Comparative Study on Sedative and Hypnotic Effects of Crude and Parched Semen Ziziphi Spinosae: Integration of Network Pharmacology and In Vivo Pharmacological Evaluation.

Jing Xia, Ming Cai, Bo Xu, Guang-Jing Xie, Ping Wang
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Abstract

Objective: This study aimed to investigate the medicinal properties of SZS before and after processing and provide novel insights into its potential for treating insomnia.

Methods: This study employed the network pharmacology platform to gather information on the chemical composition of SZS, human targets, genes, molecular networks, and pathways associated with insomnia treatment using SZS. Liquid chromatography-tandem mass spectrometry (LC-MS/ MS) was utilized to analyze the chemical profiles of crude SZS, parched SZS, and their combined decoction. The effects of different SZS products on p-chlorophenylalanine-induced insomnia mice were evaluated through pentobarbital-induced sleep tests, behavioral analyses, examination of brain tissue-related mRNA levels, and measurement of plasma neurotransmitters, aiming to explore the sedative and hypnotic effects of various SZS products.

Results: SZS was found to contain a total of 47 genes, including 22 target genes associated with insomnia. These genes may contribute to the sedative and hypnotic effects through 9 related pathways and 69 biological processes. The active components of SZS remained consistent before and after processing. Jujuboside B was found in higher concentrations in crude SZS, while jujuboside A was more abundant in parched SZS. Additionally, SZS exhibited reduced locomotor activity in mice, enhanced the hypnotic effect of pentobarbital sodium, and decreased the levels of acetylcholinesterase, α-1B adrenergic receptor, and solute carrier family 6 member 4 mRNA in the cortex and hippocampus of mice. The levels of acetylcholine, choline acetyltransferase, 5-hydroxyindoleacetic acid, and glutamate in plasma increased, with the hypnotic effect being proportional to the dosage of the drug.

Conclusion: SZS demonstrates sedative and hypnotic effects, potentially mediated by its influence on neurotransmitter levels and related receptors within the central nervous system. There was a slight variation in regulatory capabilities before and after SZS processing, with the combined decoction of crude and parched SZS exhibiting a more pronounced effect, particularly at higher dosages.

生、干太子参镇静催眠作用的比较研究:网络药理学与体内药理评价的结合。
目的:研究参参炮制前后的药用特性,为其治疗失眠的潜力提供新的见解。方法:利用网络药理学平台,收集SZS的化学成分、人体靶点、基因、分子网络以及与SZS治疗失眠相关的通路等信息。采用液相色谱-串联质谱法(LC-MS/ MS)分析了粗参、干燥参及其联合煎剂的化学成分。通过戊巴比妥诱导睡眠实验、行为学分析、脑组织相关mRNA水平检测、血浆神经递质测定等方法,评价不同SZS产品对对氯苯丙氨酸致失眠小鼠的影响,探讨不同SZS产品的镇静催眠作用。结果:发现SZS共包含47个基因,其中与失眠相关的靶基因22个。这些基因可能通过9条相关通路和69个生物学过程参与镇静和催眠作用。SZS有效成分处理前后基本一致。红枣苷B在粗制红枣中含量较高,而红枣苷A在干燥红枣中含量较高。此外,SZS还能降低小鼠的运动活性,增强戊巴比妥钠的催眠作用,降低小鼠皮层和海马中乙酰胆碱酯酶、α-1B肾上腺素能受体和溶质载体家族6成员4 mRNA的水平。血浆中乙酰胆碱、胆碱乙酰转移酶、5-羟基吲哚乙酸、谷氨酸水平升高,催眠效果与药物剂量成正比。结论:SZS具有镇静和催眠作用,可能是通过影响中枢神经系统的神经递质水平和相关受体介导的。深参炮制前后的调节能力略有差异,其中粗炒深参联合煎煮效果更明显,特别是在较高的剂量下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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