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. Author manuscript; available in PMC: 2009 Jun 1.
Published in final edited form as: Neuropharmacology. 2008 Mar 27;54(8):1153–1165. doi: 10.1016/j.neuropharm.2008.03.009

Table 2.

Kinetic parameters for current simulations

5-HT alone 5-HT + 5-HI

5-HT* 30 μM 30 μM
k1 1 × 107 M−1s−1 1 × 107 M−1s−1
k2 10 s−1 10 s−1
k3 0.01 s−1 0.01 s−1
β 400 s−1 400 s−1
α 1 s−1 1 s−1
kd+ 0.5 s−1 0.04 s−1
kd− 0.01 s−1 0.01 s−1
kDR 0.7 s−1 0.7 s−1
L0 3 × 106 3 × 106

5-HT concentration and rate constants used to generate simulated 5-HT3A receptor-mediated currents (Figure 10). Note that 5-HT concentration applies only to current simulation of response to continuous agonist application (Figure 10B), while current in simulated “deactivation” protocol run in agonist-free condition (Figure 10C).