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Cannabinoids modulate spontaneous neuronal activity and evoked inhibition of locus coeruleus noradrenergic neurons.

Anna Lisa Muntoni, Giuliano Pillolla, Miriam Melis, Simona Perra, Gian Luigi Gessa, Marco Pistis

European Journal of Neuroscience May 2006 DOI: 10.1111/j.1460-9568.2006.04759.x (opens in new tab)

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AI-extracted from the abstract
Characteristics Preclinical experimental study using single-unit extracellular recordings in anesthetized rats Peer reviewed
Population Anesthetized rats
Interventions WIN55212-2 Delta9-tetrahydrocannabinol SR141716A
Key findings WIN55212-2 and Delta9-tetrahydrocannabinol dose-dependently increased the firing rate of locus coeruleus noradrenergic neurons in anesthetized rats, with WIN55212-2 most efficacious. SR141716A counteracted this stimulation and slightly reduced firing by itself, and WIN55212-2 suppressed inhibition of these cells from the GABAergic nucleus prepositus hypoglossi. The authors suggest these findings implicate noradrenergic pathways in cognitive, attentional, and anxiety-related consequences of Cannabis intake.

Abstract

The noradrenergic pathway arising from the locus coeruleus (LC) is involved in the regulation of attention, arousal, cognitive processes and sleep. These physiological activities are affected by Cannabis exposure - both in humans and laboratory animals. In addition, exogenous cannabinoids, as well as pharmacological and genetic manipulation of the endocannabinoid system, are known to influence emotional states (e.g. anxiety) for which a contributory role of the LC-noradrenergic system has long been postulated. However, whether cannabinoid administration would affect the LC neuronal activity in vivo is still unknown. To this end, single-unit extracellular recordings were performed from LC noradrenergic cells in anaesthetized rats. Intravenous injection of both the synthetic cannabinoid agonist, WIN55212-2, and the main psychoactive principle of Cannabis, Delta9-tetrahydrocannabinol, dose-dependently increased the firing rate of LC noradrenergic neurons, with WIN55212-2 being the most efficacious. Similar results were obtained by the administration of these drugs into a lateral ventricle. Cannabinoid-induced stimulation of LC noradrenergic neuronal activity was counteracted by SR141716A, a cannabinoid receptor antagonist/reverse agonist, which by itself slightly reduced LC discharge rate. Moreover, WIN55212-2 suppressed the inhibition of noradrenergic cells produced by stimulation of the major gamma-aminobutyric acid (GABA)ergic afferent to the LC, the nucleus prepositus hypoglossi. Altogether, these findings suggest the involvement of noradrenergic pathways in some consequences of Cannabis intake (e.g. cognitive and attention deficits, anxiety reactions), as well as a role for cannabinoid receptors in basic brain activities sustaining arousal and emotional states.

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