Ghosh Sourav, Kumar Arvind, Sachan Neetu, Chandra Phool
School of Pharmaceutical Sciences, IFTM University, Lodhipur Rajput, Delhi Road (NH-24), Moradabad, 244 102, UP, India.
Department of Pharmaceutical Chemistry, S. D. College of Pharmacy & Vocational Studies, Bhopa Road, Muzaffarnagar, 251001, UP, India.
Heliyon. 2021 Apr 25;7(4):e06884. doi: 10.1016/j.heliyon.2021.e06884. eCollection 2021 Apr.
In this study, the anxiolytic activity of essential oil (PNEO) was evaluated in the elevated plus maze (EPM) and the antidepressant-like effect was evaluated through tail suspension test (TST) in mice. Flumazenil, a competitive inhibitor of GABA receptor in the benzodiazepine site and WAY-100635 maleate salt, a 5-HT receptor antagonist were used to find out the possible mechanism(s) of action of PNEO. To exclude the false-positive results due to the enhancement of the locomotor activity, the animals were submitted to open field test (OFT). We also measured monoamines levels of the mice brain after acute PNEO treatment. The data obtained from the study suggest that the anxiolytics and antidepressant-like effect of PNEO have observed in EPM and TST respectively in a dose-dependent manner after oral acute and repetitive treatment. WAY-100635, but not flumazenil was able to reverse the effect of PNEO in EPM and TST both, indicating the possible involvement of 5-HT receptor. The neurochemical analysis showed no alteration in monoamine levels in mice brains. Furthermore, no locomotor impairment or sign of toxicity or changes in body weight or abnormalities in the biochemical parameters, except for a significant decrease in total cholesterol level was observed after treatment with PNEO. The findings suggest that EO possesses a dual anxiolytic and antidepressant-like effect through the possible involvement of serotonergic transmission.
在本研究中,通过高架十字迷宫(EPM)评估了香精油(PNEO)的抗焦虑活性,并通过小鼠悬尾试验(TST)评估了其抗抑郁样作用。使用氟马西尼(一种苯二氮䓬位点GABA受体的竞争性抑制剂)和马来酸WAY-100635(一种5-羟色胺受体拮抗剂)来探究PNEO可能的作用机制。为排除因运动活性增强导致的假阳性结果,对动物进行旷场试验(OFT)。我们还在急性给予PNEO后测量了小鼠脑内单胺水平。研究获得的数据表明,急性口服和重复给药后,PNEO的抗焦虑和抗抑郁样作用分别在EPM和TST中呈剂量依赖性观察到。WAY-100635而非氟马西尼能够逆转PNEO在EPM和TST中的作用,表明可能涉及5-羟色胺受体。神经化学分析显示小鼠脑内单胺水平无变化。此外,用PNEO治疗后,除总胆固醇水平显著降低外,未观察到运动功能损害、毒性迹象、体重变化或生化参数异常。这些发现表明,该香精油可能通过5-羟色胺能传递发挥双重抗焦虑和抗抑郁样作用。