Early fetal like slow Na2+ current in heart cells of cardiomyopathic hamster

Molecular and Cellular Biochemistry

Volumn 176, Issue 1-2, 1997, Pages 249-256

  Jacques, Danielle ^a   Bkaily, Ghassan ^a   Jasmin, Gaétan ^b   Ménard, Daniel ^a   Proschek, Libuse ^b  

^a UNIVERSITY OF SHERBROOKE   (Canada)

^b UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

Apamin; Ca2+ blockers; Cardiomyopathic hamster; Heart cells; Hereditary cardiomyopathy; Melittin; Slow Na+ channel; TTX insensitive Na+ current; Um X7.1

Indexed keywords

MAGNESIUM ION; TETRODOTOXIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CARDIOMYOPATHY; CONTROLLED STUDY; FETUS; HAMSTER; HEART DEVELOPMENT; HEART MUSCLE CELL; HUMAN; HUMAN CELL; NEWBORN; NONHUMAN; PATCH CLAMP; SLOW INWARD CURRENT; SODIUM CURRENT; TRANSPORT KINETICS;

ANIMALIA; CRICETINAE;

EID: 0030779253     PISSN: 03008177     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1006809330667     Document Type: Article

References (38)

1. Bkaily G, Jacques D: Membrane physiopathology in hereditary cardiomyopathy. In: G Bkaily (ed). Membrane Physiopathology. Kluwer Academic Publishers, Boston, 1994, pp 13-23
2. Bkaily G, Jasmin G, Jacques D, Proschek L: Role of the slow sodium channel in hereditary cardiomyopathy. In: NS Dhalla, PK Singal, N Takeda, RE Beamish (eds) Pathophysiology of Heart Failure. Kluwer Academic Publishers, Boston, 1996, pp 109-125
3. Clark CE, Henry WL, Epstein SE: Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis. New Engl J Med 289: 709-714, 1973
4. Finkel MS, Shen L, Oddis CV, Romeo RC: Verapamil regulation of a defective SR release channel in the cardiomyopathic Syrian hamster. Life Sciences 52:1109-1119, 1993
5. Bkaily G, Pothier P, D'Orléans-Juste P, Simaan M, Jacques D, Jaalouk D, Belzile F, Boutin C, Haddad G, Neugebauer W: The use of confocal microscopy in the investigation of cell structure and function in heart, vascular endothelium and smooth muscle cells. Mol Cell Biochem 172: 171-195, 1997
6. Jasmin G, Solymoss CB, Proschek L: Therapeutic trials in hamster dystrophy. Ann NY Acad Sci 317: 338-348, 1979
7. Rouleau JL, Chuck LH, Hollosi G, Kidd P, Sievers RE, Wikman-Coffelt J, Parmley WW: Verapamil preserves myocardial contractility in the hereditary cardiomyopathy of the Syrian hamster. Circ Res 50: 405-412, 1982
8. + transport by taurine in heart and vascular smooth muscle. Adv Exp Med Biol 403: 263-273, 1996
9. Losse B, Kuhn H, Loogen F, Schulte HD: Exercise performance in hypertrophic cardiomyopathies. Eur Heart J 4: 197-208, 1983
10. Khuchua ZA, Vasiljeva EV, Clark JF, Korchazhkina OV, Branishte T, Kapelko VI, Kuznetsov AV, Ventura-Clapier R, Steinschneider AYa, Lakomkin VL et al.: The creatine kinase system and cardiomyopathy. Am J Cardiovasc Pathol 4: 223-234, 1992
11. Jasmin G, Proschek L: Paradoxical effect of isoproterenol on hamster hereditary polymyopathy. Muscle and Nerve 6: 408-415, 1983
12. Jasmin G, Pasternac A, Bkaily G, Proschek L: Modulation of calcium channels in the management of cardiomyopathies. In: L Hurwitz, D Partridge, J Leach (eds). Calcium Channels: Their Properties, Functions, Regulation and Clinical Relevance. CRC Press, Boca Raton, FL, 1991, pp 295-307
13. Lachnit WG, Phillips M, Gayman KJ, Pessah IN: Ryanodine and dihydropyridine binding patterns and ryanodine receptor mRNA levels in myopathic hamster heart. Am J Physiol 267: H1205-H1213, 1994
14. Malhotra A, Karell M, Scheuer J: Multiple cardiac contractile protein abnormalities in myopathic Syrian hamsters (BIO 53:58). J Mol Cell Cardiol 17: 95-107, 1985
15. Sapp JL, Howlett SE: Density of ryanodine receptors is increased in sarcoplasmic reticulum from prehypertrophic cardiomyopathic hamster heart. J Mol Cell Cardiol 26: 325-34, 1994
16. Kuo TH, Tsang W, Wang KK, Carlock L: Simultaneous reduction of the sarcolemmal and SR calcium ATPase activities and gene expression in cardiomyopathic hamster. Biochem et Biophys Acta 1138: 343-349, 1992
17. Dhalla NS, Afzal N, Beamish RE, Naimark B, Takeda N, Nagano M: Pathophysiology of cardiac dysfunction in congestive heart failure. Can J Cardiol 9: 873-887, 1993
18. Tsuruya Y, Ikeda U, Yamamoto K, Seino Y, Kanbe T, Shimada K: Decreased Na,K-ATPase gene expression in cardiomyopathic hamster hearts. Life Sciences 54: 71-77, 1994
19. Wilkinson M, Horackova M, Giles A: Reduction of ventricular M2 muscarinic receptors in cardiomyopathic hamster (CHF 147) at the necrotic stage of the myopathy. Pflugers Arch, Eur J Physiol 426: 516-23, 1994
20. 2+ exchange activity in cardiomyopathic Syrian hamster. Circ Res 74: 253-61, 1994
21. Kagiya T, Hori M, Iwakura K, Iwai K, Watanabe Y, Uchida S, Yoshida H, Kitabatake A, Inoue M, Kamada T: Role of increased alpha 1-adrenergic activity in cardiomyopathic Syrian hamster. Am J Physiol 260: H80-88, 1991
22. Sethi R, Bector N, Takeda N, Nagano M, Jasmin G, Dhalla NS: Alterations in G-proteins in congestive heart failure in cardiomyopathic (UM-X7.1) hamsters. Mol Cell Biochem 140: 163-170, 1994
23. Dhalla NS, Singh A, Lee SL, Anand MB, Bernatsky AM, Jasmin G: Detective membrane systems in dystrophic skeletal muscle of the OM-X7.1 strain of genetically myopathic hamster. Clin Sci Mol Med 49: 359-368, 1975
24. Bkaily G: Single heart cells as models for studying cardiac toxicology. In: G Jolles, A Cordier (eds). In vitro Methods in Toxicology. Academic Press, London, 1992, pp 289-334
25. + currents in single heart and rabbit aortic cells. Mol Cell Biochem 80: 59-72, 1988
26. + current in young embryonic heart. J Mol Cell Cardiol 23: 25-39, 1991
27. 2+ channel by PN200-110 in heart and vascular smooth muscle. Mol Cell Biochem 117: 93-106, 1992
28. + current in fetal single ventricular cells. J Mol Cell Cardiol 25: 1305-1316, 1993
29. 2+ current blocker in single heart cells. Am J Physiol 262: H463-H471, 1992
30. + currents as distinguished by melittin in 3 day old embryonic heart. Can J Physiol Pharmacol 66: 1017-1022, 1988
31. Chahine M, Bennett PB, George AL Jr, Horn R: Functional expression and properties of the human skeletal muscle sodium channel. Pflugers Arch, Eur J Physiol 427:136-42, 1994
32. Chahine M, George AL Jr, Zhou M, Ji S, Sun W, Barchi RL, Horn R: Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation. Neuron 12: 281-294, 1994
33. Roy ML, Narahashi T: Differential properties of tetrodotoxin-sensitive and tetrodotoxin-resistant sodium channels in rat dorsal root ganglion neurons. J Neurosci 12: 2104-11, 1992
34. George Jr AL, Knittle TJ, Tamkun MM: Molecular cloning of an atypical voltage-gated sodium channel expressed in human heart and uterus: evidence for a distinct gene family. Proc Natl Acad Sci USA 89: 4893-4897, 1992
35. Sculptoreanu A, Morton M, Gartside CL, Hauschka SD, Catterall WA, Scheuer T: Tetrodotoxin insensitive sodium channels in cardiac cell line from a transgenic mouse. Am J Physiol 262: C724-C730, 1992
36. Flamm RE, Birnberg NC, Kaczmarek LK: Transfection of activated ras into an excitable cell line (Alt-20) alters tetrodotoxin sensitivity of voltage-dependent sodium current. Pflugers Arch, 416: 120-125, 1990
37. Schlichter R, Bader CR, Bernheim L: Development of anomalous rectification (lie) and of a tetrodotoxin-resistant sodium current in embryonic quail neurones. J Physiol 442: 127-145, 1991
38. + channels in neurons of the rat dorsal root ganglia. Brain Res 65: 93-100, 1992