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Printable Handouts
Navigable Slide Index
- Introduction
- The role of ATP as a neurotransmitter
- Autonomic neuromuscular junction
- Innervation of mast cells
- Taenia coli
- Taenia coli – IJP’s
- Innervation of the gut: classical vs. revised view
- Searching for the neurotransmitter
- Criteria for establishing a neurotransmitter
- Research implicating ATP as the neurotransmitter
- Myenteric neurones - quinacrine
- NANC excitatory nerves in the bladder
- ATP mimics nerve stimulation
- Ectonucleotidases
- Bladder responses to nerve stimulation with ATP
- ATP is released by inhibitory nerves in the gut
- Purinergic nerve
- A busy bee called ATP
- ATP release during enteric nerve stimulation
- Some cells may release more than one transmitter
- Vas deferens: sympathetic nerve stimulation
- Vas deferens: EJP’s
- Guinea pig vas deferens: spritz 20ms
- Isolated rabbit saphenous artery response to ATP
- Rat tail artery (sympathetic cotransmission)
- Schematic of sympathetic cotransmission
- Junctional neuromodulation by NPY
- Cotransmitter hypothesis true in many nerve types
- Sympathetic cotransmission in hypertensive rats
- Purinergic component increase in pathologies
- Sensory - motor nerves
- ATP colocalised with NO in neurons in the gut
- NANC inhibitory nerves in the gut
- Skeletal neuromuscular junction
- Distinguishing two types of purinergic receptor
- Purinergic transmission
- Loewi-inspired experiments (1966)
- P1 receptor cloned, characterized & categorized
- Distinguishing two types of P2 purinergic receptors
- Initial cloning of P2 receptors
- Molecular structures of some of the P receptors
- Molecular structure of the P2X receptor
- Crystal structure of P2X4 receptor
- Neurotransmitters and their receptors
- P2X receptor subtypes
- Heteromultimer coexpression studies
- P2Y receptor subtypes
- P2X receptors found in very primitive creatures
- Fast synaptic purinergic transmission discovered
- Purinergic sympathetic transmission
- Intrinsic neurons in bladder and heart
- Non-cholinergic fast excitatory synaptic pathways
- Single channel activity with ATP
- Slow excitatory synaptic pathways
- Submucosal neurons
- Summary of purinergic signalling in the gut
- P2X3 in the CNS
- Cortical neuron activity mediated by P2X4-R's
- P2XR-mediated activity (cortex & hippocampus)
- P2XR and regulation of synaptic plasticity in CNS
- Vesicular nucleotide transporter (VNUT)
- ATP is likely released by all CNS nerves
- Expression of P2X receptors in sensory neurons
- ATP action in sensory nerve terminals
- P2X3 receptor differential expression in neurons
- ATP initiates pain on sensory endings: hypothesis
- Purinergic mechano-sensory transduction
- Distension induced discharges (P2X3 KO vs. WT)
- Double role for P2X3 (different threshold receptors)
- Distension response antagonized by TNP-ATP
- Human ureter ATP release
- Effect of ATP in sensory nerve activity
- Distension of rat colo-rectum: ATP release
- P2X3 immunoreactivity (subepithelial nerve plexus)
- Purinergic sensory pathways in gut: hypothesis
- P2X3 in sensory nerves: tooth pulp & odontoblasts
- Innervation of neuroepithelial bodies
- Purinergic signalling in acupuncture: hypothesis
- Rat tongue: sensory nerve preparation
- Rat colitis model (using TNBS enema)
- ATP in normal vs. inflamed colo-rectum
- P2X3 colocalisation with CGRP fibers in colitis
- P2X3 have a role in peristalsis and IBD
- Selective P2X antagonists with drug-like properties
- Number of papers published on P2 (1972-2012)
- Purinergic Signalling journal acknowledgements
- Further acknowledgments
Topics Covered
- Purinergic transmission and the role of ATP as a neurotransmitter
- Neuromuscular junctions and neuromodulation
- Synaptic transmission in peripheral and central nervous systems
- NANC excitatory and inhibitory nerves
- Sympathetic nerve stimulation and co-transmission
- Purinergic pathologies
- Sensory-motor nerves
- P1 and P2 purinergic receptors
- Fast and slow excitatory synaptic pathways
- Expression of P2X and P2Y receptor subtypes and their properties
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Talk Citation
Burnstock, G. (2014, April 6). Purinoceptors and fast purinergic transmission at neuromuscular junctions and synapses [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/FLOJ1646.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Geoff Burnstock has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Purinoceptors and fast purinergic transmission at neuromuscular junctions and synapses
A selection of talks on Neurology
Transcript
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0:00
I'm Geoff Burnstock.
I was brought up in a boxing family,
but then I finished a Ph.D. at
King's College and University
College.
I then did a post-doc at Mill Hill
with Feldberg and then in Oxford
with Edith Bulbring.
I went to America on a
Rockefeller Fellowship
and then took a
lectureship in Australia
because I liked the
Australians more than anybody
else when I was in Oxford.
And after 16 years, I became head
of the Department of Zoology there.
I returned to London
to UCL to take over
the chair of anatomy and
embryology from J Z Young.
And then when I stepped down
from the headship in '97,
they set up me up with the research
at the Autonomic Neuroscience
Research Institute at
the Royal Free Hospital.
And I am passionate for
research even at my age of 85.
0:60
The purinergic signaling
hypothesis-- that
is ATP is an extracellular signaling
molecule-- was proposed in 1972.
But it was not widely accepted
until the early 1990s when receptors
for ATP were cloned
and characterized.
It is now a field that
is expanding rapidly
in many different directions in both
neuronal and non-neuronal tissues.
In this talk, I will
focus on the role of ATP
as a neurotransmitter at both
autonomic neuromuscular junctions
and in the synaptic
transmission both in
the peripheral and
central nervous systems.
So I'll begin with the discovery
of purinergic neuromuscular
transmission,
but first I need to explain that
autonomic neurotransmission is
at non-synaptic sites.
Varicose fibers involve release
of transmitter en passage,
so they are a transient
contact with effector cells
to form neuromuscular injunctions.
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