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 |
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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. |
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ISSN: | 0363-6143 0002-9513 1522-1563 |
DOI: | 10.1152/ajpcell.1995.268.6.c1381 |