Olivier J D A, Van Der Hart M G C, Van Swelm R P L, Dederen P J, Homberg J R, Cremers T, Deen P M T, Cuppen E, Cools A R, Ellenbroek B A
Department of Cognitive Neuroscience: Psychoneuropharmacology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
Neuroscience. 2008 Mar 27;152(3):573-84. doi: 10.1016/j.neuroscience.2007.12.032. Epub 2008 Jan 1.
Human studies have shown that a reduction of 5-HT transporter (SERT) increases the vulnerability for anxiety and depression. Moreover, women are more vulnerable to develop depression and anxiety disorders than men. For that reason we hypothesized that homozygous 5-HT transporter knockout rat (SERT(-/-)) models, especially female, are valuable and reliable animal models for humans with an increased vulnerability for anxiety- and depression-related disorders. As rats are extensively used in neuroscience research, we used the unique 5-HT transporter knockout rat, that was recently generated using N-ethyl-N-nitrosurea (ENU) -driven mutagenesis, to test this hypothesis. Behavioral testing revealed that male and female SERT(-/-) rats spent less time in the center of the open field and spent less time on the open arm of the elevated plus maze compared with wild-type 5-HT transporter knockout rats (SERT(+/+)). In the novelty suppressed feeding test, only male SERT(-/-) rats showed a higher latency before starting to eat in a bright novel arena compared with SERT(+/+) controls. Both male and female SERT(-/-) rats showed a higher escape latency from their home cage than SERT(+/+) littermates. Moreover, SERT(-/-) rats were less mobile in the forced swim test, and sucrose consumption was reduced in SERT(-/-) rats relative to SERT(+/+) rats. Both effects were sex-independent. Neurochemically, basal extracellular 5-HT levels were elevated to a similar extent in male and female SERT(-/-) rats, which was not influenced by the selective 5-HT reuptake inhibitor citalopram. 5-HT immunostaining revealed no difference between SERT(+/+) and SERT(-/-) rats in the dorsal raphe nuclei, in both males and females. These findings demonstrate that SERT(-/-) rats show anxiety and depression-related behavior, independent of sex. Genetic inactivation of the SERT has apparently such a great impact on behavior, that hardly any differences are found between male and female rats. This knockout rat model may provide a valuable model to study anxiety- and depression-related disorders in male and female rats.
人体研究表明,5-羟色胺转运体(SERT)减少会增加患焦虑症和抑郁症的易感性。此外,女性比男性更容易患抑郁症和焦虑症。因此,我们推测纯合子5-羟色胺转运体基因敲除大鼠(SERT(-/-))模型,尤其是雌性模型,对于易患焦虑症和抑郁症相关疾病的人类来说是有价值且可靠的动物模型。由于大鼠在神经科学研究中被广泛使用,我们使用了最近通过N-乙基-N-亚硝基脲(ENU)驱动的诱变产生的独特的5-羟色胺转运体基因敲除大鼠来验证这一假设。行为测试表明,与野生型5-羟色胺转运体基因敲除大鼠(SERT(+/+))相比,雄性和雌性SERT(-/-)大鼠在旷场中央停留的时间更少,在高架十字迷宫开放臂上停留的时间也更少。在新奇环境抑制摄食试验中,与SERT(+/+)对照组相比,只有雄性SERT(-/-)大鼠在明亮的新奇环境中开始进食前的潜伏期更长。雄性和雌性SERT(-/-)大鼠从其家笼逃脱的潜伏期均比SERT(+/+)同窝大鼠长。此外,SERT(-/-)大鼠在强迫游泳试验中的活动较少,相对于SERT(+/+)大鼠,SERT(-/-)大鼠的蔗糖消耗量减少。这两种效应均与性别无关。神经化学方面,雄性和雌性SERT(-/-)大鼠的基础细胞外5-羟色胺水平均升高到相似程度,这不受选择性5-羟色胺再摄取抑制剂西酞普兰的影响。5-羟色胺免疫染色显示,雄性和雌性大鼠的中缝背核中SERT(+/+)和SERT(-/-)大鼠之间没有差异。这些发现表明,SERT(-/-)大鼠表现出与焦虑和抑郁相关的行为,与性别无关。SERT的基因失活显然对行为有如此大的影响,以至于雄性和雌性大鼠之间几乎没有发现差异。这种基因敲除大鼠模型可能为研究雄性和雌性大鼠的焦虑症和抑郁症相关疾病提供一个有价值的模型。