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N Akaike

Publications and source records attributed to N Akaike.

At least 343 records · Page 19Linked to original sources

Contribution of chloride shifts to the fade of gamma-aminobutyric acid-gated currents in frog dorsal root ganglion cells.

1. The contribution of Cl- redistribution to the decay phase of the GABA (gamma-aminobutyric acid) response was investigated in isolated frog sensory neurones, using a suction-pipette technique which allows for internal perfusion under conditions of voltage clamp. 2. In neurones perfused with 120 mM [Cl-]i and [Cl-]o at driving forces (delta VH) of less than 15 mV, no shift of GABA equilibrium potential (EGABA) occurred during a continuous application of GABA, at various concentrations. However, increases of delta VH towards negative or positive potentials over 15 mV induced EGABA shifts. 3. The degree of EGABA shift was governed by the total amount of Cl- flux across the soma membrane, an event which depends upon delta VH, GABA concentration and drug application time. 4. The time-dependent EGABA shift due to Cl- redistribution during GABA application induced a current run-down resulting from a decreased Cl- gradient and a diminished Cl- conductance (gCl), the latter brought about by a drop in the intracellular ionic density of Cl-. 5. The EGABA shift during a continuous GABA application was also affected by [Cl-]i; e.g. the shift more readily occurred at lower [Cl-]i. 6. In neurones perfused with internal and external solutions containing 120 mM-Cl- at a delta VH of less than 10 mV, the change of gCl occurred with no shift of EGABA during the continuous application of GABA at concentrations over 6 x 10(-5) M, thereby indicating a 'real' GABA receptor desensitization. The desensitization depended solely upon the agonist concentrations but not upon the amount of ICl. Under these conditions, the time course of recovery from GABA desensitization was estimated. The decrease of gCl at the desensitization phase was a single exponential. 7. At a delta VH greater than 15 mV, therefore, the decay of ICl induced by GABA concentrations over 6 x 10(-6) M consists of the sum of both the 'real' GABA receptor desensitization and the current run-down brought about by Cl- shifts. The gCl at the current decay phase consisted of a double exponential. In the present experiments we chose experimental conditions with which Cl- shift become negligible. 8. The 'pure' GABA receptor desensitization during a continuous application of GABA developed rapidly at GABA concentrations over 10(-5) M. The speed of desensitization was facilitated by increasing the magnitude of desensitization.

Action Potentials↗

Sodium-dependent suppression of gamma-aminobutyric-acid-gated chloride currents in internally perfused frog sensory neurones.

1. The effects of the Na+ electrochemical potential gradient on gamma-aminobutyric acid (GABA)-induced Cl- currents (ICl) in frog sensory neurones were studied, using a suction pipette technique with which internal perfusion can be accomplished under current- and voltage-clamp conditions. 2. Under current clamp, the depolarizing response to GABA decreased in the presence of external Na+. A similar external Na+-dependent reduction in the GABA-induced inward ICl was observed under voltage clamp. The reversal potential of GABA-induced ICl (EGABA) was nearly equal to the Cl- equilibrium potential (ECl), irrespective of the presence or absence of external Na+. 3. Varying the Na+ influx by changing the holding membrane potential (VH) altered the GABA response: the GABA-induced ICl decreased progressively as VH became more negative. 4. The effects of changing the external and internal Na+ concentrations ([Na+]o and [Na+]i) on the GABA-induced ICl were also studied. Increasing [Na+]o at a constant [Na+]i reduced this current while increasing [Na+]i at a fixed [Na+]o facilitated it. 5. A high temperature coefficient of about 3 was estimated with respect to the percentage reduction in GABA-induced ICl due to [Na+]o. 6. These results indicate that the [Na+]o-dependent suppression of GABA-induced ICl was mediated chiefly by the uptake of GABA subserved by a Na-GABA co-transport mechanism. 7. GABA dose-response measurements were made with and without external Na+. The [Na+]o-induced suppression was more pronounced in relative amount at lower concentrations and in absolute amount at intermediate concentrations. Analysis of these data indicates, however, that the Na+-coupled GABA influx kept increasing at GABA concentrations high enough to nearly saturate GABA-induced ICl, and the same saturating level was observed as in the Na+-free case. This indicates that the electrogenic co-transport current was much smaller so that our measurements of GABA-induced ICl' were contaminated very little. Thus, the present method based on recording of GABA-induced ICl was legitimate for the analysis of the Na-GABA co-transport. 8. By analysing the [Na+]o-dependent suppression of GABA-induced ICl, the stoichiometric ratio of the underlying co-transport was estimated to be one: one Na+ ion per GABA molecule. 9. The ICl induced by GABA agonists such as beta-alanine, taurine, l-GABOB (l-gamma-amino-beta-hydroxybutyric acid) and muscimol was not affected by the amount of external Na+ present, suggesting difference in the affinity between receptor and transport carrier.

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Kinetic properties of the pentobarbitone-gated chloride current in frog sensory neurones.

1. The kinetic properties of the activation and inactivation (desensitization) phases of pentobarbitone (PB)-induced inward Cl- current (ICl) were studied in isolated frog sensory neurones, following suppression of Na+, K+ and Ca2+ currents, using the concentration jump technique which combines the internal perfusion and the rapid exchange of the external solutions surrounding a neurone with time constants of 2-3 ms. The results were compared with those of the gamma-aminobutyric acid (GABA)-gated ICl. 2. The PB dose-response curve was bell-shaped and the maximum peak value was less than the current induced by 1.7 X 1.5(-5) M-GABA, the concentration at which GABA evoked a half-maximum response. 3. The activation and inactivation phases of PB-induced ICl consisted of double-exponential, fast and slow components, respectively. The time constant of the fast component (tau af) of the activation was relatively stable in a concentration range between 3 X 10(-4) and 6 X 10(-3) M. The time constant of the slow component (tau as) of the activation decreased with increasing PB concentrations. Both the fast and slow components (tau if and tau is) of the inactivation decreased with increasing PB concentrations. 4. Over a wide range of concentrations the tau af and tau as values of the PB-induced ICl were 10-30 times greater than the respective values of GABA-induced ICl. 5. At concentrations below 10(-3) M the PB-induced ICl was voltage dependent at more negative potentials than -20 mV. 6. The PB-induced ICl was blocked by bicuculline and by picrotoxin, but in a different manner. Bicuculline increased the time constants of the activation and inactivation. Picrotoxin had little effect on the activation phase but markedly facilitated the inactivation phase. 7. High concentrations of PB (over 10(-3) M) led to a decline in both the peak and plateau currents of the PB-induced ICl. A transient 'hump' current appeared with wash-out of the external solutions containing high concentrations of PB. This hump current was blocked by bicuculline in a dose-dependent manner. 8. The results suggest the possibilities that the PB receptor-ionophore complexes consist of at least two different components having different affinities and kinetics and that the PB and GABA binding sites are closely located.

Animals↗

Hypothalamus and sodium-potassium pump activity in skeletal muscles of DOCA-hypertensive rats.

The effects of hypothalamic lesions on Na+ and K+ content ([Na+]i and [K+]i) in both slow tonic muscle [soleus (SOL)] and fast-twitch muscle [extensor digitorum longus (EDL)] were investigated in deoxycorticosterone acetate (DOCA)-salt hypertensive rats. In DOCA-treated rats, [Na+]i was increased and [K+]i decreased in both SOL and EDL muscles compared with controls. Cellular K+ loss and Na+ accumulation in SOL were restored after tibial nerve sectioning (delta [Na+]i, -14.2 +/- 2.6 and delta [K+]i, 13.9 +/- 2.6 mmol/l fiber water (FW), n = 18, P less than 0.01) or bilateral lesioning of the ventromedial hypothalamic nucleus (VMH) (delta [Na+]i, -15.5 +/- 1.5 and delta [K+]i, 17.4 +/- 4.6 mmol/l FW, n = 6, P less than 0.01 and P less than 0.05). On the other hand, the anomalous electrolyte content in EDL was counteracted by lesions of anteroventral portion of the third ventricle (AV3V) (delta [Na+]i, -8.8 +/- 1.6 and delta [K+]i, 5.2 +/- 1.2 mmol/l FW, n = 6, P less than 0.01 and P less than 0.05) or paraventricular hypothalamic nucleus (PVN) (delta [Na+]i, -6.8 +/- 0.6 and 5.7 +/- 1.2 mmol/l FW, n = 6, P less than 0.01 and P less than 0.05), but aggravated by denervation (delta [Na+]i, 13.4 +/- 1.8 and delta [K+]i, -9.6 +/- 1.8 mmol/l FW, n = 18, P less than 0.01). These results suggest that there are at least two hypothalamic mechanisms of suppression of muscle Na-K pump activity in DOCA-hypertensive rats; i.e., neurally mediated inhibition in SOL by the VMH and, presumably, humorally mediated inhibition originating from the AV3V or PVN with greater influence in EDL.

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Modulation of the gamma-aminobutyric acid-gated chloride current by intracellular calcium in frog sensory neurones.

The effects of the voltage-dependent Ca2+ inward current (ICa) on gamma-aminobutyric acid (GABA)-induced Cl- current (ICl) in isolated frog sensory neurones were examined using the "concentration clamp" technique, an approach which combines internal perfusion by a suction pipette with a rapid external solution change method. A preceding ICa suppressed the GABA-activated ICl. While the inhibition was not influenced by changes of membrane potential between -40 and -100 mV, it was reduced when the internal EGTA concentration was increased. A preceding ICa shifted the GABA dose-response curve to the right without affecting the maximum current or the Hill coefficient (n = 2). Inhibition of the GABA-activated ICl by ICa showed a recovery in a single exponential manner, the time constant of which depended upon the extent of Ca2+ influx. At a low temperature (10 degrees C), however, the recovery from Ca2+-mediated inhibition was only slight. We conclude that, as a result of the voltage-dependent Ca2+ influx, a subsequent increase of intracellular Ca2+ concentration modulates the GABA-gated ICl in the soma membrane. Possible mechanisms are discussed.

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Hypothalamic regulation of sodium-potassium pump activity in skeletal muscle.

The suppression of active Na+-K+ transport in rat skeletal muscle during hypokalemia was counteracted by bilateral electrolytic lesion of the ventromedial hypothalamic nucleus. This reversal effect was unaffected even after pancreatectomy or adrenalectomy. The anomalous electrolyte content in hypokalemic rat muscles was aggravated by lesion of the dorsomedial hypothalamic nucleus and of the anterior hypothalamus. The results indicate that the hypothalamus is involved in the regulation of the Na+-K+ transport system in skeletal muscle during hypokalemia.

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Effects of n-alkanols on the calcium current of intracellularly perfused neurons of Helix aspersa.

The effects of n-alkanols on the calcium current (ICa) were studied in molluscan neurons perfused intracellularly and voltage clamped using a suction pipette technique. All n-alkanols employed in this experiment (methanol, ethanol and butanol) decreased the peak amplitude of ICa and caused acceleration of the decay of ICa in a dose-dependent manner at all membrane potentials. The concentrations of n-alkanols required for these actions decreased as the hydrocarbon chain increased in length. The results suggest that these effects on the ICa of molluscan neurons may be related to the lipophilic properties of n-alkanols.

1-Butanol↗

Are sulfhydryl groups essential for function of the glutamate-operated receptor-ionophore complex?

We monitored glutamate- or kainic acid-induced inward currents in pyramidal neurons of the rat hippocampus to determine a possible chemical modification of sulfhydryl residues on glutamate-receptor-ionophore complexes. Organic and inorganic mercury compounds such as HgCl2 and n-chloromercuribenzoate, 5,5'-dithiobis (2-nitrobenzoic acid) and N-ethylmaleimide depressed glutamate- or kainate-induced responses while the mercury compounds inhibited the kainate response, in a non-competitive manner. The responses inhibited by these agents were dose-dependently recovered by adding cysteine or glutathione. These observations suggest that the excitatory glutamate-receptor-ionophore complex includes sulfhydryl residues, components which may play a role in related functions.

Animals↗

Hypokalemia modulates alpha- and beta-adrenoceptor bindings in rat skeletal muscle.

Changes in the population of adrenergic alpha- and beta-receptors were examined in rat soleus muscles during hypokalemia by their direct determination using radiolabeled ligands. Only beta-adrenoceptors were detected in the normal rat muscles. Hypokalemia led to a pronounced decrease in beta-adrenoceptors, the number of [3H]DHA binding sites, by 50%, as compared with that in the normal rats. There was a genesis of alpha 1-adrenoceptors in hypokalemic rat muscles, since the competitive potency of adrenergic drugs against [3H]prazosin binding was in the order prazosin much greater than phentolamine greater than (+/-)-noradrenaline greater than yohimbine much greater than (+/-)-isoproterenol. The reduction of [3H]DHA binding sites was accompanied by an increase of an approximately equal amount in high-affinity [3H]prazosin binding sites. The Kd determined by kinetic analysis of [3H]prazosin binding was calculated from the ratio K-1/K1 that gave a value of 3.05 nM, which generally agreed with the 1.83 nM determined by saturation experiments (Scatchard plot). This phenomenon of a reduction in the beta-adrenoceptors and the occurrence of alpha 1-adrenoceptors in muscles during hypokalemia is discussed. alpha- and beta-adrenoceptors on soleus muscle membrane may play important but opposite roles in modulating potassium release from the muscle cells.

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Diazepam action on gamma-aminobutyric acid-activated chloride currents in internally perfused frog sensory neurons.

The Cl- current (ICl) in gamma-aminobutyric acid (GABA)-sensitive frog sensory neuron was separated from other Na+, Ca2+, and K+ currents using a suction pipette technique which allows internal perfusion under a single-electrode voltage clamp. Diazepam (DZP) itself evoked no response but facilitated the dose- and time-dependently GABA-induced ICl without changing the GABA equilibrium potential (EGABA) at concentrations ranging widely, from 3 X 10(-9) to 10(-4) M. In the presence of DZP, the GABA dose-response curve shifted to the left without changing the maximum current, indicating that DZP modifies the interaction between GABA and its receptor rather than affecting directly the channel activation step. The enhancement of the GABA-induced ICl by DZP depended neither on the membrane voltage nor on the inward or outward direction of the ICl. DZP also potentiated the ICl elicited by GABA agonists such as beta-alanine, taurine, homotaurine, 5-aminovaleric acid, l-GABOB, d-GABOB, glycine, and muscimol. The GABA response enhanced by pentobarbital (PB) was further enhanced by adding DZP, indicating that DZP and PB do not act in the same way. Ro5-3663, a diazepam analogue, enhanced the GABA-induced ICl only in a narrow range of the concentrations but inhibited the current at concentrations higher than 2 X 10(-6) M.

Animals↗

Persistent calcium inward current in internally perfused snail neuron.

The inactivation process of the calcium current (ICa) was investigated in a molluscan neuron which was perfused intracellularly and voltage-clamped using a suction pipette technique. The decay phase of the ICa contained a very slowly inactivated component (persistent inward current; PIC). The decay time constant of this component was over 10 sec. An increase in the amplitude of the ICa or the intracellular Ca2+ concentration caused a decrease in the decay time constant of the PIC. Replacing Ba2+ with extracellular Ca2+ increased the decay time constant of the PIC. The differences in the amplitude and the decay kinetics between the ICa and the IBa resulted from changes in the amplitude and the decay time constant of the PIC. These observations support the conclusion that the inactivation of the PIC is calcium dependent [Chad, J., Eckert, R., and Ewald, D. (1984). J. Physiol. (Lond.) 347:279-300].

Animals↗

Pipecolic acid enhancement of GABA response in single neurons of rat brain.

Using unit recording and microelectrophoresis, influence of pipecolic acid (PA), a major metabolite of lysine in the brain, on GABA and glycine responses was studied in the cerebral cortical and hippocampal pyramidal neurons of rats. With small currents, PA had no effect on the single neuron activities but enhanced GABA response without affecting glycine response. The finding provides a new evidence that PA may have a connection with central GABA system.

Action Potentials↗

The anion selectivity of the gamma-aminobutyric acid controlled chloride channel in the perfused spinal ganglion cell of frog.

The selectivity of the GABA-controlled Cl- channel in the membrane of the dorsal root ganglion cell of the frog has been measured in internally perfused cells by means of current and voltage clamp. When Cl- was replaced by various anions, the 10(-5) or 10(-4) M GABA-induced reversal potentials (EGABA) for Br-, I-, NO3-, ClO4-, SCN-, BF4- and ClO3- were more negative than that for Cl-, despite the fact that, in solution, the test anions are either larger than or similar in size to Cl-.

Animals↗

Effects of hypothalamic lesions on active sodium-potassium transport in the extensor digitorum longus muscles of hypokalemic rat.

The CNS-induced suppression on muscle Na+-K+ pump was studied in "twitch" muscle, extensor digitorum longus (EDL), of hypokalemic rats which were fed a K+ deficient diet for several weeks. Peripheral nerve section or bilateral lesion of the ventromedial hypothalamic nucleus had no effect on the Na+ and K+ contents in EDL of hypokalemic rats. However, lesions of the paraventricular nucleus caused the net Na+ loss and the net K+ uptake in the muscles. Lesions in either the dorsomedial nucleus or anterior hypothalamus also caused significant net K+ uptake but the net Na+ loss was not significant. The results were compared with those of "tonic" muscle, soleus, reported previously.

Animals↗

Differences in the actions of organic and inorganic Ca2+-antagonists on the inactivation of the Ca2+ channel in a molluscan neurone.

The actions of organic and inorganic Ca2+-antagonists on an inactivation of the Ca2+ channel was studied in molluscan neurones using a suction pipette technique. Both Ca2+-antagonists decreased the peak amplitude of Ca2+ current (ICa). The organic Ca2+-antagonists verapamil and diltiazem hastened the decay of ICa, while the inorganic Ca2+-antagonists Co2+ and Cd2+ delayed it. The difference in the action of the Ca2+-antagonists on the decay of ICa may result from the different effects of the agents on a voltage-dependent inactivation of the Ca2+ channel.

Animals↗

The electrogenic Na-pump and spontaneous contraction of the hypokalemic rat duodenum.

The effects of the electrogenic Na-pump on spontaneous contraction in the isolated, longitudinal muscle of the duodenum of rats which had been on a potassium-deficient diet for 7 weeks, have been investigated. Intracellular levels of Na+ are increased by this diet. The spontaneous contraction of the duodenal muscle was stopped, transiently, by 0.5 to 120 mM-K+ Krebs solution. The period of decrease of tone and amplitude occurring immediately after adding K+ was shortened when the external K+ concentration ([K]o) was increased from 0.5 to 120 mM. The decrease in tone and amplitude induced by K+ was abolished by exposure of the tissue to 0 mM [K]o, by exposure to a temperature below 14 degrees C, and in the presence of ouabain (3 X 10(-5)-10(-4) M). The spontaneous contraction of 'Na-rich' duodenum in bathing medium containing 15 mM K+ and following inhibition of the electrogenic Na-pump with cooling or ouabain was much the same as in the duodenum from rats fed balanced diets: i.e., increase of contractile tone immediately after adding K+. To activate the Na-pump in 'Na-rich' duodenum, the external K+ could be replaced by Rb+, Cs+, NH4+ and Tl3+. The effectiveness was in the order K+ greater than Rb+ greater than Cs+ greater than NH4+ greater than Tl3+. The possible existence of a neuronal or hormonal inhibitory mechanism affecting the active Na-K transport in rat smooth muscle in situ, under conditions of hypokalemia, is discussed.

Animals↗

'Concentration-clamp' study of gamma-aminobutyric-acid-induced chloride current kinetics in frog sensory neurones.

Kinetics of the activation and desensitization phases of gamma-aminobutyric acid (GABA)-induced Cl- current (ICl) were studied in single frog sensory neurones using the 'concentration-clamp' technique which enables perfusion of drugs with the time constant of about 3 ms. Both activation and desensitization phases of GABA response consisted of a single exponential at low concentrations and a double exponential at high concentrations. The time constant of the fast kinetic component in each phase was relatively stable, about 5 ms for activation and 3 s for desensitization over concentrations from 3 X 10(-5) to 3 X 10(-4) M, whereas those of the slow kinetic component decreased with increasing concentrations. The two kinetic components in both phases showed the same reversal potential. The slow and fast activation components recovered sensitivity from desensitization with different time courses: the recovery rate of the fast activation component was slow and that of the slow one, rapid. The peak ICl elicited at GABA concentrations below 10(-5) M increased disproportionally at more negative membrane potentials, thereby suggesting that the activation kinetics is voltage dependent. The steady-state ICl-voltage relationship obtained with less than 10(-5) M-GABA showed a non-linearity, probably due to voltage dependence of activation rather than that of desensitization kinetics. These results suggest the presence of at least two different GABA receptor-Cl- ionophore complexes with a different affinity and kinetics.

Action Potentials↗