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Departamento de Bioquimica (J.G., M.T.M.-P.) and
E. U. Optica
(J.P.), Facultad de Veterinaria, Universidad Complutense de Madrid,
28040 Madrid, Spain
A new family of dinucleotide derivatives, diinosine polyphosphates, has
been synthesized through the use of the enzyme 5
adenylic acid
deaminase from Aspergillus sp., starting from the corresponding diadenosine polyphosphates. Functional studies were performed on rat brain synaptic terminals in which a dinucleotide receptor has been described that is specific for adenine dinucleotides. The results demonstrated that diinosine polyphosphates did not behave
as agonists on the diadenosine polyphosphate receptor (also know as
P4 purinoceptor), but they were very efficient as
antagonists in abolishing the Ca2+ responses elicited by
diadenosine pentaphosphate. The IC50 values for diinosine
triphosphate, diinosine tetraphosphate, and diinosine pentaphosphate
were 4.90 ± 0.10 µM, 8.33 ± 0.22 µM, and 4.23 ± 0.12 nM,
respectively. The diinosine polyphosphates also antagonized the ATP
receptors present in synaptic terminals, showing IC50 values of 100.08 ± 5.72 µM for diinosine
triphosphate, 29.51 ± 1.40 µM for diinosine
tetraphosphate and 27.75 ± 1.65 µM for
diinosine pentaphosphate. The antagonistic ability of these diinosine
nucleotides was studied in comparison with other P1 and
P2 purinoceptor antagonists, such as suramin,
pyridoxalphosphate-6-azophenyl-2
,4
-disulfonic acid, and
8-cyclopentyl-1,3-dipropylxanthine. These purinergic antagonists did
not inhibit the response of the P4 purinoceptor; only the
diinosine polyphosphates were able to act as antagonists on the
dinucleotide receptor. Suramin and
pyridoxalphosphate-6-azophenyl-2
,4
-disulfonic acid attenuated the
responses elicited by ATP, as did the diinosine polyphosphate
compounds. The most antagonistic diinosine polyphosphate for the
dinucleotide and ATP receptors was diinosine pentaphosphate, which was
6000 times more selective for the P4 purinoceptor than it
was for the ATP receptor.
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