Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

Boehm, S.
ATP stimulates sympathetic transmitter release via presynaptic P2X purinoceptors.
J Neurosci. 1999; 19(2):737-746 Doi: 10.1523/JNEUROSCI.19-02-00737.1999
Web of Science PubMed FullText FullText_MUG

 

Leading authors Med Uni Graz
Böhm Stefan
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
ATP is a fast transmitter in sympathetic ganglia and at the sympathoeffector junction. In primary cultures of dissociated rat superior cervical ganglion neurons, ATP elicits noradrenaline release in an entirely Ca2+-dependent manner. Nevertheless, ATP-evoked noradrenaline release was only partially reduced (by approximately 50%) when either Na+ or Ca2+ channels were blocked, which indicates that ATP receptors themselves mediated transmembrane Ca2+ entry. An "axonal" preparation was obtained by removing ganglia from explant cultures, which left a network of neurites behind; immunostaining for axonal and dendritic markers revealed that all of these neurites were axons. In this preparation, ATP raised intraaxonal Ca2+ and triggered noradrenaline release, and these actions were not altered when Ca2+ channels were blocked by Cd2+. Hence, Ca2+-permeable ATP-gated ion channels, i.e., P2X purinoceptors, are located at presynaptic sites and directly mediate Ca2+-dependent transmitter release. These presynaptic P2X receptors displayed a rank order of agonist potency of ATP >/= 2-methylthio-ATP > ATPgammaS > alpha,beta-methylene-ATP approximately beta,gamma-methylene-L-ATP and were blocked by suramin or PPADS. ATP, 2-methylthio-ATP, and ATPgammaS also evoked inward currents measured at neuronal somata, but there these agonists were equipotent. Hence, presynaptic P2X receptors resemble the cloned P2X2 subtype, but they appear to differ from somatodendritic P2X receptors in terms of agonist sensitivity. Suramin reduced depolarization-evoked noradrenaline release by up to 20%, when autoinhibitory mechanisms were inactivated by pertussis toxin. These results indicate that presynaptic P2X purinoceptors mediate a positive, whereas G-protein-coupled P2Y purinoceptors mediate a negative, feedback modulation of sympathetic transmitter release.
Find related publications in this database (using NLM MeSH Indexing)
Adenosine Triphosphate - pharmacology Adenosine Triphosphate - physiology
Animals -
Animals, Newborn -
Cadmium - pharmacology
Calcium - metabolism
Cells, Cultured -
Dendrites - drug effects Dendrites - metabolism
Electrophysiology -
Feedback - physiology
Ganglia, Spinal - cytology Ganglia, Spinal - metabolism
Neurons - metabolism
Neurotransmitter Agents - metabolism
Norepinephrine - metabolism
Presynaptic Terminals - drug effects Presynaptic Terminals - metabolism
Rats -
Rats, Sprague-Dawley -
Receptors, Presynaptic - drug effects Receptors, Presynaptic - metabolism
Receptors, Purinergic P2 - drug effects Receptors, Purinergic P2 - metabolism
Sympathetic Nervous System - cytology Sympathetic Nervous System - drug effects Sympathetic Nervous System - metabolism
Tetrodotoxin - pharmacology

Find related publications in this database (Keywords)
rat superior cervical ganglion neurons
noradrenaline release
ATP
P2X receptors
presynaptic modulation
intracellular Ca2+
© Med Uni GrazImprint