Altered E-C coupling in triads isolated from malignant hyperthermia-susceptible porcine muscle

R. el-Hayek, M. Yano, B. Antoniu, J. R. Mickelson, C. F. Louis and N. Ikemoto Department of Veterinary Biology, University of Minnesota, St. Paul 55108, USA. Triad vesicles were isolated from normal (N) and homozygous malignant hyperthermia-susceptible (MHS) porcine skeletal muscle, and two types of...

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Veröffentlicht in:American Journal of Physiology: Cell Physiology 1995-06, Vol.268 (6), p.C1381-C1386
Hauptverfasser: el-Hayek, R, Yano, M, Antoniu, B, Mickelson, J. R, Louis, C. F, Ikemoto, N
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Sprache:eng
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Zusammenfassung:R. el-Hayek, M. Yano, B. Antoniu, J. R. Mickelson, C. F. Louis and N. Ikemoto Department of Veterinary Biology, University of Minnesota, St. Paul 55108, USA. Triad vesicles were isolated from normal (N) and homozygous malignant hyperthermia-susceptible (MHS) porcine skeletal muscle, and two types of sarcoplasmic reticulum Ca2+ release were investigated: 1) polylysine-induced Ca2+ release (direct stimulation of the junctional foot protein), and 2) depolarization-induced Ca2+ release (stimulation of the junctional foot protein via the dihydropyridine receptor). At submaximal concentrations of polylysine, the rates of induced Ca2+ release from the MHS triads were greater than from normal triads. The T tubules of polarized triads were depolarized by the K(+)-to-Na+ ionic replacement protocol. Higher grades of T-tubule depolarization resulted in higher rates of Ca2+ release from both MHS and normal triads but, when compared at a given grade of T-tubule depolarization, the release rate was always greater from the MHS than from normal triads. Thus the activity of the SR Ca2+ release channel is always higher in MHS than in normal muscle at a given submaximal dose of release trigger. This difference is observed when the channel is stimulated directly by polylysine or indirectly via a depolarization-induced activation of the T-tubule dihydropyridine receptor.
ISSN:0363-6143
0002-9513
1522-1563
DOI:10.1152/ajpcell.1995.268.6.c1381