Mean Membrane Potential Research Articles

Novel Pulse-Mode Neural Circuits Based on an AlGaAs-GaAs Multi-Quantum Well Diode

A novel approach to the hardware implementation of artificial, electronic pulse-mode neural circuits is described based on a new compound semiconductor device called a multi-quantum well injection mode device (MQW-IMD). The device exhibits a novel s-type current- voltage characteristic which has been theoretically modeled and experimentally verified. When operated with an resistance-capacitance (RC) load, the device switches periodically between the low conductance off state and high conductance on state generating a pulse mode output. The operation is analogous to that of the axon hillock or trigger zone of the neuron, exhibiting a threshold behavior and a nonlinear (exponential-like) dependence of the pulse frequency on the input voltage (mean membrane potential). Electronic synapses are proposed for accepting pulse-mode inputs, with both excitatory and inhibitory inputs possible. Signal integration over multiple inputs is shown to be feasible with individual synaptic weighting. Operation is shown to be possible at low voltages and powers with pulse amplitudes comparable to and pulse frequencies equal to or larger than its biological counterpart. This paper will focus on the neural-like characteristics of circuits based on this novel MQW-IMD diode.

Novel heterostructure device for electronic pulse-mode neural circuits

A new approach to the hardware implementation of artificial, electronic pulse-mode neural circuits is proposed and demonstrated based on the use of a novel heterostructure device that exhibits an S-type current-voltage characteristic. The new device consists of a multi-period quantum well structure with heavily doped n+ GaAs quantum wells and undoped AlGaAs barriers between an n+ GaAs cathode and p+ GaAs anode. When operated with an RC load, the device switches periodically between a low-conductance off state and a high-conductance on state generating a pulse-mode output. The operation is analogous to that of the axon hillock or trigger zone of the neuron, exhibiting a threshold behavior and a nonlinear dependence of the pulse frequency on the input voltage (mean membrane potential). Low-voltage and room-temperature operation are shown to be feasible.

Association between cell membrane potential and breast cancer.

Cell membrane potentials were measured in breast tissue and in breast epithelial cells to explore the relation between cell membrane potentials, oncogenesis and electrical potentials previously measured on the surface of the breast. The mean membrane potential in breast biopsy tissue from 9 women with infiltrating ductal carcinoma was significantly depolarized, compared with values measured in tissue from 8 women with benign breast disease. Depolarization was also observed in transformed breast epithelial cells, compared with normal breast cells; the transformed cells were particularly sensitive to the action of K+ channel blockers. The results were consistent with previous observations of electropositivity of skin sites over malignant tumors of the breast.

Amiloride-sensitive sodium conductance in human B lymphoid cells

The Na+ conductance of RPMI 8226 human B lymphoblastoid cells was examined using whole cell patch clamp. When the bath solution contained RPMI 1640 and the pipette solution contained (in mM) 100 potassium gluconate, 30 KCl, 10 NaCl, 0.5 ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA), and 20 N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES), as well as < 10 nM free Ca2+, pH 7.25, the mean membrane potential was -58 +/- 4.5 mV (n = 18). Cells were voltage clamped from -160 to +40 mV in 20-mV increments. The inward conductance was 767 +/- 221 pS/10 pF, and the outward conductance was 1,212 +/- 272 pS/10 pF (n = 12). Superfusion with 2 microM amiloride significantly hyperpolarized the cells by 7.4 +/- 2.2 mV (P = 0.004), significantly reduced the inward conductance to 221 +/- 65 pS/10 pF (P = 0.028), but had no effect on the outward conductance (1,294 +/- 236 pS/10 pF, P = 0.820, after amiloride). Next, the pipette and bath solutions were changed to (in mM) 150 sodium gluconate, 0.5 EGTA, and 20 HEPES, as well as < 10 nM free Ca2+, pH 7.25. Under these conditions amiloride significantly reduced (50%, P < 0.05; n = 7) the whole cell currents. When potassium gluconate was substituted for sodium gluconate, amiloride had no effect. Thus amiloride inhibited a Na(+)-specific conductance expressed by B lymphoid cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Membrane potential oscillations and corticothalamic connectivity in rat associational thalamic neurons in vitro

Thalamic relay neurons were recorded from the dorsolateral and lateroposterior nuclei of the rat thalamus in a superfused explant preparation. The mean membrane potential of these cells was -67 +/- 7 mV, input resistance 114 +/- 31 M omega and spike amplitude 75 +/- 6 mV. Low-threshold slow membrane potential oscillations (1-4 Hz) were present in about 46% of the neurons. They occurred either spontaneously or following a membrane potential perturbation. In a subpopulation of cells, we also observed a high-threshold membrane oscillation when cells were depolarized above -45 mV. This oscillation consisted of bursts of low-amplitude spikes interrupted by rhythmic after-hyperpolarizations. Stimulation of the corticothalamic pathway elicited prolonged inhibitory postsynaptic potentials in associational thalamic neurons. In the presence of picrotoxin, corticothalamic input evoked prominent excitatory postsynaptic responses that showed marked short-term synaptic plasticity. Our results suggest that associational thalamic neurons maintained in vitro have a strong tendency to exhibit membrane oscillations. In addition, they receive a direct excitatory cortical input that remained functional in explant preparation.

Divergent kinetics of 201Tl and 99mTc-SESTAMIBI in cultured chick ventricular myocytes during ATP depletion.

Thallous chloride (201Tl) and hexakis(2-methoxyisobutyl isonitrile) technetium (I) (99mTc-SESTAMIBI) are myocardial perfusion imaging agents with biological properties that also reflect tissue viability. Initial myocellular uptake rates of 201Tl reflect activity of Na,K-ATPase, whereas those of 99mTc-SESTAMIBI reflect mean plasma membrane potential. To better understand the mechanistic responses of these tracers to myocellular injury, cultured chick embryo cardiac myocytes were metabolically inhibited in iodoacetate (1 mM) and rotenone (10 microM) for up to 2 hours, and initial uptake rates of each agent were determined at successive intervals along with correlative cellular contents of ATP, sodium, and potassium and lactate dehydrogenase release. ATP content fell from 30.5 +/- 1.4 to 2.7 +/- 0.9 nmol.(mg protein)-1 within 2 minutes, whereas sodium and potassium contents ran down their thermodynamic gradients more slowly (t 1/2 approximately 60 minutes). Modestly severe cell injury was produced at 2 hours as estimated by lactate dehydrogenase release (18% of total). Initial uptake rates of 201Tl declined from 6.9 +/- 0.8 to 4.0 +/- 0.4 fmol.(mg protein)-1.(nMo)-1.(min)-1 by 20 minutes and remained depressed and ouabain (100 microM)-insensitive at 30 +/- 13% of control. Conversely, initial uptake rates of 99mTc-SESTAMIBI increased from 10.6 +/- 0.8 to 15.0 +/- 0.6 fmol.(mg protein)-1.(nMo)-1.(min)-1 within 10 minutes, remained elevated for 40-60 minutes, and later declined to low values. Injury-induced enhancement of initial uptake rates of 99mTc-SESTAMIBI were insensitive to ouabain (100 microM), carbonyl cyanide-m-chlorophenyl hydrazone (5 microM), and valinomycin (1 microgram/ml) but were significantly inhibited by 130 mM Ko buffer, Ba2+ (1 mM), glybenclamide (100 microM), and quinacrine (10 microM). Uptake rates of 201Tl monotonically decline, correlating with Na-K pump inhibition from ATP depletion. Conversely, uptake rates of 99mTc-SESTAMIBI at first increase above control for 40-60 minutes, indicating a mean plasma membrane hyperpolarization possibly resulting from opening of ATP-sensitive and arachidonic acid-activated potassium channels, before declining to low values with more severe cell injury. Correlative non-flow-dependent relations between 201Tl and 99mTc-SESTAMIBI contain information regarding the degree of myocellular injury.

Mechanism of pHi regulation by locust neurones in isolated ganglia: a microelectrode study.

1. We have measured membrane potential (Em) and intracellular pH (pHi), and sodium and chloride activities (aNai and aCli) in exposed dorsal unpaired median neurones in isolated metathoracic ganglia from the desert locust, Schistocerca gregaria using eccentric double-barrelled ion-sensitive microelectrodes. 2. In the absence of added HCO3- the steady-state pHi was 7.21 +/- 0.13 (mean +/- S.D.) at a mean membrane potential of -37 +/- 7.0 mV (S.D.) (n = 44 cells). The pHi was always more alkaline than predicted for passive H+ distribution. 3. The pHi recovery from acid loads, induced by weak acid application or weak base removal, was pHi dependent and associated, in both the presence and absence of added CO2-HCO3-, with a transient increase in aNai. 4. In the absence of added HCO3-, application of the Na(+)-H+ exchange blocker amiloride or external Na+ removal caused intracellular acidification. Also in the absence of added HCO3- the inhibitor SITS (4-acetamido-4'-isothiocyanatostilbene-2,2'-disulphonic acid) caused an acidification of about 0.2 pH units which was not additive to the effects of the removal of external Na+. 5. We found that the application of a CO2-HCO3(-)-containing solution increased the rate of pHi recovery from acidification. 6. Intracellular chloride was decreased by intracellular acidification in the presence of added CO2-HCO3-. In the presence of amiloride, intracellular Cl- depletion inhibited pHi regulation. 7. Simultaneous application of SITS (160 microM) and removal of CO2-HCO3- revealed a continuous underlying acid load of 0.03-0.05 pH unit min-1. 8. We conclude that locust neurones possess at least two pHi-regulating mechanisms which operate against a continuous acid load. One is a Na(+)-H+ exchanger which can be blocked by amiloride, while the second is a Na(+)-dependent Cl(-)-HCO3- exchanger. The latter mechanism appears to be able to operate in the absence of added HCO3- and can recover pHi to around pH 7.4; it is probably the main pHi regulating mechanism. The Na(+)-H+ exchanger appears to activate at more acid pHi and being less energy efficient may serve a protective role.

Mathematical modeling of fluctuations of the neuronal membrane potential during activation of exciting and inhibiting synapses

A probabilistic model of impulse activation of single neurons is proposed. The mean membrane potential and its limiting values are determined for the case when the impulses reaching the exciting and inhibiting synapses form a Poisson input or an arbitrary renewal process.

Calcium Current Measurements in Acutely Isolated Neonatal Cardiac Myocytes

Action potentials and voltage clamp-induced ionic currents were recorded in acutely isolated neonatal rabbit cardiac myocytes using the whole-cell voltage clamp technique. Time- and voltage-dependent Ca2+ currents in neonatal myocytes were elicited by depolarizations from a holding potential of -80 mV to various clamp potentials. The maximal measured inward Ca2+ current was 206 +/- 10 pA (mean +/- SEM, n = 51). The peak current occurred at a mean membrane potential of 7.8 +/- 1.3 mV (n = 51). The Ca2+ current voltage relation was shifted 26 mV in the positive direction when the external Ca2+ concentration was increased 10-fold. Ca2+ current rundown was observed with a half-time of approximately 20 min. Cells dialyzed with solution containing the Ca2+ chelating agent, EGTA (0.04 mM), had action potential durations similar to those previously reported in papillary muscle. In contrast, a higher concentration of EGTA (14 mM) prolonged the action potential duration. Control of the cell internal ionic composition was achieved by dialysis of the cell with a time constant for Na+ ions of 1.2 to 2.6 min. Tetrodotoxin (10 microM), included in some experiments to block Ca2+ entry via Na+ channels, was shown to be more than 98% effective. These results characterize the whole-cell voltage clamp technique as applied to immature heart cells.

Morphology and electrical properties of Schwann cells around the giant axon of the squids Loligo forbesi and Loligo Vulgaris

The first successful dye-fills of Schwann cells around the split giant axon of Loligo show them to be spindle-shaped cells ca. 600 microns long and 20 microns wide lying parallel to the axonal axis. There are some 50,000 Schwann cells per cm2 of axonal membrane. Only a small part (ca. 6% of each Schwann cell membrane) is in contact with the periaxonal space, the remainder is overlain by adjacent Schwann cells, or applied to the basal lamina. The mean membrane potential of the Schwann cells in artificial seawater (ASW) varies from around -40 mV in fresh split-axon preparations to around -60 to -70 mV after 1-2 h; this hyperpolarization is not seen in preparations dissected and maintained in Ca2(+)-free ASW. Electrical- and dye-coupling (abolished by prior octanol treatment) is present between Schwann cells, but is weaker in cells with lower (less negative) membrane potentials. The implications for potassium homeostasis around the axon are briefly discussed.

Mechanism of potassium uptake in neuropile glial cells in the central nervous system of the leech

1. Ion-selective double-barreled microelectrodes (ISME) were used to measure intracellular K+ (aKi), Na+ (aNai), and Cl- (aCli) activities of neuropile glial (NG) cells in the central nervous system of the medicinal leech Hirudo medicinalis. Ion fluxes were induced by an increase in extracellular K+ concentration [( K+]o) and analyzed to elucidate the ionic mechanism of the K+ uptake occurring under such conditions. 2. In addition, the K+ concentration of the extracellular space of the nerve cell body region (NCBR) and the neuropile (N) was measured with neutral carrier K(+)-ISME. In normal saline (4 mM K+), a concentration of 4.2 mM was measured in both extracellular spaces. No differences between the K+ concentration of the bathing fluid and the extracellular spaces were found at higher (i.e., 10 and 40 mM) K+ concentrations. 3. In normal saline, the mean membrane potential (Em) was -68 mV, and the mean aKi, aNai, and aCli were found to be 77, 10, and 7 mM, respectively. The corresponding equilibrium potentials were -81, 56, and -66 mV. The chloride equilibrium potential (ECl) was similar to Em, and it is concluded that chloride is passively distributed across the NG cell membrane. 4. When [K+]o was transiently increased 10-fold (i.e., to 40 mM), aKi and a Cli increased transiently by 22 and 25 mM, respectively, and the membrane depolarized to -28 mV, which was similar to both K+ equilibrium potential (EK) and ECl. The KCl uptake was accompanied by a transient decrease in aNai to 5 mM. 5. After incubation for at least 1 h in Na(+)-free saline, NG cells accumulated K+ in the absence of extracellular Na+ to levels similar to those observed in the presence of Na+. Therefore the uptake of K+ was not dependent on external--and probably also internal--Na+. 6. Changes in cell volume induced by the increase in [K+]o were estimated by loading NG cells with choline and monitoring its intracellular concentration with Corning-K(+)-ISME. In saline containing 40 mM K+, NG cell volume increased to approximately 150% of its volume in normal saline. 7. It is concluded that the mechanism of K+ uptake in NG cells is by passive KCl and water influx, which causes cell swelling.

The activity pattern of phrenic motoneurons during the aspiration reflex: an intracellular study

Membrane potential trajectories and discharge characteristics were measured intracellularly in 29 phrenic motoneurons of anesthetized, paralyzed and artificially ventilated cats during hypercapnic respiration and the aspiration reflex. Fifteen ‘active’ cells discharged spontaneously during inspiration, and the remaining 14 ‘quiescent’ cells exhibited no discharge in spite of strong central respiratory drive. The mean membrane potential of the quiescent cells during inspiration (−62 ± 4 mV) was significantly lower than the threshold level determined for the active cells (−52 ± 4 mV). The mean axonal conduction velocity was slower for the active (60.4 ± 8.7 m/s) than quiescent cells (67.4 ± 6.9 m/s). All phrenic motoneurons discharged during the aspiration reflex with maximum instantaneous frequencies ranging from 6 to 357 Hz. No differences were found for the maximum discharge frequency during the reflex between the active and quiescent cells. Although there were differences in the slopes of the depolarization during inspiration between the groups of cells, no such difference existed in the slopes during the aspiration reflex. The threshold level for the first spike during the reflex was the same as that during inspiration but the level for successive spikes became progressively less negative while spike amplitude decreased and duration increased. Stimulation of the nasopharynx to elicit the aspiration reflex was found to alter the timing of the subsequent respiratory cycles.

Membrane current underlying muscarinic cholinergic excitation of motoneurons in lobster cardiac ganglion.

1. We studied the effect of cholinergic agonists on motoneurons of the lobster cardiac ganglion under voltage clamp. 2. In unclamped neurons, acetylcholine (ACh) caused a depolarization and increase in burst potential frequency. By the use of nicotinic and muscarinic agonists, we determined that both types of receptors are present on the neurons. We therefore used specific muscarinic agonists to further study ionic mechanisms underlying the muscarinic cholinergic current (Imch). 3. Muscarinic agonists produced detectable inward current at doses above 10(-6) M, and maximum effect was seen at doses above 10(-3) M. 4. Imch was voltage-dependent. When the membrane holding potential was shifted to levels negative to the resting potential, the response declined, nulling but not reversing at -80 to -100 mV. The response enlarged with membrane depolarization, reaching a maximum at between -30 and -10 mV. With further depolarization, the response declined and then reversed at potentials around +20 mV. 5. The muscarinic response varied as a function of extracellular Na+ concentration and was completely blocked in Na+-free solutions. The relationship between response amplitude and external Na+ was well described by the electrodiffusion equation for Na+ driving force. 6. Imch amplitude also varied as a function of extracellular potassium concentration, becoming larger with low external K+ and smaller at higher concentrations. Shifting the Cl- equilibrium potential did not affect the properties of the Imch. 7. Tetrodotoxin (TTX) had no effect on Imch. In concentrations of 1-10 mM, such K+-channel blocking agents as Ba2+, Cs+, 4-aminopyridine (4-AP), or tetraethylammonium (TEA), and such Ca2+-channel blockers as Co2+ or Mn2+, when applied externally, did not suppress Imch. Above 30 mM, TEA did inhibit the response, and combinations of K+-channel blocking agents, each at concentrations insufficient alone to block the current, also inhibited Imch. 8. Current-voltage (I-V) curves obtained during muscarinic agonist perfusion consistently crossed the control I-V curves at a mean membrane potential of +24 mV. The reversal potential shifted to a more negative value in low extracellular Na+. 9. Although no reversal of Imch was seen when agonists were applied to cells clamped at negative holding potentials, the averaged curve of Imch, obtained by subtracting control ramp I-V curves from those obtained in the presence of agonist, did show a small net outward current at membrane potentials negative to -100 mV.(ABSTRACT TRUNCATED AT 400 WORDS)

Pre- and post-synaptic actions of the cerebral ventral giant cell on buccal muscles ofPhiline

The cerebral ventral giant cell ofPhiline exterts a selective presynaptic inhibitory modulatory action on the terminals of a buccal excitatory motoneuron in two buccal muscles. Other excitatory inputs to the muscles are not affected. The ventral giant cell also makes direct synaptic contacts on the fibres of the same muscles. In the retractor muscle M4, 5 the junction potentials are usually depolarising when measured in sea water, but in the fibres of M6 they may have either polarity. The mean membrane potential of the fibres of M4, 5 and M6 was −74.7±0.65 mV and −64±0.95 mV respectively. Depolarization of the muscles fibres by around 15 mV by immersion in 20 mM K saline abolished the junction potential in M4, 5 and converted the depolarizing potential in M6 to a hyperpolarizing response.

Membrane properties of identified embryonic nerve and glial cells of the leech central nervous system

The membrane potential of identified nerve (Retzius) cells and neuropil glial cells from 11 (±1) day-old embryos of the leechHirudo medicinalis was recorded using conventional intracellular microelectrodes. At this stage all ganglia of the segmental nervous system are formed. The membrane potential of Retzius cells was −68±4 mV (±SD,n=8), and showed a slope of 42 mV between 10 mM and 100 mM external K concentration. Retzius cells were able to fire action potentials which had a fast Na-dependent component, and, under appropriate conditions, also generated slow Ca (Ba) action potentials. The mean membrane potential of the neuropil glial cell at physiological K concentration (4 mM) was −83±5 mV (±SD,n=10), and showed a dependence of 56 mV for a tenfold change in the external K concentration (> 4mM). Neuropil glial cells showed no signs of voltage-activated excitability, but they repeatedly depolarized in the presence of 0.1 mM 5-HT.

Sex differences in membrane potential in the intact perfused rat liver.

The electrical potential difference across the plasma membrane was compared in paired livers from male and female rats perfused single-pass with Krebs-bicarbonate buffer. Variability in the membrane potential measured for different cells within the same liver was small (SD = 1.3 mV). The mean membrane potential was 5.1 mV more negative for male livers than for female livers (-30.3 +/- 0.6 vs. -25.2 +/- 1.0 mV, P less than 0.001), and the male liver had a more negative membrane potential than the female liver in all nine pairs studied. No correlation between membrane potential and perfusion rate was seen. Variability among female livers was more than twice as great (range -19.6 to -30.0 mV) as for male livers (range -26.7 to -31.9 mV). These results suggest that hepatic membrane potential may be modulated by sex hormone levels, which are more variable in female animals. Because the hepatic uptake of bile acids such as taurocholate and organic anions such as bilirubin may involve net movement of electrical charge across the plasma membrane, the current results may explain previously reported sex differences in the uptake of these and other electrogenically transported molecules.

Correlated electrophysiology and morphology of the ependyma in rat hypothalamus

The ependyma lines the ventricular system of the vertebrate brain and spinal cord. Although its embryology and morphology have been studied extensively, little is known of its physiological properties, particularly in mammals. Tanycytes are modified ependymal cells that are found predominantly lining the floor of the third ventricle, overlying the median eminence. Their processes accompany and enwrap neuroendocrine axons that course from hypothalamic nuclei to terminals in the median eminence, but the significance of this interaction is not yet understood. Intracellular recording and injection techniques were used to study ependymal cells and tanycytes of the rat in the hypothalamic slice preparation after differentiating their respective regions morphologically. With extracellular [K+] = 6.24 mM, the mean membrane potential (+/- SD) for common ependyma was -79.9 +/- 1.40 mV and for tanycytes, -79.5 +/- 1.77 mV. Input resistances (Rin) were very low (much less than 1 M omega). Single-cell injection of Lucifer yellow revealed dye coupling among 2-70 ependymal cells and 5-48 tanycytes. In both freeze-fractured replicas and thin sections, large numbers of gap junctions were found between adjacent ependymal cells and between adjacent tanycytes. The observations of numerous gap junctions, extensive dye coupling and low input resistance demonstrated that both populations are strongly coupled networks. Perhaps for this reason, attempts to uncouple these cells using sodium propionate or CO2 were unsuccessful. Electrical stimulation of the arcuate nucleus did not elicit any detectable synaptic response in impaled tanycytes, so that the functional significance of synaptoid contacts between neuroendocrine neurons and the postsynaptic tanycytes is not yet apparent. Ependymal cells and tanycytes demonstrated a near-Nernstian response to changes in extracellular [K+] between 3 and 20 mM. This finding, as well as their high negative resting potential, low Rin, extensive coupling and absence of spontaneous electrical excitability demonstrate that ependymal cells possess numerous glial characteristics and may therefore have similar functions. In the hypothalamus, ependyma probably take up K+ released from adjacent endocrine neurons and shunt it to the ventricular space.

The Action of the Prostaglandins on Isolated Human Ureteric Smooth Muscle

Summary— A study has been carried out on the actions of the prostaglandins E2 and F2α and their synthesis inhibitors, indomethacin and diclofenac sodium, upon isolated human ureteric smooth muscle, using the technique of microsuperfusion designed to ensure good tissue viability. Indomethacin and diclofenac sodium were shown to abolish almost completely the contractile response of ureteric muscle to electrical field stimulation. Contractile activity, in the presence of the inhibitors, could be restored by prostaglandin E2 or F2α or by increasing the external potassium concentration, [K+]o, of the superfusate. Prostaglandin E2 or F2α alone were shown to increase dramatically both the phasic and tonic component of the electrically stimulated contractions, on occasions inducing spontaneous activity. A possible mechanism of action was elucidated with an electrophysiological technique using intracellular microelectrodes. The mean membrane potential recorded was 54.7 mV (SD ± 10 mV, n=15). The depolarising action of raising [K+]o was demonstrated and prostaglandin F2α (3 times 10-6M) was shown to produce a small depolarisation of the ureteric muscle cell membrane.

The action of the prostaglandins on isolated human ureteric smooth muscle.

A study has been carried out on the actions of the prostaglandins E2 and F2 alpha and their synthesis inhibitors, indomethacin and diclofenac sodium, upon isolated human ureteric smooth muscle, using the technique of microsuperfusion designed to ensure good tissue viability. Indomethacin and diclofenac sodium were shown to abolish almost completely the contractile response of ureteric muscle to electrical field stimulation. Contractile activity, in the presence of the inhibitors, could be restored by prostaglandin E2 or F2 alpha or by increasing the external potassium concentration, [K+]O, of the superfusate. Prostaglandin E2 or F2 alpha alone were shown to increase dramatically both the phasic and tonic component of the electrically stimulated contractions, on occasions inducing spontaneous activity. A possible mechanism of action was elucidated with an electrophysiological technique using intracellular microelectrodes. The mean membrane potential recorded was 54.7 mV (SD +/- 10 mV, n = 15). The depolarising action of raising [K+]O was demonstrated and prostaglandin F2 alpha (3 x 10(-6) M) was shown to produce a small depolarisation of the ureteric muscle cell membrane.

Gating current harmonics. IV. Dynamic properties of secondary activation kinetics in sodium channel gating

The kinetics for sodium channel gating appear to involve three coupled processes: (a) "primary" activation, (b) "secondary" activation, and (c) inactivation. Gating current data obtained in dynamic steady states with sinusoidal voltage-clamp were analyzed to give further details about the secondary activation process in sodium channel gating. Unlike primary activation and inactivation, the secondary activation kinetics involve physical processes that become defined when the data are analyzed as a function of the sinusoid frequency in addition to mean membrane potential. The effects of these processes are described, and a physical interpretation is presented.