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
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.