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UBH 汤:通过抑制 NF-κB 介导的诱导型一氧化氮合酶预防急性炎症的草药配方。

U-Bang-Haequi Tang: A Herbal Prescription that Prevents Acute Inflammation through Inhibition of NF-κB-Mediated Inducible Nitric Oxide Synthase.

机构信息

Department of Ophthalmology, Otolaryngology & Dermatology, Daegu Haany University, Daegu 706-828, Republic of Korea.

Medical Research Center for Globalization of Herbal Formulation, College of Oriental Medicine, Daegu Haany University, Daegu 706-828, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2014;2014:542825. doi: 10.1155/2014/542825. Epub 2014 May 15.

Abstract

Since antiquity, medical herbs have been prescribed for both treatment and preventative purposes. Herbal formulas are used to reduce toxicity as well as increase efficacy in traditional Korean medicine. U-bang-haequi tang (UBT) is a herbal prescription containing Arctii fructus and Forsythia suspensa as its main components and has treated many human diseases in traditional Korean medicine. This research investigated the effects of UBT against an acute phase of inflammation. For this, we measured induction of nitric oxide (NO) and related proteins in macrophage cell line stimulated by lipopolysaccharide (LPS). Further, paw swelling was measured in carrageenan-treated rats. Carrageenan significantly induced activation of inflammatory cells and increases in paw volume, whereas oral administration of 0.3 or 1 g/kg/day of UBT inhibited the acute inflammatory response. In RAW264.7 cells, UBT inhibited mRNA and protein expression levels of iNOS. UBT treatment also blocked elevation of NO production, nuclear translocation of NF-κB, phosphorylation of Iκ-Bα induced by LPS. Moreover, UBT treatment significantly blocked the phosphorylation of p38 and c-Jun NH2-terminal kinases by LPS. In conclusion, UBT prevented both acute inflammation in rats as well as LPS-induced NO and iNOS gene expression through inhibition of NF-κB in RAW264.7 cells.

摘要

自古以来,草药就被用于治疗和预防疾病。草药配方被用于降低毒性并提高传统韩国医学中的疗效。U-bang-haequi tang(UBT)是一种草药处方,其主要成分是牛蒡子和连翘,并已在传统韩国医学中治疗了许多人类疾病。本研究调查了 UBT 对炎症急性期的影响。为此,我们测量了脂多糖(LPS)刺激的巨噬细胞系中一氧化氮(NO)和相关蛋白的诱导。此外,还测量了角叉菜胶处理的大鼠的爪肿胀。角叉菜胶显著诱导炎症细胞的激活和爪体积的增加,而 0.3 或 1 g/kg/天的 UBT 口服给药抑制了急性炎症反应。在 RAW264.7 细胞中,UBT 抑制了 iNOS 的 mRNA 和蛋白表达水平。UBT 治疗还阻止了 LPS 诱导的 NO 产生、NF-κB 核易位、Iκ-Bα磷酸化的升高。此外,UBT 治疗还显著阻止了 LPS 诱导的 p38 和 c-Jun NH2-末端激酶的磷酸化。总之,UBT 通过抑制 RAW264.7 细胞中的 NF-κB,预防了大鼠的急性炎症以及 LPS 诱导的 NO 和 iNOS 基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c5/4052510/a49a4ad3850b/ECAM2014-542825.001.jpg

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