A Combination of Magnoflorine and Spinosin Improves the Antidepressant effects on CUMS Mouse Model.

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Current drug metabolism Pub Date : 2024-01-01 DOI:10.2174/0113892002284230240213064248
Fenghe Bi, Zhihui Wang, Yijing Guo, Menglin Xia, Xuehui Zhu, Wei Qiao
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Abstract

Background: Depression is a common neuropsychiatric disease. As a famous traditional Chinese medicine with significant anti-depressive and sleep-promoting effects, Ziziphi Spinosae Semen (ZSS) has attracted the attention of many researchers. Although it is well known that Magnoflorine (MAG) and Spinosin (SPI) were the main active components isolated from ZSS, there is a lack of research on the combined treatment of depression with these two ingredients.

Methods: The shaking bottle method was used to simulate the human environment for detecting the changes in oil-water partition coefficient before and after the drug combination. Cell viability was evaluated by the MTT assay. To establish a mouse model of depression and insomnia by CUMS method, and then to explore the effect of combined administration of MAG and SPI on depression in CUMS model by observing behavior and analyzing pharmacokinetics.

Results: The change in LogP values affected the lipid solubility of MAG and increased the water solubility of SPI, allowing them to penetrate more easily through the blood-brain barrier into the brain. Compared with the model group, MAG-SPI with a concentration of 60 μM significantly increased cell survival rate. In both the TST and FST experiments, the mice showed a decrease in immobilization time. Pharmacokinetic results showed that the pharmacokinetic parameters, Cmax and AUC of MAG and SPI, were increased in the case of combination, which resulted in enhancement of their relative bioavailability and improvement of in vivo effects.

Conclusions: The present study demonstrated that a combination of MAG and SPI had a synergistic antidepressant effect in CUMS mouse model.

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木兰花碱与斯皮诺辛的联合用药可提高 CUMS 小鼠模型的抗抑郁效果
背景:抑郁症是一种常见的神经精神疾病:抑郁症是一种常见的神经精神疾病。作为一种具有明显抗抑郁和促进睡眠作用的名贵中药,酸枣仁精液(ZSS)引起了许多研究人员的关注。尽管众所周知木兰花碱(MAG)和刺五加苷(SPI)是从酸枣仁精液中分离出来的主要活性成分,但目前还缺乏对这两种成分联合治疗抑郁症的研究:方法:采用摇瓶法模拟人体环境,检测联合用药前后油水分配系数的变化。采用 MTT 法评估细胞活力。用 CUMS 法建立抑郁和失眠小鼠模型,然后通过行为观察和药代动力学分析,探讨 MAG 和 SPI 联合给药对 CUMS 模型抑郁的影响:LogP值的变化影响了MAG的脂溶性,增加了SPI的水溶性,使其更容易透过血脑屏障进入大脑。与模型组相比,浓度为 60 μM 的 MAG-SPI 能显著提高细胞存活率。在 TST 和 FST 实验中,小鼠的固定时间均有所缩短。药代动力学结果显示,MAG 和 SPI 的药代动力学参数 Cmax 和 AUC 在联合用药的情况下有所增加,从而提高了它们的相对生物利用度,改善了体内效应:结论:本研究表明,MAG和SPI复方制剂在CUMS小鼠模型中具有协同抗抑郁作用。
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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