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肉桂中的金纳米颗粒对 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的小鼠模型的作用。

Role of gold nanoparticle from Cinnamomum verum against 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) induced mice model.

机构信息

Department of Neurology, Affiliated hospital of Hebei university, Baoding, Hebei 071000, China.

Department of Neurology, Heilongjiang Provincial Hospital, Haerbin, Heilongjiang 071000, China.

出版信息

J Photochem Photobiol B. 2019 Dec;201:111657. doi: 10.1016/j.jphotobiol.2019.111657. Epub 2019 Oct 28.

Abstract

Parkinson's disease (PD) is a general neurodegenerative disorder which largely has an effect on the society of the aged populations. PD is distinguishedwith loss of dopaminergic (DA) neurons in the substantia nigra. The exceptional properties of gold nanoparticles (AuNPs) have fascinated great attention in biomedical applications. In this present study, we explored theprospective beneficial effects of AuNPs synthesized from Cinnamomum verum on PD. PD rat models were established through MPTP injection treatment and AuNPs was administered. Administration of AuNPs reduces effect of MPTP-induced oxidative stress and motor abnormalities observed in PD rats. In addition ELISA analysis demonstrated that AuNPs treatment significantly attenuates Tumor Necrosis Factor-α (TNF-α), Interleukin-1β (IL-1β) and Interleukin-6 (IL-6) expression levels. Consequently, we investigated TLR/NF-κB pathway to examine the function of AuNPs on MPTP- induced PD rats. We found that AuNPs suppressed the alterations in the pathway of TLR/NF-κB associated molecules in MPTP stimulated PD rats. Hence, our results suggest that AuNPs attenuates MPTP introduced motor disorders, oxidative stress, activated inflammatory cytokines and activated TLR/NF-κB signaling in PD rats. In conclusion, AuNPs ease PD symptoms by the inhibition of TLR/NF-κB signaling pathway and recommend promise approach in the treatment of neurodegenerative diseases such as PD.

摘要

帕金森病(PD)是一种常见的神经退行性疾病,主要影响老年人群体。PD 的特征是黑质中多巴胺能(DA)神经元的丧失。金纳米粒子(AuNPs)的特殊性质在生物医学应用中引起了极大的关注。在本研究中,我们探讨了从肉桂中合成的 AuNPs 对 PD 的潜在有益作用。通过 MPTP 注射治疗建立 PD 大鼠模型,并给予 AuNPs。AuNPs 的给药减轻了 PD 大鼠中观察到的 MPTP 诱导的氧化应激和运动异常的影响。此外,ELISA 分析表明,AuNPs 处理显著降低了肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的表达水平。因此,我们研究了 TLR/NF-κB 途径,以检查 AuNPs 对 MPTP 诱导的 PD 大鼠的作用。我们发现,AuNPs 抑制了 MPTP 刺激的 PD 大鼠 TLR/NF-κB 相关分子途径的改变。因此,我们的结果表明,AuNPs 减轻了 MPTP 引起的运动障碍、氧化应激、激活的炎症细胞因子和 PD 大鼠中激活的 TLR/NF-κB 信号。总之,AuNPs 通过抑制 TLR/NF-κB 信号通路缓解 PD 症状,为治疗帕金森病等神经退行性疾病提供了有前途的方法。

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