ArticleThe Journal of general physiology2014
Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder.
Article in The Journal of general physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed, 9 citations in OpenAlex.
- Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2.The Journal of general physiology · 2022Article
- Superfast excitation-contraction coupling in adult zebrafish skeletal muscle fibers.The Journal of general physiology · 2022Article
- CaFrontiers in physiology · 2022Article
- A proposed role for non-junctional transverse tubules in skeletal muscle as flexible segments allowing expansion of the transverse network.European journal of translational myology · 2019Article
- Small CaThe Journal of general physiology · 2018Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80-100-Hz calls lasting ∼ 500 ms interleaved with silent periods (intercall intervals) lasting ∼ 10 s. To understand the intracellular movements of Ca(2+) during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca(2+) indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca(2+) movements, including the binding and transport of Ca(2+) by the sarcoplasmic reticulum (SR) Ca(2+) pumps. The estimated total amount of Ca(2+) released from the SR during a first stimulus train is ∼ 6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca(2+) concentration ([Ca(2+)]) is below the threshold for force generation (∼ 3 µM), yet the estimated concentration of released Ca(2+) remaining in the myoplasm (Δ[CaM]) is large, ∼ 5 mM, with ∼ 80% bound to parvalbumin. At 10 s after stimulation, [Ca(2+)] is ∼ 90 nM (three times the assumed resting level) and Δ[CaM] is ∼ 1.3 mM, with 97% bound to parvalbumin. Ca(2+) movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca(2+) on parvalbumin and (b) the slow rate of Ca(2+) pumping that ensues when parvalbumin lowers [Ca(2+)] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca(2+) release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca(2+) pumping at higher [Ca(2+)].
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