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CB1 and CB2 receptors are G-protein coupled receptors for the endocannabinoids. The receptors were originally discovered in rat brain and shown to mediate the effects of both anandamide and 2-arachidonyl-glycerol. Endocannabinoids, the principal endogenous ligands for the receptors, are arachidonate derivatives that are synthesized in the brain and act peripherally to stimulate neuromuscular transmission, food intake, and other biological actions. Recent data suggest that these effects are mediated in part by the endocannabinoids acting at their receptors in the brain. In the current studies, the protein levels and distribution of the receptors were characterized in specific brain regions and spinal cord. CB1 and CB2 protein levels in rat brain were determined by immunoblotting and densitometry analyses of Western blots. Receptor levels were highest in the limbic cortex, especially in the frontal cortex. Receptor levels were highest in brainstem regions, especially in the caudal spinal cord. In the spinal cord, CB1 levels were highest in the rostral lumbar cord and lowest in the sacral cord. CB2 levels were highest in the sacral cord. Expression levels for both receptors in brain and spinal cord were compared with selected histochemical markers for specific cell populations. The cannabinoid receptors were not detected in neurofibrillary tangles of the Alzheimer’s disease brain nor in Nissl-stained neurons in Huntington’s disease brain. Double-labeling studies with 384a16bd22

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