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321 records · Page 18Linked to original sources
PubMed1996

Computer simulations of voltage clamping retinal ganglion cells through whole-cell electrodes in the soma.

1. Computer simulations of voltage-clamp experiments in retinal ganglion cells were implemented to better understand the insights that can be obtained with this physiological approach. 2. Simulation studies of voltage clamping were based on the contemporary approach of using whole-cell recordings with low resistance electrodes attached to the soma. Realistic ganglion cell morphologies were provided by cell staining experiments in the mudpuppy retina; selected cells included small-, medium-, and large-field neurons whose morphologies were entered into a computer through a neuron tracing program. 3. Values for the specific membrane resistance (Rm) varied from 5,000 to 100,000 omega/cm2 to conform to the range of Rm values obtained with intracellular sharp electrodes and whole-cell recordings. 4. Synaptic input currents were simulated by injecting current with and without an underlying conductance change into different regions of the dendritic tree. The time-variant waveform of the current included a combined transient and sustained component similar to the waveform of ON-bipolar activation. 5. Simulations were base on 1) intact structures, which included the soma and the entire dendritic tree, and 2) a more limited cell geometry that included representation of the soma, but only part of the dendritic tree, to represent the restricted morphology that might be rendered after cutting the retina into 150-microns cross sections for retinal slice experiments. 6. The results of this study indicate that voltage clamping from the soma, with optimal, low resistance electrodes and series resistance compensation, provides an error-free voltage clamp for slow signals that are generated within a small electrotonic distance from the soma (approximately 0.1 lambda). 7. The ideal voltage-clamp conditions are optimized when synaptic conductances are small and nonlinear membrane elements are minimally activated: small-field neurons best approximate these conditions, but clamping errors are evident in these cells when more distal branches are activated. The degree of error in voltage clamping was much greater when medium-and large-field neurons were evaluated. 8. It was not possible to clamp action potentials (nonpropagating) even when they were generated near the soma in any of the three model cells examined. 9. Experimental paradigms were developed to demonstrate that inadequate voltage clamping can lead to errors in the interpretation of experimental data when relevant variables are not taken into consideration. Suggestions are made for determining and optimizing favorable clamp conditions.

Action Potentials↗
PubMed2001

Number of K(Ca) channels underlying spontaneous miniature outward currents (SMOCs) in mudpuppy cardiac neurons.

Spontaneous miniature outward currents (SMOCs) in parasympathetic neurons from mudpuppy cardiac ganglia are caused by activation of TEA- and iberiotoxin-sensitive, Ca(2+)-dependent K(+) (BK) channels. Previously we reported that SMOCs are activated by Ca(2+)-induced Ca(2+) release (CICR) from caffeine- and ryanodine-sensitive intracellular Ca(2+) stores. In the present study, we analyzed the single channel currents that contribute to SMOC generation in mudpuppy cardiac neurons. The slope conductance of BK channels, determined from the I-V relationship of single-channel currents recorded with cell-attached patches in physiological K(+) concentrations, was 84 pS. The evidence supporting the identity of this channel as the channel involved in SMOC generation was its sensitivity to internal Ca(2+), external TEA, and caffeine. In cell-attached patch recordings, 166 microM TEA applied in the pipette reduced single-channel current amplitude by 32%, and bath-applied caffeine increased BK channel activity. The ratio between the averaged SMOC amplitude and the single-channel current amplitude was used to estimate the average number of channels involved in SMOC generation. The estimated number of channels involved in generation of an averaged SMOC ranged from 18 to 23 channels. We also determined that the Po of the BK channels at the peak of a SMOC remains constant at voltages more positive than -20 mV, suggesting that the transient rise in intracellular Ca(2+) from ryanodine-sensitive intracellular stores in the vicinity of the BK channel reached concentrations most likely exceeding 40 microM.

Animals↗
PubMed2002

Spontaneous miniature hyperpolarizations affect threshold for action potential generation in mudpuppy cardiac neurons.

Mudpuppy parasympathetic neurons exhibit spontaneous miniature hyperpolarizations (SMHs) that are generated by potassium currents, which are spontaneous miniature outward currents (SMOCs), flowing through clusters of large conductance voltage- and calcium (Ca(2+))-activated potassium (BK) channels. The underlying SMOCs are initiated by a Ca(2+)-induced Ca(2+) release (CICR) mechanism. Perforated-patch whole cell voltage recordings were used to determine whether activation of SMHs contributed to action potential (AP) repolarization or affected the latency to AP generation. Blockade of BK channels by iberiotoxin (IBX, 100 nM) slowed AP repolarization and increased AP duration. Treatment with omega-conotoxin GVIA (3 microM) or nifedipine (10 microM) to inhibit Ca(2+) influx through N- or L-type voltage-dependent calcium channels (VDCCs), respectively, also decreased the rate of AP repolarization and increased AP duration. Elimination of CICR by treatment with either thapsigargin (1 microM) or ryanodine (10 microM) produced no significant change in AP repolarization or duration. Blockade of BK channels with IBX and inhibition of N-type VDCCs with omega-conotoxin GVIA, but not inhibition of L-type VDCCs with nifedipine, decreased the latency of AP generation. A decrease in latency to AP generation occurred with elimination of SMHs by inhibition of CICR following treatment with thapsigargin. Ryanodine treatment decreased AP latency in three of six cells. Apamin (100 nM) had no affect on AP repolarization, duration, or latency to AP generation, but did decrease the hyperpolarizing afterpotential (HAP). Inhibition of L-type VDCCs by nifedipine also decreased HAP amplitude. Inhibition of CICR by either thapsigargin or ryanodine treatment increased the number of APs generated with long depolarizing current pulses, whereas exposure to IBX or omega-conotoxin GVIA depressed excitability. We conclude that CICR, the process responsible for SMH generation, represents a unique mechanism to modulate the response to subthreshold depolarizing currents that drive the membrane potential toward the threshold for AP initiation but does not contribute to AP repolarization. Subthreshold depolarizations would not activate sufficient numbers of VDCCs to allow Ca(2+) influx to elevate [Ca(2+)](i) to the extent needed to directly activate nearby BK channels. However, the elevation in [Ca(2+)](i) is sufficient to trigger CICR from ryanodine-sensitive Ca(2+) stores. Thus CICR acts as an amplification mechanism to trigger a local elevation of [Ca(2+)](i) near a cluster of BK channels to activate these channels at negative levels of membrane potential.

Action Potentials↗
PubMed2003

Cell swelling increases intracellular calcium in Necturus erythrocytes.

This study examined the role of Ca(2+) in regulatory volume decrease by Necturus erythrocytes. Hypotonic shock (50% tonicity) stimulated an increase in cytosolic free Ca(2+), detected using epi-fluorescence microscopy and the fluorescent Ca(2+) indicator fluo-4-AM (10 microM). A similar increase in fluorescence did not occur under isosmotic conditions, unless cells were exposed to the Ca(2+) ionophore A23187 (0.5 microM). In addition, a low Ca(2+) medium (amphibian Ringer solution with 5 mM EGTA), hexokinase (2.5 U/ml, an ATP scavenger), suramin (100 microM, a P2 receptor antagonist) and gadolinium (10 microM, a stretch-activated channel blocker) each inhibited the swelling-induced increase in Ca(2+). Consistent with these studies, a low Ca(2+) Ringer solution increased osmotic fragility, whereas volume recovery following hypotonic shock (measured with a Coulter counter) was potentiated with A23187 (0.5 microM). By contrast, a low Ca(2+) extracellular medium or buffering intracellular Ca(2+) with BAPTA-AM (100 microM) reduced the rate of volume recovery following hypotonic challenge. Finally, a low Ca(2+) extracellular Ringer solution inhibited whole-cell currents that are activated during cell swelling (measured with the whole-cell patch clamp technique). Our results are most consistent with hypotonic shock causing an increase in cytosolic free Ca(2+), thereby stimulating subsequent volume decrease.

Animals↗
PubMed1996

Ketoconazole activates chloride and fluid secretion by Necturus gallbladder at low pH.

Necturus gallbladder epithelium, normally a reabsorptive epithelium, was stimulated to secrete chloride and fluid by the combined effects of ketoconazole and a reduction in perfusate pH to 7.0. The reversal in the direction of net fluid transport was accompanied by inhibition of the conductance of the apical cell membrane to sodium, potassium, and a striking stimulation of the conductance to chloride. The results are consistent with a previously unidentified mechanism for regulation of the apical cell membrane transport properties of reabsorptive epithelia.

Animals↗
PubMed1984

Retinal carbonic anhydrase: a comparative study.

Activity levels of carbonic anhydrase (E.C. 4.2.1.1) were measured in the retina and pigment epithelium of thirteen vertebrate species. The animals cover five taxonomic classes and among them illustrate four different retinal vascular supply patterns. The species can also be grouped according to their temperature regulatory mechanisms; i.e., homeothermic or poikilothermic. Significant differences are observed when the enzyme activities are examined by taxonomic class-birds and reptiles appear to have very high levels of enzyme activity; mammals and fish, moderate levels; and amphibia, low levels. When the enzyme activities are regrouped according to either vascular structure or temperature regulation, no significant differences are observed. From this, it is concluded that the level of carbonic anhydrase required by retinal tissue is not directly related to either of these factors. Carbonic anhydrase activity in kidney was compared with that in retina/pigment epithelium. Retina/pigment epithelium values are as great or greater than those in kidney but show a wider range. Only mammalian and avian kidney CA activity levels are high. We suggest that carbonic anhydrase levels in retina/pigment epithelium may be responsive to factors which influence vitreo-retinal ion and pH gradients.

Animals↗
PubMed1988

Do N-methyl-D-aspartate receptors mediate synaptic responses in the mudpuppy retina?

Whole-cell recordings of amacrine and ganglion cells in the superfused retina-eyecup preparation of the mudpuppy were obtained in order to determine which excitatory amino acid receptor (EAAR) subtype mediates the synaptic responses of these neurons. All third-order retinal neurons tested were depolarized by kainic acid (KA, N-methyl-D-aspartate (NMDA), and quisqualate (QQ). The responses evoked by NMDA were blocked by the addition of D-2-amino-5-phosphonovaleric acid (D-AP5) and D-2-amino-7 phosphonoheptonoic acid (D-AP7) to the perfusate. When the actions of exogenously applied NMDA were completely blocked by D-AP5 and D-AP7, the light-evoked responses of inner retinal neurons persisted without any apparent reduction or, alternatively, a slight enhancement of the response was observed. Light-evoked responses of bipolar, amacrine, and ganglion cells associated with the On pathway were attenuated by L-AP5 in a manner similar to its lower-order homolog L-2-amino-4-phosphonobutyrate (AP4); nevertheless, L-AP5 was not an effective NMDA antagonist. Although synaptic transmission between retinal second- and third-order neurons appears to be mediated by EAARs, the NMDA receptor does not appear to play a prominent role under our experimental conditions. Nevertheless, our results suggest that the racemic mixture of AP5 should not be used as an NMDA antagonist in retinal research, due to the AP4-like actions of its L-enantiomer.

2-Amino-5-phosphonovalerate↗
PubMed1985

Characterization of an extended glutamate receptor of the on bipolar neuron in the vertebrate retina.

The synaptic receptors of ON bipolar neurons are selectively activated by 2-amino-4-phosphonobutyrate, a glutamate analogue. This agent uniquely distinguishes these receptors from other types of excitatory amino acid receptors found in the retina. Various glutamate and aspartate analogues were used to assess the structure-activity characteristics of this receptor. The results suggest that it represents one class of glutamate receptor which can be distinguished by its preferential activation by acidic amino acid analogues that match the extended conformation of glutamate.

Aminobutyrates↗
PubMed1984

Effect of aspirin on epithelial cell membrane potentials of gastric fundic mucosa.

The effects of aspirin on epithelial cell membrane potentials of Necturus fundic mucosa were examined by in vitro experiments according to intracellular microelectrode techniques. Stable intracellular impalements were obtained with 15 to 50 M-ohm microelectrodes filled with 3M KCl. In neutral mucosal solutions (pH 7.0) aspirin (5.0 mM) resulted in a significant increase in apical cell membrane potential (Vmc) from -36.7 +/- 1.5 mV to -43.3 +/- 2.3 mV (p less than 0.001) and basolateral cell membrane potential (Vcs) from -42.7 +/- 1.8 mV to -50.6 +/- 2.4 (p less than 0.001). This hyperpolarization of the cell was associated with an increase in transmucosal potential from -5.8 +/- 0.7 to -7.4 +/- 0.9 (p less than 0.05) and an increase in the ratio of apical to basolateral membrane resistances from 5.1 +/- 1.2 to 8.8 +/- 1.9 (p less than 0.05). These changes were consistent with an increase in potassium conductance induced by the salicylate anion. In acidic mucosal solutions (pH 4.5) aspirin caused a reduction in Vmc and Vcs. This hypopolarization of the cell membrane is consistent with acidification of the epithelial cells. These observations support the proposed mechanisms of aspirin injury: (1) back diffusion of H+ into the cells and (2) influx of the salicylate anions into the cells, which may interfere with intracellular metabolism.

Animals↗
PubMed1981

Intracellular sodium activity and transcellular sodium transport in gallbladder.

As stated in the introduction, the purpose of this report has been to illustrate how the measurement of steady-state intracellular ionic activities, a technique that has proved to be of great importance in studying the energetics of transmembrane ionic transfer processes, can, with appropriate assumptions, be used to obtain information concerning the kinetics of these processes. Specifically, our analysis has focussed on transcellular Na+ transport in Necturus gallbladder and has shown that, given the steady-state values of Em, a1Na, and apical Na+ conductance for a particular set of conditions, it is possible to obtain estimates of net baso-lateral Na+ efflux (Na+ pump rate), net (and/or unidirectional) diffusive apical Na+ influx, and net coupled NaCl influx. It should be emphasized that the analysis outlined above is a preliminary essay in this direction. We present it here in the hope that, wit appropriate refinements, it may prove useful in unraveling the mechanisms by which drugs, hormones and other specific agents affect membrane function in epithelial and other systems.

Animals↗
PubMed1994

Membrane properties of two types of basal cells in Necturus taste buds.

Necturus taste buds contain two types of basal cells: presumptive stem cells and Merkel-like basal cells. Both types of basal cells are small round cells located at the base of the taste bud, indistinguishable from each other with light microscopy. However, with electron microscopy, autoradiography, or immunocytochemistry, these two types of basal cells can be easily distinguished. We isolated basal cells from taste buds, characterized their voltage-dependent currents using gigaseal whole-cell recordings, and processed the cells for electron microscopy or immunocytochemistry. We were able to distinguish two cell types electrophysiologically and to correlate cell type with membrane properties. Isolated Merkel-like basal cells had several voltage-activated currents: transient, TTX-sensitive, inward Na+ current; sustained, saturating outward K+ current; and slowly inactivating inward Ca2+ current. These currents are similar to those observed in taste receptor cells. In contrast, presumptive stem cells from Necturus taste buds only had outward K+ currents.

Animals↗
PubMed1994

Bidirectional synaptic transmission in Necturus taste buds.

Pairs of taste cells were impaled with intracellular recording microelectrodes in intact taste buds in slices of Necturus lingual epithelium. Applying short pulses of 140 mM KCl or 200 mM CaCl2 solutions to the apical pore elicited receptor potentials in taste receptor cells. Chemostimulation of receptor cells elicited postsynaptic responses in basal cells in the taste bud. Postsynaptic responses in basal cells had a threshold for activation and did not saturate with increasing doses of chemical stimulus applied to the receptor cells. We directly depolarized individual receptor cells and tested whether this would evoke postsynaptic responses in basal cells. Depolarizing receptor cells to approximately 0 mV evoked small depolarizing responses in basal cells in 16% of the experiments. The properties of these responses were consistent with their being mediated by a chemical synapse. A comparison of the responses in basal cells evoked by depolarizing single receptor cells, with responses evoked by stimulating the entire receptor cell population with KCl suggests that there is extensive synaptic convergence from receptor cells onto each basal cell. We also tested whether electrical excitation of basal cells would elicit (retrograde) synaptic responses in receptor cells. Single depolarizing pulses (up to 1 sec duration) applied to basal cells through the intracellular recording microelectrode never evoked synaptic responses in receptor cells. However, when repetitive electrical stimuli were applied to basal cells (four to six 1 sec depolarizations to approximately 0 mV every 12 sec) we observed prolonged effects on receptor cells in 11 of 23 experiments. These effects included an increase in the amplitude of receptor potentials elicited by KCI (mean +/- SD = +19 +/- 5%), an increase in membrane input resistance of receptor cells (+27 +/- 11%), and a hyperpolarization of receptor cells (3-10 mV). In control experiments, repetitive stimulation of one receptor cell never elicited such effects in another receptor cell. We investigated the possibility that serotonin (5-HT), released from basal cells, mediated the above modulatory effects on receptor cells. Bath-applied 5-HT (100 microM) mimicked the effects produced by repetitive basal cell stimulation (KCI responses increased by 23 +/- 12%; input resistance increased by 24 +/- 11%; hyperpolarization of 5-15 mV; N = 14). We conclude that basal cells release 5-HT onto adjacent taste receptor cells and that this enhances the electrotonic propagation of receptor potentials from the apical (chemosensitive) tip to the basal (synaptic) processes of receptor cells. The net effect is that activation of basal cells effectively increases the chemosensitivity of taste receptor cells.

Animals↗
PubMed1991

Biogenic amine localization in cardiac ganglion intrinsic neurons: electron microscopic histochemistry of SIF cells.

The parasympathetic cardiac ganglion in the mudpuppy, N. maculosus, contains postganglionic nerve cells and intrinsic neurons, many of which are small intensely fluorescent (SIF) cells. Several bioactive substances have been localized in the intrinsic nerve cells which may have integrative effects at synapses within the ganglion. Ganglionic intrinsic neurons can be identified electron microscopically by the presence of numerous cytoplasmic granular vesicles 80-120 nm in diameter. Throughout the ganglion there are bundles of unmyelinated fibers some of which are filled with granular and agranular vesicles and axosomatic terminals with similar vesicles synapsing on principal parasympathetic nerve cells. To understand the aminergic contribution to ganglionic synaptic circuitry the chromaffin reaction was used. The intrinsic neurons (i.e., SIF cells) were readily identified by their characteristic intracellular granule population. All intrinsic nerve cells identified showed granules which were positively labelled by the chromaffin reaction. Granular vesicles in synaptic profiles on principal cells (P cells) were also labelled indicating a direct aminergic synaptic innervation to these cells. The cell bodies of intrinsic neurons, ensheathed with supportive glial-like cellular processes, rarely received synapses. Elemental microanalysis was used to verify the chromium content of the electron dense product within the granular vesicles. These studies demonstrated direct aminergic synaptic input to at least a subpopulation of principal parasympathetic cells in the cardiac ganglion of mudpuppy.

Animals↗