TY - JOUR T1 - Cannabinoids Cause Central Sympathoexcitation and Bradycardia in Rabbits JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 707 LP - 713 VL - 294 IS - 2 AU - Nathalie Niederhoffer AU - Bela Szabo Y1 - 2000/08/01 UR - http://jpet.aspetjournals.org/content/294/2/707.abstract N2 - Systemically administered cannabinoids elicit marked cardiovascular effects, and the role of the central and the peripheral nervous system in these effects is not clarified. The aim of this study was to characterize the actions of cannabinoids on cardiovascular regulatory centers in conscious rabbits. A catheter for administration of drugs into the cisterna cerebellomedullaris and an electrode for recording renal sympathetic nerve activity were implanted under halothane anesthesia. Experiments were carried out later in conscious animals. Two cannabinoid receptor agonists were injected intracisternally: the aminoalkylindole WIN55212-2 (0.1, 1, and 10 μg kg−1) and the bicyclic Δ9-tetrahydrocannabinol analog CP55940 (0.1, 1, and 10 μg kg−1). WIN55212-2 and CP55940 dose dependently increased renal sympathetic nerve activity and the plasma noradrenaline concentration and also lowered the heart rate. The highest doses of WIN55212-2 and CP55940 increased blood pressure. In contrast, intracisternal injection of WIN55212-3 (0.1, 1, and 10 μg kg−1), an enantiomer of WIN55212-2 with very low affinity for cannabinoid binding sites, had no effects. The CB1cannabinoid receptor antagonist SR141716A (0.5 mg kg−1, i.v.) attenuated the effects of intracisternally administered WIN55212-2 (0.1, 1, and 10 μg kg−1). The results indicate that cannabinoids, acting directly on cardiovascular regulatory centers, elicit sympathoactivation and bradycardia. These effects were likely mediated by CB1 cannabinoid receptors, because they were elicited by two cannabinoid agonists belonging to different chemical classes (WIN55212-2 and CP55940), but not by the inactive enantiomer WIN55212-3, and because they were attenuated by the CB1 cannabinoid receptor antagonist SR141716A. The American Society for Pharmacology and Experimental Therapeutics ER -