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Biochem Biophys Res Commun ; 295(4): 929-36, 2002 Jul 26.
Article in English | MEDLINE | ID: mdl-12127984

ABSTRACT

We have investigated the effect of hypoxia on the excitatory synaptic transmission in the substantia gelatinosa neurons using perforated-patch-clamp configuration. Brief periods of hypoxia induced a depression in the evoked excitatory postsynaptic current (eEPSC) amplitude. The hypoxia-induced depression of eEPSC was not observed in the presence of theophylline, a nonselective adenosine receptor antagonist, and DPCPX, a selective adenosine receptor A1 antagonist. Application of adenosine (100 microM) also depressed eEPSC in a similar way as with hypoxia. This adenosine-induced depression of eEPSC was inhibited by DPCPX. Hypoxia and exogenous adenosine decreased the frequency of the spontaneous excitatory postsynaptic current (sEPSC) but not the amplitude of sEPSC and increased the paired-pulse ratio. From these results, it is suggested that acute hypoxia depresses the excitatory synaptic transmission by activating the presynaptic adenosine A1 receptor.


Subject(s)
Hypoxia/metabolism , Neurons/metabolism , Substantia Gelatinosa/metabolism , Theophylline/pharmacology , Adenosine/metabolism , Adenosine/pharmacology , Analgesics/pharmacology , Animals , Electrophysiology , Patch-Clamp Techniques , Phosphodiesterase Inhibitors/pharmacology , Rats , Rats, Sprague-Dawley , Receptors, Purinergic P1/metabolism , Synapses/metabolism , Time Factors
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