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对黄连解毒汤(HLJDD)中潜在生物活性成分进行计算机辅助靶点筛选,并阐明其治疗脓毒症的分子机制。

In silico target fishing for the potential bioactive components contained in Huanglian Jiedu Tang (HLJDD) and elucidating molecular mechanisms for the treatment of sepsis.

作者信息

Ma Shi-Tang, Feng Cheng-Tao, Dai Guo-Liang, Song Yue, Zhou Guo-Liang, Zhang Xiao-Lin, Miao Cheng-Gui, Yu Hao, Ju Wen-Zheng

机构信息

Food and Drug College, Anhui University of Science and Technology, Fengyang 233100, China; College of Pharmacy, Nanjing University of Traditional Chinese Medicine, Nanjing 210023, China.

Anhui University of Science and Technology, Huainan 232001, China.

出版信息

Chin J Nat Med. 2015 Jan;13(1):30-40. doi: 10.1016/S1875-5364(15)60004-8.

Abstract

The present study was designed to target fish for potential bioactive components contained in a Huang Lian Jie Du decoction (HLJDD) and identify the underlying mechanisms of action for the treatment of sepsis at the molecular level. he bioactive components database of HLJDD was constructed and the sepsis-associated targets were comprehensively investigated. The 3D structures of the PAFR and TXA2R proteins were established using the homology modelling (HM) method, and the molecular effects for sepsis treatment were analysed by comparing the bioactive components database and the sepsis targets using computational biology methods. The results of the screening were validated with biological testing against the human oral epidermal carcinoma cell line KB in vitro. We found that multiple bioactive compounds contained in the HLJDD interacted with multiple targets. We also predicted the promising compound leads for sepsis treatment, and the first 28 compounds were characterized. Several compounds, such as berberine, berberrubine and epiberberine, dose-dependently inhibited PGE2 production in human KB cells, and the effects were similar in the presence or absence of TPA. This study demonstrates a novel approach to identifying natural chemical compounds as new leads for the treatment of sepsis.

摘要

本研究旨在针对含有黄连解毒汤(HLJDD)的鱼类潜在生物活性成分,并在分子水平上确定其治疗脓毒症的潜在作用机制。构建了HLJDD的生物活性成分数据库,并全面研究了脓毒症相关靶点。使用同源建模(HM)方法建立了PAFR和TXA2R蛋白的三维结构,并通过计算生物学方法比较生物活性成分数据库和脓毒症靶点来分析脓毒症治疗的分子效应。筛选结果在体外针对人口腔表皮癌细胞系KB进行生物学测试验证。我们发现HLJDD中含有的多种生物活性化合物与多个靶点相互作用。我们还预测了脓毒症治疗有前景的化合物先导物,并对前28种化合物进行了表征。几种化合物,如小檗碱、小檗红碱和表小檗碱,在人KB细胞中剂量依赖性地抑制PGE2的产生,并且在有或没有佛波酯(TPA)的情况下效果相似。本研究展示了一种鉴定天然化合物作为脓毒症治疗新先导物的新方法。

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