Intracellular pH changes induced by calcium influx during electrical activity in molluscan neurons

Simultaneous measurements of electrical activity and light absorbance have been made on nerve cell bodies from Archidoris monteryensis injected with indicator dyes. pH indicators, phenol red and bromocresol purple, and arsenazo III, which under normal conditions is primarily a calcium indicator have been employed. Voltage clamp pulses which induced calcium influx caused an absorbance decrease of the pH dyes indicating an internal acidification. The onset of the pH drop lagged the onset of Ca2+ influx by 200-400 ms, and pH continued to decrease for several seconds after pulse termination which shut off Ca2+ influx. Trains of action potentials also produced an internal pH decrease. Recovery of the pH change required periods greater than 10 min. The magnitude of the pH change was largely unaffected by external pH in the range 6.8-8.4. The voltage dependence of the internal p/ change was similar to the voltage dependence of calcium influx determined by arsenazo III, and removal of calcium from the bathing saline eliminated the pH signal. In neurons injected with EGTA (1-5 mM), the activity- induced internal Ca2+ changes were reduced or eliminated, but the internal pH drop was increased severalfold in magnitude. After the injection of EGTA, voltage clamp pulses produced a decrease in arsenazo III absorbance instead of the normal increase. Under these conditions the dye was responding primarily to changes in internal pH. Injection of H+ caused a rise in internal free calcium. The pH buffering capacity of the neurons was measured using three different techniques: H+ injection, depressing intrinsic pH changes with a pH buffer, and a method employing the EGTA-calcium reaction. The first two methods gave similar measurements: 4-9 meq/unit pH per liter for pleural ganglion cells and 13-26 meq/unit pH per liter for pedal ganglion cells. The EGTA method gave significantly higher values (20-60 meq/unit pH per liter) and showed no difference between pleural and pedal neurons.

[1]  P. C. Caldwell Studies on the internal pH of large muscle and nerve fibres , 1958, The Journal of physiology.

[2]  JOHN W. Moore,et al.  Liquid Junction and Membrane Potentials of the Squid Giant Axon , 1960, The Journal of general physiology.

[3]  C. S. Spyropoulos CYTOPLASMIC pH OF NERVE FIBRES , 1960, Journal of neurochemistry.

[4]  M. Paillard Direct intracellular pH measurement in rat and crab muscle , 1972, The Journal of physiology.

[5]  R. Keynes,et al.  Calcium and potassium systems of a giant barnacle muscle fibre under membrane potential control , 1973, The Journal of physiology.

[6]  S. Hagiwara Ca spike. , 1973, Advances in biophysics.

[7]  R. Meech The sensitivity of Helix aspersa neurones to injected calcium ions , 1974, The Journal of physiology.

[8]  R. Thomas Intracellular pH of snail neurones measured with a new pH‐sensitive glass micro‐electrode , 1974, The Journal of physiology.

[9]  A. Scarpa,et al.  Ionized magnesium concentration in axoplasm of dialyzed squid axons , 1975, FEBS letters.

[10]  J. A. Coles,et al.  Effects of increased intracellular pH-buffering capacity on the light response of Limulus ventral photoreceptor. , 1976, Biochimica et biophysica acta.

[11]  W. Boron,et al.  Intracellular pH transients in squid giant axons caused by CO2, NH3, and metabolic inhibitors , 1976, The Journal of general physiology.

[12]  R. Thomas The effect of carbon dioxide on the intracellular pH and buffering power of snail neurones. , 1976, The Journal of physiology.

[13]  F. Jöbsis,et al.  Spectrophotometric studies on the pH of frog skeletal muscle. PH change during and after contractile activity , 1976, The Journal of general physiology.

[14]  P. K. Brown,et al.  Detection of light‐induced changes of intracellular ionized calcium concentration in Limulus ventral photoreceptors using arsenazo III , 1977, The Journal of physiology.

[15]  R. Meech,et al.  The effect of calcium injection on the intracellular sodium and pH of snail neurones. , 1977, The Journal of physiology.

[16]  C. Ashley,et al.  Increase in free Ca2+ in muscle after exposure to CO2 , 1978, Nature.

[17]  J. Connor,et al.  Measurement of calcium influx under voltage clamp in molluscan neurones using the metallochromic dye arsenazo III. , 1979, The Journal of physiology.

[18]  J. Connor Calcium current in molluscan neurones: measurement under conditions which maximize its visibility. , 1979, The Journal of physiology.

[19]  W F Boron,et al.  Intracellular pH. , 1981, Physiological reviews.