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人参皂苷 Rg3 在小鼠疼痛模型中的镇痛作用及相关氨基酸调节。

Analgesic effect and related amino acids regulation of ginsenoside Rg3 in mouse pain models.

机构信息

School of Pharmacy, Jinzhou Medical University, Jinzhou, PR China.

Dalin Fusheng Natural Medicine Development Co. Ltd., Dalian, PR China.

出版信息

Life Sci. 2019 Dec 15;239:117083. doi: 10.1016/j.lfs.2019.117083. Epub 2019 Nov 20.

Abstract

AIMS

The present study aims to evaluate the analgesic effect of ginsenoside Rg3 in different mouse pain models.

MAIN METHODS

Formalin-, carrageenan- and S180 tumor cells induced mouse pain models were built in the study. The licking and biting time and PEG2 contents in the inflammatory sites were measured. The excitatory and inhibitory amino acids in the brains were determined by pre-column derivation FLD-HPLC method.

KEY FINDING

We have found that ginsenoside Rg3 treated the pain phases and decreased the PGE2 in formalin and carrageenan induced models, respectively. It significantly increased the contents of EAAs (Asp and Glu) in the brains of S180 tumor inducing pain mice, meanwhile, the IAAs (Gly, Tau and GABA) decreased.

SIGNIFICANCE

Our results revealed that ginsenoside Rg3 acted central and peripheral analgesic effect and regulated the inflammatory factors and pain-related amino acids. It could re-balance the abnormal EAAs/IAAs value when the pain occurred. The analgesic mechanism and the clinical application of ginsenoside Rg3 need be evaluated furtherly.

摘要

目的

本研究旨在评估人参皂苷 Rg3 在不同小鼠疼痛模型中的镇痛作用。

方法

本研究建立了福尔马林、角叉菜胶和 S180 肿瘤细胞诱导的小鼠疼痛模型。测量了炎症部位的舔舐和咀嚼时间以及 PEG2 含量。通过预柱衍生 FLD-HPLC 法测定脑内兴奋性和抑制性氨基酸。

主要发现

我们发现人参皂苷 Rg3 可治疗疼痛阶段,并分别降低福尔马林和角叉菜胶诱导模型中的 PGE2。它显著增加了 S180 肿瘤诱导疼痛小鼠脑中 EAAs(天冬氨酸和谷氨酸)的含量,同时 IAAs(甘氨酸、tau 和 GABA)减少。

意义

我们的结果表明,人参皂苷 Rg3 具有中枢和外周镇痛作用,并调节炎症因子和与疼痛相关的氨基酸。当疼痛发生时,它可以重新平衡异常的 EAAs/IAAs 值。人参皂苷 Rg3 的镇痛机制和临床应用需要进一步评估。

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