ELEC ENG 3BB3: Cellular Bioelectricity - McMaster …ibruce/courses/EE3BB3_2011/EE3BB3... ·...

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ELEC ENG 3BB3: Cellular Bioelectricity Notes for Lecture #12 Thursday, January 27, 2011

Transcript of ELEC ENG 3BB3: Cellular Bioelectricity - McMaster …ibruce/courses/EE3BB3_2011/EE3BB3... ·...

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ELEC ENG 3BB3:

Cellular Bioelectricity

Notes for Lecture #12Thursday, January 27, 2011

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Temperature effects:The temperature of an excitable cell affects:1. the Nernst equilibrium potentials, e.g.,

2. and the rate constants (α

and β) of the gating particles.

In the latter case, a temperature-dependent scaling constant Q

(or Q10

) is utilized.

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Temperature effects (cont.):For example, the rate constants for the HH model were obtained at a temperature of 6.3°C. In order to correctly scale the rate constants for other temperatures T

(in units of °C), the Q

value is

calculated according to:

where:

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Temperature effects (cont.):The differential equations describing the gating particle kinetics then become:

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Active transport:When the membrane is at rest, there is a steady influx of sodium and a steady efflux of potassium.During an action potential these fluxes grow very large (see the sodium and potassium currents in Fig. 5.16 of Plonsey and Barr).Without the action of ion pumps and exchangers, the intra- and extra-cellular concentrations would become identical over time, such that a Donnan equilibrium is reached, i.e., the Nernst equilibrium potentials are identical for all ion species. Note that it is impossible to generate action potentials when at a Donnan equilibrium.

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Active transport (cont.):In an experiment by Hodgkin and Keynes, efflux of radioactively-labelled sodium was linear on a log- linear scale. This indicates a constant pump rate, i.e., the efflux is proportional to the intracellular concentration [24Na+]:

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Application of the metabolic inhibitor DNP greatly reduced sodium efflux, indicating inhibition of an active sodium pump.

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Pump stoichiometry:The sodium pump stoichiometry is:

where the best fit of the experimental data is obtained with x

= 3

and y

= 2.

That is, one mole of ATP

is reduced to ADP + Pi

to drive the process of three moles of sodium ions being pumped out and two moles of potassium being pumped in ⇒ A net efflux of one mole of cations, i.e., a positive transmembrane current Ip

.

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Including pump in steady-state model:The total steady-state transmembrane current is now:

and Eqn. (3.30) becomes:

and Eqn. (3.31) becomes:

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Calcium channels and “other” membrane models:The Hodgkin–Huxley equations only incorporate sodium and potassium channels that have linear conductances when open.However:

some excitable cells have other significant ionic channels, especially calcium channels, and

some channels exhibit non-linear conductances when open.

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Frankenhaeuser-Huxley equations:The Frankenhaeuser–Huxley (F–H) model of the vertebrate node of Ranvier incorporates non-linear instantaneous conductances. For example, the F–H potassium channel has the following current- voltage relationship based on the GHK current equation (5.90):

where the potassium permeability is:

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Frankenhaeuser-Huxley equations (cont.):The potassium activation dynamics described by the activation particle n

are identical to the HH

equations, and the rate constants are:

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Calcium currents:Macroscopic voltage-clamp data for a calcium channel:

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Calcium currents (cont.):The following current-voltage relationship explains the macroscopic behaviour of the calcium channel shown in the previous slide:

This channel exhibits very strong inward rectification for calcium. However, this channel is also slightly permeable to potassium, which somewhat reduces the rectification and greatly reduces the reversal potential of the channel.

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Calcium currents (cont.):

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Luo-Rudy cardiac model:Heart action potentials are two orders of magnitude longer in duration than action potentials in nerve or striated muscle.

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Luo-Rudy cardiac model (cont.):The Luo-Rudy (L-R) cardiac cell model greatly expands on the HH formulation.

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Luo-Rudy cardiac model (cont.):The L-R model includes:

INa

: a fast Na+

current, which includes a slow

inactivation parameter j

in addition to the HH activation and inactivation parameters m3

and

h, respectively.

IK

: a time-dependent potassium current, with an activation parameter X2

and an inactivation

parameter Xi

. Additionally, the maximum potassium conductance is not assumed to be constant but rather depends on [K]o

, and the reversal potential allows for a small sodium current through the potassium channel.

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Luo-Rudy cardiac model (cont.):

IK1

: a time-independent potassium current, which again has a maximum potassium conductance that is not assumed to be constant but rather depends on [K]o

. This channel has an activation parameter that acts instantaneously.

IK

: a potassium plateau current, which is time independent and is insensitive to [K]o

.

ICa

: a calcium current, with instantaneous activation and inactivation parameters d

and f,

respectively. Its I-V

relationship is described by the GHK current equation, and potassium and sodium flux through the channel is considered.

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Families of ion channels:

(Hille 2001)

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Families of ion channels (cont.):

(Hille 2001)

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Families of ion channels (cont.):

(Hille 2001)

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Families of ion channels (cont.):

(Hille 2001)