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Neuronal responses to delta 9-tetrahydrocannabinol in the solitary tract nucleus.

T Himmi, M Dallaporta, J Perrin, J C Orsini

European Journal of Pharmacology October 3, 1996 DOI: 10.1016/0014-2999(96)00490-6 (opens in new tab)

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AI-extracted from the abstract
Characteristics Ex vivo extracellular recording study in rat brain slices Peer reviewed
Population Neurons in the subpostremal division of the nucleus tractus solitarii in rat brain slices
Interventions Delta 9-tetrahydrocannabinol Clonidine 1-phenylbiguanide
Topics Cannabis
Key points THC significantly altered spontaneous firing in 54.8% of recorded subpostremal nucleus tractus solitarii neurons. Glucose-responsive (putative nutrition-related) neurons were selectively sensitive to THC, and THC-sensitive neurons were depressed by clonidine, suggesting an adrenergic or noradrenergic identity. The authors propose these catecholaminergic, glucose-responsive neurons might mediate cannabinoid effects on feeding, and that opposite responses to THC and a 5-HT3 agonist may relate to cannabinoid nausea reduction.

Abstract

The effects of delta 9-tetrahydrocannabinol on single-unit activity in the subpostremal division of the nucleus tractus solitarii were investigated by extracellular recording in rat brain slices. The spontaneous firing rate of 54.8% of the recorded neurons was significantly changed after bath applications of delta 9-tetrahydrocannabinol. Putative nutrition-related neurons responding to a moderate increase in glucose concentration were selectively sensitive to delta 9-tetrahydrocannabinol. The delta 9-tetrahydrocannabinol-sensitive neurons were depressed by clonidine and are therefore likely to be adrenergic or noradrenergic. These observations suggest that some catecholaminergic, glucose-responsive neurons in the subpostremal nucleus tractus solitarii might mediate the influence of cannabinoids on feeding behaviour. Furthermore, most delta 9-tetrahydrocannabinol-sensitive neurons in the nucleus tractus solitarii showed opposite responses to delta 9-tetrahydrocannabinol and the 5-HT3 receptor agonist 1-phenylbiguanide, and might therefore be involved in the nausea-reducing effects of cannabinoids.

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