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Voltage concentration dependence

Figure 4. Concentration-dependent ion channel blockade by (R)-JV-methylanatoxinol. The patterns identified as bursts and separated by long (>8 msec) closed intervals are indicated with a bar, the figure was designed to show approximately 2 bursts per trace. The dose-related decrease in mean channel open time resulted from the blockade of the open channel by the (R)-A -methylanatoxinol. The channel amplitude is related to membrane voltage (as was given in Figure 3) by the slope conductance such that 1 pA is equivalent to 30 mV. Continued on next page. Figure 4. Concentration-dependent ion channel blockade by (R)-JV-methylanatoxinol. The patterns identified as bursts and separated by long (>8 msec) closed intervals are indicated with a bar, the figure was designed to show approximately 2 bursts per trace. The dose-related decrease in mean channel open time resulted from the blockade of the open channel by the (R)-A -methylanatoxinol. The channel amplitude is related to membrane voltage (as was given in Figure 3) by the slope conductance such that 1 pA is equivalent to 30 mV. Continued on next page.
A voltmeter joined between the two electrodes of a galvanic cell shows a characteristic voltage, which depends on the concentration and nature of participating reactants. For example, in the Cu-Zn cell, if Cu2+ and Zn2+ are at 1 mol dm-3 (1 M) concentrations and the temperature is 298 K, the voltage measured would be 1.10 V. This voltage is characteristic of the reaction as shown below ... [Pg.636]

Here, Ws is the work function of electrons in the semiconductor, q is the elementary charge (1.6 X 1CT19 C), Qt and Qss are charges located in the oxide and the surface and interface states, respectively, Ere is the potential of the reference electrode, and Xso is the surface-dipole potential of the solution. Because in expression (2) for the flat-band voltage of the EIS system all terms can be considered as constant except for tp (which is analyte concentration dependent), the response of the EIS structure with respect to the electrolyte composition depends on its flat-band voltage shift, which can be accurately determined from the C-V curves. [Pg.219]

The same principles apply for oxygen in solutions as diverse as liquid metals or blood. Because the oxygen is dissolved, the voltage measured depends upon the activity of the oxygen in the solution. For low concentrations, the activity can be approximated to the concentration, hence ... [Pg.284]

Mutanguha EM, Valentine ZH, Symington SB (2010) Pyrethroid inhibition of a human T-type voltage-sensitive calcium channel is structural specific and concentration -dependent. 49th Annual Society of Toxicology, Salt Lake City, UT... [Pg.71]

CONCENTRATION DEPENDENCE OF EQUILIBRIUM CELL VOLTAGE THE GENERAL NERNST EQUATION... [Pg.57]

Equation (5.9) is the general Nemst equation giving the concentration dependence of the equilibrium cell voltage. It will be used in Section 5.4 to derive the equilibrium electrode potential for metal/metal-ion and redox electrodes. [Pg.59]

In order to confirm the possible interaction of ethanol and crocin on NMDA receptors, we also performed whole-cell patch recording with primary cultured hippocampal neurons and measured membrane currents induced by the application of NMDA in a voltage-clamped condition. Application of 100 pM NMDA induced an inward current of 100.2 9.8 pA (n=10) at a holding potential of -60 mV. The NMDA-induced inward current was not affected by 10 pM CNQX (data not shown), but was completely abolished by 30 pM APV, supporting the fact that the response was mediated by NMDA receptors. Ethanol inhibited NMDA-induced currents in a concentration-dependent manner. Crocin (10 pM) had no effect on NMDA-induced currents by itself (data not shown), but attenuated the inhibitory effect of ethanol on NMDA-induced currents. The concentration-effect curve for ethanol was shifted to the right by the presence of crocin [22]. [Pg.319]

Unlike genistein (42), quercetin (29) [308,309] and myricetin (31) [310] enhanced the calcium current carried by L-type calcium channels of the myocytes from rat tail artery. The character of voltage-, concentration-, and frequency-dependent calcium current changes induced by myricetin (31) [310] allowed the conclusion that this flavonoid exerted its effect on L-type calcium channels by binding preferentially to the channels in the inactivated state. Quercetin stimulated L-type calcium channels in rat pituitary GH3 cells in a dose-dependent manner [309]. The EC50 value was about 7 xM, and many facts suggested direct interaction between ion channels and flavonoid. In NG 108-15 neuronal cells quercetin (29) caused inhibition of TTX-sensitive sodium current. [Pg.291]


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See also in sourсe #XX -- [ Pg.540 , Pg.541 , Pg.542 , Pg.543 ]




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