Department of Pharmacology, JSS Medical College, JSS Academy of Higher Education and Research, Mysuru, India.
Department of Neurology, Saint Francis Hospital and Medical Center, Trinity Health Of New England, Hartford, CT, USA.
Pharm Biol. 2022 Dec;60(1):1656-1668. doi: 10.1080/13880209.2022.2101669.
L. (Magnoliaceae) has been known since ancient times for its rich medicinal properties.
The ethanol extract of leaves (EEMC) was evaluated on depression and anxiety using and studies.
Swiss albino mice were divided into control, standard, 100 and 200 mg/kg b.w. EEMC groups and for drug administration using oral gavage. The antidepressant activity was evaluated using forced swim test (FST) and tail suspension test (TST) whereas the anxiolytic activity through elevated plus maze and light and dark tests. The studies included molecular docking against human potassium channel KCSA-FAB and human serotonin transporter, and ADME/T analysis.
Open arm duration and entries were comparable between 200 mg/kg b.w. group (184.45 ± 1.00 s and 6.25 ± 1.11, respectively) and that of diazepam treated group (180.02 s ± 0.40 and 6.10 ± 0.05, respectively). Time spent in the light cubicle was higher (46.86 ± 0.03%), similar to that of diazepam (44.33 ± 0.64%), suggesting its potent anxiolytic activity. A delayed onset of immobility and lowered immobility time was seen at both the treatment doses (FST: 93.7 ± 1.70 and 89.1 ± 0.40 s; TST: 35.05 ± 2.75 and 38.50 ± 4.10 s) and the standard drug imipramine (FST: 72.7 ± 3.72 and TST: 30.01 ± 2.99 s), indicative of its antidepressant ability. studies predicted doripenem to induce anxiolytic and antidepressant activity by inhibiting human potassium channel KCSA-FAB and human serotonin transporter proteins, respectively.
EEMC is a rich source of bioactive compounds with strong antidepressant and anxiolytic properties.
叶子(木兰科)自古以来就因其丰富的药用特性而闻名。
采用 和 研究评估叶乙醇提取物(EEMC)对抑郁和焦虑的作用。
将瑞士白化病小鼠分为对照组、标准组、100 和 200mg/kg 体重 EEMC 组,并通过口服灌胃进行药物给药。使用强迫游泳试验(FST)和悬尾试验(TST)评估抗抑郁活性,而通过高架十字迷宫和明暗试验评估抗焦虑活性。 研究包括针对人钾通道 KCSA-FAB 和人血清素转运蛋白的分子对接,以及 ADME/T 分析。
200mg/kg 体重组(分别为 184.45±1.00s 和 6.25±1.11)和地西泮治疗组(180.02s±0.40 和 6.10±0.05)的敞口臂持续时间和进入次数相当。在光舱中的停留时间更高(46.86±0.03%),与地西泮相似(44.33±0.64%),表明其具有有效的抗焦虑活性。在两个治疗剂量(FST:93.7±1.70 和 89.1±0.40s;TST:35.05±2.75 和 38.50±4.10s)和标准药物丙咪嗪(FST:72.7±3.72 和 TST:30.01±2.99s)中,观察到潜伏期延长和不动时间缩短,这表明它具有抗抑郁作用。研究预测多立培南通过抑制人钾通道 KCSA-FAB 和人血清素转运蛋白分别诱导抗焦虑和抗抑郁活性。
EEMC 是一种丰富的生物活性化合物来源,具有强烈的抗抑郁和抗焦虑特性。