POTENTIAL OF ANTHOCYANIN BASED POLY (METHYL METHACRYLATE) NANOPARTICLES SPECIFIC ACTIVATED MICROGLIA IN MANAGEMENT INFLAMMATORY PAIN ON HERNIATED NUCLEUS PULPOSUS: A LITERATURE REVIEW

I. Widyadharma, Agung B S Satyarsa, F. Sanjaya, Ni Made Gitari, I. Niryana, T. E. Purwata, I. M. Jawi, Dewa Ngurah Suprapta, A. Sudewi
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引用次数: 1

Abstract

Pain is an unpleasant sensory and emotional experience that can affect the quality of life and leads to decreased productivity in patients. Low back pain (LBP) is one of the significant causes of disability worldwide with lifelong incidence. The purpose of this literature review describes the potential of anthocyanin-based Poly (Methyl Methacrylate) (PMMA) nanoparticles as the management of inflammatory pain in the Hernia Nucleus Pulposus (HNP ). The method used is a literature study by entering the keyword. Of the 77 journals reviewed, 47 journals were found by the topic and used as a reference for this work. The anthocyanin-based PMMA nanoparticles act as anti-nociceptors by inhibiting microglia that produce inflammatory mediators in HNP. Poly (Methyl Methacrylate) nanoparticles have specific targets in microglia. Anthocyanins have the effect of inhibiting inflammatory pain through many destinations. Anthocyanin inhibits the synthesis of nitric oxide (NO ) and prostaglandin E2 (PGE 2) and inhibits the activation of p38 MAPK and NF-kB pathways that express TNF-α and IL-1β genes as anti-nociceptive. The anthocyanin-based PMMA nanoparticles have potential as a novel therapy for inflammatory pain in HNP. There has been no research between these modalities. Therefore, further research is needed to find out the exact potential of anthocyanin-based PMMA nanoparticles.
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基于花青素的聚甲基丙烯酸甲酯纳米颗粒特异性激活小胶质细胞治疗髓核突出性炎症性疼痛的潜力:文献综述
疼痛是一种不愉快的感觉和情绪体验,可影响患者的生活质量并导致生产力下降。腰痛(LBP)是世界范围内致残的重要原因之一,具有终生发病率。本文献综述的目的是描述花青素基聚甲基丙烯酸甲酯(PMMA)纳米颗粒作为治疗髓核疝(HNP)炎症性疼痛的潜力。使用的方法是通过输入关键词进行文献研究。在77种期刊中,有47种期刊被该主题找到,并被用作本工作的参考。花青素基PMMA纳米颗粒通过抑制HNP中产生炎症介质的小胶质细胞而起到抗伤害感受器的作用。聚甲基丙烯酸甲酯纳米颗粒在小胶质细胞中具有特异性靶点。花青素具有通过许多目的地抑制炎症性疼痛的作用。花青素抑制一氧化氮(NO)和前列腺素E2 (pge2)的合成,抑制表达TNF-α和IL-1β基因的p38 MAPK和NF-kB通路的激活,起到抗伤害性作用。花青素基PMMA纳米颗粒有潜力成为治疗HNP炎症性疼痛的新疗法。目前还没有关于这些模式之间的研究。因此,需要进一步研究花青素基PMMA纳米颗粒的确切潜力。
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