Lecture 9 Flashcards
(28 cards)
Role of myelin
membranous wrapping of insulation around axons. Not all neurons are myelinated. Myelination status affects conduction velocity of action potentials
continuous propagation
occurs in unmyelinated axons. Channels open sequentially-depolarisation of one regio then depolarisation of adjacent region and so on. slow
saltatory propagation
occurs in myelinated axons. myelin sheath prevents leak (insulator). Action potentials ‘jump’ between Nodes of Ranvier fast (>100m/s)
Myelin as insulator
myelin blocks leaky channels = decrease ion leakage = less current loss = current travels further before dissipating below threshold levels = action potential regenerated at next Node of Ranvier
axon diameter and conduction velocity
increase axon diameter = decrease resistance (from membrane) = increase conduction velocity
factors influencing conduction velocity
myelination = increase conduction
increase axon diameter = increase conduction
increase temperature = increase conduction
type A axon fibres
myelinated, large diameter (4-20 um), fast conduction (>100m/s)
type B axon fibres
myelinated, smaller diameter (2-4 um), moderate conduction (18m/s)
type c axon fibres
unmyelinated, smaller diameter (<2um), slow conduction
different sizes
not all fibres are fast to compromise between speed and space. increase diameter and myelination increase bulk. type A fibres reserved for essential motor and sensory signalling
electrical synapse
pre and post synaptic membranes ‘locked together’. AP always propagated. Rare (vestibular nuclei, eye)
chemical synapse
cells not directly coupled, use neurotransmitters. AP not always propagated. Most common synapse
neurotransmitter storage in vesicles
vesicles of neurotransmitter stored in pre-synaptic terminals that are released on demand. terminals also contain many mitochondria to fuel metabolism and transport. High mitochondria produce energy to maintain Na+ pump for membrane potential.
small neurotransmitter synthesis
e.g ACh, amines are synthesised and packaged in the synaptic terminals. In synaptic vesicles
Peptide neurotransmitter synthesis
synthesised and packaged in cell body. travels to synaptic terminals as protein synthesis is more efficient in cell body and also, to stop them diffusing all over the cell, they are packaged there and then transported. Less efficient.
Neurotransmitter release
When an action potential reaches the end of the axon Ca2+ moves in allowing neurotransmitter release.Neurotransmitters diffuse across the synaptic cleft to bind with receptors on the post synaptic membrane. Neurotransmitters are broken down by enzymes or undergo re-uptake into the presynaptic neuron.
ligand-gated ion channel
ionotropic, fast response, ion channels open and ions immediately flood in/out of cells
G-protein coupled receptor
Metatropic. slow response, ion channels opening relies on an intermediary 2ndary messenger
Acetylcholine
most common neurotransmitter. Found in CNS, PNS, between neurons and muscle cells. Receptors include nicotinic (ligand-gated) and muscarinic (g-protein)
Cholinergic
Synapses that release ACh
Cholinergic signalling at NMJ
occurs in skeletal muscle fibres. Inactivation gives muscles ability to turn on and off quickly
Cholinergic signalling at NMJ steps
- An arriving action potential depolarises the synaptic knob
- Ca2+ enters the cytoplasm and after a brief delay. ACh is released through the exocytosis of synaptic vesicles.
- ACh binds to Na+ channel receptors on the postsynaptic membrane producing a graded depolarisation
- Depolarisation ends as ACh is broken down into acetate and choline by ACh enzyme.
- Synaptic knob reabsorbs choline from the synaptic cleft and uses it to synthesise new ACh molecules.
noradrenaline
brain and ANS, GPCR, usually excitatory
dopamine
CNS, GPCR, excitatory and inhibitory