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Receptors & Transmitters DENT/OBHS 131 Neuroscience 2009.

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Presentation on theme: "Receptors & Transmitters DENT/OBHS 131 Neuroscience 2009."— Presentation transcript:

1 Receptors & Transmitters DENT/OBHS 131 Neuroscience 2009

2 Learning Objectives Know what criteria are used to define a neurotransmitter Recall the major different categories of transmitters Know the names of the principle neurotransmitters in the CNS (including: glutamate, GABA, acetylcholine, norepinephrine, serotonin and dopamine) Compare and contrast small the synthesis and action of small molecular weight and peptide transmitters Identify the brainstem nuclei associated with the biogenic amine transmitters Compare and contrast ligand-gated and G-protein coupled receptors

3 You are a neurotransmitter if you…. are produced within a neuron, and are present in the presynaptic terminal are released during depolarization (action potential-dependent manner) act on receptors to cause a biological effect have a mechanism of termination

4 More strictly, to be a transmitter.. a particular substance, when applied to the post- synaptic cell in quantities equal to that released by the pre-synaptic cell, produces the same post-synaptic response as does a pre-synaptic action potential

5 Learning Objective #2 & 3 Recall the major different categories of transmitters Know the names of the principle neurotransmitters in the CNS (including: glutamate, GABA, acetylcholine, norepinephrine, serotonin and dopamine)

6 The keys Small molecular weight: Acetylcholine (ACh) Amino acids: Glutamate, GABA, glycine Biogenic amines: Catecholamines: Dopamine, Norepinephrine (Epinephrine) Indolamines: Serotonin (5-HT), Histamine Nucleotides ATP, Adenosine

7 More keys... Neuropeptides Unconventional (what?) (yes, I want to be a transmitter but I’m not going to tell you exactly how)

8 Learning Objective #4 Compare and contrast small the synthesis and action of small molecular weight and peptide transmitters

9 Small Molecules

10 Neuropeptides

11 Back to transmission…..

12 Where are the transmitters?

13 Amino Acids Glutamate everywhere in CNS major excitatory transmitter in CNS most projection neurons in cortex use glutamate GABA everywhere in CNS major inhibitory transmitter in CNS found (not always) in local circuit neurons (interneurons) Glycine major inhibitory transmitter in brainstem and spinal cord

14 L -Glutamate

15 Synthesis and Degradation: GABA Kreb’s Cycle  -ketoglutarate glutamate GABA (release & uptake) The GABA Shunt glutamic acid decarboxylase (GAD) succinic semialdehyde succinic acid

16 Distribution: Acetylcholine 5% Ventral horn spinal motor neurons (PNS) to skeletal muscle Brain stem motor nuclei Striatum (local) Septal nuclei to hippocampus Nucleus basalis to cortex, amygdala, thalamus PNS - autonomic Cognition - memory Motor (striatum)

17 Learning Objective #5 Identify the brainstem nuclei associated with the biogenic amine transmitters

18 Locus coeruleus to everywhere attention, alertness circadian rhythms memory formation mood Distribution: Norepinephrine (NE) 1%

19 Rostral raphe nuclei to nearly all regions of the brain Caudal raphe nuclei to spinal cord mood sleep / wake cycles pain modulation Distribution: serotonin (5-HT) 1%

20 Substantia nigra to striatum Ventral tegmentum to: Amygdala, nucleus Accumbens & prefrontal cortex Arcuate nucleus to median eminence of hypothalamus movement motivation sex hormones Distribution: Dopamine 3%

21 DopamineTyrosine L-DOPA tyrosine hydroxylase dopa decarboxylase HO CH 2 -CH-NH 3 COOH + HO CH 2 -CH-NH 3 COOH OHOH + HO OHOH CH 2 -CH-NH 3 H + (these steps occur within the cytoplasm) Synthesis: Dopamine

22 dopamine-  -hydroxylase (DBH) Dopamine Norepinephrine HO OHOH CH 2 -CH-NH 3 H + HO OHOH CH-CH 2 -NH 3 OH + (these steps occur within the synaptic vesicle) Synthesis: Norepinephrine

23 Transmitter termination Clinical relevance: Neurotransmitter transporters: MAOs: disease (epilepsy, ALS, Parkinson’s) drug abuse (cocaine, amphetamine) treatment (depression, OCD)

24 Learning Objective #6 Compare and contrast ligand-gated and G-protein coupled receptors

25 Classes of Neurotransmitter Receptors Ionotropic Receptors Ligand-gated ion channels Fast synaptic transmission (1 ms) Are closed (impermeable to ions) in absence of transmitter Neurotransmitter binding opens receptor (direct) Metabotropic Receptors G-protein coupled receptors (GPCRs) Slow onset and longer duration of effects (100 ms & longer) Ligand binding activates GTP-binding proteins (indirect)

26 Ligand-gated / G-protein Coupled

27 Transmitter and receptor pairing Both ionotropic and metabotropic receptors: glutamate acetylcholine GABA 5HT (serotonin) Just ionotropic: glycine Just metabotropic: other biogenic amines (DA & NE)

28 Each subunit has multiple membrane spanning domains Glutamate: 3 All others: 4 Multimers Glutamate: 4 All others: 5 Glutamate Receptor SubunitsAll Other Receptor Subunits Ligand-gated ion channels

29 Allosteric “other” binding sites

30 Congenital myasthenia Single channel lifetime shortened open slower & close faster (Wang et al, 1999)

31 Structure of G-protein Coupled Receptors Single polypeptide with 7 TM domains (no subunits) 2nd & 3rd cytoplasmic loops plus part of the intracellular tail bind to appropriate G protein

32 Agonist binding causes conformational change that activates the G-protein cholera toxin pertussis toxin

33 Direct modulation of Ca 2+ channels

34 Modulation Through 2 nd Messenger Pathway

35 “Retro” transmitters NO endocannanbinoids

36 Definitions… Agonist = activates (opens) the receptor when it binds Antagonist = binds to the receptor and inhibits its function different types Allosteric modulators = act at a site different from agonist Desensitization = response decrease although the agonist is still present or repetitively applied Ligand gated ion channels: Gating = opening / closing of the channel Kinetics = how long processes take Affinity = tightness of the agonist binding Efficacy = how readily the channel opens


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