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具有遗传血清素转运体和脑源性神经营养因子缺陷的小鼠中脑单胺和焦虑样行为的性别依赖性调节。

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

作者信息

Ren-Patterson Renee F, Cochran Lauren W, Holmes Andrew, Lesch Klaus-Peter, Lu Bai, Murphy Dennis L

机构信息

Laboratory of Clinical Science, NIMH, Bethesda, MD 20892-1264, USA.

出版信息

Cell Mol Neurobiol. 2006 Jul-Aug;26(4-6):755-80. doi: 10.1007/s10571-006-9048-6. Epub 2006 Sep 22.

Abstract
  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 SERTxBDNF-deficient mice, female SERTxBDNF 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 SERTxBDNF-deficient mice demonstrated no increases in the anxiety-like behaviors previously found in males. 4. Furthermore, female SERTxBDNF mice did not manifest the approximately 40% reduction in the expression of TrkB receptors or the approximately 30% reductions in dopamine and its metabolites that male SERTxBDNF did. After estradiol implantation in male SERTxBDNF 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 genexgenexgender interactions in studies of SERT and BDNF gene polymorphisms in human genetic diseases such as anxiety disorders and depression.
摘要
  1. 脑源性神经营养因子(BDNF)支持血清素能神经元的发育,我们最近的研究发现,携带一个BDNF基因等位基因缺失的杂合小鼠与雄性血清素转运体(SERT)基因敲除小鼠杂交后,其脑组织中血清素浓度的降低幅度更大,焦虑样行为的增加幅度更大,对应激的促肾上腺皮质激素反应也比单独的SERT基因敲除小鼠更大。2. 我们在此进行研究,通过将最初的研究扩展到雌性小鼠,以及研究卵巢切除术和他莫昔芬对这些雌性小鼠的影响,还有对雄性小鼠进行21天的17-β雌二醇植入,来探究SERT和BDNF联合缺陷的这些后果是否存在性别差异。3. 我们发现,与雄性SERTxBDNF缺陷小鼠不同,雌性SERTxBDNF小鼠似乎受到性别的保护,相对于对照组,其下丘脑和其他脑区血清素浓度的降低幅度明显小于雄性。同样,在高架十字迷宫实验中,雌性SERTxBDNF缺陷小鼠并未表现出之前在雄性小鼠中发现的焦虑样行为增加。4. 此外,雌性SERTxBDNF小鼠没有表现出雄性SERTxBDNF小鼠中出现的TrkB受体表达约40%的降低,也没有出现多巴胺及其代谢产物约30%的降低。在雄性SERTxBDNF小鼠中植入雌二醇后,与植入溶剂的小鼠相比,下丘脑血清素显著增加。这些发现支持了这样一种假说,即雌激素可能通过其TrkB受体增强BDNF功能,导致血清素回路发生改变,从而调节焦虑样行为。5. 这种双突变小鼠模型有助于扩充知识库,这将有助于在人类遗传疾病如焦虑症和抑郁症的研究中理解SERT和BDNF基因多态性中的基因×基因×性别相互作用。

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