The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats

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The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats. / Sass, Amdi; Wörtwein, Gitta.

In: Behavioural Brain Research, Vol. 228, No. 1, 2012, p. 169-75.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sass, A & Wörtwein, G 2012, 'The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats', Behavioural Brain Research, vol. 228, no. 1, pp. 169-75. https://doi.org/10.1016/j.bbr.2011.12.006

APA

Sass, A., & Wörtwein, G. (2012). The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats. Behavioural Brain Research, 228(1), 169-75. https://doi.org/10.1016/j.bbr.2011.12.006

Vancouver

Sass A, Wörtwein G. The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats. Behavioural Brain Research. 2012;228(1):169-75. https://doi.org/10.1016/j.bbr.2011.12.006

Author

Sass, Amdi ; Wörtwein, Gitta. / The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats. In: Behavioural Brain Research. 2012 ; Vol. 228, No. 1. pp. 169-75.

Bibtex

@article{8b33fbd2c77c4f2bbfe98f4d099d7b19,
title = "The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats",
abstract = "Selective serotonin re-uptake inhibitors are increasingly used for the treatment of adolescents with behavioural disorders. However, the effect of this class of drugs during this sensitive period of brain development has not been extensively investigated. In this study we examine the effect of subchronic treatment with the selective serotonin re-uptake inhibitor, fluoxetine (10mg/kg/day, i.p.) throughout adolescence (postnatal day 28-60) on learning and memory in the rat. Learning and memory were assessed at two time points: during adolescence, while the animals were being treated with fluoxetine and in young adulthood, 40 days after the termination of fluoxetine treatment. Fluoxetine treated rats were compared to a saline injected control group with respect to spatial navigation in the water maze, object recognition and object-in-place recognition memory. Additionally open field behaviour was examined. In adolescent rats fluoxetine treatment impaired water-maze probe trial performance and object recognition at intertrial intervals of 15 and 60min, while leaving object-in-place recognition memory unaffected. In the open field the fluoxetine treated animals displayed reduced exploratory activity and higher levels of anxiety. Training the animals to a new platform position in young adulthood showed that the rats that had been treated with fluoxetine during adolescence were significantly slower to acquire this new spatial information. Adolescent fluoxetine treatment had no effect on cell proliferation in dorsal dentate gyrus and subgranular zone in young adulthood. This calls for further studies examining the long-term effects of this class of antidepressants on adolescent brain development and behaviour.",
author = "Amdi Sass and Gitta W{\"o}rtwein",
note = "Copyright {\textcopyright} 2011 Elsevier B.V. All rights reserved.",
year = "2012",
doi = "10.1016/j.bbr.2011.12.006",
language = "English",
volume = "228",
pages = "169--75",
journal = "Behavioural Brain Research",
issn = "0166-4328",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - The effect of subchronic fluoxetine treatment on learning and memory in adolescent rats

AU - Sass, Amdi

AU - Wörtwein, Gitta

N1 - Copyright © 2011 Elsevier B.V. All rights reserved.

PY - 2012

Y1 - 2012

N2 - Selective serotonin re-uptake inhibitors are increasingly used for the treatment of adolescents with behavioural disorders. However, the effect of this class of drugs during this sensitive period of brain development has not been extensively investigated. In this study we examine the effect of subchronic treatment with the selective serotonin re-uptake inhibitor, fluoxetine (10mg/kg/day, i.p.) throughout adolescence (postnatal day 28-60) on learning and memory in the rat. Learning and memory were assessed at two time points: during adolescence, while the animals were being treated with fluoxetine and in young adulthood, 40 days after the termination of fluoxetine treatment. Fluoxetine treated rats were compared to a saline injected control group with respect to spatial navigation in the water maze, object recognition and object-in-place recognition memory. Additionally open field behaviour was examined. In adolescent rats fluoxetine treatment impaired water-maze probe trial performance and object recognition at intertrial intervals of 15 and 60min, while leaving object-in-place recognition memory unaffected. In the open field the fluoxetine treated animals displayed reduced exploratory activity and higher levels of anxiety. Training the animals to a new platform position in young adulthood showed that the rats that had been treated with fluoxetine during adolescence were significantly slower to acquire this new spatial information. Adolescent fluoxetine treatment had no effect on cell proliferation in dorsal dentate gyrus and subgranular zone in young adulthood. This calls for further studies examining the long-term effects of this class of antidepressants on adolescent brain development and behaviour.

AB - Selective serotonin re-uptake inhibitors are increasingly used for the treatment of adolescents with behavioural disorders. However, the effect of this class of drugs during this sensitive period of brain development has not been extensively investigated. In this study we examine the effect of subchronic treatment with the selective serotonin re-uptake inhibitor, fluoxetine (10mg/kg/day, i.p.) throughout adolescence (postnatal day 28-60) on learning and memory in the rat. Learning and memory were assessed at two time points: during adolescence, while the animals were being treated with fluoxetine and in young adulthood, 40 days after the termination of fluoxetine treatment. Fluoxetine treated rats were compared to a saline injected control group with respect to spatial navigation in the water maze, object recognition and object-in-place recognition memory. Additionally open field behaviour was examined. In adolescent rats fluoxetine treatment impaired water-maze probe trial performance and object recognition at intertrial intervals of 15 and 60min, while leaving object-in-place recognition memory unaffected. In the open field the fluoxetine treated animals displayed reduced exploratory activity and higher levels of anxiety. Training the animals to a new platform position in young adulthood showed that the rats that had been treated with fluoxetine during adolescence were significantly slower to acquire this new spatial information. Adolescent fluoxetine treatment had no effect on cell proliferation in dorsal dentate gyrus and subgranular zone in young adulthood. This calls for further studies examining the long-term effects of this class of antidepressants on adolescent brain development and behaviour.

U2 - 10.1016/j.bbr.2011.12.006

DO - 10.1016/j.bbr.2011.12.006

M3 - Journal article

C2 - 22178317

VL - 228

SP - 169

EP - 175

JO - Behavioural Brain Research

JF - Behavioural Brain Research

SN - 0166-4328

IS - 1

ER -

ID: 37581908