Jayakumar Saikarthik, Raghunath Gunapriya, Ilango Saraswathi, Vijayakumar J, Vijayaraghavan R
Research Scholar, Department of Anatomy, Saveetha University, Chennai, Tamil Nadu, India.
Professor and Head, Department of Anatomy, Saveetha Medical College, Chennai, Tamil Nadu, India.
J Clin Diagn Res. 2017 Jun;11(6):AF01-AF06. doi: 10.7860/JCDR/2017/26958.9953. Epub 2017 Jun 1.
Stress has been known to be a potential modulator of learning and memory. Long term stress can lead to depression. Fluoxetine is a selective serotonin reuptake inhibitor group of drug used in the treatment of depression.
The present study was conducted to evaluate the potential of Fluoxetine on cold restraint induced stress in the hippocampus of Wistar rats.
A total of 18 male wistar albino rats were divided randomly into three groups (n=6). Group 1 was the control group which were kept in normal laboratory conditions. Group 2 was the negative control group which were given cold restraint stress for period of four weeks. Group 3 was the experimental group, where the animals were pretreated with fluoxetine 10 mg/kg for a period of one week followed by cold restraint stress for 30 minutes and cotreated with fluoxetine 10 mg/kg for a period of four weeks. The whole study was done for a period of five weeks followed by behavioural studies and subsequently sacrificed with removal of brain for various histological, Immunohistochemical (IHC), neurochemical and antioxidant analysis. The values were expressed as Mean±SEM. One-way analysis of variance followed by Tukey's multiple comparisons test was used for the comparison of means. A probability of 0.05 and less was taken as statistically significant using Prism Graphpad software version 6.01.
The results show there was significant improvement in the Morris water maze test after treatment with fluoxetine in Group 2. Similar results were also noted in the levels of neurotransmitters and antioxidant levels in brain and also in the number of cells counted in IHC and histological studies by H&E when Group 3 was compared with Group 2. The treatment reversed the damage in Group 2 which was comparable with the control group.
The results revealed that administration of fluoxetine 10 mg/kg given orally has a potential antistressor effect by improving the neurogenic and neuroprotective effect on the cold restraint stress induced hippocampal damage.
压力一直被认为是学习和记忆的潜在调节因素。长期压力会导致抑郁。氟西汀是一种用于治疗抑郁症的选择性5-羟色胺再摄取抑制剂类药物。
本研究旨在评估氟西汀对Wistar大鼠海马体冷束缚诱导应激的潜在作用。
总共18只雄性Wistar白化大鼠随机分为三组(n = 6)。第1组为对照组,饲养于正常实验室条件下。第2组为阴性对照组,给予四周的冷束缚应激。第3组为实验组,动物先用10 mg/kg氟西汀预处理一周,然后进行30分钟的冷束缚应激,并同时用10 mg/kg氟西汀共处理四周。整个研究为期五周,随后进行行为学研究,随后处死大鼠并取出大脑进行各种组织学、免疫组织化学(IHC)、神经化学和抗氧化分析。数据以平均值±标准误表示。采用单因素方差分析,随后进行Tukey多重比较检验来比较均值。使用Prism Graphpad软件6.01版本,概率为0.05及以下被视为具有统计学意义。
结果显示,第2组用氟西汀治疗后,在莫里斯水迷宫试验中有显著改善。当第3组与第2组比较时,在大脑神经递质水平、抗氧化水平以及IHC和苏木精-伊红染色组织学研究中计数的细胞数量方面也观察到类似结果。该治疗逆转了第2组中的损伤,与对照组相当。
结果表明,口服给予10 mg/kg氟西汀通过改善对冷束缚应激诱导的海马体损伤的神经生成和神经保护作用,具有潜在的抗应激作用。