Behavioral evaluation of male and female mice pups exposed to fluoxetine during pregnancy and lactation

被引:114
作者
Lisboa, Sabrina F. S.
Oliveira, Paulo E.
Costa, Leandro C.
Venancio, Emerson J.
Moreira, Estefania G.
机构
[1] Univ Estadual Londrina, Dept Physiol Sci, Londrina, Brazil
[2] Univ Estadual Londrina, Dept Pathol Sci, Londrina, Brazil
关键词
fluoxetine; pregnancy; lactation; developmental exposure; anxiety depression; pain sensitivity; aggressiveness;
D O I
10.1159/000103097
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background/Aims: Fluoxetine (FLX) has been widely prescribed for depression during pregnancy and/or lactation. Since serotonin is a neurotrophic factor, the use of FLX by mothers could disrupt brain development resulting in behavioral alterations in their progeny. This study evaluated the effects of developmental FLX exposure on anxiety, depression, aggressivity and pain sensitivity of male and female mice pups. Methods: Swiss dams were treated daily, by gavage, with 7.5 mg/kg of FLX during pregnancy and lactation. Pups were submitted to open-field, forced swimming, elevated plus-maze, intruder-resident and hot plate tests at adolescence and adulthood. Results and Conclusion: In male pups, exposure to FLX decreased ambulation at postnatal day (PND) 40 and tended (p = 0.07) to increase the latency to the first attack in the intruder-resident test at PND 70, suggesting decreased impulsivity. In female pups, FLX exposure increased immobility time in the forced swimming test at both PND 30 and 70, which is interpreted as depressive-like behavior. In conclusion, our results suggest that maternal exposure to FLX during pregnancy and lactation results in enduring behavioral alterations in male and female pups throughout life. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 44 条
[1]  
ALBERT PR, 1990, J BIOL CHEM, V265, P5825
[2]   5-HT1A receptors, gene repression, and depression: Guilt by association [J].
Albert, PR ;
Lemonde, S .
NEUROSCIENTIST, 2004, 10 (06) :575-593
[3]   Early-life blockade of the 5-HT transporter alters emotional behavior in adult mice [J].
Ansorge, MS ;
Zhou, MM ;
Lira, A ;
Hen, R ;
Gingrich, JA .
SCIENCE, 2004, 306 (5697) :879-881
[4]   Developmental and behavioral consequences of prenatal fluoxetine [J].
Bairy, K. L. ;
Madhyastha, S. ;
Ashok, K. P. ;
Bairy, Indira ;
Malini, S. .
PHARMACOLOGY, 2007, 79 (01) :1-11
[5]   Role of the 5-HT1A receptor in development of the neonatal rat brain: Preliminary behavioral studies [J].
Borella, A ;
Bindra, M ;
WhitakerAzmitia, PM .
NEUROPHARMACOLOGY, 1997, 36 (4-5) :445-450
[6]  
Broadhurst PL, 1960, EXPT PERSONALITY, P31
[7]  
Burt VK, 2002, J CLIN PSYCHIAT, V63, P9
[8]   DEVELOPMENTAL TOXICOLOGY STUDIES OF FLUOXETINE HYDROCHLORIDE ADMINISTERED ORALLY TO RATS AND RABBITS [J].
BYRD, RA ;
MARKHAM, JK .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 22 (04) :511-518
[9]   TRANSIENT EXPRESSION OF 5-HT1A RECEPTOR-BINDING SITES IN SOME AREAS OF THE RAT CNS DURING POSTNATAL-DEVELOPMENT [J].
DAVAL, G ;
VERGE, D ;
BECERRIL, A ;
GOZLAN, H ;
SPAMPINATO, U ;
HAMON, M .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1987, 5 (03) :171-&
[10]   Reduction of intraspecific aggression in adult rats by neonatal treatment with a selective serotonin reuptake inhibitor [J].
de Castro, RM ;
Medeiros, JMB ;
da Silva, CM ;
Ferreira, LMP ;
Guedes, RCA ;
Cabral, JE ;
Costa, JJA .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2001, 34 (01) :121-124