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基于仿生脂蛋白纳米制剂的木酸酸代谢组学和转录组学分析及其抗风湿关节炎的潜力。

Metabolomic and transcriptomic analyses of the anti-rheumatoid arthritis potential of xylopic acid in a bioinspired lipoprotein nanoformulation.

机构信息

State Key Laboratory of Natural Medicines, Clinical Metabolomics Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, No. 639 Longmian Avenue, Nanjing, 211198, China.

Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Qld, 4072, Australia.

出版信息

Biomaterials. 2021 Jan;268:120482. doi: 10.1016/j.biomaterials.2020.120482. Epub 2020 Nov 27.

Abstract

Xylopic acid (XA), a diterpene kaurene and the major active ingredient of the African spice Xylopia aethiopica (Annonaceae), is reported to possess anti-inflammatory and analgesic properties. Here, we investigated the therapeutic potential of XA for rheumatoid arthritis (RA), a debilitating autoimmune inflammatory disease characterized by joint damage, in the complete Freund's adjuvant (CFA)-induced arthritis model in rats. We synthesized bioinspired reconstituted high-density lipoprotein (rHDL) nanoparticles loaded with purified XA crystals (rHDL/XA) that passively accumulate in inflamed joints of CFA-induced arthritic rats. Treatment with rHDL/XA minimized mononuclear cell infiltration of CFA-induced arthritic sites and ameliorated disease burden. Metabolomic and transcriptomic analyses revealed that the major molecular pathways perturbed following CFA-induced arthritis correlated with amino acid and lipid metabolism, which were restored to normal states by rHDL/XA treatment. This work demonstrates the anti-RA potential of XA in a nanoformulation and uncovers its underlying therapeutic mechanisms at the transcript and metabolite levels.

摘要

木酸酸(XA)是一种双萜贝壳杉烯,也是非洲香料 Xylopia aethiopica(番荔枝科)的主要活性成分,据报道具有抗炎和镇痛作用。在这里,我们研究了 XA 在类风湿关节炎(RA)中的治疗潜力,RA 是一种以关节损伤为特征的使人衰弱的自身免疫性炎症性疾病,在完全弗氏佐剂(CFA)诱导的大鼠关节炎模型中进行了研究。我们合成了仿生再构成高密度脂蛋白(rHDL)纳米颗粒,负载纯化的 XA 晶体(rHDL/XA),这些纳米颗粒可以被动地积聚在 CFA 诱导的关节炎大鼠的炎症关节中。rHDL/XA 的治疗最小化了 CFA 诱导的关节炎部位的单核细胞浸润,并改善了疾病负担。代谢组学和转录组学分析表明,CFA 诱导的关节炎后受干扰的主要分子途径与氨基酸和脂质代谢相关,rHDL/XA 治疗可使其恢复正常状态。这项工作证明了 XA 在纳米制剂中的抗 RA 潜力,并揭示了其在转录和代谢物水平的潜在治疗机制。

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