Department of Pharmacology, Medical School, University of Athens, Athens, Greece.
Physiol Behav. 2012 Sep 10;107(2):201-6. doi: 10.1016/j.physbeh.2012.06.016. Epub 2012 Jul 3.
The rat Forced Swim Test (FST) is widely used to investigate the response to antidepressant treatment. Selective serotonin reuptake inhibitors (SSRIs) elongate swimming duration during the FST, while climbing duration is unaffected. In the present study, we aimed to correlate behavioral effects of the SSRI sertraline in the FST with respective changes in the serotonergic activity of the hippocampus and the prefrontal cortex. Male rats were subjected to the standard FST (two swim sessions in two consecutive days) and between the two sessions they received three i.p. injections of sertraline (10 mg/kg or 40 mg/kg) or vehicle. All rats were killed immediately after the second FST session. Unstressed animals received the same administration schemes and were killed in equivalent time-points. Serotonin and its metabolite 5-HIAA were assayed in the hippocampus and the prefrontal cortex with the use of high-performance liquid chromatography (HPLC-ED) and their ratio 5-HIAA/5-HT was calculated. Sertraline enhanced swimming and decreased immobility duration at both doses. Serotonergic activity was not altered by the 2-day swim stress in either brain region, while subchronic sertraline treatment enhanced 5-HT levels and decreased 5-HIAA/5-HT in the hippocampus and the prefrontal cortex. The serotonin turnover rate (5-HIAA/5-HT ratio) decrease is probably indicative of reduced 5-HT metabolism, as a result of 5-HT reuptake inhibition. This effect was significant in the prefrontal cortex of unstressed rats only after a higher dose of sertraline. In the prefrontal cortex, but not in the hippocampus, immobility duration was negatively correlated with 5-HT tissue levels, whereas swimming duration was positively correlated with 5-HT. These results indicate that after antidepressant treatment, behavior during the FST can be predictive of respective serotonergic changes, especially in the prefrontal cortex.
大鼠强迫游泳试验(FST)广泛用于研究抗抑郁治疗的反应。选择性 5-羟色胺再摄取抑制剂(SSRIs)延长 FST 中的游泳时间,而攀爬时间不受影响。在本研究中,我们旨在将 SSRIs 舍曲林在 FST 中的行为效应与海马体和前额叶皮质中相应的 5-羟色胺能活性变化相关联。雄性大鼠接受标准 FST(连续两天的两次游泳),在两次游泳之间,它们接受三次腹腔注射舍曲林(10mg/kg 或 40mg/kg)或载体。所有大鼠在第二次 FST 后立即处死。未应激的动物接受相同的给药方案,并在等效时间点处死。使用高效液相色谱法(HPLC-ED)测定海马体和前额叶皮质中的 5-羟色胺及其代谢物 5-HIAA,并计算其比值 5-HIAA/5-HT。舍曲林在两个剂量下均增强游泳并减少不动时间。在两个脑区,2 天游泳应激均未改变 5-羟色胺能活性,而亚慢性舍曲林治疗增强了海马体和前额叶皮质中的 5-HT 水平并降低了 5-HIAA/5-HT。5-HT 周转率(5-HIAA/5-HT 比值)的降低可能表明由于 5-HT 再摄取抑制导致 5-HT 代谢减少。这种作用在仅接受较高剂量舍曲林的未应激大鼠的前额叶皮质中是显著的。在前额叶皮质中,但不在海马体中,不动时间与 5-HT 组织水平呈负相关,而游泳时间与 5-HT 呈正相关。这些结果表明,在抗抑郁治疗后,FST 期间的行为可以预测相应的 5-羟色胺变化,特别是在前额叶皮质中。