PHARMACOLOGICAL CHARACTERIZATION OF P-2 PURINOCEPTOR TYPES IN RAT LOCUS-COERULEUS NEURONS

Citation
R. Frohlich et al., PHARMACOLOGICAL CHARACTERIZATION OF P-2 PURINOCEPTOR TYPES IN RAT LOCUS-COERULEUS NEURONS, European journal of pharmacology, 315(3), 1996, pp. 255-261
Citations number
40
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
315
Issue
3
Year of publication
1996
Pages
255 - 261
Database
ISI
SICI code
0014-2999(1996)315:3<255:PCOPPT>2.0.ZU;2-C
Abstract
The frequency of spontaneous action potentials of locus coeruleus neur ons was recorded extracellularly in pontine slices of the rat brain. T he adenosine 5'-triphosphate (ATP) analogues alpha,beta-methylene ATP (alpha,beta-meATP) and 2-methylthio ATP increased the firing rate with a similar potency, while uridine 5'-triphosphate (UTP) was inactive. Diadenosine 5'-pentaphosphate (Ap(5)A), diadenosine 5'-tetraphosphate (Ap(4)A) and diadenosine 5'-triphosphate (Ap(3)A) all facilitated the firing. When equimolar concentrations were compared, Ap(5)A had the la rgest effect followed by Ap(4)A and Ap(3)A. Suramin markedly inhibited responses to alpha,beta-meATP and 2-methylthio ATP; the effect of Ap( 4)A was only slightly depressed by suramin. Pyridoxalphosphate-6-azoph enyl-2,3-disulfonic acid (PPADS) strongly antagonized alpha,beta-meATP , but failed to alter the effects of 2-methylthio ATP and Ap(4)A. Reac tive blue 2 weakly antagonized alpha,beta-meATP and did not interfere with 2-methylthio ATP and Ap(4)A. Moreover, suramin depressed response s to lpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) an d N-methyl-D-aspartic acid (NMDA), but not to substance P. PPADS faile d to affect the AMPA- and NMDA-induced increases in firing. Hence, loc us coeruleus neurons may possess receptors for adenosine nucleotides ( P-2X and P-2Y purinoceptors) and dinucleotides (P-2D purinoceptors); r eceptors for uridine nucleotides (P-2U purinoceptors or pyrimidinocept ors) are probably absent.