Sulfhydryl oxidation overrides Mg(2+) inhibition of calcium-induced calcium release in skeletal muscle triads

• Published in: Biophysical journal 2000-07, Vol.79 (1), p.279-286
• Main Authors: Donoso, P, Aracena, P, Hidalgo, C
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Animals; Calcium - antagonists & inhibitors; Calcium - metabolism; Calcium - pharmacology; Dithiothreitol - pharmacology; Dose-Response Relationship, Drug; Magnesium - metabolism; Magnesium - pharmacology; Muscle, Skeletal - metabolism; Myofibrils - metabolism; Oxidation-Reduction - drug effects; Phosphorylation - drug effects; Rabbits; Ryanodine Receptor Calcium Release Channel - drug effects; Ryanodine Receptor Calcium Release Channel - isolation & purification; Ryanodine Receptor Calcium Release Channel - metabolism; Sarcoplasmic Reticulum - chemistry; Sarcoplasmic Reticulum - drug effects; Sarcoplasmic Reticulum - metabolism; Sulfhydryl Compounds - chemistry; Thimerosal - antagonists & inhibitors; Thimerosal - pharmacology
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(00)76290-4

We studied the effect of oxidation of sulfhydryl (SH) residues on the inhibition by Mg(2+) of calcium-induced calcium release (CICR) in triad-enriched sarcoplasmic reticulum vesicles isolated from rabbit skeletal muscle. Vesicles were either passively or actively loaded with calcium before eliciting CICR by dilution at pCa 4.6-4.4 in the presence of 1.2 mM free [ATP] and variable free [Mg(2+)]. Native triads exhibited a significant inhibition of CICR by Mg(2+), with a K(0.5) approximately 50 microM. Partial oxidation of vesicles with thimerosal produced a significant increase of release rate constants and initial release rates at all [Mg(2+)] tested (up to 1 mM), and shifted the K(0.5) value for Mg(2+) inhibition to 101 or 137 microM in triads actively or passively loaded with calcium, respectively. Further oxidation of vesicles with thimerosal completely suppressed the inhibitory effect of [Mg(2+)] on CICR, yielding initial rates of CICR of 2 micromol/(mg x s) in the presence of 1 mM free [Mg(2+)]. These effects of oxidation on CICR were fully reversed by SH reducing agents. We propose that oxidation of calcium release channels, by decreasing markedly the affinity of the channel inhibitory site for Mg(2+), makes CICR possible in skeletal muscle.