Satam Sonali, Raut Sanket, Shetty Yashashri C, Marathe Padmaja A, Mulkalwar Alhad, Raut Ashwinikumar, Rege Nirmala
Department of Pharmacology and Therapeutics, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, IND.
School of Psychology, University of Tasmania, Tasmania, AUS.
Cureus. 2025 Apr 9;17(4):e81962. doi: 10.7759/cureus.81962. eCollection 2025 Apr.
Background (CP), an Indian medicinal plant, is hypothesized to be effective in alcohol use disorder (AUD) based on its medicinal properties useful in CNS disorders as per ancient Ayurveda literature. Hence, it was tested in animal models of AUD. Methodology The study was conducted in Swiss albino mice (n=144) of either sex after obtaining Institutional Animal Ethics Committee permission. Three doses of seed oil of CP (CP1: 140, CP2: 280 and CP3: 560 mg/kg) were administered orally in milk (vehicle for CP). A conditioned place preference (CPP) model was used to study the effect of CP on alcohol dependence. Elevated plus maze (EPM) and open field test (OFT) were used to study its effect on alcohol withdrawal-induced anxiety. Naltrexone and diazepam were used as positive controls. Results The results in all the CP groups (CP1 (337.88±20.66s, p<0.05); CP2 (322.38±17.61s, p<0.05) and CP3 (315.50±4.24s) as evaluated by the time spent in alcohol paired compartment in CPP) showed better protection against alcohol dependence as compared to the vehicle (552.63±27.47s, p<0.05). The values in all the CP groups were comparable to the naltrexone group. In the EPM test, the CP3 group showed significantly increased time spent (170.63±19.75s) in the open arm ( the vehicle control, 12.75±11.03s, p<0.05). Also in OFT, longer time was spent in the central zone by mice in the CP3 group (23.25±6.19s 8.50±5.48s in the vehicle group, p<0.05). The results of the CP3 group were comparable to diazepam in EPM and OFT experiments. Conclusion seed oil showed a dose-dependent effect in the CPP model of alcohol dependence in mice. The highest dose of CP also prevented alcohol withdrawal-induced anxiety.
根据古代阿育吠陀文献记载,印度药用植物[植物名称未给出,用CP代替]因其对中枢神经系统疾病有益的药用特性,被推测对酒精使用障碍(AUD)有效。因此,在酒精使用障碍的动物模型中对其进行了测试。方法:在获得机构动物伦理委员会许可后,对瑞士白化小鼠(n = 144)进行了该研究,雌雄不限。将三种剂量的CP种子油(CP1:140、CP2:280和CP3:560毫克/千克)用牛奶口服给药(牛奶为CP的赋形剂)。使用条件性位置偏爱(CPP)模型研究CP对酒精依赖的影响。使用高架十字迷宫(EPM)和旷场试验(OFT)研究其对酒精戒断引起的焦虑的影响。纳曲酮和地西泮用作阳性对照。结果:在CPP中,通过在酒精配对隔室中花费的时间评估,所有CP组(CP1(337.88±20.66秒,p <0.05);CP2(322.38±17.61秒,p <0.05)和CP3(315.50±4.24秒))的结果显示,与赋形剂组(552.63±27.47秒,p <0.05)相比,对酒精依赖具有更好的保护作用。所有CP组的值与纳曲酮组相当。在EPM试验中,CP3组在开放臂中花费的时间显著增加(170.63±19.75秒)(赋形剂对照组为12.75±11.03秒,p <0.05)。同样在OFT中,CP3组的小鼠在中央区域花费的时间更长(23.25±6.19秒,赋形剂组为8.50±5.48秒,p <0.05)。在EPM和OFT实验中,CP3组的结果与地西泮相当。结论:CP种子油在小鼠酒精依赖的CPP模型中显示出剂量依赖性效应。CP的最高剂量还可预防酒精戒断引起的焦虑。