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酸枣仁生品与炒品镇静催眠作用的比较研究:网络药理学与药理评价相结合

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

作者信息

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

机构信息

Institute of Geriatrics, School of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, 430065, China.

出版信息

Curr Comput Aided Drug Des. 2025;21(5):573-586. doi: 10.2174/0115734099281920240730051328.

Abstract

OBJECTIVES

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.

摘要

目的

本研究旨在探讨酸枣仁生品与炮制品的药用特性,并为其治疗失眠的潜力提供新的见解。

方法

本研究利用网络药理学平台收集酸枣仁的化学成分、人体靶点、基因、分子网络以及与酸枣仁治疗失眠相关的通路信息。采用液相色谱 - 串联质谱法(LC-MS/MS)分析酸枣仁生品、炒酸枣仁及其合煎液的化学图谱。通过戊巴比妥诱导睡眠试验、行为分析、脑组织相关mRNA水平检测以及血浆神经递质测定,评估不同酸枣仁制品对对氯苯丙氨酸诱导的失眠小鼠的影响,旨在探讨各种酸枣仁制品的镇静催眠作用。

结果

发现酸枣仁共含有47个基因,其中包括22个与失眠相关的靶基因。这些基因可能通过9条相关通路和69个生物学过程产生镇静催眠作用。酸枣仁炮制前后的活性成分保持一致。酸枣仁生品中酸枣仁皂苷B含量较高,而炒酸枣仁中酸枣仁皂苷A含量更为丰富。此外,酸枣仁可降低小鼠的自发活动,增强戊巴比妥钠的催眠作用,并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-羟吲哚乙酸和谷氨酸水平升高,催眠作用与药物剂量成正比。

结论

酸枣仁具有镇静催眠作用,可能是通过影响中枢神经系统内神经递质水平及相关受体介导的。酸枣仁炮制前后的调节能力略有差异,生品与炒酸枣仁合煎液的作用更为明显,尤其是在较高剂量时。

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