The aim of this study was to investigate adenosine receptor sites in whole
brain membranes of the saltwater teleost fish, Mugil cephalus, using the Al
receptor selective agonist, [H-3]- N-6-cyclohexyladenosine ([H-3]-CHA). Sp
ecific binding was saturable and reversible. A single class of high-affinit
y binding sites was identify, showing K-d and B-max values of 1.43 +/- 0.26
nM and 69.5 +/- 5.4 fmol/mg protein, respectively. In competition experime
nts, the following adenosine analogues, CHA, (2-[p-(2-carboxyethyl)-phenyle
thylamino]-5'-N-ethylcarboxamidoadenosine) (CGS21680), 5'-(N-cyclopropyl)ca
rboxamidoadenosina (CPCA) and N-6-[2-(3,5-dimethoxyphenyl)-2-(2methylphenyl
)-ethyl]adenosine (DPMA), displaced [H-3]-CHA specifically bound to brain m
embranes, revealing that the high-affinity binding sites have some pharmaco
logical properties of mammalian Al adenosine receptors. Furthermore, our fi
ndings indicate that in captivity chemical pollution determines a decrease
of the K-d value corresponding to a 5-fold increase in affinity, whereas it
does not induce any variation of the receptor density. (C) 1998 Elsevier S
cience Ltd. All rights reserved.