3. Overview Course introduction Neural Processing: Basic Issues Neural Communication: Basics Vision, Motor Control: Models

4. Neurons cell body dendrites (input structure)  receive inputs from other neurons  perform spatio-temporal integration of inputs  relay them to the cell body axon (output structure)  a fiber that carries messages (spikes) from the cell to dendrites of other neurons

5. postsynaptic neuron science-education.nih.gov

6. Synapse site of communication between two cells formed when an axon of a presynaptic cell “connects” with the dendrites of a postsynaptic cell

7. Synapse axon of presynaptic neuron dendrite of postsynaptic neuron bipolar.about.com/library

8. Synapse a synapse can be excitatory or inhibitory arrival of activity at an excitatory synapse depolarizes the local membrane potential of the postsynaptic cell and makes the cell more prone to firing arrival of activity at an inhibitory synapse hyperpolarizes the local membrane potential of the postsynaptic cell and makes it less prone to firing the greater the synaptic strength, the greater the depolarization or hyperpolarization

10. Neural Communication: 1 Communication within and between cells

11. Transmission of information Information must be transmitted within each neuron and between neurons

12. The Membrane The membrane surrounds the neuron. It is composed of lipid and protein.

13. The Resting Potential There is an electrical charge across the membrane. This is the membrane potential. The resting potential (when the cell is not firing) is a 70mV difference between the inside and the outside. inside outside Resting potential of neuron = -70mV + - + - + - + - + -

14. Artist’s rendition of a typical cell membrane

15. Ions and the Resting Potential Ions are electrically-charged molecules e.g. sodium (Na+), potassium (K+), chloride (Cl-). The resting potential exists because ions are concentrated on different sides of the membrane.  Na + and Cl - outside the cell.  K + and organic anions inside the cell. inside outside Na + Cl - Na + K+K+ Cl - K+K+ Organic anions (-) Na + Organic anions (-)

16. Ions and the Resting Potential Ions are electrically-charged molecules e.g. sodium (Na+), potassium (K+), chloride (Cl-). The resting potential exists because ions are concentrated on different sides of the membrane.  Na + and Cl - outside the cell.  K + and organic anions inside the cell. inside outside Na + Cl - Na + K+K+ Cl - K+K+ Organic anions (-) Na + Organic anions (-)

17. Maintaining the Resting Potential Na+ ions are actively transported (this uses energy) to maintain the resting potential. The sodium-potassium pump (a membrane protein) exchanges three Na + ions for two K + ions. inside outside Na + K+ Na +

19. Excitatory postsynaptic potentials (EPSPs) Opening of ion channels which leads to depolarization makes an action potential more likely, hence “excitatory PSPs”: EPSPs.  Inside of post-synaptic cell becomes less negative.  Na + channels (NB remember the action potential)  Ca 2+. (Also activates structural intracellular changes -> learning.) inside outside Na + Ca 2+ + -

20. Inhibitory postsynaptic potentials (IPSPs) Opening of ion channels which leads to hyperpolarization makes an action potential less likely, hence “inhibitory PSPs”: IPSPs.  Inside of post-synaptic cell becomes more negative.  K + (NB remember termination of the action potential)  Cl - (if already depolarized) K+K+ Cl - + - inside outside

21. Integration of information PSPs are small. An individual EPSP will not produce enough depolarization to trigger an action potential. IPSPs will counteract the effect of EPSPs at the same neuron. Summation means the effect of many coincident IPSPs and EPSPs at one neuron. If there is sufficient depolarization at the axon hillock, an action potential will be triggered. axon hillock

22. Neuronal firing: the action potential The action potential is a rapid depolarization of the membrane. It starts at the axon hillock and passes quickly along the axon. The membrane is quickly repolarized to allow subsequent firing.

23. Before Depolarization

24. Action potentials: Rapid depolarization When partial depolarization reaches the activation threshold, voltage-gated sodium ion channels open. Sodium ions rush in. The membrane potential changes from -70mV to +40mV. Na + - + + -

25. Depolarization

27. Action potentials: Repolarization Sodium ion channels close and become refractory. Depolarization triggers opening of voltage-gated potassium ion channels. K+ ions rush out of the cell, repolarizing and then hyperpolarizing the membrane. K+K+ K+K+ K+K+ Na + + -

28. Repolarization

29. Action potentials: Resuming the Resting Potential Potassium channels close. Repolarization resets sodium ion channels. Ions diffuse away from the area. Sodium-potassium transporter maintains polarization. The membrane is now ready to “fire” again. K+K+ K+K+ K+K+ K+K+ Na + K+ Na+ K+

30. The Action Potential The action potential is “all-or-none”. It is always the same size. Either it is not triggered at all - e.g. too little depolarization, or the membrane is “refractory”; Or it is triggered completely.

31. Course of the Action Potential The action potential begins with a partial depolarization (e.g. from firing of another neuron ) [A]. When the excitation threshold is reached there is a sudden large depolarization [B]. This is followed rapidly by repolarization [C] and a brief hyperpolarization [D]. There is a refractory period immediately after the action potential where no depolarization can occur [E] Membrane potential (mV) [A] [B] [C] [D] excitation threshold Time (msec) -70 +40 0 0 1 2 3 [E][E]

32. Action Potential Local Currents depolarize adjacent channels causing depolarization and opening of adjacent Na channels Question: Why doesn’t the action potential travel backward?

34. Conduction of the action potential. Passive conduction will ensure that adjacent membrane depolarizes, so the action potential “travels” down the axon. But transmission by continuous action potentials is relatively slow and energy-consuming (Na + /K + pump). A faster, more efficient mechanism has evolved: saltatory conduction. Myelination provides saltatory conduction.

35. Myelination Most mammalian axons are myelinated. The myelin sheath is provided by oligodendrocytes and Schwann cells. Myelin is insulating, preventing passage of ions over the membrane.

36. Saltatory Conduction Myelinated regions of axon are electrically insulated. Electrical charge moves along the axon rather than across the membrane. Action potentials occur only at unmyelinated regions: nodes of Ranvier. Node of RanvierMyelin sheath

37. Synaptic transmission Information is transmitted from the presynaptic neuron to the postsynaptic cell. Chemical neurotransmitters cross the synapse, from the terminal to the dendrite or soma. The synapse is very narrow, so transmission is fast.

38. terminal dendritic spine synaptic cleft presynaptic membrane postsynaptic membrane extracellular fluid Structure of the synapse An action potential causes neurotransmitter release from the presynaptic membrane. Neurotransmitters diffuse across the synaptic cleft. They bind to receptors within the postsynaptic membrane, altering the membrane potential.

39. Neurotransmitter release Synaptic vesicles, containing neurotransmitter, congregate at the presynaptic membrane. The action potential causes voltage-gated calcium (Ca 2+ ) channels to open; Ca 2+ ions flood in. vesicles Ca 2+

40. Neurotransmitter release Ca 2+ causes vesicle membrane to fuse with presynaptic membrane. Vesicle contents empty into cleft: exocytosis. Neurotransmitter diffuses across synaptic cleft. Ca 2+

42. Ionotropic receptors (ligand gated) Synaptic activity at ionotropic receptors is fast and brief (milliseconds). Acetylcholine (Ach) works in this way at nicotinic receptors. Neurotransmitter binding changes the receptor’s shape to open an ion channel directly. ACh

44. Ionotropic Receptors

45. Metabotropic Receptors (G-Protein)

47. Postsynaptic potentials Depending on the type of ion channel which opens, the postsynaptic cell membrane becomes either depolarized or hyperpolarized. Ions will tend to follow the concentration gradient from high to low concentration, and the electrostatic gradient towards the opposite charge.

48. Postsynaptic Ion motion

49. Requirements at the synapse For the synapse to work properly, six basic events need to happen: Production of the Neurotransmitters  Synaptic vesicles (SV) Storage of Neurotransmitters  SV Release of Neurotransmitters Binding of Neurotransmitters  Lock and key Generation of a New Action Potential Removal of Neurotransmitters from the Synapse  reuptake

50. Three Nobel Prize Winners on Synaptic Transmission Arvid Carlsson discovered dopamine is a neurotransmitter. Carlsson also found lack of dopamine in the brain of Parkinson patients. Paul Greengard studied in detail how neurotransmitters carry out their work in the neurons. Dopamine activated a certain protein (DARPP-32), which could change the function of many other proteins. Eric Kandel proved that learning and memory processes involve a change of form and function of the synapse, increasing its efficiency. This research was on a certain kind of snail, the Sea Slug (Aplysia). With its relatively low number of 20,000 neurons, this snail is suitable for neuron research.

51. Neuronal firing: the action potential The action potential is a rapid depolarization of the membrane. It starts at the axon hillock and passes quickly along the axon. The membrane is quickly repolarized to allow subsequent firing.

52. Overview Course introduction Neural Processing: Basic Issues Neural Communication: Basics Vision, Motor Control: Models

54. Motor Control: Basics

55. Motor Control Basics Reflex Circuits –Usually Brain-stem, spinal cord based –Interneurons control reflex behavior –Central Pattern Generators Cortical Control

57. Hierarchical Organization of Motor System Primary Motor Cortex and Premotor Areas

58. Primary motor cortex (M1) Foot Hip Trunk Arm Hand Face Tongue Larynx

59. postsynaptic neuron science-education.nih.gov

60. Flexor- Crossed Extensor Reflex (Sheridan 1900) Painful Stimulus Reflex Circuits With Inter-neurons

63. Gaits of the cat: an informal computational model

64. Vision and Action

65. Cortical Motor System Pre-motor cortex Movement planning/sequencing Many projections to M1 But also many projections directly into pyramidal tract Damage => more complex motor coordination deficits Stimulation => more complex mov’t Two distinct somatotopically organized subregions SMA (dorso-medial) May be more involved in internally generated movement Lateral pre-motor May be more involved in externally guided movement

66. Somatotopy of Action Observation Foot Action Hand Action Mouth Action Buccino et al. Eur J Neurosci 2001

67. Rizzolatti et al. 1998 A New Picture

68. Somato-Centered Bimodal RFs in area F4 (Fogassi et al. 1996)

69. The fronto-parietal networks Rizzolatti et al. 1998

70. F5c-PF

71. The F5c-PF circuit Links premotor area F5c and parietal area PF (or 7b). Contains mirror neurons. Mirror neurons discharge when: Subject (a monkey) performs various types of goal- related hand actions and when: Subject observes another individual performing similar kinds of actions

73. Murata et al. J Neurophysiol. 78: 2226-2230, 1997 F5 Canonical Neurons

74. Vision

75. Overview of the Visual System

80. Physiology of Color Vision © Stephen E. Palmer, 2002 Cones cone-shaped less sensitive operate in high light color vision Rods rod-shaped highly sensitive operate at night gray-scale vision Two types of light-sensitive receptors

81. The Microscopic View

84. How They Fire No stimuli: –both fire at base rate Stimuli in center: –ON-center-OFF-surround fires rapidly –OFF-center-ON-surround doesn’t fire Stimuli in surround: –OFF-center-ON-surround fires rapidly –ON-center-OFF-surround doesn’t fire Stimuli in both regions: –both fire slowly

93. Visual Processing

94. http://www.iit.edu/~npr/DrJennifer/visual/retina.html Rods and Cones in the Retina

95. What Rods and Cones Detect Notice how they aren’t distributed evenly, and the rod is more sensitive to shorter wavelengths

96. Center / Surround Strong activation in center, inhibition on surround The effect you get using these center / surround cells is enhanced edges top: the stimuli itself middle: brightness of the stimuli bottom: response of the retina You’ll see this idea get used in Regier’s model http://www-psych.stanford.edu/~lera/psych115s/notes/lecture3/figures1.html

97. How They Fire No stimuli: –both fire at base rate Stimuli in center: –ON-center-OFF-surround fires rapidly –OFF-center-ON-surround doesn’t fire Stimuli in surround: –OFF-center-ON-surround fires rapidly –ON-center-OFF-surround doesn’t fire Stimuli in both regions: –both fire slowly