Gender-dependent modulation of brain monoamines and anxiety-like behaviors in mice with genetic serotonin transporter and BDNF deficiencies

被引:81
|
作者
Ren-Patterson, Renee F.
Cochran, Lauren W.
Holmes, Andrew
Lesch, Klaus-Peter
Lu, Bai
Murphy, Dennis L.
机构
[1] NIMH, Clin Sci Lab, Bethesda, MD 20892 USA
[2] NIAAA, Sect Behav Genom, Bethesda, MD USA
[3] Univ Wurzburg, D-97070 Wurzburg, Germany
[4] NICHD, Dev Neurobiol Lab, Rockville, MD USA
关键词
neurotrophins; serotonin; knockout; gene interaction; estrogen; TrkB; dopamine; NEUROTROPHIC FACTOR BDNF; FACTOR MESSENGER-RNA; MOTOR-NEURONS; RAT-BRAIN; IN-VITRO; VAL66MET POLYMORPHISM; PROTEIN EXPRESSION; STRIATAL DOPAMINE; RIBONUCLEIC-ACID; ESTROUS-CYCLE;
D O I
10.1007/s10571-006-9048-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. Brain-derived neurotrophic factor (BDNF) supports serotonergic neuronal development and our recent study found that heterozygous mice lacking one BDNF gene allele interbred with male serotonin transporter (SERT) knockout mice had greater reductions in brain tissue serotonin concentrations, greater increases in anxiety-like behaviors and greater ACTH responses to stress than found in the SERT knockout mice alone. 2. We investigated here whether there might be gender differences in these consequences of combined SERT and BDNF deficiencies by extending the original studies to female mice, and also to an examination of the effects of ovariectomy and tamoxifen in these female mice, and of 21-day 17-beta estradiol implantation to male mice. 3. We found that unlike the male SERT x BDNF-deficient mice, female SERT x BDNF mice appeared protected by their gender in having significantly lesser reductions in serotonin concentrations in hypothalamus and other brain regions than males, relative to controls. Likewise, in the elevated plus maze, female SERT x BDNF-deficient mice demonstrated no increases in the anxiety-like behaviors previously found in males. 4. Furthermore, female SERT x BDNF mice did not manifest the similar to 40% reduction in the expression of TrkB receptors or the similar to 30% reductions in dopamine and its metabolites that male SERT x BDNF did. After estradiol implantation in male SERT x BDNF mice, hypothalamic serotonin was significantly increased compared to vehicle-implanted mice. These findings support the hypothesis that estrogen may enhance BDNF function via its TrkB receptor, leading to alterations in the serotonin circuits, which modulate anxiety-like behaviors. 5. This double-mutant mouse model contributes to the knowledge base that will help in understanding gene x gene x gender interactions in studies of SERT and BDNF gene polymorphisms in human genetic diseases such as anxiety disorders and depression.
引用
收藏
页码:755 / 780
页数:26
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