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)
Study at a glance
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.
Citations in the library
Cited by 4
- Cannabinoids Elicit Antidepressant-Like Behavior and Activate Serotonergic Neurons through the Medial Prefrontal Cortex Journal of Neuroscience October 24, 2007
- The cannabinoid CB 1 receptor and the endocannabinoid anandamide: possible antidepressant targets Expert Opinion on Therapeutic Targets October 14, 2008
- NMDA receptor adjusted co-administration of ecstasy and cannabinoid receptor-1 agonist in the amygdala via stimulation of BDNF/Trk-B/CREB pathway in adult male rats. Brain Research Bulletin April 2017
- The synthetic cannabinoid HU210 induces spatial memory deficits and suppresses hippocampal firing rate in rats. British Journal of Pharmacology July 2007
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