Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Barium Compounds”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 847 records · Page 47Linked to original sources
PubMed1995

Barium inhibits the endothelium-dependent component of flow but not acetylcholine-induced relaxation in isolated rabbit cerebral arteries.

An increase in blood flow can cause vasodilation through a local action on the blood vessel wall. We examined the involvement of potassium channels in the relaxation of segments of the rabbit middle cerebral artery to intraluminal infusion of physiological saline. In segments with intact endothelium, intraluminal flow (20 microliters/min) produced a relaxation of 81.7 +/- 3.0% of pre-flow tone. This relaxation was significantly reduced upon endothelium removal (43%, n = 5) or inhibition of nitric oxide synthase (34%, n = 6). Inhibition of nitric oxide synthase had no effect on the relaxation in endothelium denuded preparations. This suggests that the overall response to flow is a combination of endothelium/nitric oxide dependent and smooth muscle components. Barium chloride (10 and 300 microM) reduced flow-induced relaxations by 30 and 61%, respectively, in intact arteries but had no effect following endothelium removal or nitric oxide synthase inhibition. Micromolar concentrations of barium are thought to block selectively the inward rectifier potassium channel. These concentrations of barium were without effect on the relaxation produced by the endothelium-dependent vasodilator acetylcholine. Blockers of other potassium channels, glibenclamide (10 microM, ATP-sensitive K+ channel), charybdotoxin (100 nN) and tetraethylammonium (0.3 mM, Ca(++)-activated K+ channel) and 4-aminopyridine (1 mM, delayed rectifier K+ channel) did not effect either endothelium-dependent or endothelium-independent flow-induced relaxation. Our results suggest that flow-induced shear stress activates endothelial cell inward rectifier potassium channels leading to increased synthesis/release of nitric oxide.(ABSTRACT TRUNCATED AT 250 WORDS)

Acetylcholine↗
PubMed1995

Proarrhythmia of a class Ic drug: suppression by combination with a drug prolonging repolarization in the dog late after infarction.

Encainide treatment in patients after myocardial infarction is associated with increased risk of sudden cardiac death. This may relate to drug-induced changes in the electrophysiologic milieu, thus predisposing the patient to sustained ventricular tachyarrhythmias. The goals of this study were to first develop a model of class Ic-induced ventricular tachycardia (VT) and then to design treatments to oppose this prodysrhythmic activity. Dogs with time-dependent loss of inducible sustained VT in the antiarrhythmic drug-free state were studied late after infarction. These dogs received a series of three loading and maintenance infusions of O-demethyl encainide (ODME) to achieve concentrations of 60 +/- 31, 136 +/- 46 and 339 +/- 171 ng/ml. Drug maintenance continued until programmed stimulation induced monomorphic sustained VT. When ODME infusion allowed this induction, barium chloride infusions were added. ODME treatment allowed induction of monomorphic sustained VT in 9 of 10 dogs studied. Prodysrhythmic monomorphic VT was significantly related (P < .01) to prolongation of conduction velocity in the peri-infarct zone. ODME modestly increased ventricular refractoriness at some but not all peri-infarct sites. Infusion of barium chloride in the above nine dogs caused their hearts to return to the noninducible state. Prolongation of refractoriness in the peri-infarct zone was correlated to this suppression of prodysrhythmia. Prolongation of conduction velocity in the absence of substantial prolongation of refractoriness may underlie ODME-facilitated induction of monomorphic VT. Prolongation of refractoriness in the peri-infarct zone by combination treatment with barium chloride reversed prodysrhythmic VT in all of the dogs.

Animals↗
PubMed1995

Parenteral copper and selenium supplementation of sheep on legume-grass pastures: biochemical and production responses in lambs to maternal treatment.

Liver and kidney copper (Cu) and selenium (Se) concentrations were studied over a 7-month period after parenteral supplementation using Cu heptonate and barium (Ba) selenate in 44 8-month-old South African (SA) Mutton Merino wethers. Responses in plasma Cu and blood Se concentrations, as well as fecundity were also measured in a breeding flock of SA Mutton Merino ewes for 3 consecutive years. The effect of maternal supplementation with Cu and Se was assessed in terms of biochemical parameters and production responses in 654 lambs produced by these ewes. Parenteral treatments with Cu and Se raised liver and kidney concentrations (P < or = 0.05) for up to 7 months in wethers under conditions where liver Cu and Se respectively declined to concentrations below 30 mg/kg DM and 300 micrograms/kg dry matter (DM) in spring. Plasma Cu concentrations of breeding ewes which received Cu heptonate were increased (P < or = 0.05) by 18% relative to the control group in which concentrations declined to 91 micrograms/dl during late pregnancy. Blood Se concentrations of control ewes exceeded 200 ng/ml, and were unaffected by parenteral Se supplementation. Survival of progeny of Cu heptonate treated ewes tended (P < or = 0.10) to be improved by 13% (0.68 vs 0.60). This tendency was accompanied by generally higher (P < or = 0.10) plasma Cu concentrations of these lambs relative to control lambs at 10 - 20 and 45 - 55 d of age. Lambs of Cu supplemented ewes that died prior to weaning, had higher (P < or = 0.05) liver Cu concentrations than control group contemporaries.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMedDate not supplied

[Use of barium salts of pentoso-1-phosphoric acids in the enzymatic synthesis of ribothymidine and bromvinyldeoxyuridine].

The use of barium salts of ribose 1-phosphate and 2-deoxyribose-1-phosphate as the donors of the carbohydrate part of the required nucleosides in the reaction of enzymatic glycosylation of heterocyclic bases was studied. It was shown that application of indicated substrates in the synthesis of modified nucleosides-ribothymidine and bromovinyldeoxyuridine, catalyzed by the nucleoside phosphorylases from Escherichia coli BM-11, leads to the 96-98% yield of required products even at an equimolar ratio of original pentose 1-phosphates and heterocyclic bases in the reaction mixtures.

Barium Compounds↗
PubMed1995

Regulation of [Na+]i in resting and stimulated submandibular salivary ducts.

In the preceding manuscript (Zhao, H., Xu, X., Diaz, J., and Muallem, S. (1995) J. Biol. Chem. 270, 19599-19605), we described a Kout(+)-dependent H+/HCO3- and Na+ influx pathway in the luminal membrane of salivary duct cells. In the present studies, we further characterized this pathway to show that the Kout(+)-dependent Na+ influx was not mediated by the luminal amiloride-sensitive Na+ channel, the Na+/H+ exchangers, or any electroneutral or conductive Cl(-)-dependent transport pathway. Thus, K+ efflux probably maintained electroneutrality during Na+ influx induced by removal of Kout+. Accordingly, Na+ influx was largely inhibited by 2.5mM external Ba2+. The K+ site of the Kout(+)-dependent Na+ influx showed the selectivity sequence Cs+ > K+ > NH4+ >> > Li+ which is different from that of several known K+ channels. More importantly, Na+ influx is 50% inhibited at about 20 mM Kout+, and significant Na+ influx occurred even at 80 mM Kout+. This is a critical property for the pathway to play a role in Na+ reabsorption and K+ secretion by the duct. The large Na+ influx in resting duct cells is matched by high activity of the ductal Na+ pump which is about 8-fold faster than that of acinar cells. Stimulation of submandibular ducts with various agonists increased [Na+]i in an agonist-specific manner. The parasympathetic agonist epinephrine was more effective than isoproterenol and sympathetic agonist carbachol. The use of various inhibitors of Na+ and K+ transporters suggests that different pathways mediate Na+ influx in stimulated acinar and duct cells of the gland. In duct cells, Na+ influx was inhibited only by extracellular Cs+ and Ba2+. The overall findings support a significant role for the Kout(+)-dependent pathway(s) in Na+ reabsorption and K+ and HCO3- secretion and explain several features of transepithelial electrolyte transport by salivary ducts.

Amiloride↗
PubMed1995

All-trans retinoic acid inhibits fluctuations in intracellular Ca2+ resulting from changes in extracellular Ca2+.

Previous studies have shown that all-trans retinoic acid (RA) preserves fibroblast viability and stimulates their proliferation, in part, by reducing the extracellular Ca2+ requirement (Am J Pathol 1990, 130:1275). Based on this observation, we have in the present study examined the effects of RA on Ca2+ mobilization in human dermal fibroblasts. For these studies we used the Ca(2+)-binding dyes, Fluo-3 and Indo-1. Using fluorescence of Fluo-3-loaded cells or Indo-1-loaded cells as indicators of intracellular free Ca2+, we observed that treatment of the cells with RA did no, by itself, alter the concentration of intracellular Ca2+. Nor did it interfere with the rapid, transient rise in intracellular Ca2+ induced by treatment with ionomycin. However, treatment of the cells with RA prevented re-equilibration of intracellular Ca2+ when the cells were initially equilibrated in low Ca2+ (0.15 mmol/L) culture medium and then switched to high Ca2+ (1.4 mmol/L) medium or when cells were first equilibrated in high Ca2+ medium and then switched to low Ca2+ medium. This effect of RA could be seen within seconds after treatment and the effect was observed 1 day after treatment (longest time point examined). The effect was concentration dependent and concentrations of RA that modulated Ca2+ re-equilibration (0.3 to 3.0 mumol/L) were the same as those that have previously been shown to promote fibroblast survival and growth. A biologically inactive retinoid did not have this effect. Specificity of the response was suggested by the finding that concentrations of RA that modulated Ca2+ movement had no effect on Ba2+ transport. These data suggest that RA prevents re-equilibration of intracellular Ca2+ in human dermal fibroblasts by interfering with Ca2+ movement across the plasma membrane.

Aniline Compounds↗
PubMed1995

Putative pre- and postsynaptic ATP-sensitive potassium channels in the rat substantia nigra in vitro.

Pre- and postsynaptic adenosine 5'-triphosphate-sensitive potassium (ATP-K+) currents were studied using whole-cell recordings from substantia nigra zona compacta "principal" neurons in midbrain slices. The GABAA and GABAB receptor-mediated synaptic potentials were unaffected by the ATP-K+ channel inhibitor glibenclamide (30 microM) or by the opener diazoxide (500 microM), indicating that ATP-K+ channels on GABA-ergic terminals are not active, nor can they be activated pharmacologically, under control conditions. However, application of a glucose-free solution to reduce intracellular ATP levels caused a reduction of the GABAB IPSP in all neurons. This was substantially reversed by the sulfonylurea inhibitor tolbutamide (300 microM) in 50% of the neurons tested. The reduction of the GABAB IPSP was a presynaptic effect since postsynaptic hyperpolarizations induced by the GABAB receptor agonist baclofen (10 microM) were unaffected by glucose-free solutions. Diazoxide (500 microM) induced a slowly developing hyperpolarization or outward current in 64% of principal neurons, which was tolbutamide- (100-300 microM) or glibenclamide- (30 microM) sensitive. In contrast, the GABAB receptor agonist baclofen (30 microM) induced a rapid hyperpolarization or outward current in all neurons tested that was unaffected by tolbutamide (300 microM). Although both the diazoxide-induced current and the baclofen-induced current were inhibited by Ba2+ (300 microM), the currents elicited by diazoxide and baclofen summated. The reversal potential for the diazoxide-induced current was also less negative than that for baclofen, which was close to EK. In the presence of intracellular cesium, diazoxide induced a tolbutamide-sensitive inward current in a proportion of neurons, indicating that it has other actions in addition to activating a potassium current. Our results suggest that functional ATP-K+ channels exist both pre- and postsynaptically in the SN, where they modulate the activity of principal neurons. They are different to the potassium channels activated by the GABAB receptor agonist baclofen.

6-Cyano-7-nitroquinoxaline-2,3-dione↗
PubMed1995

Swelling-induced chloride currents in neuroblastoma cells are calcium dependent.

The effects of osmotic stress on chloride (CI-) currents in the human neuroblastoma cell line CHP-100 were evaluated. Following exposure to hypoosmotic solution, an increase in whole-cell CI- current was observed. This current was blocked by the CI- channel blocker 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB). In cells loaded with the CI- permeability marker 125I, exposure to hypoosmotic solution increased 125I efflux by 197 +/- 14% (n = 41, p < 0.05) over controls. This increase was sensitive to NPPB. Hypoosmotic stress also increased cytosolic calcium levels (Ca2+) in fura-2-loaded cells. Pretreatment with EGTA inhibited the increase in cytosolic Ca2+, 125I efflux, and whole-cell CI- current produced by hypoosmotic solution. Antagonists of N-, L-, and T-type Ca2+ channels did not alter stimulation in 125I efflux or cytosolic Ca2+ levels during osmotic stress. However, omega-conotoxin MVIIC, a P-type Ca2+ channel blocker, inhibited hypoosmotically activated whole-cell CI- currents and increases in cytosolic Ca2+. It is concluded that a Ca(2+)-dependent change in CI- permeability is activated in CHP-100 cells in response to osmotic stress.

Barium Compounds↗
PubMed1995

Potassium currents responsible for inward and outward rectification in rat neostriatal spiny projection neurons.

Many of the nonlinear membrane properties displayed by neostriatal spiny projection neurons are conferred by their voltage-gated potassium (K+) currents, including an inwardly rectifying current (IKir), fast (IAt), and slowly (IAs)-inactivating A-currents, and a slow, noninactivating current. The relative contribution of these K+ currents to the pronounced inward and outward rectification of the current-voltage (I-V) relationship of spiny neurons was investigated in a neostriatal slice preparation. Manipulation of the equilibrium potential for K+ (EK) showed that the voltage dependence of activation of inward rectification was identical to that of IKir. In addition, application of barium (100 microM), which is known to reduce IKir in a time- and voltage-dependent manner, had equivalent effects on inward rectification. Subsequent application of cesium (3 mM) or tetraethylammonium (TEA, 25 mM) blocked inward rectification in a solely voltage-dependent fashion consistent with the action of these blockers on IKir. Administration of 4-aminopyridine (4-AP, 100 microM) at concentrations that selectively depress IAs, reduced outward rectification of spiny neurons at subthreshold membrane potentials. Higher concentrations of 4-AP (2 mM), which block both IAs and IAt, revealed an early transient overshoot in voltage deflections at potentials near spike threshold, but rectification persisted at the end of the responses. The transient overshoot and the residual rectification were eliminated by TEA (25 mM), a blocker of the slow, noninactivating K+ current. Collectively, these results indicate that all three depolarization-activated K+ currents contribute to outward rectification at different times and membrane potentials defined by their voltage dependence of activation and kinetics of inactivation. The spontaneous activity of neostriatal spiny neurons recorded in intact animals is characterized by sustained and limited shifts in membrane potential from relatively hyperpolarized potentials to depolarized potentials near spike threshold. The present data suggest that the hyperpolarized state is determined principally by IKir and the limits on the depolarized state are defined by IAf, IAs, and the noninactivating current. These outward K+ currents also are hypothesized to govern the spike discharge characteristics once the depolarized state has been reached.

4-Aminopyridine↗
PubMedDate not supplied

[Long-term results and perspectives of various radio-endovascular embolization in the treatment of patients with renal parenchyma cancer].

Various types of x-ray endovascular embolization were carried out in 256 patients with renal parenchymatous carcinoma over the period of 1979 to 1991. Iodolipol chemoembolization with dioxadet, a fat-soluble preparation, significantly improved three- and five-year cumulative survival of operable patients to 82.5 and 77%, respectively, vs. embolization without dioxadet, when only 58% of patients survived for three and 51% for five years. In inoperable patients five-year survival after fatty chemoembolization was 24.5% vs. null in the group administered embolization without dioxadet. Ferrochemoembolization appears still more promising.

Antineoplastic Agents↗
PubMed1994

Unusual pharmacology of (+)-tubocurarine with rat neuronal nicotinic acetylcholine receptors containing beta 4 subunits.

We have investigated the functional properties of four rat neuronal nicotinic acetylcholine receptor types expressed in Xenopus oocytes after injection of pairwise combinations of mRNA encoding alpha 2 or alpha 3 receptor subunits with mRNA encoding beta 2 or beta 4 receptor subunits. Current responses evoked by rapid application of cholinergic agonists (acetylcholine, nicotine, or 1,1-dimethyl-4-phenylpiperazinium) were recorded from voltage-clamped oocytes. Substituting BaCl2 for CaCl2 in the external solution increased the apparent Kd values of beta 4 subunit-containing receptors for acetylcholine but decreased the apparent Kd values of beta 2 subunit-containing receptors. Inhibition curves for the cholinergic antagonist (+)-tubocurarine were measured in BaCl2 medium at low agonist concentrations. (+)-Tubocurarine was a competitive antagonist of acetylcholine at neuronal nicotinic acetylcholine receptors that coexpressed the beta 2 subunit; the estimated Kb values were 3.6 microM (alpha 2 beta 2 receptors) and 390 nM (alpha 3 beta 2 receptors). In contrast, (+)-tubocurarine enhanced the peak responses evoked by low acetylcholine concentrations at alpha 2 beta 4 and alpha 3 beta 4 neuronal nicotinic acetylcholine receptors, without being a partial agonist. The maximal increase was observed at 5 microM and 10 microM (+)-tubocurarine for alpha 2 beta 4 and alpha 3 beta 4 receptors, respectively. Higher (+)-tubocurarine concentrations inhibited cholinergic responses, thus yielding a "bell-shaped" concentration-response curve.

Animals↗
PubMed1994

Effects of somatostatin-28 on rat locus coeruleus neurons.

The effects of somatostatin-28 (SS-28) on rat locus coeruleus (LC) neurons were investigated with techniques of brain slice and intracellular recording. SS-28 was applied by micropressure ejection through a micropipette. SS-28 (500 microM, 10 or 20 psi, 1 msec - 5 sec) reversibly decreased the firing rate of all neurons of the locus coeruleus tested. In addition to inhibition of spontaneous firing, larger concentrations of SS-28 also hyperpolarized the neurons of the locus coeruleus and simultaneously decreased the input resistance. At the greatest concentration (20 psi x 5sec) applied, SS-28 produced complete inhibition of firing of all neurons tested; the inhibition was associated with a 11-mV hyperpolarization and decreased input resistance 9 percent. The voltage-current relationship of the resting cell revealed an inward-going rectification that became enhanced after the pressure application of SS-28. The reversal potential for the SS-28-induced hyperpolarization was -116 mV, which is approximately the potassium equilibrium potential. The results also showed that BaCl2 blocked the SS-28-induced hyperpolarization, but apamin did not. We conclude that the inhibitory actions of SS-28 are due to opening the inward-going rectification potassium channels and that SS-28 and somatostatin-14 exert similar electrophysiological actions on LC neurons.

Animals↗
PubMed1994

Voltage-dependent effects of opioid peptides on hippocampal CA3 pyramidal neurons in vitro.

Opioid peptides, and especially the dynorphins, have been localized to several circuits in the CA3 hippocampal region, yet electrophysiological studies often find mixed effects of opiates on the excitability of CA3 neurons. Reasoning that these mixed effects might involve voltage-dependent actions, we tested the effect of several opiates on CA3 pyramidal neurons using single-electrode voltage-clamp recording in a slice preparation of rat hippocampus. In most CA3 neurons, the voltage-dependent K+ current known as the M-current (IM) was uniquely sensitive to the opioid peptides, with the direction of response dependent upon the opiate type and concentration. Thus, an opiate selective for kappa receptors, U-50,488H, significantly augmented IM. The kappa-selective agonists dynorphin A and dynorphin B, which exist in mossy fiber afferents to CA3 pyramidal neurons, also markedly augmented IM at low concentrations (20-100 nM). By contrast, dynorphin A at higher concentrations (1-1.5 microM) often reduced IM. Similarly, several opiates [e.g., D-Ala2,D-Leu5-enkephalin: (DADL), [D-Pen2,5]-enkephalin (DPDPE)] known to act on the delta receptor subtypes reduced the M-current, with partial reversal of this effect by naloxone. Neither the selective mu-receptor agonist [D-Ala2, NMe-Phe4, Gly-ol]-enkephalin (DAMGO) nor the nonopioid fragment of dynorphin, des-Tyr-dynorphin, consistently altered IM. These opiate effects on IM were accompanied by changes in conductance and holding current consistent with their respective effects on IM. Dynorphin A did not measurably affect the Q-current, a conductance known to contribute to inward rectification in hippocampal pyramidal neurons. The opiate effects on IM were not altered by pretreatment with Cs+ (which blocks IQ) or Ca2+ channel blockers. The opposing effects of the dynorphins (both A and B) and DADL on IM were antagonized by naloxone (1-3 microM), and the dynorphin-induced augmentations of IM were usually reversed by the kappa receptor antagonist norbinaltorphimine. These results suggest that the opiates can have opposing effects on the same voltage-dependent K+ channel type (the M channel) in the rat CA3 pyramidal neuron, with the direction of the response depending on which receptor subtype is activated. These data not only help explain the mixed effects of opiates seen in other studies, but also suggest a potential postsynaptic function for the endogenous opiates contained in the CA3 mossy fibers.

3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cycloh↗
PubMed1994

CO2 binding by Baralyme in three different carrier gases.

The absorptive properties of Baralyme and Sodasorb for CO2 in a container were studied by measuring the lifetime T0.5 of the unit, i.e., the time until the exit concentration of CO2 reaches 0.5%. The container size, the inlet gas flow rate, and the inlet CO2 concentration were varied. The experiments were repeated with either He, N2, or SF6 as the inert gas to evaluate the effect of increased gas density due to hyperbaric conditions on scrubber performance. It was found that T0.5 is best described by an exponential function of the type b (ttr)a, where ttr is the transit time of the gas through the container. The exponent a equals about 1.5 and varies relatively little. The constant b, however, is strongly dependent on inert gas density and on CO2 concentration in the inlet gas; it is independent of container size and gas flow rate. In addition, the amount of absorber reaching up to time T0.5 was measured in all conditions. It is strongly dependent on CO2 concentration; however, surprisingly it is nearly independent of inert gas properties. These results are compared with a mathematical model of scrubber behavior that is based on the chemical reaction rate of an imaginary absorber. The model neglects possible effects of CO2 diffusion in the gas phase, of ash formation, and of heat produced by the reaction. Differences between our experimental data and the model are analyzed as a function of these effects. The results give some simple predictive equations for the lifetime and the amount of absorber reacting.

Barium Compounds↗
PubMed1993

Effects of hydrochlorothiazide on contraction and 86Rb efflux in rat aorta.

Hydrochlorothiazide (HCT) (0.1, 0.3 mmol.L-1) inhibited the contraction of rat aortic strips induced by low (< 40 mmol.L-1), not higher concentrations of KCl. HCT (0.3 mmol.L-1) did not inhibit the CaCl2-induced contraction of the aortic strips depolarized with high K+ (KCl 80 mmol.L-1). The inhibitory effect of HCT (0.1 mmol.L-1) on KCl (20 mmol.L-1)-induced contraction was markedly antagonized by BaCl2 (0.1 mmol.L-1) and tetraethylammonium (TEA) (0.3 mmol.L-1), but not by glibenclamide (Gli, 0.01 mmol.L-1). With norepinephrine (NE) or 5-HT as agonists, HCT (0.3 mmol.L-1) also inhibited the contractions of rat aortic strips. In the 2 components of NE-induced contraction, HCT inhibited only the tonic component depending on Ca2+ influx, but not the phasic component elicited by the release of intracellular Ca2+. The inhibitory action of HCT was endothelium-independent. That the HCT (3 mmol.L-1) increased the 86Rb efflux rate coefficient was antagonized by BaCl2 (0.1 mmol.L-1), but not by Gli (0.01 mmol.L-1). The results indicated that the inhibitory effect of HCT on the contraction of rat aorta was attributable to the opening of membrane potassium channels.

Animals↗
PubMed1994

Effects of toosendanin on electric and mechanical properties of guinea pig papillary muscles.

Effects of toosendanin (TS) on the action potentials and contractile force in guinea pig papillary muscles were examined using a standard microelectrode technique. TS concentration-dependently increased the action potential duration at 90% repolarization (APD90) of the fast action potentials. In the presence of a Ikl channel blocker BaCl2, the effects of TS on lengthening the APD90 were completely abolished, thereby suggesting that TS inhibited the inward rectifier K+ current Ikl. The APD and contractile force of aminophylline-induced slow action potentials were potentiated by TS in a concentration-dependent manner. In the presence of BaCl2, both effects of TS were completely abolished. The effect of TS on enhancing contractile force was abolished by the addition of CdCl2, with the prolongation of APD preserved. Thus, TS selectively inhibited the inward rectifier K+ current Ikl with a positive inotropic effect, resulting from a delay in Ca channel inactivation which was secondary to delay in ventricular repolarization.

Action Potentials↗