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首页> 外文期刊>Molecular medicine reports >Therapeutic targets of thunder god vine (Tripterygium wilfordii hook) in rheumatoid arthritis
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Therapeutic targets of thunder god vine (Tripterygium wilfordii hook) in rheumatoid arthritis

机译:雷霆神藤(Tregterygium wilfordi钩)在类风湿性关节炎的治疗目标

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摘要

Celastrol and triptolide, chemical compounds isolated from Tripterygium wilfordii hook (also known as thunder god vine), are effective against rheumatoid arthritis (RA). Celastrol targets numerous signaling pathways involving NF-kappa B, endoplasmic reticulum Ca2+-ATPase, myeloid differentiation factor 2, toll-like receptor 4, pro-inflammatory chemokines, DNA damage, cell cycle arrest and apoptosis. Triptolide, inhibits NF-kappa B, the receptor activator of NF-kappa B (RANK)/RANK ligand/osteoprotegerin signaling pathway, cyclooxygenase-2, matrix metalloproteases and cytokines. The present review examined the chemistry and bioavailability of celastrol and triptolide, and their molecular targets in treating RA. Clinical studies have demonstrated that T. wilfordii has several promising bioactivities, but its multi-target toxicity has restricted its application. Thus, dosage control and structural modification of T. wilfordii are required to reduce the toxicity. In this review, future directions for research into these promising natural products are discussed.
机译:Celastrol和Triptolide,从赛德韦福德钩(又称雷神藤蔓)中分离的化学化合物,对类风湿性关节炎(RA)有效。 Celastrol靶向涉及NF-Kappa B,内质网Ca2 + -ATP酶,骨髓分化因子2,损伤趋化因子,DNA损伤,细胞循环抑制,细胞循环抑制和细胞凋亡的信号传导途径。雷丝酮,抑制NF-Kappa B,NF-κB(等级)/等级配体/骨盆信号传导途径,环氧氧酶-2,基质金属蛋白酶和细胞因子的受体激活剂。本综述检测了Celastrol和Triptolide的化学和生物利用度,以及它们在治疗RA的分子靶标。临床研究表明,T.Wilfordii有几个有前景的生物活性,但其多目标毒性已经限制了其应用。因此,需要D.Wilfordii的剂量控制和结构改性来降低毒性。在这篇综述中,讨论了未来的研究进入这些有前途的天然产品的方向。

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