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January 1, 1968The Journal of Physiology283 citationsOpen Access

The action of caffeine on the activation of the contractile mechanism in striated muscle fibres

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HLH C LüttgauHOH. Oetliker

Key Result

Caffeine caused reversible contractures and shifted the potassium concentration required for half-maximal tension from 30 to 16 mM-K in isolated frog muscle fibres.

Key Points

  • This research aims to investigate how caffeine influences the contractile mechanisms in striated muscle fibers.
  • Isolated twitch muscle fibers from frogs were used.
  • Tension was recorded with a mechano-electrical transducer in varying potassium solutions and caffeine concentrations.
  • Mechanical activity was tested with tetracaine and temperature variations.
  • Caffeine induced reversible contractures at 6-10 mM, with peak tension achieved in 2-4 seconds.
  • Subthreshold caffeine shifted potassium effective concentration significantly, indicating lower activation thresholds.
  • Tetracaine altered tension thresholds and modulated caffeine-induced contractility, reinforcing the role of membrane potential.

Structured PICO

P
Population
Isolated twitch muscle fibres of the frog
I
Intervention
Caffeine (1.5 mM to 10 mM) in Ringer solution or 95 mM-K(2)SO(4) solution
O
Outcome
Initiation of isometric tension (contractures)surrogate

Caffeine induces reversible contractures and increases sensitivity to potassium in frog muscle fibers, suggesting it acts on the sarcotubular system.

Abstract

The effect of caffeine on the initiation of isometric tension in isolated twitch muscle fibres of the frog was recorded with a mechano-electrical transducer.2. In Ringer solution as well as in solutions containing 95 mM-K(2)SO(4), caffeine (6-10 mM) caused reversible contractures. Tension of maximal potassium contractures was reached with a half-time of 2-4 sec.3. Caffeine caused a shift to lower potassium concentrations of the S-shaped curve which relates peak tension to log. K(o) or membrane potential. In subthreshold concentrations of caffeine (1.5 mM) the potassium concentration at which half of maximal tension was reached shifted from 30 to 16 mM-K (-39 to -53 mV).4. In the ;steady state' the ability of fibres to develop tension is related to log. K(o) or membrane potential by an S-shaped curve whose half value shifted from 28 to 45 mM-K (-41 to -29 mV) when 1.5 mM caffeine was applied.5. Fibres were most sensitive to caffeine at membrane potentials between -50 and -20 mV.6. The mechanical activity caused by caffeine was ;stabilized' by an increase in Ca(o) or Mg(o) resembling the stabilizing action of these ions on potassium contractures or on the sodium permeability of excitable membranes.7. Tetracaine in low concentrations (0.04-0.1 mM) increased the threshold for mechanical activation and shortened the plateau of potassium contractures. Higher concentrations (1-2 mM) suppressed mechanical activity completely.8. Tetracaine, 0.04 mM, was sufficient to suppress tension caused by a 100 times stronger concentration of caffeine. With higher concentrations of caffeine the inhibitory action of tetracaine could be reversed.9. Fibres which were immersed in subthreshold concentrations of caffeine either in Ringer solution or in a solution with 95 mM-K(2)SO(4) developed a strong contracture after a sudden drop in temperature from 20 to 1-3 degrees C.10. The fast activation of the whole cross-section of the muscle fibre caused by caffeine and its dependence on membrane potential, tetracaine and external alkali earth ions favours the idea that the drug acts at some part of the sarcotubular system which is easily accessible for external ions and drugs and in close connextion with the surface membrane.

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Cite This Study

Lüttgau et al. (1968) studied Isolated twitch muscle fibres of the frog. Caffeine was evaluated on Initiation of isometric tension. Caffeine caused reversible contractures and shifted the potassium concentration required for half-maximal tension from 30 to 16 mM-K in isolated frog muscle fibres.

synapsesocial.com/papers/6a62eec83eb69703d1b6e150https://doi.org/10.1113/jphysiol.1968.sp008394
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