Antony Lourdu Jafrin, Paruchuri Venkata Naveen Kumar, Ramanan Ramchandar
Assistant Professor, Department of Pharmacology, Sri Manakula Vinayagar Medical College , Pondicherry, India .
Final Year Student, Sri Manakula Vinayagar Medical College , Pondicherry, India .
J Clin Diagn Res. 2014 Jun;8(6):HC05-7. doi: 10.7860/JCDR/2014/9679.4445. Epub 2014 Jun 20.
Depression is the most common mental disorder in community settings, and is a major cause of disability across the world. Antidepressants such as SSRI (Selective Serotonin Reuptake Inhibitor) and TCA (Tricyclic antidepressants) are used. These drugs affect the adrenergic and serotonergic pathways. These drugs have an unfavorable side effect profile, take longer time to act and are not very effective in resistant cases. Alternate pathways involving the glutamate receptors have also been linked with depression, hence Ketamine an NMDA antagonist was evaluated for the antidepressant effect.
To study the antidepressant effect of ketamine in subanaesthetic doses in male albino mice.
STUDY DESIGN, MATERIALS AND METHODS: The study was a randomized controlled animal study done on 30 male albino BALB/c mice divided into five groups with Imipramine (10mg/kg) as the standard drug and Ketamine in varying doses (5, 7.5, 10 mg/kg) as the test drug. The animal model used was the forced swim test. The reduction in immobility time was taken as the index of the antidepressant effect.
The data were analysed with the one way ANOVA test using SPSS version 12.
The data analysis showed that Ketamine at a dose lower dose of Ketamine (5mg/kg) did not show a significant antidepressant effect in contrast to the higher doses (7.5 and 10mg/kg) which showed significant antidepressant effect ('p' > 0.05). The inference of this study is that Ketamine has significant antidepressant property at variable dose ranges and further studies can be done on these lines.
抑郁症是社区环境中最常见的精神障碍,也是全球致残的主要原因。人们使用了如SSRI(选择性5-羟色胺再摄取抑制剂)和TCA(三环类抗抑郁药)等抗抑郁药。这些药物影响肾上腺素能和5-羟色胺能途径。这些药物具有不良的副作用,起效时间较长,并且在难治性病例中效果不佳。涉及谷氨酸受体的替代途径也与抑郁症有关,因此对NMDA拮抗剂氯胺酮的抗抑郁作用进行了评估。
研究亚麻醉剂量氯胺酮对雄性白化小鼠的抗抑郁作用。
研究设计、材料与方法:该研究是一项随机对照动物研究,对30只雄性白化BALB/c小鼠进行,分为五组,以丙咪嗪(10mg/kg)作为标准药物,不同剂量(5、7.5、10mg/kg)的氯胺酮作为受试药物。所使用的动物模型是强迫游泳试验。不动时间的减少被作为抗抑郁作用的指标。
使用SPSS 12版的单因素方差分析对数据进行分析。
数据分析表明,与较高剂量(7.5和10mg/kg)显示出显著抗抑郁作用相比,较低剂量(5mg/kg)的氯胺酮未显示出显著的抗抑郁作用(“p”>0.05)。本研究的推断是氯胺酮在不同剂量范围内具有显著的抗抑郁特性,可以在此基础上进行进一步研究。