Effects of acute or repeated paroxetine and fluoxetine treatment on affective behavior in male and female adolescent rats

被引:18
作者
Amodeo, Leslie R. [1 ]
Greenfield, Venuz Y. [1 ]
Humphrey, Danielle E. [1 ]
Varela, Veronica [1 ]
Pipkin, Joseph A. [1 ]
Eaton, Shannon E. [1 ]
Johnson, Jelesa D. [1 ]
Plant, Christopher P. [1 ]
Harmony, Zachary R. [1 ]
Wang, Li [1 ]
Crawford, Cynthia A. [1 ]
机构
[1] Calif State Univ San Bernardino, Dept Psychol, San Bernardino, CA 92407 USA
关键词
Selective serotonin reuptake inhibitors (SSRI); Adolescents; Anhedonia; Antidepressants; Anxiety; MAJOR DEPRESSIVE DISORDER; ELEVATED PLUS-MAZE; ACOUSTIC STARTLE; GENDER-DIFFERENCES; SUICIDAL-BEHAVIOR; ANXIETY DISORDERS; GENE-EXPRESSION; MDMA ECSTASY; SHORT-TERM; SEROTONIN;
D O I
10.1007/s00213-015-4003-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale The SSRI antidepressant fluoxetine is one of the few drugs that is effective at treating depression in adolescent humans. In contrast, the SSRI paroxetine has limited efficacy and is more at risk for inducing suicidal behavior. Objective The purpose of the present study was to more fully characterize the differential actions of paroxetine and fluoxetine. Methods In experiment 1, male and female rats were injected with paroxetine (2.5 or 10 mg/kg), fluoxetine (10 mg/kg), or vehicle for 10 days starting on postnatal day (PD) 35, and affective behaviors were assessed using sucrose preference and elevated plus maze tasks. A separate set of rats were used to examine monoamine levels. In experiment 2, rats were injected with paroxetine (2.5, 5, or 10 mg/kg), fluoxetine (5, 10, or 20 mg/kg), or vehicle during the same time frame as experiment 1, and anxiety-like behaviors were measured using elevated plus maze, light/dark box, and acoustic startle. Results Repeated SSRI treatment failed to alter sucrose preference, although both paroxetine and fluoxetine reduced time spent in the open arms of the elevated plus maze and light compartment of the light/dark box. Paroxetine, but not fluoxetine, enhanced acoustic startle and interfered with habituation. Serotonin turnover was decreased by both acute and repeated fluoxetine treatment but unaltered by paroxetine administration. Discussion These results show that repeated treatment with paroxetine and fluoxetine has dissociable actions in adolescent rats. In particular, paroxetine, but not fluoxetine, increases acoustic startle at low doses and may increase sensitivity to environmental stressors.
引用
收藏
页码:3515 / 3528
页数:14
相关论文
共 75 条
[1]   Lower anxiogenic effects of serotonin agonists are associated with lower activation of amygdala and lateral orbital cortex in adolescent male rats [J].
Arrant, Andrew E. ;
Coburn, Elizabeth ;
Jacobsen, Jacob ;
Kuhn, Cynthia M. .
NEUROPHARMACOLOGY, 2013, 73 :359-367
[2]   INTERACTIONS OF FLUOXETINE WITH METABOLISM OF DOPAMINE AND SEROTONIN IN RAT-BRAIN REGIONS [J].
BALDESSARINI, RJ ;
MARSH, ER ;
KULA, NS .
BRAIN RESEARCH, 1992, 579 (01) :152-156
[3]   Acute anxiogenic-like effects of selective serotonin reuptake inhibitors are attenuated by the benzodiazepine diazepam in BALB/c mice [J].
Birkett, Melissa A. ;
Shinday, Nina M. ;
Kessler, Eileen J. ;
Meyer, Jerrold S. ;
Ritchie, Sarah ;
Rowlett, James K. .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2011, 98 (04) :544-551
[4]   EFFECTS OF SHORT-TERM AND LONG-TERM ADMINISTRATION OF FLUOXETINE ON THE MONOAMINE CONTENT OF RAT-BRAIN [J].
CACCIA, S ;
FRACASSO, C ;
GARATTINI, S ;
GUISO, G ;
SARATI, S .
NEUROPHARMACOLOGY, 1992, 31 (04) :343-347
[5]   Prenatal cocaine exposure potentiates paroxetine-induced desensitization of 5-HT2A receptor function in adult male rat offspring [J].
Chen, Z ;
Waimey, K ;
Van de Kar, LD ;
Carrasco, GA ;
Landry, M ;
Battaglia, G .
NEUROPHARMACOLOGY, 2004, 46 (07) :942-953
[6]   Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis [J].
Cipriani, Andrea ;
Furukawa, Toshiaki A. ;
Salanti, Georgia ;
Geddes, John R. ;
Higgins, Julian P. T. ;
Churchill, Rachel ;
Watanabe, Norio ;
Nakagawa, Atsuo ;
Omori, Ichiro M. ;
McGuire, Hugh ;
Tansella, Michele ;
Barbui, Corrado .
LANCET, 2009, 373 (9665) :746-758
[7]   Anatomic and physiologic substrates of emotion in an animal model [J].
Davis, M .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1998, 15 (05) :378-387
[8]   Effects of chronic treatment with fluvoxamine and paroxetine during adolescence on serotonin-related behavior in adult mate rats [J].
de Jong, TR ;
Snaphaan, LJAE ;
Pattij, T ;
Veening, JG ;
Waldinger, MD ;
Cools, AR ;
Olivier, B .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2006, 16 (01) :39-48
[9]  
deAngelis L, 1996, N-S ARCH PHARMACOL, V354, P379
[10]   Effects of acute fluoxetine, paroxetine and desipramine on rats tested on the elevated plus-maze [J].
Drapier, Dominique ;
Bentue-Ferrer, Daniele ;
Laviolle, Bruno ;
Millet, Bruno ;
Allain, Herve ;
Bourin, Michel ;
Reymann, Jean-Michel .
BEHAVIOURAL BRAIN RESEARCH, 2007, 176 (02) :202-209