Literature DB >> 8538672

Porcine malignant hyperthermia: genotype and contractile threshold of immature muscles.

E M Gallant1, R C Jordan.   

Abstract

We investigated whether malignant hyperthermia (MH)-related contractile abnormalities, such as lowered contractile threshold, were expressed in MH-susceptible (MHS) immature muscles and myotubes. Muscles from neonatal piglets homozygous for Arg615 (normal) or for Cys615 (MHS) ryanodine receptor alleles, and heterozygotes were used. Intact cell bundles from piglet muscles generally were similar in contractile properties to adult muscles of the same genotype. Thresholds for K contractures in normal, heterozygous, and MHS piglet muscles (40 mmol/L, 25 mmol/L and 15 mmol/L K+, respectively) differed significantly. Cultured myotubes were subjected to a series of square pulses of varying strengths (-50 to +50 mV) and durations (25-300 ms) using whole cell patch-clamp techniques. Threshold for contraction differed significantly among the three genotypes, for example, with 300 msec pulses thresholds were -6.9 +/- 0.9, -12.4 +/- 1.6, and -22.6 +/- 2.6 mV for normal, heterozygous and MHS myotubes, respectively. Thus a significantly lower than normal threshold for contraction was expressed in MHS and heterozygous piglet muscles and myotubes. Further, these developmentally immature preparations are likely to express other differences characteristic of adult MHS muscles, and thus provide suitable preparations for clinically relevant studies of MH-related cellular abnormalities.

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Year:  1996        PMID: 8538672     DOI: 10.1002/(SICI)1097-4598(199601)19:1<68::AID-MUS9>3.0.CO;2-6

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  6 in total

1.  Functional effects of central core disease mutations in the cytoplasmic region of the skeletal muscle ryanodine receptor.

Authors:  G Avila; R T Dirksen
Journal:  J Gen Physiol       Date:  2001-09       Impact factor: 4.086

2.  Malignant hyperthermia mutation Arg615Cys in the porcine ryanodine receptor alters voltage dependence of Ca2+ release.

Authors:  B Dietze; J Henke; H M Eichinger; F Lehmann-Horn; W Melzer
Journal:  J Physiol       Date:  2000-08-01       Impact factor: 5.182

3.  Distinct effects on Ca2+ handling caused by malignant hyperthermia and central core disease mutations in RyR1.

Authors:  Robert T Dirksen; Guillermo Avila
Journal:  Biophys J       Date:  2004-09-03       Impact factor: 4.033

4.  Voltage-dependent calcium release in human malignant hyperthermia muscle fibers.

Authors:  A Struk; F Lehmann-Horn; W Melzer
Journal:  Biophys J       Date:  1998-11       Impact factor: 4.033

5.  A retrograde signal from RyR1 alters DHP receptor inactivation and limits window Ca2+ release in muscle fibers of Y522S RyR1 knock-in mice.

Authors:  Zoita Andronache; Susan L Hamilton; Robert T Dirksen; Werner Melzer
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-25       Impact factor: 11.205

6.  Relationships between resting conductances, excitability, and t-system ionic homeostasis in skeletal muscle.

Authors:  James A Fraser; Christopher L-H Huang; Thomas H Pedersen
Journal:  J Gen Physiol       Date:  2011-06-13       Impact factor: 4.086

  6 in total

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