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CB1 cannabinoid receptor ligands augment the antidepressant‐like activity of biometals (magnesium and zinc) in the behavioural tests
Objective During the last few decades, endocannabinoid system has emerged as a novel possible target for antidepressant treatment. Although the medical literature provides information on the mood‐changing effects of CB1 ligands, little is known about the possible interaction between the simultaneous...
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Published in: | Journal of pharmacy and pharmacology 2018-04, Vol.70 (4), p.566-575 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective
During the last few decades, endocannabinoid system has emerged as a novel possible target for antidepressant treatment. Although the medical literature provides information on the mood‐changing effects of CB1 ligands, little is known about the possible interaction between the simultaneous activation or inhibition of the CB1 receptor and administration of other agents that possess antidepressant potential. The main goal of our study was to evaluate the influence of the CB1 cannabinoid receptor ligands (oleamide – an endogenous agonist and AM251 – an inverse agonist/antagonist) on the antidepressant‐like activity of biometals (i.e. magnesium and zinc).
Methods
The forced swim test and the tail suspension test in mice were used to determine the antidepressant‐like activity.
Key findings
Concomitant intraperitoneal administration of per se inactive doses of oleamide (5 mg/kg) or AM251 (0.25 mg/kg) and the tested biometals (i.e. magnesium, 10 mg/kg or zinc, 5 mg/kg) shortened the immobility time of animals in the forced swim test and the tail suspension test. The observed effect was not associated with an increase in spontaneous locomotor activity of mice.
Conclusions
The simultaneous modulation of the cannabinoid system and supplementation of magnesium or zinc produce at least additive antidepressant‐like effect. |
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ISSN: | 0022-3573 2042-7158 |
DOI: | 10.1111/jphp.12880 |