Involvement of the cerebellar adenosine A1 receptor in cannabinoid-induced motor incoordination in the acute and tolerant state in mice

Cannabinoids are known to impair motor function in humans and laboratory animals. We have demonstrated an accentuation of cannabinoid (CP55,940)-induced motor incoordination in mice by the adenosine A(1) receptor-selective agonist Nb-cyclohexyladenosine (CHA) (4 ng) using an intracerebellar (ICB) microinjection method. This effect was mediated by the A(1) receptor because pre-treatment with ICE 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) (100 ng), an adenosine A(1) receptor selective antagonist, completely abolished the accentuation. Furthermore. ICE pre-treatment with DPCPX (100 ng) before ICE CP55,940 (15 mug) attenuated the motor incoordination suggesting a modulation by an endogenous adenosine A(1) system. ICE microinjection of CHA or DPCPX prior to ICE vehicle had no effect on normal motor coordination. ICB microinjection of dipyridamole (25 mug). an adenosine transport inhibitor, significantly accentuated the motor incoordination by ICE CP55,940 (15 (mug). providing further support for the involvement of endogenous adenosine in the action of CP55,940. Tolerance to the motor incoordinating effect of ICE CP55,940 was demonstrated following 3 days of i.p. CP55,940 (0.1. 1 or 2 mg/kg every 12 or 24 h: total of six or three injections, respectively). Interestingly, animals which exhibited tolerance to ICE CP55,940 also demonstrated tolerance to the accentuating effect of ICE CHA suggesting cross-tolerance between adenosine agonists and cannabinoids. Cross-tolerance was also demonstrated following 3 days of i.p. CHA (0.25 or 1 mg/kg every 24 h; total of three injections) as further evidence of the modulatory role of the cerebellar adenosine system in the acute manifestation of CP55,940-induced motor incoordination. The involvement of cerebellar adenosine and the A(1) receptor in cannabinoid actions is circumstantially supported by previous evidence that CB1 receptors and A(1) receptors are both localized on cerebellar granule cell parallel fiber terminals and basket cell neurons where they serve to inhibit the release of neurotransmitters, (C) 2001 Elsevier Science B.V. All rights reserved.