莨菪亭和芦丁能减轻小鼠条件性位置偏好试验中的乙醇奖赏

Vijayapandi Pandy , Kamini Vijeepallam , Nurul Fatin Amira Roslan , Arif Sajat , Yew Chang Wai , Phani Sai Vennela Ramisetty , Vulli Naga Jyothi
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引用次数: 0

摘要

引言 在传统中医学中,海巴戟的叶、果、花、根和树皮等各部分都被用作滋补品,可治疗发热、皮肤、眼睛、喉咙和牙龈问题,以及恶心、呕吐和神经系统疾病。以前的研究表明,M. citrifolia Linn.果实及其果汁可降低小鼠的乙醇条件性位置偏好(CPP),其中莨菪亭(SCOP)和芦丁(RUT)被认为是产生这种效果的主要生物活性化合物。本研究旨在利用小鼠的 CPP 试验评估 SCOP 和 RUT 对乙醇奖赏的影响。方法 CPP 方案包括为期 3 天的适应阶段、1 天的预调节阶段、10 天的调节、休息日和调节后日。药物-盐水对照组和药物-乙醇对照组口服 1 % w/v 的羧甲基纤维素钠(CMC)溶液,剂量为 10 毫升/千克。口服 SCOP 和 RUT 的剂量为 0.05 至 1 毫克/千克体重(bw),而阿坎酸(ACAM)的剂量为 300 毫克/千克体重(bw),均在后调节前一小时进行。结果在第 16 天进行后条件测试前一小时口服 SCOP(0.05、0.1 和 0.5 毫克/千克体重)和 RUT(0.05 毫克/千克体重)可显著降低小鼠的乙醇 CPP。此外,所有测试剂量(0.05-1 毫克/千克体重,口服)的 SCOP 和 RUT 都不会引起小鼠正常运动活动的任何变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Scopoletin and rutin attenuate ethanol reward in mouse-conditioned place preference test

Scopoletin and rutin attenuate ethanol reward in mouse-conditioned place preference test

Introduction

In Traditional Chinese Medicine (TCM), Morinda citrifolia Linn. (Hai ba ji), is utilized for its various parts such as leaves, fruits, flowers, roots, and bark, serving as a tonic and addressing ailments including fever, skin, eye, throat, and gum issues, as well as nausea, vomiting, and neurological diseases. Previous research indicated that M. citrifolia Linn. fruit and its juice reduced ethanol-conditioned place preference (CPP) in mice, with scopoletin (SCOP) and rutin (RUT) proposed as the main bioactive compounds responsible for this effect. This study aimed to evaluate the impact of SCOP and RUT on ethanol reward using the CPP test in mice.

Methods

The CPP protocol consisted of a habituation phase spanning 3 days, a 1-day preconditioning phase, 10 days of conditioning, a rest day, and a post-conditioning day. The vehicle-saline control and vehicle-ethanol control groups received oral administration of a 1 % w/v solution of sodium carboxymethyl cellulose (CMC) at a dosage of 10 ml/kg. SCOP and RUT were administered orally at doses ranging from 0.05 to 1 mg/kg body weight (bw), while acamprosate (ACAM) was administered at a dosage of 300 mg/kg bw, all one hour before postconditioning. Statistical analyses utilized both repeated measures two-way and one-way ANOVA.

Results

Oral administration of SCOP (0.05, 0.1, and 0.5 mg/kg bw) and RUT (0.05 mg/kg bw) one hour before postconditioning testing on day 16 markedly reduced ethanol CPP in mice. Additionally, SCOP and RUT at all tested doses (0.05–1 mg/kg bw, p.o.) did not induce any changes in normal locomotor activity in mice.

Discussion

These results suggest that SCOP and RUT diminish ethanol reward in mice, underscoring the therapeutic potential of these phytochemicals in managing alcohol use disorder.

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