Psych 181: Dr. Anagnostaras

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1 Psych 181: Dr. Anagnostaras Lecture 5 Synaptic Transmission Introduction to synaptic transmission Synapses (Gk., to clasp or join) Site of action of most psychoactive drugs 6.5 1

2 Synapses Know basic terminology: Soma Axon Dendrite Synaptic vesicles Synaptic cleft Postsynaptic Presynaptic Glia 6.2 Synapses Dendrites & spines 3.10 Synapses Types of cell-cell junctions Tight junctions membranes fused Gap junctions close juxtaposition (2-4 nm) electrical synapse Chemical synapses synaptic cleft (20-30 nm) polarized 2

3 Multiple types of synapses Vesicle varieties Multiple types of synapses Multiple patterns of connectivity Axodendritic Dendrodendritic Axoaxonic Axosomatic etc. 6.1 Steps in synaptic transmission Synthesis Transport Storage Release Inactivation 3

4 Release Excitation-secretion coupling Depolarization Open voltage-gated Ca ++ channels Ca ++ influx Bind to Ca ++ -calmodulin protein kinase Phosphorylation of synapsin I Movement of vesicles to release site Exocytosis Diffusion Exocytosis 6.17 Inactivation Reuptake transporters Enzymatic degradation metabolism excretion cycling

5 Sample question In which of the following are the events listed in the correct temporal order (i.e., the temporal order associated with excitation-secretion coupling)? (a) Depolarization > calcium influx > phosphorylation of synapsin > activation of calcium-calmodulin protein kinase > exocytosis (b) Depolarization > calcium influx > activation of calcium-calmodulin protein kinase > phosphorylation of synapsin > reuptake > exocytosis (c) Exocytosis > phosphorylation of synapsin > calcium influx > activation of calcium-calmodulin protein kinase > depolarization > calcium influx (d) Enzymatic degradation > exocytosis > activation of calciumcalmodulin protein kinase > phosphorylation of synapsin > calcium influx > depolarization (e) Depolarization > calcium influx > activation of calcium-calmodulin protein kinase > phosphorylation of synapsin > exocytosis > enzymatic degradation Neurotransmitters Two major types: Classical small water soluble molecules with amine formed from dietary precursors Neuropeptides protein synthesis Neurotransmitters Phenylethylamines DA, NE, E, tyramine, etc. Indoleamines 5-HT, tryptamine, melatonin, etc. Cholinergics Amino acids Neuropeptides Enkephalins, substance P, neurotensin, etc. Nonpeptide hormones 5

6 Receptors 6.5 Receptors Classification GABA By Location Postsynaptic ACH DA Receptors Classification GABA By Location Postsynaptic Autoreceptors ACH DA 6

7 Autoreceptors Presynaptic Somatodendritic Terminal GABA Release-modulating Synthesis-modulating Impulse-modulating ACH DA Receptors Classification: By Transduction Mechanism Outside cell Inside cell Membrane Effector Drug, transmitter or hormone Receptor Transduction Receptor Superfamilies 1. Ligand-gated channels binding site coupled to ion channel transmitter (or drug) gates the channel ionotropic receptors 7

8 Receptor Superfamilies 1. Ligand-gated channels 2. G protein-coupled receptor coupled to G protein G protein activates effector metabotropic receptors Ligand-gated channels Ligand opens channel Ions flow down conc. gradient Rapid Rapidly reversible 5.9 Ligand-gated channels Examples: Nicotinic acetylcholine receptor coupled to sodium channel drugs: nicotine, curare GABA A receptor coupled to chloride channel drugs: sedativehypnotics 8

9 G protein-coupled receptors G protein-coupled receptors Large family all with 7 membranespanning regions Receptor coupled to G protein, and G protein stimulates effector Slower than ion-coupled 6.22 G protein-coupled receptors Two classes: G protein directly coupled to ion channel effector is ion channel G protein coupled to 2nd messenger system effector is enzyme that promotes formation of intracellular second messenger 9

10 G protein-coupled receptors Examples: Cholinergic muscarinic GABA B 5-HT Opioid Dopamine Norepinephrine Second messengers Are many: Calcium cgmp Phosphoinositides (IP 3, diacylglycerol) camp camp (cyclic adenosine 3,5- monophosphate) camp

11 Protein phosphorylation Changes structure/function of protein Consequence depends on function of protein ion channel proteins enzymes cytoskeletal proteins vesicular proteins receptors gene regulatory proteins Second messengers and protein kinases have many targets from P. Greengard, Science, 2001 from P. Greengard, Science,

12 Gene regulation Second messengers can alter gene regulation: Activate transcription factors Regulate transcription enhance or supress If enhance - new gene products Gene regulation Two phases of gene activation: Initial phase induction of immediate-early genes (IEGs) (e.g., cfos, c-jun, zif-268, etc.) protein products initiate 2nd phase Second phase induction of late-onset genes products that alter cellular function Gene regulation by camp R= regulatory subunit C= catalytic subunit Transcription factor: CREB (camp response element binding protein) CREB stimulates gene transcription (eg., IEGs)

13 Convergence on CREB kinases Multiple signalling pathways can alter gene transcription via same transcription factor 2nd messengers 6.35 Summary Drugs of abuse are very effective in inducing IRGs c-fos mrna Expression Saline Amphetamine Home Novel 13

14 Sites of drug action 6.2 Sample question Which of the following classes of drug action would have in common the effect of increasing synaptic transmission? (a) facilitation of release; block reuptake; inhibition of synthesis (b) blockade of the release modulating autoreceptor; facilitation of release; receptor agonist (c) receptor agonist; receptor antagonist; synthesis inhibition (d) reuptake blocker; facilitation of release; receptor antagonist (e) blocks metabolism; block reuptake; inhibits synthesis 14

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