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author | bnewbold <bnewbold@robocracy.org> | 2017-01-16 15:45:26 -0800 |
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committer | bnewbold <bnewbold@robocracy.org> | 2017-01-16 15:45:26 -0800 |
commit | c08fefa5e30e680e348acf7817201193b1a9634f (patch) | |
tree | 62c2a706547c7b01b59cc3aef8b8210cadbd63ad /examples/hodgkin_huxley/model.modelica | |
parent | 90d533e03132bab1032adde78fae3c10903d05cc (diff) | |
download | modelthing-c08fefa5e30e680e348acf7817201193b1a9634f.tar.gz modelthing-c08fefa5e30e680e348acf7817201193b1a9634f.zip |
clean up hodgkin-huxley
Diffstat (limited to 'examples/hodgkin_huxley/model.modelica')
-rw-r--r-- | examples/hodgkin_huxley/model.modelica | 46 |
1 files changed, 27 insertions, 19 deletions
diff --git a/examples/hodgkin_huxley/model.modelica b/examples/hodgkin_huxley/model.modelica index 782cb20..7e44547 100644 --- a/examples/hodgkin_huxley/model.modelica +++ b/examples/hodgkin_huxley/model.modelica @@ -1,24 +1,32 @@ model HodgkinHuxley - "Predator-Prey Model" - parameter Real G_Na =120 "conductance"; - parameter Real G_K =36 "conductance"; - parameter Real G_lk =0.3 "conductance"; - parameter Real C =1.0 "membrane capacitance"; + "Model of action potential in squid neurons (1952)" + parameter Real C_m =1.0 "membrane capacitance"; + parameter Real g_Na =120 "conductance"; + parameter Real g_K =36 "conductance"; + parameter Real g_L =0.3 "conductance"; parameter Real V_Na =115 "potential"; parameter Real V_K =-12 "potential"; - parameter Real V_lk =-49.387 "leakage"; - Real n; - Real alpha_n; - Real beta_n; - Real m; - Real alpha_m; - Real beta_m; - Real h; - Real alpha_h; - Real beta_h; + parameter Real V_lk =-49.387 "leak reveral potential"; + parameter Real E_Na =-190 "equilibrium potential"; + parameter Real E_K =-63 "equilibrium potential"; + parameter Real E_lk =-85.613 "equilibrium potential"; + parameter Real n =0.31768 "dimensionless; 0 to 1"; + parameter Real m =0.05293 "dimensionless; 0 to 1"; + parameter Real h =0.59612 "dimensionless; 0 to 1"; + Real V_m "membrane voltage potential"; + Real I =1.0 "membrane current"; + Real alpha_n, alpha_m, alpha_h "rate constants"; + Real beta_n, beta_m, beta_h "rate constants"; equation - C * der(V_m) = - G_Na * (Vm - E_Na) - G_K * (V_m - E_K) - G_lk * (V_m - V_lk); - der(n) = - (alpha_n + beta_n) * n + alpha_n; - der(m) = - (alpha_m + beta_m) * m + alpha_m; - der(h) = - (alpha_h + beta_h) * h + alpha_h; + C_m * der(V_m) = I - g_Na * m^3 * h * (V_m - E_Na) - g_K * n^4 * (V_m - E_K) - G_lk * (V_m - E_lk); + der(n) = alpha_n - n * (alpha_n + beta_n); + der(m) = alpha_m - m * (alpha_m + beta_m); + der(h) = alpha_h - h * (alpha_h + beta_h); + + alpha_n = 0.01 * (V_m + 10) / (e^((V_m + 10)/10) - 1); + alpha_m = 0.1 * (V_m + 25) / (e^((V_m + 25)/10) - 1); + alpha_h = 0.07 * e^(V_m / 20); + beta_n = 0.125 * e^(V_m / 80); + beta_m = 4*e^(V_m/18); + beta_h = 1 / (e^((V_m + 30)/10) + 1); end HodgkinHuxley; |