Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathy

Cardiovascular Research

Volumn 45, Issue 4, 2000, Pages 860-865

  Jarreta, Diana ^a   Orús, Josefina ^a   Barrientos, Antoni ^b   Miró, Oscar ^a   Roig, Eulàlia ^a   Heras, Magdalena ^a   Moraes, Carlos T ^b   Cardellach, Francesc ^a   Casademont, Jordi ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Cardiomyopathy; Energy metabolism; Gene therapy; Mitochondria; Oxidative phosphorylation

Indexed keywords

CITRATE SYNTHASE; CYTOCHROME B; CYTOCHROME C OXIDASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SUCCINATE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE;

ADULT; ARTICLE; CLINICAL ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; ENERGY METABOLISM; ENZYME ACTIVITY; FEMALE; GENE THERAPY; GENETIC POLYMORPHISM; HEART DILATATION; HEART MITOCHONDRION; HEART TRANSPLANTATION; HUMAN; HUMAN TISSUE; MALE; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; RESPIRATORY CHAIN;

ADULT; ANALYSIS OF VARIANCE; CARDIOMYOPATHY, DILATED; CASE-CONTROL STUDIES; CITRATE (SI)-SYNTHASE; CYTOCHROME B GROUP; ELECTRON TRANSPORT; ELECTRON TRANSPORT COMPLEX I; ELECTRON TRANSPORT COMPLEX II; ELECTRON TRANSPORT COMPLEX III; ELECTRON TRANSPORT COMPLEX IV; ENERGY METABOLISM; FEMALE; HUMANS; LINEAR MODELS; MALE; MIDDLE AGED; MITOCHONDRIA, HEART; MULTIENZYME COMPLEXES; MYOCARDIAL ISCHEMIA; NADH, NADPH OXIDOREDUCTASES; OXIDATIVE PHOSPHORYLATION; OXIDOREDUCTASES; SEQUENCE ANALYSIS, DNA; SPECTROPHOTOMETRY; SUCCINATE DEHYDROGENASE;

EID: 0342445429     PISSN: 00086363     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6363(99)00388-0     Document Type: Article

References (31)

1. Dec G.W., Fuster V. Idiopathic dilated cardiomyopathy. New Engl J Med. 8:1994;1564-1575.
2. Suomalainen A., Paetau A., Leinonen H., et al. Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA. Lancet. 340:1992;1319-1320.
3. Li Y.Y., Hengstenberg C., Maisch B. Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy. Biochem Biophys Res Commun. 210:1995;211-218.
4. Bobba A., Giannattasio S., Pucci A., et al. Characterization of mitochondrial DNA in primary cardiomyopathies. Clin Chim Acta. 243:1995;181-189.
5. Li Y.Y., Maisch B., Rose M.L., Hengstenberg C. Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy. J Mol Cell Cardiol. 29:1997;2699-2709.
6. Vilarinho L., Santorelli F.M., Rosas M.J., et al. The mitochondrial A3243G mutation presenting as severe cardiomyopathy. J Med Genet. 34:1997;607-609.
7. Rustin P., Chretien D., Bourgeon T., et al. Biochemical and molecular investigations in respiratory chain deficiencies. Clin Chim Acta. 228:1994;35-51.
8. Chretien D., Rustin P., Bourgeron T., et al. Reference charts for respiratory chain activities in human tissues. Clin Chim Acta. 228:1994;53-70.
9. Bradford M. A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 72:1976;248-254.
10. Miró O., Cardellach F., Barrientos A., et al. Cytochrome c oxidase assay in minute amounts of human skeletal muscle using single wavelength spectrophotometers. J Neurosci Methods. 80:1998;107-111.
11. Ausubel F.M., Brent R., Kingston R.E., et al. Current protocols in molecular biology, unit 2.9A. 1993;Wiley, New York.
12. Anderson S., Bankier A.T., Barrell B.G., et al. Sequence and organization of the human mitochondrial genome. Nature. 290:1981;457-465.
13. Brown M.D., Voljavec A.S., Lott M.T., et al. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics. 130:1992;163-173.
14. Howell N., Halvorson S., Burns J., McCullough D.A., Poulton J. When does bilateral optic atrophy become Leber hereditary optic neuropathy? Am J Hum Genet. 53:1993;959-963.
15. Kelly D.P., Strauss A.W. Inherited cardiomyopathies. New Engl J Med. 330:1994;913-919.
16. Bohlega S., Tanji K., Santorelli F., et al. Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy. Neurology. 46:1996;1329-1334.
17. Anan R., Nakagawa M., Miyata M., et al. Cardiac involvement in mitochondrial diseases. Circulation. 91:1995;955-961.
18. Marin-Garcia J., Goldenthal M.J., Pierpont M.E., Ananthakrishnan R. Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis. J Card. Failure. 1:1995;285-291.
19. Buchwald A., Till H., Unterberg C., et al. Alterations of the mitochondrial respiratory chain in human dilated cardiomyopathy. Eur Heart J. 11:1990;509-516.
20. Bornstein B., Huertas R., Ochoa P., et al. Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases. Biochim Biophys Acta. 1406:1998;85-90.
21. Maurer I., Zierz S. Myocardial respiratory chain enzyme activities in idiopathic dilated cardiomyopathy, and comparison with those in atherosclerotic coronary artery disease and valvular aortic stenosis. Am J Cardiol. 72:1993;428-433.
22. Bakker H.D., Scholte H.R., van den Bogert C., et al. Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis: a new mitochondrial defect. Pediatr Res. 33:1993;412-417.
23. Briones P., Vilaseca M.A., Ribes A., et al. A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60. J Inherit Metab Dis. 20:1997;569-577.
24. Zeviani M., Servidei S., Gellera C., et al. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature. 339:1989;309-311.
25. Moraes C.T., Shanske S., Tritschler H.J., et al. MtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases. Am J Hum Genet. 48:1991;492-501.
26. Sarov V.G., Goussev A., Lesch M., Goldstein S., Sabbah H.N. Abnormal mitochondrial function in myocardium of dogs with chronic heart failure. Mol Cell Cardiol. 30:1998;1757-1762.
27. Kalsi K.K., Smolenski R.T., Pritchard R.D., et al. Energetics and function of the failing human heart with dilated or hypertrophic cardiomyopathy. Eur J Clin Invest. 29:1999;469-477.
28. Yücel D., Aydogdu S., Çehreli S., et al. Increased oxidative stress in dilated cardiomyopathic heart failure. Clin Chem. 44:1998;148-154.
29. Corral-Debrinski M., Stepien G., Shoffner J.M., et al. Hypoxemia is associated with mitochondrial DNA damage and gene induction. J Am Med Assoc. 266:1991;1812-1816.
30. Corral-Debrinski M., Shoffner J.M., Lott M.T., Wallace D.C. Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease. Mutat Res. 275:1992;169-180.
31. Knight J.A. Free radicals: their history and current status in aging and disease. Ann Clin Lab Sci. 28:1998;331-346.