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M Galvan

Publications and source records attributed to M Galvan.

At least 55 records · Page 3Linked to original sources
PubMed1983

Fast inward-rectifying current accounts for anomalous rectification in olfactory cortex neurones.

The somatic membrane of guinea-pig olfactory cortex neurones in vitro (23 degrees C) was voltage clamped by means of a single-micro-electrode sample-and-hold technique. In most cells the current-voltage (I-V) relationship showed inward (anomalous) rectification with increasing hyperpolarization beyond the resting potential (ca. -80 mV). Under current-clamp conditions a time-dependent 'sag' of the hyperpolarizing electrotonic potentials was observed following an initial overshoot. No depolarizing after-potential was seen on return to the resting potential. Inward rectification was activated between -100 and -110 mV (irrespective of pre-set resting potential) and increased the membrane input conductance by up to three-fold. The rectification was unaffected by tetrodotoxin or Cd2+. Under somatic voltage clamp, hyperpolarization beyond -110 mV activated a rapid inward relaxation fitted by a single exponential. The relaxation time constant (tau on) decreased e-fold for a 40 mV hyperpolarization. (Typical values: 28 ms at -110 mV declining to 13 ms at -140 mV; external K+ concentration 3 mM, 23 degrees C). More extreme hyperpolarizations evoked a slower 'inactivation' phase (tau = 40-60 ms). A transient outward-decaying 'tail' current reflecting deactivation of inward rectification was seen on stepping from -140 mV to more positive potentials. tau off became slower with hyperpolarization. The tail current disappeared at a potential close to the expected VK but was rarely inverted to an inward-decaying tail. It is proposed that the fast inward-rectifying current of olfactory neurones (If.i.r.) is a K+ current analogous to the anomalous K+ rectifier of marine egg and frog muscle membranes. The behaviour of the inward rectifier was dependent on external K+ concentration in accordance with the unique 'V--VK' dependence of classical anomalous rectification; however, of several agents tested (external Cs+, Ba2+, Rb+, Tl+ or tetraethylammonium), only Cs+ and Ba2+ blocked If.i.r. in a time- and voltage-dependent manner. The effect of tetraethylammonium resembled that of an increase in external K+. The possible contribution of the inward rectifier to the passive cell membrane properties is discussed.

Action Potentials↗
PubMed1982

A transient outward current in rat sympathetic neurones.

Voltage-clamped rat sympathetic neurones exhibited a transient outward current similar to that previously described in invertebrate neurones and marine egg cells. It had an activation threshold of about -60 mV and displayed both voltage and time-dependent inactivation. In current clamp, this current manifested as a pronounced outward rectification at the onset of electrotonic potentials, increasing the latency to directly-evoked action potentials. The amplitude of the current was dependent on the external K+ concentration and was reduced by 4-aminopyridine.

Adrenergic Fibers↗
PubMed1982

Control of calcium current in rat sympathetic neurons by norepinephrine.

Inward voltage-dependent calcium currents were recorded from clamped rat sympathetic ganglion cells using either one or two microelectrodes. Suppression of potassium current was achieved by applying tetraethylammonium (TEA) externally and TEA plus cesium internally. Peak ICa was observed at 0 mV. ICa was abolished by perfusing cadmium or low calcium medium. ICa was reduced by adding norepinephrine (1-50 micrometers). This effect was not accompanied by any major change in the voltage sensitivity or time course of the residual calcium current. It is suggested that norepinephrine acts by reducing the number of available calcium channels.

Animals↗
PubMed1982

Convulsant actions of 4-aminopyridine on the guinea-pig olfactory cortex slice.

The effects of bath-applied 4-aminopyridine on neurones and extracellular potassium and calcium concentrations were recorded in slices of guinea-pig olfactory cortex. Neurones were orthodromically activated by stimulating the lateral olfactory tract. 4-Aminopyridine (3-10 microM) had the following effects: (1) an increase in the frequency and amplitude of spontaneous postsynaptic potentials; (2) a prolongation and oscillatory behaviour of orthodromically evoked postsynaptic potentials; (3) induction of spontaneous or stimulus-evoked seizure-type discharges which were accompanied by large rises in extracellular potassium and falls in calcium concentration; (4) a prolongation of the lateral olfactory tract population fibre spike. Prior to paroxysmal depolarization, membrane potential, input resistance and soma spike duration were unaffected. In the seconds before seizure discharges, a late hyperpolarizing potential (evoked by orthodromic stimulation) was reduced in amplitude or abolished. Diphenylhydantoin (50 microM) or magnesium ions (5 mM) prevented paroxysmal activity. Our results show that 4-aminopyridine can produce seizure-type discharges in a brain slice preparation. The role of increased spontaneous potentials and possible loss of synaptic inhibition as causal factors for such discharges is discussed.

4-Aminopyridine↗
PubMed1982

Extracellular K+ concentration during electrical stimulation of rat isolated sympathetic ganglia, vagus and optic nerves.

Recordings of extracellular potassium concentration ( [K+]e) were made in rat isolated sympathetic ganglia, vagus and optic nerves using ion sensitive microelectrodes. Repetitive orthodromic stimulation of ganglia resulted in [K+]e increases of up to 7 mmol/l above resting level (6 mmol/l), which were followed by post-stimulus undershoots. Activation of vagal A and B fibres did not significantly alter [K+]e but C-fibre activity induced rises of up to 5 mmol/l. Repetitive stimulation of the predominantly myelinated optic nerve resulted in [K+]e rises of up to 2.5 mmol/l. In the ganglion and vagus nerve, application of ouabain (30-1000 mumol/l) led to a raised baseline [K+]e concentration, an increase in the peak achieved during stimulation and a reduced undershoot amplitude. The amplitude of the undershoot in normal solution was shown to be dependent on the duration of the preceding stimulation period as well as the amplitude of the preceding [K+]e rise. In ganglia and vagus nerves, bath application of gamma-aminobutyric acid (10-100 mumol/l) and carbachol (10-100 mumol/l) also elevated [K+]e. It is concluded that repetitive activity in rat peripheral and central nerve fibres leads to significant changes in extracellular K+ ion-concentration and that the restoration of these levels is strongly dependent on the intact activity of the membrane Na+/K+ pump.

Animals↗
PubMed1980

Intracellularly-recorded effects of glutamate and aspartate on neurones in the guinea-pig olfactory cortex slice.

The effects of bath-applied glutamate, aspartate (and some related amino acids) on neurones of the guinea pig olfactory cortex slice were recorded intracellularly. Neurones were activated either by intracellularly-applied current or orthodromically by stimulating the lateral olfactory tract. In response to orthodromic stimuli several neurones displayed a late hyperpolarizing potential (LHP) after the usual sequence of EPSP, spike and IPSP. Glutamate and aspartate evoked 3 types of response: (a) a depolarization with apparent increase in input conductance; (b) a depolarization with no detectable conductance change; and (c) a hyperpolarization with conductance increase. Some possible mechanisms by which these 3 response-types could be generated are discussed. Depolarizations evoked by the glutamate analogue, kainate, were usually irreversible. Our results emphasize that glutamate and aspartate can evoke a variety of neuronal responses from olfactory cortex neurones. Several of these responses were previously undetected in experiments based on extracellular recordings.

Animals↗
PubMed1980

Presynaptic actions of 4-aminopyridine and gamma-aminobutyric acid on rat sympathetic ganglia in vitro.

Responses to bath-applications of 4-aminopyridine(4-AP) and gamma-aminobutyric acid (GABA) were recorded intracellularly from neurones in the rat isolated superior cervical ganglion. 4-aminopyridine (0.1-1.0 mmol/l) usually induced spontaneous action potentials and excitatory postsynaptic potentials (EPSPs), which were blocked by hexamethonium. Membrane potential was unchanged; spike duration was slightly increased. Vagus nerve B- and C-fibre potentials were prolonged. In 4-AP solution (0.2-0.3 mmol/l), GABA (0.1 mmol/l), 3-aminopropanesulphonic acid or muscimol evoked "bursts" of spikes and EPSPs in addition to a neuronal depolarization. These "bursts", which were not elicited by glycine, glutamate, taurine or (+/-)-baclofen, were completely antagonised by hexamethonium, tetrodotoxin or bicuculline methochloride. It is concluded that: (a) 4-AP has a potent presynaptic action on sympathetic ganglia; (b) presynaptic actions of GABA can be recorded postsynaptically in the presence of 4-AP; and (c) the presynaptic GABA-receptors revealed in this condition are similar to those on the postsynaptic membrane.

Action Potentials↗
PubMed1980

Influence of cellular transport on the interaction of amino acids with gamma-aminobutyric acid (GABA)-receptors in the isolated olfactory cortex of the guinea-pig.

1 Freshly cut guniea-pig olfactory cortex slices contained 2.2 mmol gamma-aminobutyric acid (GABA)/kg tissue weight. This declined during in vitro incubation at 25 degrees C in the absence of exogenous GABA, but increased to 6.95 mmol/kg after 1.5 h incubation in 1 mM GABA. 2 Uptake of [3H]-GABA (1 microM) was inhibited by 1 mM (+/-)-nipecotic acid (-83%), beta-amino-n-butyric acid (BABA) (-59%), L-2,4-diaminobutyric acid (DABA) (-63%), (+/-)cis-3-aminocyclohexane carboxylic acid (ACHC) (-53%), and 3-aminopropanesulphonic acid (3-APS) (-26%), but was increased by beta-alanine (BALA) (+23%). 3 Autoradiographs showed steep concentration gradients of radioactivity across slices incubated for short periods in [3H]-GABA. 4 Efflux of [3H]-GABA from pre-loaded slices was accelerated strongly by nipecotic acid, BABA, DABA and ACHC but weakly or not all by BALA or 3-APS. 5 Nipecotic acid (1 mM) potentiated the surface-depolarization of the slice produced by GABA but not that produced by 3-APS. 6 The depolarizing actions of DABA, BABA, nipecotic acid and ACHC, but not that of 3-APS or BALA, were potentiated when the endogenous GABA content of slices was raised. 7 It is concluded that: (a) the depolarizing action of exogenous GABA is limited by cellular uptake; (b) surface-depolarizations produced by nipecotic acid, DABA, BABA and ACHC may be mediated by the release of GABA; and (c) neuronal, rather than glial, transport systems are responsible for these effects.

Amino Acids↗
PubMed1979

Responses of the guinea-pig isolated olfactory cortex slice to gamma-aminobutyric acid recorded with extracellular electrodes.

1. Potential changes between the pial and cut surfaces of slices of guinea-pig olfactory cortex in vitro produced by gamma-aminobutyric acid (GABA) were recorded with extracellular electrodes. 2. GABA, superfused over the pial surface (0.1 to 10 mM), produced a pial-negative potential deflection, accompanied by inhibition of the postsynaptic response to lateral olfactory tract (LOT) stimulation. 3. This effect was replicated by the following compounds (potency relative to GABA = 1, in brackets): 3-aminopropanesulphonic acid (5.3), epsilon-aminovaleric acid (0.07), beta-alanine (0.07), beta-amino-nibutyric acid 0.05), epsilon-aminocaproic acid, alpha-amino-isobutyric acid, L-leucine (less than 0.02). 4. L-Glutamate (1 to 10 mM) produced a very large surface negative shift, with relatively less synaptic inhibition. Glycine (1 to 10 mM) produced less surface negatively, accompanied by synaptic inhibition. 5. Responses to GABA were antagonized more effectively than those to glycine by bicuculline (3 to 30 micrometer) and picrotoxin (1 to 30 micrometer). Strychnine (1 to 10 micrometer) incompletely inhibited responses to glycine. 6. It is concluded that, while the locus within the slice of these effects is uncertain, the preparation may be useful for testing the interaction of drugs with cerebral GABA receptors.

Action Potentials↗
PubMed1977

Influence of neuroglial transport on the action of gamma-aminobutyric acid on mammalian ganglion cells.

1 The effect of inhibiting the transport of gamma-aminobutyric acid (GABA) by neuroglial cells on the depolarizing action of exogenous amino acids on isolated superior cervical ganglia of the rat was studied. 1 Transport (measured by uptake of [3H]-GABA) was inhibited by (a) reducing external [na+] from 143 to 2mM and (b) administering alternative carrier-sbustrates, 3-amino-n-butyric acid (beta-amino-butyric acid, BABA) and (+/-)-nipecotic acid at a concentration of 1 mM. 3 All three procedures enhanced the depolarization produced by low concentrations of GABA (less than or equal to 10 muM) but did not alter the maximum response, nor the response to 3-aminopropanesulphonic acid (a gabamimetic with low affinity for the neuroglial carrier). 4 It is concluded that the neuroglial uptake process can limit the action of exogenous GABA upon neurones, by reducing the interstitial GABA concentration.

Alkanesulfonates↗