Armadillidium vulgare Latreille水提物通过抑制IL-12-IFN-γ-IFNGR-CXCL10通路介导的神经元-星形胶质细胞串扰减轻神经性疼痛

IF 4.8 2区 医学 Q1 CHEMISTRY, MEDICINAL
Yujie Yang , Shen Zhang , Jin Yang , Changheng Yao , Xue Li , Wenling Dai , Jihua Liu
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引用次数: 0

摘要

民族药理学相关性:药虫的干燥体,最早记载于《神农本草经》。作为动物性中药中常见的镇痛药,主要用于止痛、利尿、解乏等。我们的研究表明,AV可以减轻各种类型的急性和慢性疼痛,包括神经性疼痛(NP)。转录组测序分析显示,AV可抑制CXCL10缓解NP,但CXCL10合成的上游机制尚不清楚。研究目的:本研究的目的是确定AV调节CXCL10改善NP的机制。材料和方法:术后14 d采用坐骨神经慢性收缩损伤(CCI)诱导NP模型。为了识别细胞信号通路,使用了各种方法,包括转录组测序,western blotting,免疫荧光以及ELISA。体外实验包括神经元PC12细胞和星形胶质细胞C6细胞的培养。结果:体内和体外实验结果均表明,IL-12/IL-18可增强脊髓神经元中IFN-γ的产生,其作用于神经元和星形胶质细胞上的IFN-γ受体,上调神经元和星形胶质细胞中CXCL10的表达,说明IL-12在神经元和星形胶质细胞间的串聊中起着关键作用。首次阐明了IL-12在神经系统疼痛调节中的作用。此外,它与IL-18在下游IFN-γ-CXCL10通路上的协同相互作用显著改变了神经元和星形胶质细胞的激活。AV可通过介导IL-12-IFN-γ-IFNGR信号通路抑制CXCL10缓解NP。结论:通过调控神经元-星形细胞串扰,探索了NP的新靶点,为AV的临床应用提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The aqueous extract of Armadillidium vulgare Latreille alleviates neuropathic pain via inhibiting neuron-astrocyte crosstalk mediated by the IL-12-IFN-γ-IFNGR-CXCL10 pathway

The aqueous extract of Armadillidium vulgare Latreille alleviates neuropathic pain via inhibiting neuron-astrocyte crosstalk mediated by the IL-12-IFN-γ-IFNGR-CXCL10 pathway

Ethnopharmacological relevance

Armadillidium vulgare Latreille (AV), the dried body of pillbug, was originally described in Shennong's Classic of Materia Medica. As a common analgesic in animal-based traditional Chinese medicine, it is mainly used to relieve pain, promoting diuresis, relieving fatigue and so on. Our work demonstrated that AV could alleviate various types of acute and chronic pain including neuropathic pain (NP). And transcriptome sequencing analysis revealed that AV could suppress CXCL10 to alleviate NP, however, the upstream mechanisms governing CXCL10 synthesis remain vague.

Aim of the study

The research's goal was to identify the mechanism via which AV regulates CXCL10 to ameliorate NP.

Materials and methods

Chronic constriction injury (CCI) to the sciatic nerve was used to induce the NP model 14 days following surgery. To identify cell signaling pathways, various approaches were used, including transcriptome sequencing, western blotting, immunofluorescence, as well as ELISA. The in vitro assay involved the cultivation of neuron PC12 cells and astrocyte C6 cells.

Results

Both in vivo and in vitro results demonstrated that IL-12/IL-18 enhanced IFN-γ production in spinal neurons, which acted on IFN-γ receptors on neurons and astrocytes to upregulate CXCL10 expression in these cells, illustrating the pivotal role of IL-12 in the crosstalk between neurons and astrocytes. The role of IL-12 in pain regulation was elucidated for the first time within the nervous system. Additionally, its synergistic interaction with IL-18 on the downstream IFN-γ-CXCL10 pathway dramatically altered the activation of neurons and astrocytes. And AV could suppress CXCL10 to alleviate NP by mediating the IL-12-IFN-γ-IFNGR signaling pathway.

Conclusions

We explored a new target for NP by regulating neuron-astrocyte crosstalk and provided a theoretical basis for AV in clinical use.
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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