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Research ArticleNEUROPHARMACOLOGY

Cannabinoid CB1 Receptor Agonists Produce Cerebellar Dysfunction in Mice

Sachin Patel and Cecilia J. Hillard
Journal of Pharmacology and Experimental Therapeutics May 2001, 297 (2) 629-637;
Sachin Patel
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Cecilia J. Hillard
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Abstract

The purpose of these studies was to characterize the effects of agonists of the CB1 cannabinoid receptor on cerebellar function in mice. We used two measures specific for cerebellar function: gait analysis and the bar cross test. CB1receptor agonists CP55940, Win 55212-2, Δ9-tetrahydrocannabinol, arachidonylethanolamide (AEA), and two AEA analogs with high affinity for the CB1 receptor (arachidonyl-2-chloroethylamide and arachidonylcyclopropylamide) all produced increases in gait width, a measure of truncal ataxia. All of the CB1 agonists tested significantly increased the number of slips on the bar cross test, which is consistent with motor incoordination. Pretreatment with the CB1 receptor antagonist SR141716 attenuated both the change in gait width and number of slips induced by CP55940 and AEA. Neither cannabidiol nor Win 55212-3 affected these measures, further evidence that this effect is mediated by the CB1 receptor. Pretreatment with the dopamine receptor agonists apomorphine or bromocriptine did not attenuate the diminished performance on the bar cross or the gait abnormality induced by CP55940. These data indicate that the assays used in this study are specific for cerebellar-mediated behavioral deficits, and that these deficits are not mediated by the basal ganglia or cannabinoid-induced alterations in nigrostriatal dopaminergic transmission. Other well known effects of cannabinoids in mice, such as hyperreflexia exemplified by jumping or “popcorn” behavior and postural hypotonia are discussed in relationship to cerebellar dysfunction and a working model of the effects of CB1receptor activation on cerebellar circuitry is presented.

Footnotes

  • Send reprint requests to: Cecilia J. Hillard, Ph.D., Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI 53226. E-mail:chillard{at}mcw.edu

  • This work was supported by National Institutes of Health Grants DA08098 and DA09155.

  • Abbreviations:
    THC
    Δ9-tetrahydrocannabinol
    GABA
    γ-aminobutyric acid
    CB1
    neuronal cannabinoid receptor
    AEA
    N-arachidonylethanolamine
    ACEA
    arachidonyl-2-chloroethylamide
    ACPA
    arachidonyl-cyclopropylamide
    • Received October 2, 2000.
    • Accepted January 13, 2001.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 297 (2)
Journal of Pharmacology and Experimental Therapeutics
Vol. 297, Issue 2
1 May 2001
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Research ArticleNEUROPHARMACOLOGY

Cannabinoid CB1 Receptor Agonists Produce Cerebellar Dysfunction in Mice

Sachin Patel and Cecilia J. Hillard
Journal of Pharmacology and Experimental Therapeutics May 1, 2001, 297 (2) 629-637;

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Research ArticleNEUROPHARMACOLOGY

Cannabinoid CB1 Receptor Agonists Produce Cerebellar Dysfunction in Mice

Sachin Patel and Cecilia J. Hillard
Journal of Pharmacology and Experimental Therapeutics May 1, 2001, 297 (2) 629-637;
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