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Biomedical subjects

R Ochi

Publications and source records attributed to R Ochi.

At least 37 records · Page 2Linked to original sources

Single-channel mechanism of beta-adrenergic enhancement of cardiac L-type calcium current.

The cardiac L-type Ca2+ channel current is enhanced by beta-adrenergic stimulants by phosphorylation mediated by an increase in cyclic AMP. Single-channel studies have revealed that the Ca2+ channels are not always allowed to open at test steps from large negative holding potentials and beta-agonists increase the ratio of current-containing sweeps (availability, Ps). The duration of available (Ts) and unavailable states (TF) are measurable by applying a large number of test pulses. beta-Agonists shorten TF and prolong TS, possibly by enhancing channel phosphorylation by activating cyclic AMP-dependent protein kinase and by inhibiting channel dephosphorylation by phosphorylating phosphatase inhibitor 1, respectively, if the available state reflects the phosphorylated state of the channel. The modulation of the slow gating process, the increase in PS, plays a primary role in increasing the L-type Ca2+ current at moderate increase in sympathetic activity. When a larger increase in cyclic AMP is resulted, moduration of burst-kinetics including mode 2 openings also produced by phosphorylation enhances further the Ca2+ current.

Adrenergic beta-Agonists↗

[Recent progress of research on cardiac ion channels].

The paper summarizes the recent progress of research on the structure, function and regulation of cardiac ion channels. The primary structures of voltage-gated Na and Ca channels are homologous, with identical voltage sensors and homologous pore structure. The voltage-gated channels are modulated by sympathetic and vagal transmitters. beta-Stimulants phosphorylate various channels by activating cyclic AMP-dependent kinase, while acetylcholine antagonizes this phosphorylation. The phosphorylation inhibits the Na current by promoting inactivation, increases the L-type Ca current by increasing the channel availability, increases the delayed rectifying K current and induces Cl current. Acetylcholine induces a K current in nodal and atrial cells via a direct binding of beta gamma subunit of GTP-binding protein (GK) to the K channel.

Acetylcholine↗

Adrenoceptor-mediated effects on calcium channel currents are antagonized by 5'-(N-ethyl)-carboxamido-adenosine in guinea-pig atrial cells.

In guinea-pig atrial myocytes, the effects of the adenosine analogue 5'-(N-ethyl)-carboxamido-adenosine (NECA) in the presence of isoprenaline (ISO) on Ca2+ channel activity were analyzed. Single Ca2+ channel currents were recorded from cell-attached patches by application of several hundred 100 ms depolarizing steps. Under control conditions, burstlike activity of channel openings during some depolarizing steps were followed by variably long periods of quiescence (blank sweeps). During superfusion with ISO (100 nmol/l), ensemble-averaged (mean) current was increased by about 150%. The underlying mechanism was found to be a significant increase in the channel availability, defined as the ratio of current-containing sweeps to the total number of sweeps. In addition, the ISO-induced reduction of blank sweeps was combined with slightly but not significantly higher values of the open probability in the current-containing sweeps. Open time and shut time histograms could be fitted by single and double exponential curves, respectively, which remained rather unaffected in the presence of ISO; accordingly, mean open time and mean shut time of the channel were not significantly changed by ISO. After the addition of NECA (1 mumol/l) in the presence of ISO, the ISO-induced increase in mean current was abolished. This effect of NECA on mean current was due to a reduction of the channel availability and a slight decrease in the open probability. The purinoceptor blocking agent 8-phenyltheophylline (10 mumol/l) antagonized the inhibitory action of NECA on the ISO-induced increase in Ca2+ channel activity.(ABSTRACT TRUNCATED AT 250 WORDS)

Adenosine↗

[Acid-base balance and contraction of the cardiac muscle].

In cardiac muscle, intracelular pH (pHi) is regulated to close to 7.1, both by membrane transport systems (Na-H and Cl-HCO3 exchange) and intracellular H+ buffers. Internal acidosis depresses the contraction, while alkalosis increases it. Internal proton depresses the contraction even without altering the internal concentration of Ca (Cai). The proton blocks the Ca channels. However, as it releases membrane-bound Ca and the influx of Na via Na-H exchange increases Ca influx through Na-Ca exchange, pHi decrease is often accompanied by the Cai increases. The internal proton also affects the uptake and release of sarcoplasmic reticulum, Ca binding to troponin, actomyosin dynamics and variable catalytic processes.

Acid-Base Equilibrium↗

Whole-cell K+ currents in isolated rabbit corneal epithelial cells.

Membrane currents were recorded from enzymatically isolated cells from basal layers of rabbit corneal epithelium by the whole-cell clamp technique. Pipettes contained 140.4 mM KCl and extracellular K+ concentration was varied. The membrane currents on step voltage changes were rectangular currents with some fluctuations. The fluctuations disappeared near the zero-current potential. The reversal potential in normal Tyrode's solution with 5.4 mM K+ was -57.8 +/- 6.2 mV (mean +/- S.D., n = 10). Increasing [K+]o from 5.4 to 140.4 mM shifted the reversal potentials in the positive direction with a slope of 41.0 mV/decade. Concomitant depolarization of the resting potential was observed on increasing [K+]o. The whole-cell currents were blocked by Cs+ or Ba2+. These suggest that the major current component in the corneal epithelial cells in K+.

Animals↗

Modulation of slow gating process of calcium channels by isoprenaline in guinea-pig ventricular cells.

1. The mechanism of enhancement of Ca2+ current by isoprenaline was studied by recording single-channel activity from cell-attached patches on isolated guinea-pig ventricular cells using patch pipettes containing 50 or 100 mM-Ba2+. 2. Isoprenaline (100 nM) increased the amplitude of ensemble average currents by increasing the rate of non-blank sweeps (availability). The current decay during 400 ms steps was significantly slowed by isoprenaline. However, the open probability for the non-blank sweeps elicited by 100 ms steps was only slightly increased by the application of isoprenaline. 3. The durations of the available state (TS) and the unavailable state (TF) were estimated by the number of non-blank and blank sweeps per run, respectively, applying repetitively 100 ms steps at 2 Hz. 4. At large negative holding potentials the distribution of TS was well fitted by an exponential curve, whose time constant was increased from 1.6 to 3.1 sweeps by 100 nM-isoprenaline, while TF distributed approximately single exponentially with a time constant of 2.0 sweeps in control and 1.3 sweeps in the presence of the drug. 5. At depolarized holding potentials a slow voltage-dependent component appeared in the histogram of TF and its time constant was markedly decreased by 100 nM-isoprenaline. 6. The availability-voltage relationship was simulated by the Boltzmann equation with a maximal value of 0.4 in the control. The maximal value was increased to 0.7 and the curve was shifted to a depolarizing direction by 7 mV by 100 nM-isoprenaline. 7. Isoprenaline increased the availability of cardiac Ca2+ channels by increasing the forward rate constant and decreasing the backward rate constant in both voltage-dependent and independent slow state transitions.

Animals↗

Mechanism of adenosine-induced inhibition of calcium current in guinea pig ventricular cells.

The mechanism of adenosine-induced inhibition of Ca2+ currents was studied by recording single-channel Ca2+ currents from cell-attached patches on isolated guinea pig ventricular cells with pipettes containing 50 or 100 mM Ba2+. Numerous 100-msec depolarization steps were applied repetitively at 2 Hz from the resting potential of approximately -70 mV. The addition of 0.1 mM adenosine to the superfusate in the presence of 100 nM isoproterenol depressed the isoproterenol-induced increase in ensemble-averaged current: in peak amplitude, from 258 +/- 105% (mean +/- SD) (p less than 0.01) that of control in the presence of isoproterenol to 153 +/- 41% (n = 7) (p less than 0.05) by the addition of adenosine. In these patches, adenosine did not much affect the open probability in nonblank sweeps (control, 0.10 +/- 0.05; isoproterenol, 0.11 +/- 0.08; adenosine and isoproterenol, 0.08 +/- 0.05), but significantly decreased channel availability, defined as the rate of current-containing sweeps in total sweeps (control, 0.36 +/- 0.17; isoproterenol, 0.69 +/- 0.16 [p less than 0.01]; adenosine and isoproterenol, 0.45 +/- 0.20 [p less than 0.01]). The decrease of channel availability by adenosine was due to the shortening of the duration of the available state and the prolongation of that of the unavailable state. The depressive action of adenosine was suppressed by 0.1 mM theophylline. The single-channel conductance in the presence of 100 mM Ba2+ and Bay K 8644 was 26 pS and was not affected by isoproterenol or adenosine. We conclude that adenosine decreases Ca2+ current under beta-adrenergic stimulation mainly by reducing channel availability.

Adenosine↗

[Experimental study of periodontal tissue regeneration using biodegradable membranes].

This study was designed to investigate the effect on new attachment formation using a biodegradable membrane as a barrier to the regeneration of periodontal tissue. One-wall wide periodontal osseous defects with exposed root surfaces were prepared in three adult mongrel dogs. After surgical debridement of the periodontal defects, 3 types of biodegradable membranes, [Poly(L-lactic acid); (P-L-LA)] membrane, [Poly(lactic acid-co-glycolic acid); (PLGA)] (81: 19 mole%) membrane and PLGA (50: 50 mole%) membrane, were arranged to cover the denuded root surfaces. Specimen blocks were removed 8 weeks postoperatively for histological evaluation of their effect on the regeneration of periodontal tissue. The results were as follows: 1. Gingival regions containing P-L-LA or PLGA (81: 19 mole%) membranes showed delayed wound healing macroscopically. 2. Almost all P-L-LA membranes were present in the experimental sites failing to be resorbed during the 8-week experimental period. PLGA (81: 19 mole%) membranes were also present but showed with some degree of resorption and fragility, while PLGA (50: 50 mole%) membranes were completely resorbed. 3. This showed that the membranes used in this experiment are possible barriers to the generation of new attachment. It is important to make sure keeping the membrane. 4. There was no relationship between osteogenesis and cementogenesis. It seems that osteogenesis was depressed by membrane shrinkage and the gingival pressure which limited "the regenerative space of bone." 5. Moderate resorption was observed on the root surface, and new cementum was formed at the resorbed surface. 6. Ankylosis was observed between the new cementum and bone at the experimental sites. Newly formed cementum was seen on coronal sections of this area.

Animals↗

Voltage-dependent decrease in the availability of single calcium channels by nitrendipine in guinea-pig ventricular cells.

1. The mechanism of Ca2+ channel block by nitrendipine was studied by recording single-channel activity from cell-attached patches on guinea-pig ventricular cells using patch pipettes containing 50 mM-Ba2+. Test depolarization pulses to around 10 mV with a duration of 100 ms were applied repetitively at 2 Hz. 2. The percentage of non-blank sweeps was maximal (about 40%) at a holding potential between -65 and -130 mV and decreased sigmoidally with its depolarization. Nitrendipine shifted the availability-voltage relationship in a hyperpolarizing direction. 3. From the number of consecutive non-blank sweeps and that of blank sweeps, the duration of the available state and that of the unavailable state were estimated. 4. The histogram of the duration of the available state showed a single-exponential distribution. Its mean duration was about 1.5 s and was shortened by nitrendipine. Correspondingly, the decay of the mean current during the depolarization step was accelerated by nitrendipine. 5. In the presence of 100 nM-nitrendipine the histogram of the duration of the unavailable state at large negative holding potentials was simulated as the sum of two exponential components, one with a time constant similar to that in the control and the other with a time constant of 6-7 s. 6. The histogram of the duration of the unavailable state at depolarized holding potentials was simulated by a double-exponential curve also in the control. The duration of the slow component was prolonged by nitrendipine. 7. The prolongation of the unavailable states initiated by drug binding during depolarization steps and maintained during depolarized holding potentials is the mechanism of the blockade. The rate constants of the state transitions between an available state and two unavailable states were estimated.

Action Potentials↗

Maitotoxin-activated single calcium channels in guinea-pig cardiac cells.

1. In order to clarify the mechanism of Ca-dependent excitatory action of maitotoxin (MTX), the most potent marine toxin known, patch-clamp techniques were used to analyse electrophysiological effects of MTX on guinea-pig isolated cardiac myocytes. 2. The whole-cell recordings showed that MTX (0.3 ng ml-1) produced a sustained inward current that was enhanced by adrenaline (2 microM) and abolished by Cd2+ (1 mM). 3. This current was predominantly carried by Ca2+ or Ba2+ and has an almost linear current-voltage relationship. 4. In cell-attached patches, MTX added to the pipette solution activated Ca channels with novel properties. The opening events of these channels occurred as long bursts, and the channel gating showed little voltage-dependence. 5. The unitary conductance was 12 pS in the presence of 50 mM Ba2+. Within a burst, the distribution of opening times was a single exponential with a mean open time of 10.4 ms. 6. The channel described here represents either a new class of voltage-independent Ca channel or an entirely modified form of voltage-gated Ca channel. This channel may account for the mechanism of enhanced Ca2+ influx through the cell membrane induced by MTX, and presumably regulates some ionic movements in myocardial cells.

Animals↗

Beta-adrenergic modulation of the slow gating process of cardiac calcium channels.

Single Ca channel currents were recorded from isolated guinea pig ventricular myocytes in the presence of 50 mM Ba by the patch clamp technique under cell-attached configuration. When a constant short depolarizing pulse was applied repetitively, a single Ca channel opened in bursts during some depolarizing steps but completely failed to open in other steps. The opening probability of Ca channels in current-containing sweeps was little affected by adrenaline. There was a tendency for either failure, or success, in inducing a burst, to occur in clusters. The histogram of the number of successes between two failures showed a single exponential distribution with a time constant of 1-2 sec in controls and 2-4 sec in the presence of adrenaline (2 X 10(-6) M). The mean number of failures between two successes was diminished considerably by adrenaline. In ventricular myocytes adrenaline seems to increase the Ca current mainly by decreasing the rate of the Ca channel for the transition between one mode at which the channel is allowed to open on depolarization and other modes.

Adrenergic beta-Agonists↗

Elementary currents through Ca2+ channels in guinea pig myocytes.

Elementary Ca2+ and Ba2+ currents were recorded from cell-attached membrane patches of ventricular myocytes from adult guinea pig hearts using the improved patch-clamp technique (Hamill et al. 1981). High concentrations of Ba2+ or Ca2+ (50 or 90 mM) were used in the pipettes to increase the signal-to-noise ratio. All data were derived from elementary current analyses in patches containing only one channel. 1) In response to voltage steps, channel openings occurred singly or in bursts of closely spaced unitary current pulses separated by wider shut intervals. During depolarizations of small amplitude from the resting potential, channel openings occurred almost randomly, whereas during larger depolarizations the events were grouped preferentially at the beginning. 2) Channel openings became more probable with increased depolarization; simultaneously, unitary current amplitudes declined in an ohmic manner. Elementary current amplitudes were slightly larger, when 50 mM Ba2+ replaced 50 mM Ca2+ in the pipettes (slope conductances 9 and 10 pS, respectively), but more than doubled, when Ba2+ was increased to 90 mM (slope conductance 18 pS). Clear outward currents through Ca2+ channels were not observed under these conditions. 3) Peak amplitudes of reconstructed mean currents doubled when 50 mM Ba2+ replaced 50 mM Ca2+ and were larger still when 90 mM Ba2+ was used in the pipettes. The current-voltage relations of the reconstructed mean currents showed a positive shift along the voltage axis as Ba2+ was increased or substituted equimolarly by Ca2+. correspondingly, the open state probability-voltage relations (activation curves) showed a parallel shift as Ba2+ was increased, which was less pronounced when Ba2+ was replaced equimolarly by Ca2+. 4) Determination of Ca2+ channel inactivation using 90 mM Ba2+ in the pipettes indicated an overlap with channel activation in a limited voltage range, resulting in a steady-state "window" current. Inactivation can occur without divalent cation influx. 5) Formation of an inside-out patch resulted in a fast rundown of elementary Ca2+ channel currents. 6) Channel openings were often grouped in bursts. The lifetimes of the open state, the bursts, and the closed states were estimated for Ba2+ and Ca2+ as permeating ions. At least two exponentials were needed to fit the histogram of the lifetimes of all closed states. The lifetimes of the individual openings and bursts were mono-exponentially distributed. The kinetics of the Ca+ channel depended on the voltage and the permeating ion. During +30 mV depolarizations, no significant effect on the permeating ion on channel gating could be detected.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗

Inhibition of the slow inward current and the time-dependent outward current of mammalian ventricular muscle by gentamicin.

The aminoglycoside antibiotic, gentamicin (GM), depressed the plateau phase and shortened the duration of the action potential in guinea pig papillary muscle. Its effect on the membrane currents was studied by a single sucrose gap voltage clamp method. The slow inward current (is) was remarkably diminished by GM with little change in its time course, in the voltage-dependency of the steady-state inactivation and activation or in its reversal potential. The maximal amplitude of is, obtained by subtracting the Co2+-resistant current, was reduced to 57% by 0.1 mmol/l GM and almost reduced to zero by 1 mmol/l GM. The efficacy of GM in inhibiting (is) was reduced by increasing the external Ca2+ concentration from 1.8 to 5.4 or 10.8 mmol/l, but not by the application of adrenaline. The time-dependent outward current (ik) was also decreased by GM but only at higher concentrations. It is proposed that the depressant action of GM on is was due to a blockade of slow channels, whereby GM may have dislocated Ca from the binding sites at slow channels on the external surface of the membrane.

Action Potentials↗

Electrical decoupling by Sr action potentials in guinea-pig papillary muscle.

The membrane constants of guinea-pig papillary muscle have been derived by cable analysis, utilizing a single sucrose gap and micro-electrode recordings. In Na-free 20 mmol/l Sr Tyrode, the longitudinal resistance (ri) was increased by 210% from the control value after the passage of ten action potentials (APs) and by 457% after twenty APs but this increase in ri was reversibly abolished by perfusing with Na-containing solutions. ri was not affected by stimulation in Na-containing 20 mmol/l Sr Tyrode. Concomitant with the increase in ri, the conduction velocity of Sr APs was decreased from the control level of 8.6 to 3.1 cm/s after about twenty evoked Sr APs. The twitches elicited in the Na-free Sr Tyrode were large but the relaxation time was comparatively slow (20-30s), whereas those elicited in the Na-containing Sr Tyrode had a large amplitude and relaxation occurred within a few seconds. It is suggested that the increase in ri is due to junctional decoupling, produced either directly, by an intracellular accumulation of Sr2+, or indirectly by an increase in intracellular H+.

Action Potentials↗

Effect of acetylcholine on membrane currents in guinea-pig papillary muscle.

1. The effect of acetylcholine (ACh) on the membrane current components in guinea-pig papillary muscle was studied by the single sucrose gap voltage clamp method. 2. The slow inward current (is) elicited by various depolarizations from the holding potential of -40 mV was evidently diminished by ACh greater than 5 x 10(-7) M. The amplitude of is, estimated as the difference between the peak of is and the current at 150 msec, was reduced to 56.8 +/- 12.9% (mean +/- S.D., n = 34) by 2 x 10(-8) M-ACh when estimated at the membrane potential where the amplitude was maximal. 3. is was suppressed almost completely by 2 mM-Co2+, is obtained by subtracting the current remaining in 2 mM-Co2+ was also diminished to the same extent by 2 x 10(-6) M-Ach with little change in its time course; the degree of decrease was not dependent on the membrane potential. 4. The time-dependent outward current during the depolarizing pulse was also diminished by 2 x 10(-6) M-Ach. Correspondingly, the positive tail current obtained when the membrane was repolarized to the holding potential of -40 mV after various 1 sec depolarizations was reduced in a proportionate manner to 68.6 +/- 7.3% (n = 10). 5. The time-independent inward rectifying outward current was not affected by 2 x 10(-6) M-Ach. 6. Atropine (10(-6) M) restored is and the time-dependent outward current which had been previously depressed by 2 x 10(-6) M-ACh. 7. ACh may decrease tension development by depressing is, thereby preserving the duration of the action potential with relatively little change, since, different from atrial muscle, ACh does not increase the outward current in mammalian ventricular muscle.

Acetylcholine↗

The ionic mechanism of prolongation of action potential duration of cardiac ventricular muscle by anthopleurin-A and its relationship to the inotropic effect.

Anthopleurin-A (AP-A) prolonged the duration of action potential and increased the developed tension of isolated guinea-pig and canine ventricular muscle. Voltage clamp experiments by using a single sucrose gap method were performed to investigate the ionic mechanism of the prolongation of the action potential in guinea-pig ventricular muscle. The prolongation of action potential by AP-A was accompanied by a decreased net outward current in a quasi-steady state. The slow inward current and the delayed potassium current were not changed by AP-A. The prolongation of action potential by AP-A was reversed by tetrodotoxin, thus it was concluded that AP-A induced tetrodotoxin-sensitive inward current which lasted long after the initial fast Na current. Modification of the AP-A-induced positive inotropic effect was also examined by using the canine blood-perfused ventricular muscle and was consistent with the above electrophysiological effects; tetrodotoxin, not nifedipine, suppressed percent changes produced by AP-A and also that by veratrine.

Action Potentials↗