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Nicotine, but not mecamylamine, enhances antidepressant-like effects of citalopram and reboxetine in the mouse forced swim and tail suspension tests.

作者信息

Andreasen Jesper T, Redrobe John P

机构信息

Department of Affective Disorders, Neurosearch A/S, 93 Pederstrupvej, DK-2750 Ballerup, Denmark.

出版信息

Behav Brain Res. 2009 Jan 30;197(1):150-6. doi: 10.1016/j.bbr.2008.08.016. Epub 2008 Aug 22.


DOI:10.1016/j.bbr.2008.08.016
PMID:18786574
Abstract

Current literature suggests that nicotinic acetylcholine receptors (nAChRs) are involved in major depression. In rodents, antidepressant-like effects of both nicotine and the non-selective nAChR antagonist mecamylamine have been reported. Nicotine increases serotonergic and noradrenergic neuronal activity and facilitates serotonin and noradrenaline release. Thus, we hypothesise that nicotine may enhance the behavioural effects of serotonin (e.g., citalopram) and/or noradrenaline (e.g., reboxetine) reuptake inhibitors. Here, we tested if nicotine enhanced the activity of citalopram or reboxetine in the mouse forced swim test (mFST) and the mouse tail suspension test (mTST). The potential for mecamylamine to augment antidepressant drug action was also investigated. Sub-threshold and threshold doses of citalopram (3 and 10mg/kg) or reboxetine (3, 10 and 20mg/kg) were tested alone and in combination with nicotine (0.3 and 1.0mg/kg) and mecamylamine (1 and 3mg/kg). Locomotor activity experiments were performed to rule out non-specific stimulant effects. Nicotine (1.0mg/kg) enhanced the effect of 10mg/kg citalopram and 20mg/kg reboxetine in the mFST. Similarly, nicotine (1.0mg/kg) enhanced the effect of 3 and 10mg/kg citalopram and 3 and 10mg/kg reboxetine in the mTST. No concomitant locomotor stimulation was observed at the tested dose combinations. Mecamylamine was effective on its own in some tests, but did not augment the effects of citalopram or reboxetine at the doses tested. The data show that nicotine enhances the effects of both serotonin and noradrenaline reuptake inhibitors, possibly reflecting nicotine's facilitating effects on the release of these two neurotransmitters, and indicating that nicotine may enhance antidepressant action.

摘要

相似文献

[1]
Nicotine, but not mecamylamine, enhances antidepressant-like effects of citalopram and reboxetine in the mouse forced swim and tail suspension tests.

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[3]
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[6]
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引用本文的文献

[1]
Ropanicant (SUVN-911), an α4β2 nicotinic acetylcholine receptor antagonist intended for the treatment of depressive disorders: pharmacological, behavioral, and neurochemical characterization.

Psychopharmacology (Berl). 2022-7

[2]
Cholinergic regulation of mood: from basic and clinical studies to emerging therapeutics.

Mol Psychiatry. 2018-8-17

[3]
Nicotine and networks: Potential for enhancement of mood and cognition in late-life depression.

Neurosci Biobehav Rev. 2017-8-30

[4]
Nicotine Significantly Improves Chronic Stress-Induced Impairments of Cognition and Synaptic Plasticity in Mice.

Mol Neurobiol. 2016-7-12

[5]
Behavioral effects of nicotinic antagonist mecamylamine in a rat model of depression: prefrontal cortex level of BDNF protein and monoaminergic neurotransmitters.

Psychopharmacology (Berl). 2015-3

[6]
The catecholaminergic-cholinergic balance hypothesis of bipolar disorder revisited.

Eur J Pharmacol. 2015-4-15

[7]
New Insights into the Mechanisms of Action of Cotinine and its Distinctive Effects from Nicotine.

Neurochem Res. 2015-10

[8]
Molecules and circuits involved in nicotine addiction: The many faces of smoking.

Neuropharmacology. 2013-4-28

[9]
Potential therapeutic uses of mecamylamine and its stereoisomers.

Pharmacol Biochem Behav. 2013-4-18

[10]
The nicotinic acetylcholine receptor as a target for antidepressant drug development.

ScientificWorldJournal. 2012

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