Figure 10. Open- and closed-time distributions of N-methyl-D-aspartate receptors recorded in the outside-out configuration. (A) The open-duration histogram was fitted with the sum of two exponential functions that had fast and slow time constants (ms) and relative areas of tau1= 0.74 ms, a10.26, tau2= 3.6 ms, a2= 0.75. (B) In the presence of 1 micro Meter ketamine, tau1= 0.81 ms, a10.2, tau2= 4.1 ms and a2= 0.81. (C) The closed-duration histograms were best fit with three exponential functions. Under control conditions, tau1= 0.60 ms, a1= 0.6, tau2= 8.11 ms, a2= 0.16, tau3= 39.47 ms, a3= 0.25, whereas tau1= 0.8 ms, a1= 0.6, tau sub 2 = 7.6 ms, a2= 0.09, tau3= 65 ms and a3= 0.34 in the presence of ketamine (D).

Figure 10. Open- and closed-time distributions of N-methyl-D-aspartate receptors recorded in the outside-out configuration. (A) The open-duration histogram was fitted with the sum of two exponential functions that had fast and slow time constants (ms) and relative areas of tau1= 0.74 ms, a10.26, tau2= 3.6 ms, a2= 0.75. (B) In the presence of 1 micro Meter ketamine, tau1= 0.81 ms, a10.2, tau2= 4.1 ms and a2= 0.81. (C) The closed-duration histograms were best fit with three exponential functions. Under control conditions, tau1= 0.60 ms, a1= 0.6, tau2= 8.11 ms, a2= 0.16, tau3= 39.47 ms, a3= 0.25, whereas tau1= 0.8 ms, a1= 0.6, tau sub 2 = 7.6 ms, a2= 0.09, tau3= 65 ms and a3= 0.34 in the presence of ketamine (D).

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