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Auto‐inhibition of rat parallel fibre–Purkinje cell synapses by activity‐dependent adenosine release
Author(s) -
Wall Mark J.,
Dale Nicholas
Publication year - 2007
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2006.126417
Subject(s) - adenosine , extracellular , purkinje cell , adenosine a1 receptor , adenosine receptor , cerebellum , biophysics , neuroscience , chemistry , purinergic signalling , electrophysiology , neuroprotection , microbiology and biotechnology , biology , receptor , biochemistry , agonist
Adenosine is an important signalling molecule involved in a large number of physiological functions. In the brain these processes are as diverse as sleep, memory, locomotion and neuroprotection during episodes of ischaemia and hypoxia. Although the actions of adenosine, through cell surface G‐protein‐coupled receptors, are well characterized, in many cases the sources of adenosine and mechanisms of release have not been defined. Here we demonstrate the activity‐dependent release of adenosine in the cerebellum using a combination of electrophysiology and biosensors. Short trains of electrical stimuli delivered to the molecular layer in vitro , release adenosine via a process that is both TTX and Ca 2+ sensitive. As ATP release cannot be detected, adenosine must either be released directly or rapidly produced by highly localized and efficient extracellular ATP breakdown. Since adenosine release can be modulated by receptors that act on parallel fibre–Purkinje cell synapses, we suggest that the parallel fibres release adenosine. This activity‐dependent adenosine release exerts feedback inhibition of parallel fibre–Purkinje cell transmission. Spike‐mediated adenosine release from parallel fibres will thus powerfully regulate cerebellar circuit output.