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Potassium current levels

The long-lasting cardiac action potential is a consequence of such an evolutionary compromise in the development of potassium currents in the heart. Early work on these channels [5] showed that they could be divided into two classes channels that close on depolarization, Iki, and channels that open during depolarization, including the various components of Ik and the transient outward current, it0. At rest, Iki is switched on and holds the resting potential at a very negative level, where the other K+ currents are switched off. On depolarization iki rapidly switches off, while the other currents take time to activate and cause repolarization. This analysis of the potassium channels in cardiac muscle formed the basis of the first biophysically detailed model [6] and remains the basis of all subsequent models [7-9]. [Pg.261]

Similarly, if renal system function is insufficient or nonexistent (failure), reabsorption and excretion of electrolytes may occur without response to the feedback mechanism or consideration of current levels of electrolytes. For example, in renal failure, potassium may be not be excreted and may even be reabsorbed, although the potassium level is already high because there is a failure of the usual feedback mechanism. Table 1-3 is a summary of regulation mechanisms for representative electrolytes. [Pg.36]

Figure 13.10 Voltage clamp data (current vs. time) for (a) Hodgkin-Huxley ( delayed rectifier )-type potassium current and (b) calcium-activated potassium current i . Noisy traces are experimental data, smooth curves are model simulations. Note that has no inactivation, so current remains at higher level, while / contains inactivation, so that current reaches a peak and declines. (Adapted from Buchholtz et ah, 1992.)... Figure 13.10 Voltage clamp data (current vs. time) for (a) Hodgkin-Huxley ( delayed rectifier )-type potassium current and (b) calcium-activated potassium current i . Noisy traces are experimental data, smooth curves are model simulations. Note that has no inactivation, so current remains at higher level, while / contains inactivation, so that current reaches a peak and declines. (Adapted from Buchholtz et ah, 1992.)...
Modern solutions fall mainly into three types (a) the plain cyanide bath which contains typically 20-25 g/1 of copper cyanide, 25-30 g/1 total sodium cyanide (6.2 g/1 free sodium cyanide), and is operated at 21-38 C and 110-160 A/m (b) the Rochelle copper bath to which is added 35-50g/1 of Rochelle salt and which is used at 66 C at up to 645 A/m and (c) the high-efficiency cyanide baths which may contain up to 125 g/1 of copper cyanide, 6-11 g/1 of free sodium or potassium cyanide, 15-30 g/1 of sodium or potassium hydroxide, and are operated at up to 6-9A/dm and 65-90 C. Most bright cyanide copper baths are of the high-efficiency type and, in addition, contain one or more of the many patented brightening and levelling agents available. Periodic reverse (p.r.) current is also sometimes used to produce smoother deposits. [Pg.518]

The quality of the refined metal, and the current efficiency strongly depend on the soluble vanadium in the bath and the quality of the anode feed. As the amount of vanadium in the anode decreases, the current efficiency and the purity of the refined product also decrease. A laboratory preparation of the metal with a purity of better than 99.5%, containing low levels of nitrogen (30-50 ppm) and of oxygen (400-1000 ppm) has been possible. The purity obtainable with potassium chloride-lithium chloride-vanadium dichloride and with sodium chloride-calcium chloride-vanadium dichloride mixtures is better than that obtainable with other molten salt mixtures. The major impurities are iron and chromium. Aluminum also gets dissolved in the melt due to chemical and electrochemical reactions but its concentrations in the electrolyte and in the final product have been found to be quite low. The average current efficiency of the process is about 70%, with a metal recovery of 80 to 85%. [Pg.720]

Other potassium channels also play important roles here. For example, Kv4.3/ KChIP complex conducts the transient outward current, Ito, responsible for the descending phase 1 of the cardiac action potential, whereas Kvl.5 is underlying the ultra rapid delayed rectifying current, IKur, responsible for descending phase 2. Finally, inward rectifier potassium channel (Kir2 family) is responsible for IKl current, which maintains the action potential close to or at the resting level (phase 4). [Pg.391]

Symptomatic or prior-symptomatic fluid retention responds well to treatment with diuretics and salt restriction if LVEF is reduced. This will usually improve current HF symptoms. Especially, an aldosterone antagonist like spironolactone should be added in selected patients with advanced HF symptoms and reduced LVEF with preserved renal function. Potassium has to be normal and should be carefully monitored. Patients with renal dysfunction and with serum creatinine levels >2.5 mg/dl in men and >2.0 mg/dl in women are contraindicated for aldosterone antagonists. [Pg.596]

Preparation of Potassium Hydroxide by the Electrolysis of a Potassium Chloride Solution. Assemble an electrolyzer (see Fig. 130, p. 231). Place small cylinder 2 (8 cm in height and 4 cm in diameter) made from uncalcined clay into 0.5-litre thick-walled beaker 1. Pour a saturated potassium chloride solution into both vessels so that the level of the liquid in them will be the same. Add a few drops of phenolphthalein to the electrolyte. Use carbon rod 4 as the anode and thick iron wire 3 as the cathode. Secure both electrodes with corks in the electrolyzer lid. A d-c source at 10 V is needed for the experiment. After assembling the electrolyzer, switch on the current. What happens in the anode and cathode compartments Write the equations of the reactions. What substances can form in the absence of a diaphragm ... [Pg.188]

It is normal to use additionally a mixture of both benzoic and sorbic acids, added as their sodium and potassium salts respectively. Current UK preservative regulations permit a maximum level of 300 mg/1 of sorbic acid and 150 mg/1 of benzoic acid, both at drinking strength. For this reason it is normal to suggest on the product label a dilution ratio, which can then be used as a factor in calculating the amount of these preservatives to be used. An example is set out in Table 6.7. [Pg.138]


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