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K Kaila

Publications and source records attributed to K Kaila.

At least 73 records · Page 4Linked to original sources
PubMed1990

Dependence of intracellular free calcium and tension on membrane potential and intracellular pH in single crayfish muscle fibres.

The dependence of intracellular free calcium ([Ca2+]i) and tension on membrane potential and intracellular pH (pHi) was studied in single isolated fibres of the crayfish claw-opener muscle using ion-selective microelectrodes. Tension (T) was quantified as a percentage of the maximum force, or as force per cross-sectional area (N/cm2). In resting fibres, pHi had a mean value of 7.06. Contractions evoked by an increase extracellular potassium [( K+]0) produced a fall in pHi of 0.01-0.05 units. The lowest measured levels of resting [Ca2+]i corresponded to a pCai (= -log [Ca2+]i) of 6.8. Intracellular Ca2+ transients recorded during K(+)-induced contractions did not reveal any distinct threshold for force development. Both the resting [Ca2+]i and resting tension were decreased by an intracellular alkalosis and increased by an acidosis. The sensitivity of resting tension to a change in pHi (quantified as -dT/dpHi) showed a progressive increase during a fall in pHi within the range examined (pHi 6.2-7.5). The pHi/[Ca2+]i and pHi/tension relationships were monotonic throughout the multiphasic pHi change caused by NH4Cl. A fall of 0.5-0.6 units in pHi did not produce a detectable shift in the pCai/tension relationship at low levels of force development. The results indicate that resting [Ca2+]i is slightly higher than the level required for contractile activation. They also show that the dependence of tension on pHi in crayfish muscle fibres is attributable to a direct H+ and Ca2+ interaction at the level of Ca2+ sequestration and/or transport. Finally, the results suggest that in situ, the effect of pH on the Ca2+ sensitivity of the myofibrillar system is not as large as could be expected on the basis of previous work on skinned crustacean muscle fibres.

Ammonium Chloride↗
PubMed1990

Postsynaptic fall in intracellular pH and increase in surface pH caused by efflux of formate and acetate anions through GABA-gated channels in crayfish muscle fibres.

H(+)-selective microelectrodes and a two- or three-microelectrode voltage clamp were used to examine the influence of weak-acid, carboxylate anions on the actions of GABA on postsynaptic intracellular pH, surface pH and on membrane potential in fibres of the crayfish leg opener muscle. Substitution of 30 mM Cl- by formate or acetate promoted a GABA-induced decrease in intracellular pH, which was coupled to an increase in surface pH and to a depolarization. Such effects were not seen in the presence of an equivalent amount of lactate, methanesulphonate or glucuronate. Both the GABA-induced depolarization and the fall in internal pH promoted by formate and acetate were blocked by picrotoxin, and the fall in pH was reversibly inhibited by a K(+)-induced depolarization. The rate of the fall in intracellular pH produced by GABA (0.2 mM) was about 0.02 pH units/min in the presence of formate and 0.03 pH units/min in the presence of acetate. Under steady-state conditions, both 30 mM formate and acetate (but not lactate) induced a positive shift in the reversal potential of GABA-activated current, which was accounted for by a relative permeability vs Cl- of formate and acetate of 0.5 and 0.15, respectively. The conductance sequence of the anions was identical to the permeability sequence, i.e. Cl- greater than formate greater than acetate greater than lactate approximately equal to 0. This sequence is strictly correlated to the Stokes diameter of the anions. The relative permeabilities of the anions indicate that the effective diameter of the GABA-gated channel is about 0.5 nm. The fact that the GABA-induced acidosis was slower in the presence of formate than in the presence of acetate suggests that, in the former case, the rate-limiting step in the fall in internal pH is the entry of non-dissociated formic acid. All the above results are consistent with a scheme where GABA induces a channel-mediated efflux of permeant weak-acid anions, which gives rise to an inward (depolarizing) current and to an intracellular acidosis. A comparison of the permeability properties of crayfish and vertebrate GABA-gated channels suggests that effects similar to those seen in this work are likely to occur in mammalian and other vertebrate neurons in the presence of permeant weak-acid anions.

Acetates↗
PubMed1990

Mechanism of action of GABA on intracellular pH and on surface pH in crayfish muscle fibres.

1. The mode of action of gamma-aminobutyric acid (GABA) on intracellular pH (pHi) and surface pH (pHs) was studied in crayfish muscle fibres using H(+)-selective microelectrodes. The extracellular HCO3- concentration was varied (0-30 mM) at constant pH (7.4). 2. GABA (5 x 10(-6)-10(-3) M) produced a reversible fall in pHi which showed a dependence on the concentrations of both GABA and HCO3-. The fall in pHi was associated with a transient increase in pHs and it was inhibited by a K(+)-induced depolarization. 3. In the presence of 30 mM-HCO3-, a near-saturating concentration of GABA (0.5 mM) produced a mean fall in pHi of 0.43 units. This change in pHi accounted for about two-thirds of the GABA-induced decrease (from -66 to -29 mV) in the sarcolemmal H+ driving force, while the rest was due to the simultaneous depolarization. 4. The apparent net efflux of HCO3- (JHCO3e) produced by a given concentration of GABA was estimated on the basis of the instantaneous rate of change of pHi. In the presence of 30 mM-HCO3-, JHCO3e following exposure to 0.5 mM-GABA had a mean value of 8.0 mmol l-1 min-1. Under steady-state conditions (at plateau acidosis), the intracellular acid load produced by 0.5 mM-GABA was about 25% of that seen at the onset of the application. 5. The GABA-induced HCO3- permeability, calculated on the basis of the flux data, showed a concentration dependence similar to that of the GABA-activated conductance described in previous work. 6. The GABA-induced increase in pHs was immediately blocked by both a membrane-permeant inhibitor of carbonic anhydrase (acetazolamide, 10(-6) M) and by a poorly permeant inhibitor (benzolamide, 10(-6) M). 7. Application of acetazolamide (10(-4) M) for 5 min or more produced a decrease of up to 60% in the maximum rate of fall of pHi at GABA concentrations higher than 20 microM. 8. The recovery of the GABA-induced acidosis was associated with a fall in pHs. The recovery was completely blocked in solutions devoid of Na+ or of Cl-, as well as by DIDS (4,4'-diisothiocyanostilbene-2,2'-disulphonic acid, 10(-5) M). This indicates that the maintenance of a non-equilibrium H+ gradient at plateau acidosis and the recovery of pHi are attributable to Na(+)-dependent Cl(-)-HCO3- exchange. 9. We conclude that the effects of GABA on pHi and pHs are due to electrodiffusion of HCO3- across postsynaptic anion channels.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1989

Fall in intracellular pH and increase in resting tension induced by a mitochondrial uncoupling agent in crayfish muscle.

1. The influence of the mitochondrial uncoupling agent carbonylcyanide-m-chlorophenylhydrazone (CCCP) upon resting tension and intracellular pH (pHi) was studied in the dactyl opener muscle of the crayfish. pHi was measured with liquid sensor H+-selective microelectrodes. 2. CCCP (10(-6)-10(-5) mol l-1) induced a reversible, tonic contracture which was associated with a depolarization of the membrane potential. Both effects were augmented by a fall and inhibited by a rise in extracellular pH. The action of CCCP on tension was not mimicked by cyanide + oligomycin or by cyanide + dicyclohexylcarbodiimide nor was it inhibited by pre-exposure to these agents. 3. CCCP produced an initial alkalosis of less than 0.1 units and thereafter a fall in pHi of 0.4-0.6 units during which the sarcolemmal H+ driving force decreased from 61 to 15 mV. The apparent influx of H+ due to CCCP had a maximum of 2.7 mequiv l-1 min-1. The CCCP-induced acidosis was unaffected by iodacetate (0.5 mmol l-1) but it was inhibited by a depolarization of the membrane potential. 4. The contraction caused by CCCP was not due to the simultaneous fall in pHi since an intracellular acidosis of equal magnitude, produced by propionate (50 mmol l-1), did not lead to force generation. In addition, propionate had an inhibitory effect on the depolarization and contracture caused by CCCP. 5. Both the depolarization and the contracture caused by CCCP were inhibited by gamma-aminobutyric acid (GABA). The contracture was blocked by Cd2+, Mn2+ and by a nominally Ca2+ -free medium but not by a pre-exposure to caffeine (20 mmol l-1). Cd2+ and Mn2+ had no influence on the fall of pHi caused by CCCP. 6. It is concluded that CCCP induces a sarcolemmal H+ conductance which leads to a fall in pHi and to a depolarization of the membrane potential. This depolarization activates sarcolemmal, voltage-dependent calcium channels and thereby induces an increase in tension. The initial alkalosis produced by CCCP may be due to a transient uptake of H+ by mitochondria.

Animals↗
PubMed1989

Influence of GABA-gated bicarbonate conductance on potential, current and intracellular chloride in crayfish muscle fibres.

1. The effects of gamma-aminobutyric acid (GABA) on membrane potential and conductance as well as on the intracellular Cl- activity (aiCl) and intracellular pH (pHi) were studied in crayfish muscle fibres using a three-microelectrode voltage clamp and ion-selective microelectrodes. In the presence of CO2-HCO3-, the intracellular HCO3- activity (aiHCO3) was estimated from pHi. 2. In a nominally HCO3(-)-free solution, a near-saturating concentration of GABA (0.2 mM) produced a marked increase in membrane conductance but little change in potential. In a solution containing 30 mM-HCO3- (equilibrated with 5% CO2 + 95% air; pH 7.4), the GABA-induced increase in conductance was associated with a depolarization of about 15 mV, with an increase in aiCl and with a decrease in aiHCO3. All these effects were blocked by picrotoxin (PTX). The depolarizing action of GABA was augmented following depletion of extracellular and intracellular Cl-. 3. The GABA-induced increase in aiCl which took place in the presence of HCO3- was blocked by clamping the membrane potential at its resting level. This indicates that the increase in aiCl was due to passive redistribution of Cl-. In both the presence and absence of HCO3-, the GABA-activated transmembrane flux of Cl- showed reversal at the level of the resting potential, which indicates that under steady-state conditions the Cl- equilibrium potential (ECl) is identical to the resting potential. 4. In a Cl(-)-free, 30 mM-HCO3(-)-containing solution, 0.5 mM-GABA produced a PTX-sensitive increase in conductance which amounted to 15% of the conductance activated in the presence of Cl-. In the absence of both Cl- and HCO3-, the respective figure was 2.8%. Assuming constant-field conditions, the conductance data yielded a permeability ratio PHCO3/PCl of 0.42 for the GABA-activated channels. 5. In a Cl(-)-containing, HCO3(-)-free solution, the reversal potential of the GABA-activated current (EGABA) was, by about 1 mV, less negative than the resting membrane potential (RP). In a solution containing Cl- and 30 mM-HCO3-, EGABA-RP was 12 mV. Simultaneous measurements of EGABA, aiCl and aiHCO3 (pHi) gave a PHCO3/PCl value of 0.33. 6. In a Cl(-)-free, HCO3(-)-containing solution EGABA was close to the HCO3- equilibrium potential (EHCO3) and an experimental acidosis which produced a negative shift in EHCO3 was associated with a similar shift in EGABA.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1988

Effect of repetitive activity upon intracellular pH, sodium and contraction in sheep cardiac Purkinje fibres.

1. The influence of repetitive activity upon intracellular pH (pHi), intracellular Na+ activity (aNA(i)) and contraction was examined in isolated sheep cardiac Purkinje fibres. Ion-selective microelectrodes were used to measure intracellular Na+ and H+ ion activity. Twitch tension was elicited by field stimulation or by depolarizing pulses applied using a two-microelectrode voltage clamp. Experiments were performed in HEPES-buffered solution equilibrated either with air or 100% O2. 2. An increase in action potential frequency from a basal rate of 0.1 to 1-4 Hz induced a reversible fall in pHi and a reversible rise in aNa(i). These effects reached a steady state 3-10 min following an increase in stimulation frequency, and showed a linear dependence on frequency with a mean slope of 0.023 pH units Hz-1 and 0.57 mmol l-1 Hz-1, respectively. The rise in total intracellular acid and aNa(i) associated with a single action potential was estimated as 5.3 mu equiv l-1 of acid and 3.5 mu equiv l-1 of Na+. 3. At action potential frequencies greater than 1 Hz, the rate-dependent rise in aNa(i) was usually accompanied by a positive force staircase. 4. The fall in pHi following a rate increase also occurred when fibres were bathed in Tyrode solution equilibrated with 23 mM-HCO3- plus nominally 5% CO2/95% O2. In these cases, however, the fall in pHi was halved in magnitude. 5. In fibres exposed to strophanthidin (0.5 microM), the rate-dependent fall in pHi was doubled in magnitude and its time course was more variable than under drug-free conditions. The rate-dependent rise in aiNa was also usually larger in strophanthidin. 6. In order to examine the influence of the rate-dependent acidosis on developed tension, the acidosis was reversed experimentally by adding 2 mmol l-1 NH4Cl to the bathing solution. This produced a rise in pHi accompanied by a large increase in twitch tension. Such an effect of pHi upon tension was quantitatively similar to that observed in previous work on Purkinje fibres (Vaughan-Jones, Eisner & Lederer, 1987). 7. It is concluded that the rate dependence of pHi will influence both the magnitude and the time course of an inotropic response to a change in heart rate.

Action Potentials↗
PubMed1988

Mechanism of rate-dependent pH changes in the sheep cardiac Purkinje fibre.

1. The mechanism of the rate-dependent decrease in intracellular pH (pHi) and its recovery were studied in isolated sheep cardiac Purkinje fibres. Intracellular Na+ activity (aiNa) and pHi were measured using ion-selective microelectrodes. Twitches were elicited by field stimulation or by depolarizing pulses applied using a two-microelectrode voltage clamp. 2. A 3 Hz train of short (50 ms) depolarizing voltage-clamp pulses induced a reversible fall in pHi which was accompanied by a reversible increase in aiNa. A train of longer (200 ms) pulses also produced a fall in pHi which was now paralleled by a decrease in aiNa. These observations indicate that the rate-dependent acidosis is not dependent upon a rise in aiNa. 3. Neither the fall in pHi nor the increase in aiNa seen upon an increase in action potential frequency was inhibited by amiloride (1 mmol l-1) which indicates that Na+-H+ exchange is not involved in the generation of the acidosis. Furthermore, the rate-dependent acidosis was not abolished in Na+-free solution (Li+ or N-methyl glucamine substituted) indicating that other Na+-requiring processes (such as Na+-Ca2+ exchange) are not a necessary requirement. Rate-dependent pHi changes were also unaffected by the stilbene compound DIDS indicating no participation by Cl--HCO-3 exchange. 4. The rate-dependent acidosis was inhibited by the organic calcium antagonist D600 (20 mumol l-1) which also inhibited twitch tension. This suggests that the acidosis is related to the activation by Ca2+ of developed tension. D600 also inhibited the rate-dependent rise in aiNa (field stimulation). 5. The rate-dependent acidosis was not inhibited by cyanide (2 mmol l-1) but it was blocked by iodoacetate (0.5 mmol l-1) and by 2-deoxyglucose (DOG) (10 mmol l-1, applied in glucose-free solution). These results suggest that the acidosis is generated metabolically via stimulation of glycolysis, following an increase in contraction. Contributions from aerobic metabolism are likely to be small. 6. Twitch tension was inhibited by ryanodine (10 mumol l-1) but the drug had little inhibitory effect on the rate-dependent acidosis. A tonic component of tension was observed, however, in the presence of ryanodine. The lack of effect of ryanodine upon the rate-induced acidosis is discussed. 7. The half-time of pHi recovery from the frequency-dependent acidosis was consistently shorter than that from an intracellular acid load induced by adding and then removing external NH4Cl (10 mmol l-1).(ABSTRACT TRUNCATED AT 400 WORDS)

Amiloride↗
PubMed1987

Stimulation-induced changes in the intracellular sodium activity of the crayfish stretch receptor.

Changes in intracellular Na+ activity (aiNa) caused by mechanical stimulation in the slowly adapting stretch receptor of the crayfish were examined using Na+-selective microelectrodes. A series of brief stretches (each giving rise to a brief receptor potential and a single action potential) induced a reversible increase in aiNa which was proportional to the stimulation frequency in the range examined, 0-9.5 Hz. At 9.5 Hz, aiNa increased by 4-5 mM from the resting value of 7-10 mM. Tetrodotoxin (TTX) reduced, but did not abolish the stimulation-dependent increase in aiNa indicating the involvement of a Na+-influx pathway in addition to the potential-dependent, TTX-sensitive sodium channels of the neuronal plasma membrane. A likely candidate for this TTX-resistant pathway are the cationic transducer channels of the dendrites.

Animals↗
PubMed1987

Influence of sodium-hydrogen exchange on intracellular pH, sodium and tension in sheep cardiac Purkinje fibres.

1. The influence of sarcolemmal Na+-H+ exchange upon intracellular Na+ activity (aiNa), intracellular pH (pHi), extracellular surface pH (pHs) and tonic tension was investigated in sheep cardiac Purkinje fibres. Intracellular ion activities were measured with liquid sensor ion-selective micro-electrodes. A two-micro-electrode voltage-clamp was also used to control membrane potential while simultaneously recording tonic tension. 2. Inhibition of the sarcolemmal Na+-K+ pump by strophanthidin (10 mumol/l) produced a rise in aiNa, an increase in [Ca2+]i as evidenced by a rise in tonic tension, and a fall in pHi of 0.1-0.3 units. The intracellular acidosis has been shown previously to be linked to the rise in [Ca2+]i (Vaughan-Jones, Lederer & Eisner, 1983). 3. Amiloride (1-2 mmol/l), an inhibitor of Na+-H+ exchange, produced a small reversible decrease in pHi and aiNa. Both effects became more pronounced in strophanthidin-exposed fibres. In addition, pHi decreased during application of strophanthidin and this decrease was reversibly inhibited by amiloride. It is concluded that sarcolemmal Na+-H+ exchange is stimulated following inhibition of the Na+-K+ pump. 4. In strophanthidin-exposed fibres, a rise in [Ca2+]i resulted in an intracellular acidosis which could still be observed in the presence of amiloride (1 mmol/l). This suggests that the fall in pHi was not caused by a modulatory effect of [Ca2+]i on sarcolemmal Na+-H+ exchange. 5. Tetrodotoxin (TTX) produced a small fall in aiNa (ca. 0.5 mmol/l) which was not augmented in the presence of strophanthidin. Furthermore, the effects on aiNa of TTX and amiloride were additive. Thus the influence of amiloride on aiNa does not involve blockade of voltage-gated Na+ channels. 6. The stoicheiometry of Na+-H+ exchange, estimated from the rates of change of pHi and aiNa in amiloride, appeared to be electroneutral (1:1). The stoicheiometry was unaffected by changes in pHi. 7. In strophanthidin-exposed fibres (i.e. aiNa is elevated), the recovery of pHi from an intracellular acidosis (brought about by brief exposure to NH4Cl) was slowed greatly by amiloride (1-2 mmol/l). The rise in aiNa that occurred during pHi recovery was also reduced by amiloride. It is concluded that Na+-H+ exchange can be stimulated by a fall in pHi under conditions where aiNa is elevated. However, at a given pHi, its rate of recovery was slower in the presence than in the absence of strophanthidin.(ABSTRACT TRUNCATED AT 400 WORDS)

Amiloride↗
PubMed1987

Regulation of intracellular pH in sheep cardiac Purkinje fibre: interactions among Na+, H+, and Ca2+1.

Experiments were performed on sheep cardiac Purkinje fibres using pH- and sodium-selective microelectrodes, while simultaneously measuring tension, to determine if the fall in intracellular pH (pHi) following a rise in intracellular Na+ activity (aiNa) is caused by inhibition or reversal of acid extrusion on Na+-H+ exchange. A rise in aiNa was induced either by using the cardioactive steroid strophanthidin to inhibit the sarcolemmal Na+-K+ pump or by increasing the frequency of stimulation (0-4 Hz). Both of these manoeuvres led to an increase in aiNa and a decrease in pHi. Following exposure to strophanthidin, amiloride (an inhibitor of sarcolemmal Na+-H+ exchange) produced a decrease in both pHi and aiNa. These effects of amiloride increased with decreasing pHi, indicating that acid extrusion on Na+-H+ exchange is stimulated by the fall in pHi. The changes in intracellular Na+ and H+ caused by amiloride were quantitatively consistent with an electroneutral stoichiometry. The fall in pHi during strophanthidin exposure is therefore not caused by inhibition or reversal of acid extrusion Na+-H+ exchange. It is likely that the fall in pHi during a rate increase is also independent of Na+-H+ exchange. This is because (i) it has been shown previously to occur in the presence of amiloride and (ii) the calcium antagonist D600 completely abolished the stimulation-dependent fall in pHi. It is concluded that the intracellular acidosis following inhibition of the sarcolemmal Na+-K+ pump or following an increase in the rate of stimulation is secondary to a rise in intracellular calcium.

Amiloride↗
PubMed1986

Quantitative measurements of the cytosolic Ca2+ activity within isolated guinea pig nerve-endings using entrapped arsenazo III and quin2.

The absorbance changes of intrasynaptosomally entrapped arsenazo III have been converted into values of free Ca2+ concentration by correcting for the nonlinear response of arsenazo III at different concentrations of the dye as well as for changes in internal pH. An average resting value for free Ca2+ concentration around 0.4 microM is obtained. Depolarization with veratridine or gramicidin increases this value to around 3 microM. Measurements of cytosolic free Ca2+ with the quin2 method gives much lower values in similar conditions. The release of prelabelled [14C]noradrenaline from the nerve-endings is maximally activated when the internal free Ca2+ concentration rises as measured with arsenazo III to about 4 microM when titrated with increasing concentrations of ionophore A23187.

Aminoquinolines↗
PubMed1986

Development of a neural phenotype in differentiating ganglion cell-derived human neuroblastoma cells.

Human neuroblastoma cells (clone SHSY-5Y) induced to differentiate by 12-O-tetradecanoylphorbol-13-acetate (TPA) are shown to possess properties characteristic of mature ganglion cells. Elevation of the external K+ concentration, exposure to Ca2+ ionophore A23187, and acetylcholine all stimulate the release of preloaded 3H-noradrenaline in the presence but not in the absence of added Ca2+. Acetylcholine causes a fall in the 86Rb+ or 14C-TPMP equilibrium potential across the plasma membrane and stimulates 86Rb+ efflux. These responses are prevented by atropine. Acetylcholine and muscarine but not nicotine stimulate an increase in 45Ca2+ influx, an effect blocked by atropine. None of these responses have been observed in nondifferentiating cells. Muscarinic receptors, however, as measured by the binding of tritiated quinuclidinyl benzilate (3H-QNB), were present to a similar extent in control and differentiated cells. Both cell types also exhibit an accelerated release of Ca2+ in response to acetylcholine, but the control cells were at least 1 order of magnitude more sensitive to the agonist.

Acetylcholine↗
PubMed1986

The sensitivity of liquid sensor, ion-selective microelectrodes to changes in temperature and solution level.

Current procedures for the manufacture of ion-selective microelectrodes using liquid ion sensors result in two kinds of electrode, one with a short (10-100 micron) column of sensor at the tip and one with a long column (greater than 1 mm). We report here that the signal from a long-column microelectrode is very sensitive to small fluctuations in bath temperature and solution level when a recording is made above room temperature. This sensitivity is explained by the effects of temperature on the potentials developed at the interfaces between the ion sensor and the bordering aqueous solutions (the internal filling solution of the electrode and the test solution). If the temperature at the two interfaces is changed by different amounts, these interfacial potentials will also change by different amounts resulting in a change in the output of the electrode. Such an effect occurs for long-column electrodes because the column of sensor is usually not completely immersed in the heated test solution. Hence fluctuations in solution temperature and level will induce fluctuations in temperature along the column of sensor producing variations in the electrical signal from the electrode. In contrast, sensitivity to temperature and solution level is virtually absent in short-column microelectrodes since their column of sensor is fully immersed in the test solution and thereby at uniform temperature. In conclusion, in order to produce noise-free recordings of ion activities, the use of short-column microelectrodes is recommended for experiments performed above (or below) room temperature.

Electrophysiology↗
PubMed1985

Dependence of cytoplasmic calcium transients on the membrane potential in isolated nerve endings of the guinea pig.

The relation of changes in internal, free Ca2+, measured with arsenazo III, to the membrane potential, measured with the cyanine dye di-S-C2(5) or 86Rb+ distribution ratio, was studied in isolated guinea pig cortical nerve endings. Depolarization of the plasma membrane with veratridine or gramicidin as well as addition of ionophore A23187 led to an increase in cytosolic Ca2+. Only the response to veratridine was inhibited by tetrodotoxin. The dependence of the depolarization-induced increase in intraterminal, free Ca2+ on the membrane potential between about -50 to 0 mV was sigmoidal. A maximal increase in cytosolic Ca2+ was reached when the membrane potential was depolarized from the resting level, about -64 mV, to about -40 mV. These results show that in isolated nerve endings the activation of voltage-sensitive Ca2+ channels concomitantly leads to an increase in cytosolic, free Ca2+. Comparison of the results of the present study with the previous electrophysiological observations indicate that Ca2+ channels in synaptosomes, presynaptic nerve terminals of the squid giant synapse and cardiac cells have essentially similar voltage dependency.

Animals↗
PubMed1984

Depolarization of the mitochondrial membrane potential increases free cytosolic calcium in synaptosomes.

Intracellular calcium transients in synaptosomes, isolated from the guinea pig brain, were measured using entrapped metallochromic indicator arsenazo III. Addition of 1 microM carbonyl cyanide p-trifluoromethoxyphenyl hydrazone (FCCP) increased rapidly the absorbance of the entrapped arsenazo III, indicating an increase in the cytosolic free calcium. The FCCP-induced increase in cytoplasmic free Ca2+ was not blocked by 200 microM verapamil, while the increment in calcium caused by 40 microM veratridine was verapamil-sensitive. The absorbance changes induced by FCCP were not significantly increased when the extracellular potassium concentration was elevated from 5.4 to 50 mM. These data indicate that in nerve endings of mammalian brain, cytoplasmic free calcium, which is essential for the release of transmitter, is increased on depolarization of major intracellular calcium buffers, mitochondria.

Animals↗
PubMed1984

Use-dependent block of GABA-activated chloride channels in crayfish muscle fibers by picrate.

In crayfish muscle fibers studied with intracellular microelectrodes the protein-binding agent, picrate (2,4,6-trinitrophenolate; 10(-5)-2 X 10(-4) M) was found to have a specific and dose-dependent inhibitory effect on the chloride conductance activated by bath-applied gamma-aminobutyric acid (GABA). A kinetic analysis showed that picrate did not interfere with GABA binding to its receptor. The blocking action of picrate was not increased by lowering the extracellular Cl- concentration which indicates that picrate is not likely to bind to the ionic selectivity site of the postsynaptic Cl- channel. In fibers first exposed to picrate (1-2 X 10(-4) M) and then, in the continuous presence of this drug, to GABA (5 X 10(-4) M), the latter induced a transient increase in the chloride conductance with an apparent rate constant of decay of about 40 sec. It is tentatively suggested that the site of action of picrate is a positively charged amino acid residue that is exposed through the action of GABA and critically involved in the chemical gating of the postsynaptic chloride channel.

Animals↗