Cell Membrane Resistance Research Articles

Functional and structural properties of Na+/K+‐ATPase enzyme in neonatal erythrocytes

The Na+/K(+)-pump is the main regulator enzyme of intracellular monovalent cation concentration. There are only limited data available concerning its structure and function in healthy neonates, in comparison with data available regarding its structure and function in children. Samples of 100 microL of anticoagulated blood were taken from 53 healthy neonates (age under 6th postnatal day, median age 3.5 days) and 61 healthy children (median age 12.4 months, range 6-36 months,). The Na+/K(+)-ATPase activity, its sensitivity to ouabain (a digoxin-analogue substance) and the expression of Na+/K(+) ATPase subunit isoforms were determined. The enzyme activity (429.2 +/- 17.2 versus 295.5 +/- 10.2 U, P < 0 x 0.001) and I50 value for ouabain inhibition (1.50 +/- 0.10 versus 0.96 +/- 0.10 mumol L-1, P < 0.05) was higher in neonates. More alpha 1 subunits (relative density: 1.16 +/- 0.10 versus 0.75 +/- 0.03, P < 0.001) and higher alpha 1/ alpha 2 ratio (4.14 +/- 0.21 versus 2.02 +/- 0.16, P < 0.01) were detected. This is the first study demonstrating changes of Na+/K(+) -ATPase molecules not only in enzyme activity, but also on protein level. Our results might contribute to the understanding of the resistance of neonatal cell membranes toward the pharmacodynamic actions of cardiac glycosides.

Effect of inhibitors of ethylene biosynthesis and action, as well as calcium and magnesium on rose shoot rooting, shoot-tip necrosis and leaf senescence in vitro

Microcuttings of easy-to-root dwarf rose cv. Starina, showing early symptoms of leaf senescence and shoot-tip necrosis in rooting stage, were chosen for the study. The effects of inhibitors of ethylene biosynthesis (AOA, AIB) and action (AgNO3), and Ca2+ and Mg2+ were studied in relation to rooting, leaf senescence and shoot-tip necrosis. The effects of these substances were examined with respect to IAA presence in a medium, which stimulated leaf yellowing and shoot-tip necrosis. AOA strongly inhibited rooting of microcuttings, but did not affect ethylene biosynthesis. AIB at 250 mg·l−1 and AgNO3 2.5 mg·l−1 in the presence of IAA did not affect rooting but effectively prevented leaf senescence. Ca2+ alone or combined with Mg2+ at raised concentration, or an ethylene action inhibitor Ag+, reduced shoot-tip necrosis in microcuttings treated with IAA. Addition of Ag+ to IAA medium drastically increased ethylene production by the shoots. Interaction between endogenous levels of auxin, ethylene and calcium in relation to rooting, shoot-tip necrosis and leaf senescence was discussed. Ethylene could enhance tissue sensitivity to auxin. Moreover, the tissue of rose shoots is very sensitive in the in vitro condition on standard medium because of the calcium deficiency. Thus, the raised Ca/Mg level counteracted shoot-tip necrosis through enhancing cell membrane and wall resistance to ethylene and IAA.

Antagonist properties of (−)‐pindolol and WAY 100635 at somatodendritic and postsynaptic 5‐HT1A receptors in the rat brain

1. The aim of the present work was to characterize the 5-hydroxytryptamine1A (5-HT1A) antagonistic actions of (-)-pindolol and WAY 100635 (N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl) cyclohexane carboxamide). Studies were performed on 5-HT1A receptors located on 5-hydroxytryptaminergic neurones in the dorsal raphe nucleus (DRN) and on pyramidal cells in the CA1 and CA3 regions of the hippocampus in rat brain slices. 2. Intracellular electrophysiological recording of CA1 pyramidal cells and 5-hydroxytryptaminergic DRN neurones showed that the 5-HT1A receptor agonist 5-carboxamidotryptamine (5-CT) evoked in both cell types a concentration-dependent cell membrane hyperpolarization and a decrease in cell input resistance. On its own, (-)-pindolol did not modify the cell membrane potential and resistance at concentrations up to 10 microM, but it antagonized the 5-CT effects in a concentration-dependent manner. Similar antagonism of 5-CT effects was observed in the CA3 hippocampal region. (-)-Pindolol also prevented the 5-HT1A receptor-mediated hyperpolarization of CA1 pyramidal cells due to 5-HT (15 microM). In contrast, the 5-HT-induced depolarization mediated by presumed 5-HT4 receptors persisted in the presence of 3 microM (-)-pindolol. 3. In the hippocampus, (-)-pindolol completely prevented the hyperpolarization of CA1 pyramidal cells by 100 nM 5-CT (IC50=92 nM; apparent KB=20.1 nM), and of CA3 neurones by 300 nM 5-CT (IC50=522 nM; apparent KB= 115.1 nM). The block by (-)-pindolol was surmounted by increasing the concentration of 5-CT, indicating a reversible and competitive antagonistic action. 4. Extracellular recording of the firing rate of 5-hydroxytryptaminergic neurones in the DRN showed that (-)-pindolol blocked, in a concentration-dependent manner, the decrease in firing elicited by 100 nM 5-CT (IC50=598 nM; apparent KB= 131.7 nM) or 100 nM ipsapirone (IC50= 132.5 nM; apparent KB= 124.9 nM). The effect of (-)-pindolol was surmountable by increasing the concentration of the agonist. Intracellular recording experiments showed that 10 microM (-)-pindolol were required to antagonize completely the hyperpolarizing effect of 100 nM 5-CT. 5. In vivo labelling of brain 5-HT1A receptors by i.v. administration of [3H]-WAY 100635 ([O-methyl-3H]-N-(2-(4-(2-methoxyphenyl)-1 -piperazinyl)ethyl-N-(2-pyridyl)cyclo-hexane-carboxamide) was used to assess their occupancy following in vivo treatment with (-)-pindolol. (-)-Pindolol (15 mg kg[-1]) injected i.p. either subchronically (2 day-treatment before i.v. injection of [3H]-WAY 100635) or acutely (20 min before i.v. injection of [3H]-WAY 100635) markedly reduced [3H]-WAY 100635 accumulation in all 5-HT1A receptor-containing brain areas. In particular, no differences were observed in the capacity of (-)-pindolol to prevent [3H]-WAY 100635 accumulation in the DRN and the CAI and CA3 hippocampal areas. 6. Intracellular electrophysiological recording of 5-hydroxytryptaminergic DRN neurones showed that WAY 100635 prevented the hyperpolarizing effect of 100 nM 5-CT in a concentration-dependent manner (IC50=4.9 nM, apparent KB=0.25 nM). In CA1 pyramidal cells, hyperpolarization induced by 50 nM 5-CT was also antagonized by WAY 100635 (IC50 = 0.80 nM, apparent KB= 0.28 nM).

Dissecting the frog inner ear with Gaussian noise. II. Temperature dependence of inner ear function

The temperature dependence of the response of single primary auditory nerve fibers ( n = 31) was investigated in the European edible frog, Rana esculenta (seven ears). Nerve fiber responses were analyzed with Wiener kernel analysis and polynomial correlation. The responses were described with a cascade model, consisting of a linear bandpass filter, a static nonlinearity, and a linear lowpass filter. From the computed Wiener kernels and the polynomial correlation functions, the characteristics of the three model components were obtained. With increasing temperature (1) tuning of the first filter increased in the majority ( n = 16) of amphibian papilla fibers (best excitatory frequency, BEF < 1 kHz, n = 21) but remained unchanged in the majority ( n = 10) of basilar papilla fibers (BEF > 1 kHz, n = 11), (2) the gain of the first filter remained unchanged, (3) the shape of nonlinear 10 function remained unchanged, (4) the combined gain of the static nonlinearity and the second filter usually increased, but displayed considerable scatter across fibers (from −0.7 dB/†C to 3 dB/†C), and (5) the cutoff frequency of the second lowpass filter increases, with average 0.13 oct/°C. The immunity of the shape of the nonlinearity is considered evidence of a temperature independent gating mechanism in the transduction channels. The temperature dependence of the second filter may have resulted from a decrease of the hair cell membrane resistance, but may also reflect changes in subsequent staging of nerve fiber excitation.

Luminal acid increases apical cell membrane resistance in isolated Necturus antral mucosa

BACKGROUND & AIMS: The gastric mucosa must have efficient protective mechanisms to maintain physiological intracellular pH. The aim of this study was to investigate the effect of low luminal pH on apical membrane permeability. METHODS: Chambered Necturus antral mucosa was perfused with Ringer's/95% O2-5% CO2 at pH 7.25. The mucosal side was exposed to pH 4.0-2.0 with four microelectrodes placed in surface cells. Two-dimensional cable analysis was used to measure apical, basolateral, and shunt resistances. In some experiments, liquid sensor pH or Na(+)-selective microelectrodes were used. RESULTS: Luminal acidification hyperpolarized apical cell membrane potential and increased apical cell membrane resistance from 21.3 +/- 2.6 (pH 7.25) to 38.0 +/- 2.3 k omega.cm2 (pH 3.0; n = 8). The increase in apical cell membrane resistance was preceded by transient intracellular acidosis from 7.32 +/- 0.07 (pH 4.0) to 7.23 +/- 0.06 (pH 3.0; n = 6). Similar intracellular acidosis (provoked by NH4+ prepulse) failed to cause the effects observed with luminal acid. The increase in apical cell membrane resistance caused by luminal acid was eliminated when N- methyl-D-glucamine+, but not Na+, was substituted for all cations in the luminal solution. CONCLUSIONS: Luminal acidification (pH 3.0-2.0) closes apical amiloride-blockable Na+ channels. Protons are probably able to pass and even block these channels, but their effect in closing the channels does not occur intracellularly. (Gastroenterology 1997 Sep;113(3):875-83)

Membrane time constant as a tool to assess cell degeneration

Changes in neuronal surface area may be monitored by measuring the plasma membrane capacitance [8]. Membrane time constant ( τ m) is given by the product of the membrane resistance ( r m) and membrane capacitance ( c m), τ m= r m c m. Thus, when membrane resistance is kept constant at a steady state (resting), membrane time constant can reflect the size of neuronal surface area. Membrane time constant is the time for the potential to fall from the resting to a fraction (1−1/e), or 63%, of its final value in the charging curve during the application of a small negative current pulse [9]. Negative voltage shift from the resting potential hardly activates any voltage-dependent ion channel, resulting in nominal changes in cell membrane resistance. Although elaborated methods for mathematical models and simulations are available for the electrophysiological assessment of neuron geometry in order to estimate subthreshold potential attenuation during the propagation of synaptically mediated electrical signals [1, 4, 10], they involve a number of critical assumptions for the convenience to each model, and some of these assumptions are unlikely to be valid [7]. With these restrictive assumptions, very little can be determined about the electrotonic structure of a neuron beyond the measurement of neuronal membrane resistance and membrane time constant. Alternatively, numerous tracers are available to visualize morphologies of neurons intracellularly and extracellularly. These anatomical methods provide direct and quantitative evidence for neuron geometry; however, they involve tissue processing and a series of chemical reactions, some of which are time- and effort-demanding. The purpose of the present paper is to show that membrane time constant can be effectively used as a tool to assess diminution in cell surface area without involving extensive mathematical theories and/or neuroanatomical techniques. This approach is particularly effective in electrotonically compact cells such as hippocampal neurons [1]. Recent development in the technique of the whole-cell patch clamp recording in the slice preparation yielded longer time constant with better resolution due to the absence of the leak conductance associated with microelectrode impalement [10]. Indeed, when membrane time constant was measured with the whole-cell patch clamp recording technique, it successfully detected the reduction in dendritic arbors (dendritic degeneration) in dentate granule cells in the pilocarpine model of chronic epilepsy, and this finding is supported by the neuroanatomical evidence that was obtained from the same specimen samples [6]. Membrane time constant is an easy-to-measure “passive membrane property” and can be used as a reliable probe by itself for detecting dendritic degeneration, or as a tool for decision-making in introducing neuroanatomical technique in combination with slice neurophysiology.

Cardiac swelling-induced chloride current depolarizes canine atrial myocytes.

The effect of the cardiac swelling-induced chloride current (I(Cl,swell)) on the transmembrane potential was examined. Osmotic swelling affected the resting potassium current through an apparent dilution of intracellular potassium. Inflating cells by applying positive pressure to the patch electrode prevented the effect on the resting potassium current. Inflation depolarized dog atrial myocytes when the recording electrodes contained either 17 or 42 mM Cl-. The depolarization coincided with activation of I(Cl,swell) and was antagonized by the chloride-channel blocker niflumic acid. Substituting extracellular chloride with the more permeant ion SCN- shifted the reversal potential for I(Cl,swell) to more negative values and antagonized inflation-induced depolarization. The depolarization was accentuated by replacing extracellular chloride with a less permeant ion, aspartate. We conclude that activation of I(Cl,swell) in atrial cells causes significant depolarization of the resting membrane. The outward rectification of I(Cl,swell) and the high cell membrane resistance during the action potential plateau suggest that I(Cl,swell) will also have significant effects on atrial action potential configuration.

Effect of low oxygen concentration on the electrical properties of cortical cells of wheat roots

Short-term effect of oxygen-deficiency on the membrane potential difference (PD), membrane resistance of cortical cells and electrical coupling between cortical cells was investigated using excised wheat roots. Hypoxia rapidly depolarised the membrane potential of the cortical cells by about 60 mV, while hypoxia had little effect on the membrane resistance of the cells. No significant change in membrane resistance by potassium channel blockers, TEA+ and verapamil, under hypoxia was observed. The electrical coupling ratio, which is a measure of plasmodesmatal resistance, between cortical cells of wheat roots was 5.9 % in aerated solution and was not affected by the low oxygen treatment, suggesting that solute transport through cytoplasmic annulus of plasmodesmata could not be affected. The possible involvement of the endoplasmic reticulum in intercellular transport of solute and water is discussed.

Serotonergic modulation of evoked responses in turtle cerebellar Purkinje cells.

1. Immunocytochemical studies of the turtle brain revealed the presence of serotonin (5-hydroxytryptamine, 5-HT) immunoreactive (5-HT-ir) processes in the granule and Purkinje cell layers, but not in the molecular layer (ML), of the cerebellar cortex. Immunoreactive axonal profiles were present throughout the granule cell layer (GCL) where they generally coursed in an anteroposterior direction and could frequently be seen to ascend toward the Purkinje cell layer (PCL). Occasional 5-HT-ir processes were observed adjacent to Purkinje cell somata. 2. The effects of exogenously applied serotonin on mossy fiber and parallel fiber evoked responses in turtle Purkinje cells were examined by use of intrasomatic and intradendritic recordings in an intact cerebellar preparation in vitro. 3. Bath application of serotonin (0.2-1.0 microM) produced a dose-dependent reduction in Purkinje cell membrane resistance, which was not correlated with changes in postsynaptic response amplitude. At 5-HT concentrations > 1.0 microM (0.01-5 mM), resistance values returned to control levels. No consistent changes in spike width or postspike afterhyperpolarization were seen in response to serotonin application, nor were endogenous pacemaker-like discharges affected. Firing rate, assessed as threshold response to depolarizing current injection (0.3-1.0 nA, 1 s duration), was increased in 51% and decreased in 40% of cells tested. 4. Single stimuli delivered to either the cerebellar peduncle or the GCL resulted in the activation of fast excitatory postsynaptic potentials (fEPSP). These responses were dose dependently reduced in amplitude by bath application of serotonin (0.2-1.0 microM). At concentrations ranging from 10 to 100 microM, the response amplitude following agonist application plateaued at approximately 70% of control value. With higher dose applications (0.5-5 mM) of serotonin, the response amplitude exhibited a steep reduction (from 65-10% of control value). 5. Brief trains of stimuli (5 stimuli, 50 Hz) delivered to either the cerebellar peduncle or the GCL resulted in the activation of slow excitatory postsynaptic potentials (sEPSP). The peak amplitude of this response was unaffected by bath application of serotonin at concentrations ranging from 0.2 to 100 microM. At higher concentrations (0.5-5 mM), the sEPSP peak amplitude was dose-dependently reduced, with the largest amplitude reduction seen after peduncular stimulation. 6. It is suggested that serotonin acts as a modulator of fast excitatory synaptic activity in the cerebellar cortex, while exerting little affect on slow excitatory events. The fact that serotonin preferentially affects fast excitatory transmission may have important implications for the integration of incoming sensory signals at both the granule and Purkinje cell level.

Thyroid eye disease.

Effects of warm hypoxia and ischemia on electrophysiologic properties of isolated perfused mouse proximal straight tubules were studied. Oxyrase (5 to 10 microliters/mL) was added to the hypoxic and ischemic solutions to lower the oxygen tension to 5 mm Hg. The ischemic solution also simulated acidosis, K+ and lactate accumulation, and substrate deprivation. Twenty-minute tubular perfusion with the hypoxic and ischemic solutions (lumen and bath) at 37 degrees C did not significantly alter basolateral membrane potential, basolateral K+ transference number, or intracellular Na+ activity from control values of -69 +/- 1 mV (N = 91), 0.71 +/- 0.01 (N = 15), and 15.2 +/- 0.8 mM (N = 12), respectively. However, the hypoxic and ischemic perfusions decreased transepithelial potential by 40% (hypoxia: -1.7 +/- 0.1 to -1.1 +/- 0.1 mV [N = 30; P &lt; 0.001]; ischemia: -1.4 +/- 0.1 to -0.82 +/- 0.05 mV [N = 17; P &lt; 0.001]). A similar extent of reduction in transepithelial resistance was observed (hypoxia: 14.3 +/- 1.0 to 9.2 +/- 1.1 omega.cm2 [N = 7; P &lt; 0.005]; ischemia: 12.6 +/- 1.2 to 8.1 +/- 1.0 omega.cm2 [N = 6; P &lt; 0.03]). In addition, neither apical (R(ap)) nor basolateral (Rbl) cell membrane resistances were significantly altered after the ischemic perfusion (control: R(ap) = 369 +/- 48 omega.cm2; Rbl = 92 +/- 11 omega.cm2 [N = 63]; reperfusion: R(ap) = 454 +/- 88 omega.cm2; Rbl = 101 +/- 16 omega.cm2 [N = 21]). It was concluded that tubular cells are able to maintain their electrogenic ionic transport after short-term exposure to hypoxic or ischemic conditions. However, cell-to-cell junctions are damaged by these insults, which could possibly increase leakage and decrease the efficiency of the active transport.

Effects of temperature on silkmoth olfactory responses to pheromone can be simulated by modulation of resting cell membrane resistances

Electrophysiological parameters were measured at different temperatures in resting and pheromone-stimulated olfactory sensilla trichodea of male Antheraea polyphemus (Saturniidae). A method for selective cooling of either the olfactory hair or the antennal branch was developed. The resting preparation resistance increased with lower temperatures, the transepithelial potential decreased. These effects were also observed when the antennal branch was cooled, but were absent during cooling the hair, suggesting a major influence of auxiliary cells on the transepithelial potential and resistance. Together with the preparation resistance, the responses to pheromone stimuli increased with lower temperatures. Computer simulation of the current flow in the sensillum showed that the temperature dependence of responses to pheromone can be explained by modulation of resting resistances of cell membranes alone, without effects of temperature on stimulus transduction. The weak temperature dependence of transepithelial potential might be due to temperature dependence of the electrogenic pump producing the transepithelial potential. Selective cooling of the olfactory hair had no effect on the shape of nerve impulses, cooling of the antennal branch caused changes similar to that obtained by cooling the entire sensillum. This supports the idea that the nerve impulses are generated in the soma of the receptor cell.

In vitro brain slice studies of the rat's dorsal nucleus of the lateral lemniscus. III. synaptic pharmacology

1. The synaptic pharmacology of the dorsal nucleus of the lateral lemniscus (DNLL) of the rat was investigated in a brain slice preparation of the auditory midbrain. The brain slice was cut in the coronal plane and placed in a small recording chamber where warm, oxygenated saline was continuously perfused over and underneath the tissue. Intracellular recordings were made with glass microelectrodes filled with 4 M potassium acetate. Synaptic potentials were elicited by electrical stimulation of the lateral lemniscus or commissure of Probst and pharmacological effects were tested by bath application of amino acid agonists and antagonists. 2. The cells in DNLL were challenged with the excitatory amino acid (EAA) agonists, alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA), N-methyl-D-aspartic acid (NMDA) in 0 Mg2+, and L-glutamate. Each of these caused a depolarization of the cell membrane, a reduction in cell membrane resistance, and the onset of spontaneous firing. 3. Short-latency excitatory postsynaptic potentials (EPSPs) were evoked by stimulation of the lateral lemniscus in 77% of the neurons tested. The mean latency to initial depolarization was 0.9 ms. A single spike with relatively constant latency (mean 1.5 ms) was typically elicited when the strength of lemniscal stimulation was increased. A longer-latency EPSP (mean 2.9 ms) was seen in 34% of the neurons tested either with the slice in normal saline or after pharmacological block of the earlier, short-latency EPSP. The long-latency EPSP was followed by a single spike of multiple spikes with highly variable latencies (range 3.2-24 ms). In 28% of the neurons tested, both early and late EPSPs were observed in response to stimulation of a single location on the lateral lemniscus. 4. Stimulation of the commissure of Probst elicited short-latency EPSPs (mean 0.9 ms) in 37% of the neurons tested. Longer-latency EPSPs (mean 3.0 ms) were found in only 3% of the neurons in response to commissural stimulation. 5. The nonspecific EAA antagonist kynurenic acid blocked both short-and long-latency EPSPs evoked by either lemniscal or commissural stimulation. The non-NMDA antagonist 6-cyano-7-nitro-quinoxaline-2,3-dione (CNQX), at very low concentrations, blocked the short-latency EPSPs but had no effect on the longer-latency EPSPs. The short-latency EPSPs were unaffected by the NMDA antagonist D,L-2-amino-5-phosphonovaleric acid (APV). In contrast, the longer-latency EPSPs were blocked by APV, but never by CNQX. 6. DNLL neurons were affected by the inhibitory amino acid agonists gamma-aminobutyric acid (GABA) and glycine. The membrane resistance of the neurons was decreased by GABA and glycine in a solution of either normal or calcium-free saline in a concentration-dependent manner. 7. Inhibitory postsynaptic potentials (IPSPs) were elicited by stimulation of the lateral lemniscus in 53% of the neurons and the commissure of the Probst in 18% of the neurons tested. The mean latencies were 1.0 and 0.9 ms, respectively. The reversal potentials of the IPSPs were around -70 mV. 8. The IPSPs evoked by stimulation of the lateral lemniscus were blocked by the glycine receptor antagonist strychnine, but not by the GABA receptor antagonist bicuculline, whereas the IPSPs elicited by stimulation of the commissure of Probst were blocked by bicuculline but not strychnine.

Calcium entry stimulated by swelling of Madin-Darby canine kidney cells.

Cell swelling in Madin-Darby canine kidney (MDCK) cells by reduction of extracellular osmolarity (omission of 70 ad 150 mmol/l mannitol, respectively) leads to the activation of anion of channels and Ca2+ sensitive K+ channels. The K+ channel activation leads to an initial transient hyperpolarization of the cell membrane potential (PD) followed by a sustained depolarization due to activation of anion channels. The present study elucidates the role of intracellular calcium (Ca2+i) in regulatory cell volume decrease (RVD) of MDCK cells. While reduction of extracellular osmolarity by omitting 70 mmol/l mannitol did not lead to a detectable change in Ca2+i, severe cell swelling by omitting 150 mmol/l mannitol led to a transient rise in Ca2+i. PD changes, on the other hand, were not different under either condition. In addition, the response of PD to cell swelling was not altered by treatment of the cells with 12-O-tetradecanoylphorbol-13-acetate diester, pertussis toxin or cholera toxin. In the nominal absence of extracellular Ca2+, reduction of extracellular osmolarity did not lead to an increase in Ca2+i and no initial transient hyperpolarization was observed, whereas addition of 10 mumol/l ATP still led to a significant hyperpolarization. Omission of extracellular Ca2+ was followed by a strong decrease in cell membrane resistance (Rm) due to activation of a depolarizing cation conductance. Subsequent readdition of Ca2+ caused a marked increase in Ca2+i due to Ca2+ influx. This Ca2+ entry was further stimulated by cell swelling. RVD was significantly blunted in the absence of extracellular Ca2+. The results suggest that cell swelling stimulates a Ca2+-permeable pathway in the cell membrane favoring Ca2+ entry into the cell with subsequent activation of Ca2+-sensitive K+ channels.

Modulation of glomus cell membrane currents of intact rat carotid body.

1. In order to understand better the relationship between sinus nerve chemoreceptor activity and changes in glomus cell membrane current, both were measured simultaneously in rat carotid bodies in vitro. Mean membrane resistance of intact glomus cells was 1327 +/- 140 M omega (n = 104, mean +/- S.E.M.) and membrane capacitance was 7.9 +/- 0.8 pF (n = 28). 2. Over the course of 15 min following the start of whole-cell recording, outward current increased by 169 +/- 48% (n = 19), but there was no significant change in holding current or membrane resistance. Reversal potential of the tail current was not changed over this time period. Current run-up was not affected by addition of ATP, Ca2+, okadaic acid or H-7 to the pipette fluid. 3. Brief hypoxia (30-45 s duration, 0 mmHg at nadir) caused a rapid increase in nerve activity, but, on average, no significant change in cell holding current, or resistance. Outward current slightly decreased during hypoxia but failed to recover in the post-hypoxia period. 4. Tetraethylammonium (20 mM), and 4-aminopyridine (1 mM) reduced the outward current to 54 +/- 7 and 66 +/- 3% of control, respectively, but basal nerve activity was unchanged and the nerve response to hypoxia remained intact. 5. These results suggest that hypoxia modulation of glomus cell K+ current is not the primary initiating factor in the nerve response to brief periods of hypoxia in the rat carotid body.

The effect of graded hypertonia on interstitial volume, tissue resistance and synaptic transmission in rat hippocampal tissue slices

Rat hippocampal slices were exposed for 30 min to each of three levels of increased osmolarity (π o), achieved by adding 25, 50 or 100 mM mannitol to the bathing solution. The interstitial volume (ISV) determined as the relative volume of dilution of the probe ion, tetra-methyl-ammonium (TMA +), increased markedly, indicating cell shrinkage. Tissue resistance ( R o) decreased only slightly with increasing π o. The discrepancy between ISV increase and R o decrease suggests increased electrical resistance of cell membranes. TMA + dilution appears to be a more reliable measure of ISV than is R o During recovery from hypertonic treatment the previously expanded ISV frequently shrank, suggesting post-hypertonic cell swelling. Hypertonic treatment significantly depressed orthodromically transmitted population spikes and extracellular synaptic potentials (fEPSPs), and the degree of depression varied with the increase in π o. Changing recording condition due to reduced R o could not account for the depression of population spikes and fEPSPs. Following return to normal π o, orthodromic population spikes frequently overshot initial control amplitude. An isolated episode of spreading depression occurred in about half of the slices following exposure to the most severely hypertonic solution. At the end of 2.5 h recovery, orthodromic spikes did not significantly differ from those of untreated control slices observed for the same length of time. We conclude that synaptic transmission is depressed by elevation of π o and the depression is concentration dependent and reversible.

Влияние антиоксидантов на состояние перекисного окисления липидов и функцию бета-клеток у больных с впервые выявленным инсулинзависимым сахарным диабетом

Sixty-one patients with newly detected insulindependent diabetes mellitus (IDDM) and 16 normal subjects were examined. Levels of glycemia, HbAlc, basal and stimulated C- peptide, insulin requirement, and lipid peroxidation (LPO) were assessed before and 3, 6, and 12 months after the follow-up was started. Activation of lipid peroxidation detected as early as at the debut of the disease permitted the authors to propose antioxidants, alfa-tocopherol acetate and nicotinamide, among other agents, for the correction of the disorders detected. The best results characterizing the clinical course, hormonal and metabolic markers, and function of the intact beta-cells in patients with newly detected IDDM were observed in the group of patients treated with insulin, nicotinamide, and vitamin E. The number of remissions was reliably higher in this group of patients in comparison with other groups: complete remission was attained in 33%, partial in 67% of patients; stimulated C-peptide level 6 months after treatment (0.41 ± 0.06 nmol/liter) was reliably (p < 0.01) higher than in group IV (0.14 ± 0.02 nmol/liter). In group III the minimal levels of LPO products (hydroperoxides and malonic dialdehyde) and normalization of red cell membrane resistance were observed, as well as the highest activities of superoxide dismutase and glutathion peroxidase.

In Situ Membrane Resistance Measurements in Polymer Electrolyte Fuel Cells by Fast Auxiliary Current Pulses

A solid‐state current pulse generator for in situ membrane resistance measurements by superimposed square current pulses in polymer electrolyte fuel cells was designed and built. The choice of the measuring technique and of parameters of the instrumentation was based on a critical analysis of the relevant electrochemical and physical processes. The inductance of the current pulse path is very low (≈5 nH), because the last stage of the generator is directly attached to the fuel cell. This low inductance permits the generation of 5 A pulses with extremely fast (decay time ≤5 ns) trailing edges (accompanied by a moderate ringing), which in turn makes it possible to measure the voltage transient induced by the current decay, with gigahertz resolution. The voltage transient is analyzed in a time window of 200 to 700 ns after the end of the pulse. By measurements in this time window, it is possible to separate accurately the ohmic series resistance of the cell (membrane resistance) from the other overpotentials at the electrochemical interfaces. Because the pulse current path is independent of the dc loop, the resistance can be measured independently of the dc value, i.e., at open circuit and under high current density conditions. The instrument was tested, and the results were analyzed for accuracy. Resistances down to 2 mΩ can be measured with an error of <5%. The influence of the pulse length and pulse amplitude on the cell voltage response was also investigated. For cell resistances in the order of few milliohms, a current pulse amplitude of 5 A is the minimum requirement for accurate measurements.

Characterization of two distinct Cl? conductances in fused human respiratory epithelial cells

The present microelectrode experiments on fused respiratory epithelial cells of cystic fibrosis (CF) origin and non-CF origin aim at characterizing the molecular basis of the Cl- conductances regulated by cyclic adenosine monophosphate (cAMP) or respectively Ca2+, as described in the preceding publication. Cell membrane potential (Vm) and resistance (Rm) were recorded as well as their response to substitution of 90% of bath Cl- by isethionate (delta Vm,ISE), by I- (delta Vm,I), or by other halide anions. Fused CF cells had significantly (P < 0.05) higher control Vm values (-18.0 +/- 9.4 mV, +/- SD, n = 68) than fused non-CF cells (-12.5 +/- 6.6 mV, n = 69) and responded to the Ca2+ ionophore A23187 with an increase in the Vm response to Cl- substitution, but did not respond to forskolin. This indicates that CF cells express only the Ca(2+)-stimulated Cl- conductance. Injection of the antibody M3A7 against a fusion protein containing amino acids 1195 to 1480 of the CF gene product into young, forskolin-stimulated or old non-CF cells decreased delta Vm,ISE and delta Vm,I within 15 min to values observed in CF cells. This indicates inhibition of the cAMP-stimulated Cl- conductance and supports the molecular identity of this conductance with the CF gene product. However, the slow onset of inhibition does not allow secondary effects to be excluded and a slight fall in Rm remains unexplained. Stimulation of the Ca(2+)-regulated Cl- conductance was not impaired. Injection of M3A7 into CF cells or of a control antibody in non-CF cells had no effect.(ABSTRACT TRUNCATED AT 250 WORDS)

Influence of Intracellular Renin on Heart Cell Communication

The influence of intracellular renin and angiotensinogen on the control of cell-to-cell communication in heart muscle was investigated in cell pairs isolated from adult rat ventricle. Junctional conductance was measured with two separated voltage-clamp circuits. Intracellular dialysis of renin (0.2 pmol/L) caused a decrease in junctional conductance of 29 +/- 3.8% (+/- SEM, P < .05) in 7 minutes. The effect of renin on junctional conductance seems to be mainly due to the synthesis of Ang II because enalaprilat (10(-9) mol/L) dialyzed into the cell caused an appreciable reduction in the effect of renin. The intracellular administration of renin (0.2 pmol/L) plus angiotensinogen (0.4 pmol/L) produced a faster and stronger fall in junctional conductance (84.3 +/- 1.35%, P < .05), and the effect was greatly reduced by enalaprilat. The effects of both renin and angiotensinogen on junctional conductance were not related to a fall in surface cell membrane resistance or a change in series resistance. The effect of renin on junctional conductance was blocked by intracellular administration of a renin inhibitor (S 2864). Moreover, renin dialyzed into just one cell of the pair induced rectification of the junctional membrane, which was prevented by enalaprilat. The results support the view that an intracrine renin-angiotensin system in the heart regulates intercellular communication.

Electrophysiological effects of progesterone on hepatocytes

The addition of progesterone (1–100 μmol/l) to the extracellular fluid bathing rat hepatocytes led to a rapid and fully reversible depolarization of the cell membrane. The progesterone-induced depolarization was paralleled by a decrease of potassium selectivity and an increase of cell membrane resistance and was abolished in the presence of the potassium channel blocker barium. Accordingly, in whole cell recordings, progesterone led to a decrease of the cell membrane conductance. 17 α-Hydroxyprogesterone and β-estradiol were less effective by a factor of 10, whereas cholesterol, corticosterone and hydrocortisone did not significantly alter the potential difference across the cell membrane. In conclusion, acute administration of progesterone depolarized rat hepatocytes by decreasing the potassium conductance of the cell membrane.