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Chronic treatment with caffeine and its withdrawal modify the antidepressant-like activity of selective serotonin reuptake inhibitors in the forced swim and tail suspension tests in mice. Effects on Comt, Slc6a15 and Adora1 gene expression.
- Source :
-
Toxicology and applied pharmacology [Toxicol Appl Pharmacol] 2017 Dec 15; Vol. 337, pp. 95-103. Date of Electronic Publication: 2017 Nov 09. - Publication Year :
- 2017
-
Abstract
- Recent preclinical and clinical data suggest that low dose of caffeine enhances the effects of common antidepressants. Here we investigated the effects of chronic administration of caffeine (5mg/kg, twice daily for 14days) and its withdrawal on day 15th on the activity of per se ineffective doses of fluoxetine (5mg/kg) and escitalopram (2mg/kg) given on day 15th. We found decreased immobility time in the forced swim and tail suspension tests in mice in which caffeine was administered simultaneously with antidepressants on day 15th following a 14-day caffeine treatment and no alterations in the spontaneous locomotor activity. A decrease in the level of escitalopram and an increase in the level of caffeine in serum were observed after concomitant administration of these compounds, while the joint administration of caffeine and fluoxetine was not associated with changes in their levels in serum or brain. Caffeine withdrawal caused a decrease in Adora1 mRNA level in the cerebral cortex (Cx). Administration of escitalopram or fluoxetine followed by caffeine withdrawal caused an increase in this gene expression, whereas administration of escitalopram, but not fluoxetine, on day 15th together with caffeine caused a decrease in Adora1 mRNA level in the Cx. Furthermore, antidepressant-like activity observed after joint administration of the tested drugs with caffeine was associated with decreased Slc6a15 mRNA level in the Cx. The results show that withdrawal of caffeine after its chronic intake may change activity of antidepressants with concomitant alterations within monoamine, adenosine and glutamate systems.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Amino Acid Transport Systems, Neutral genetics
Amino Acid Transport Systems, Neutral metabolism
Animals
Antidepressive Agents, Second-Generation pharmacokinetics
Caffeine pharmacokinetics
Central Nervous System Stimulants pharmacokinetics
Cerebral Cortex drug effects
Cerebral Cortex metabolism
Citalopram pharmacokinetics
Depression genetics
Depression metabolism
Depression psychology
Disease Models, Animal
Drug Administration Schedule
Fluoxetine pharmacokinetics
Male
Mice
RNA, Messenger genetics
RNA, Messenger metabolism
Receptor, Adenosine A1 genetics
Receptor, Adenosine A1 metabolism
Selective Serotonin Reuptake Inhibitors pharmacokinetics
Time Factors
Antidepressive Agents, Second-Generation administration & dosage
Behavior, Animal drug effects
Caffeine administration & dosage
Central Nervous System Stimulants administration & dosage
Citalopram administration & dosage
Depression drug therapy
Fluoxetine administration & dosage
Hindlimb Suspension
Motor Activity drug effects
Selective Serotonin Reuptake Inhibitors administration & dosage
Swimming
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0333
- Volume :
- 337
- Database :
- MEDLINE
- Journal :
- Toxicology and applied pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 29107002
- Full Text :
- https://doi.org/10.1016/j.taap.2017.10.020