Effects of adenosine receptor agonists and antagonists on audiogenic seizure-sensible DBA/2 mice

We have studied the effects of selective and non-selective adenosine recept or agonists and antagonists in audiopenic-seizure-sensitive DBA/2 mice, an animal model of generalized reflex epilepsy. With the exception of the aden osine A(3) receptor agonist, N-6-(3-iodobenzyl)-5'-N-methylcarboxamidoadeno sine (IB-MECA), all the agonists studied prevented the development of audio genic seizures in a dose-dependent manner. The ED50 values against the clon ic phase of the audiogenic seizures were low, that is: 0.06 mg/kg, i.p., fo r the adenosine A(1) receptor agonist, 2-chloro-N-6-cyclopentyladenosine (C CPA), 0.02 and 0.03 mg/kg, i.p., for the adenosine A(2A) receptor agonists, 2-(4-(2-carboxyethyl)-phenylamino)-5'-N-ethylcarboxamidoadenosine (CGS 216 80) and 2-hexynyl-5'-N-ethyl-carboxamidoadenosine (2-HE-NECA), and 0.7 mg/k g, i.p., for the adenosine A(1)/A(3) receptor agonist, N-6-2-(4-aminophenyl )ethyladenosine (APNEA). Conversely, the non-selective agonist, N-ethyl-car boxamidoadenosine (NECA), was highly potent, the ED50 being 0.0005 mg/kg, i .p. In the absence of auditory stimulation, the adenosine receptor antagoni sts increased the incidence of both clonic and tonic seizures in DBA/2 mice . The ED50 values were: for caffeine, 207.5 mg/kg, i.p., for the adenosine A(1) receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), 327.8 mg/kg i.p., for the adenosine A(2A) receptor antagonists, 3,7-dimethyl-1-p ropylxanthine (DPMX), 86.7 mg/kg i.p., for the (E,18%-Z,82%)7-methyl-8-(3,4 -dimethoxystyryl)-1,3-dipropylxanthine (KF 17837), 69.1 mg/kg i.p., and 5-a mino-7-(2-phenylethyl)-2-(2-furyl)-pyrazolo-(4,3-c)1,2,4-triaxzolo(1,5-c)-p yrimidine (SCH 58261), 321.8 mg/kg i.p. The rank order of convulsant potenc y in our epileptic model, following intracerebroventricular administration, was DPCPX > DMPX > 1,3,7-trimethyl-8-(3-chlorostyryl)xanthine (CSC)> KF 17 837 > Caffeine > SCH 58261 > 5-amino-9-chloro-2-(2-furyl)-1,2,4-triazolo(1, 5-c)quinazoline (CGS 15943). Following a subconvulsant audiogenic stimulus of 83 dB, all adenosine receptor antagonists induced both tonic and clonic seizures. The ED50 values for such proconvulsant effects were: for caffeine 0.04 mg/kg, i.p., for the adenosine A(1) receptor antagonist, DPCPX, 5.84 mg/kg, i.p., for the adenosine A(2A) receptor antagonists, DMPX, 0.02 mg/kg , i.p., CGS 15943, 0.29 mg/kg i.p., KF 17837, 0.57 mg/kg, i.p., CSC 0.12 mg /kg, i.p. and SCH 58261 0.07 mg/kg, i.p., respectively. These data suggest that stimulation of adenosine A(1) and A(2A) receptors is involved in the s uppression of seizures. (C) 1999 Elsevier Science B.V. All rights reserved.