1. The action potential and cellular excitability (Chapter 9-8 of KS) 1.- The cellular action potential 4.- AP propagation and cable properties of nerve and muscle 2.- Voltage clamp, current clamp 3.- Ion channels and the AP. HH theory. Readings: 1.- HODGKIN AL, HUXLEY AF. A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol. 1952 Aug;117(4):500-44. 2.- Fenwick EM, Marty A, Neher E. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol. 1982 Oct;331:577-97. 3.- Jiang Y, Ruta V, Chen J, Lee A, MacKinnon R. The principle of gating charge movement in a voltage-dependent K+ channel. Nature. 2003 May 1;423(6935):42-8.

2. Keywords: Action potential All-or-none response Threshold, peak, refractory period Overshoot Voltage clamp, current clamp TTX, TEA, Saxitoxin Activation, inactivation, gating currents Ensemble average HH model Space constant, conduction velocity Propagated action potential

3. Problems: 1.- Describe concisely the driving forces of ion flux in excitable cells. What factors determine the direction of ion flux? 2.- Describe the ionic events that underlie the action potential. 3.- Suppose that you have a chromaffin cell under voltage and space clamp conditions. Draw the instantaneous I-V relationship for the K+ conductance. Draw the I-V relationship that you predict results from changing the ionic conditions so that now [K] o = 145 mM and [K] i =5 mM?

4. The three principal cell types to study excitability were the squid giant axon, the node of Ranvier and isolated muscle fibers.

6. Basic properties of action potentials. A, The upper panels show four graded hyperpolarizing stimuli and the Vm responses. The lower panels show four graded depolarizing stimuli and the Vm responses. Note that the two largest stimuli evoke identical action potentials. B, A stimulating electrode injects current at the extreme left of the cell. Four recording electrodes monitor Vm at equidistant sites to the right. If the stimulus is hyperpolarizing, the graded Vm responses decay with distance from the stimulus site. If the stimulus is depolarizing and large enough to evoke an action potential, a full action potential appears at each of the recording sites. However, the action potential arrives at the most distant sites with increasing delay.

7. Nerve and muscle excitability. The curve in A represents the combination of the minimum stimulus intensity and duration that is required to reach threshold and evoke an action potential.

8. Changes in ionic conductance that underlies the action potential. (Data from Hodgkin AL, Huxley AF: A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol (Lond) 117:500-544, 1952.) I strongly suggest that you read this paper! It’s a classic and led to their Nobel prize in physiology and medicine.

9. Basic properties of action potentials. A, The upper panels show four graded hyperpolarizing stimuli and the Vm responses. The lower panels show four graded depolarizing stimuli and the Vm responses. Note that the two largest stimuli evoke identical action potentials. B, A stimulating electrode injects current at the extreme left of the cell. Four recording electrodes monitor Vm at equidistant sites to the right. If the stimulus is hyperpolarizing, the graded Vm responses decay with distance from the stimulus site. If the stimulus is depolarizing and large enough to evoke an action potential, a full action potential appears at each of the recording sites. However, the action potential arrives at the most distant sites with increasing delay.

10. Voltage-clamp and space-clamp of a single nerve fiber

11. Dissection of Na+ and K+ currents by voltage-clamp analysis and pharmacology. A, In a typical voltage-clamp experiment, a sudden hyperpolarization from ­80 to ­140 mV results in a transient capacitative current, but no ionic currents. B, In a voltage- clamp experiment, a sudden depolarization from ­80 to ­20 mV results in a transient capacitative current followed first by an inward ionic current and then by an outward ionic current. C, Blockade of the outward current by tetraethylammonium leaves only the inward current, which is carried by Na+. Conversely, a blockade of the inward current by tetrodotoxin or saxitoxin leaves only the outward current, which is carried by K+.

13. Voltage dependence of ionic currents.

16. Patch clamp methods. (Data from Hamill OP, Marty A, Neher E, Sakmann B, Sigworth FJ: Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch 391:85-100, 1981.)

17. Proteins also have a bonded structure that helps them resist the constant bombardment caused by Brownian motion. Small protein ubiquitinA cartoon representation

18. The Bonded structure is dynamic, as it gets bombarded, the structure bends and bonds break and reform

19. E kT t 0 ~ 10 -12 seconds How often does Brownian motion overcomes the energy barrier and causes an ion channel to open ?

20. Brownian death Too strong Biology E = pico seconds How long do we have to wait for Brownian motion to overcome an energy barrier ? seconds 10 67 years

21. EE Control in Biology is accomplished by reducing energy barriers. Then, unlikely events will occur over short time periods