurement of malondialdehyde in biological samples. Lipids 1994;29:73-75.
25. Crapo JD, Tierney DF. Superoxide dismutase and pulmonary oxygen toxicity. Am J Physiol 1974;226:1401-1407.
26. Kimball RE, Reddy K, Pierce TH, Schwartz LW, Mustafa MG, Cross CE. Oxygen toxicity: augmentation of antioxidant defense mechanisms in rat lung. Am J Physiol 1976;230:1425-1431.
27. Campbell KP. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell 1995;80:675-679.
28. Hopf WF, Turner PR, Denetclaw WF, Reedy R, Steinhardt RA. A critical evaluation of resting intracellular free calcium regulation in dystrophic mdx muscle. Am J Physiol Cell Physiol 1996; 271:C1325-C1339.
29. Jackson MJ, Edwards RHT. Development of changes in cation content of muscles from the 129 ReJ dystrophic mouse. Comp Biochem Physiol 1987;87A:349-354.
30. Reeve JL, McArdle A, Jackson MJ. Age-related changes in muscle calcium content in dystrophin-deficient mdx mice. Muscle Nerve 1997;20:357-360.
31. Emery AEH. Some unanswered questions in Duchenne muscular dystrophy. Neuromusc Disord 1994;4:301-303.
32. Coulton GR, Morgan JK, Partridge TA, Sloper JE. The mdx mouse skeletal muscle myopathy. I. A histochemical, morphometric and biochemical investigation. Neuropathol Appl Neurobiol 1988;14:53-70.
33. Woo M, Tanabe Y, Ishii H, Nonaka I. Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx mice. J Neurol Sci 1987;82:111-122.
34. Torres LFB, Duchen LW. The mutant mdx: inherited myopathy in the mouse. Brain 1987;110:269-299.
35. Tanabe Y, Esaki K, Nomura T. Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse. Acta Neuropathol 1986;69:91-95.
36. Stedman HH, Sweeney HL, Shrager JB, Maguire HC, Panettieri RA, Petrof B, Narvsawa M, Leferovich JM, Sladkey JT, Kelly AM. The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy. Nature 1991;352:536-539.
37. Karapati G, Carpenter S, Prescott S. Small-caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophy. Muscle Nerve 1988;11:795-803.
38. Rosenbaum RM, Wittner M, Lenger M. Mitochondrial and other ultrastructural changes in great alveolar cells of oxygen-adapted and poisoned rats. Lab Invest 1969;20:516-528.
39. Crapo JD, Barry BE, Foscue HA, Sheiburne J. Structural and biochemical changes in rat lungs occurring during exposures to lethal and adaptive doses of oxygen. Am Rev Respirat Dis 1980;122:123-145.
40. Barja De Quiroga G, Gil P, Lopez-Torres M. Physiological significance of catalase and glutathione peroxidases, and in-vivo peroxidation in selected tissues of the toad Discoglossus pictus (Amphibia) during acclimation to normobaric hyperoxia. J Comp Physiol B 1988;158:583-590.
41. Arzueto A, Brassard JM, Andrade FH, Lawrence RA, Maxwell LC, Levine SM, Jenkinson SG. Effects of hyperoxia on rat diaphragm function. J Appl Physiol 1994;77:63-68.
42. Porter JD, Baker RS, Ragusa RJ, Brueckner JK. Extraocular muscles: basic and clinical aspects of structure and function. Surv Ophthalmol 1995;39:451-484.
43. Porter JD, Baker RS. Muscles of a different 'color': the unusual properties of the extraocular muscles may predispose or protect them in neurogenic and myogenic disease. Neurology 1996;46:30-37.
44. Muller-Hocker J, Seibel P, Schneiderbanger K, Kadenbach B. Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly. Virchows Arch A Pathol Anat Histopathol 1993;422:7-15.
45. Borchert MS. Diseases of the ocular muscles. In: Albert DM, Jakobiec FA, editors. Principals and practice of ophthalmology, vol. 4. Philadelphia: WB Sanders, 1994:2490-2498.
46. Bakker AJ, Head SI, Williams DA, Stephenson DG. Calcium levels in myotubes grown from the skeletal muscle of dystrophic (mdx) and normal mice. J Physiol 1993;460:1-13.
47. Turner RR, Fong P, Denetclaw WF, Steinhardt RA. Increased calcium influx in dystrophic muscle. J Cell Biol 1991;115:1701-1712.
48. Fong P, Turner PR, Denetclaw WF, Steinhardt RA. Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin. Science 1990;250:673-676.
49. Khurana TS, Prendergast RA, Alameddine H, Tome FMS, Fardeau M, Arahata K, Sugita H, Kunkel LM. Absence of extraocular muscle pathology in Duchenne muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing. J Exp Med 1995;182:467-475.
50. Celio MR, Heizmann CW. Calcium-binding protein parvalbumin is associate with fast contracting muscle fibres. Nature 1982;297:504-506.
51. Kaminski HJ, Al-Hakim M, Leigh RJ, Katiriji MB, Ruff RL. Extraocular muscles are spared in advanced Duchenne dystrophy. Ann Neurol 1992;32:586-588.