Discovery of synergistic anti-inflammatory compound combination from herbal formula GuGe FengTong Ta

来源 :中国天然药物 | 被引量 : 0次 | 上传用户:scv100
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Multi-components in herbal formulae exert holistic effects in synergistic or additive manners.However,appropriate strategies and supportive evidences are still lacking to uncover the synergistic or additive combinations.The present investigation aimed at seeking a screening strategy to identify the targeted combinations in GuGe FengTong Tablet (GGFTT),an herbal formula.Two compounds,belonging to different chemical classes,were combined with different concentration ratios and their anti-inflammation effects were investigated.The most significant anti-inflammatory combinations were evaluated by combination index (CI) method (additive effect,CI =1;synergism,CI < 1;antagonism,CI > 1).The modulating effects of candidate combinations on pro-inflammatory cytokines and MAPKs signaling pathway were also detected.Two combinations,“biochanin A + 6-gingerol” (Bio-6G) and “genistein + 6-gingerol” (Geno6G),showed synergistic effects (CI < 1),and Bio-6G was selected for further study.Compared with single compound,Bio-6G could synergistically inhibit the production of pro-inflammatory cytokines (TNF-a,IL-1β,and IL-6) and the activation of MAPKs signaling pathway in LPS-stimulated RAW264.7 cells.The combined results showed that Bio-6G was a synergistic anti-inflammatory combination in GGFTT.Our results could provide a useful strategy to screen the synergistic combinations in herbal formulae.
其他文献
The present study was designed to evaluate the therapeutic potential of bioactive compounds from chloroform extract of the leaves of Hylocereus undatus in the formation of advanced glycation end products (AGEs) in vitro.Bioactivity-guided fractionation of
Romipeptides A and B (1 and 2),two new romidepsin derivatives,and three known compounds,chromopeptide A (3),romidepsin (4) and valine-leucine dipeptide (5) were isolated from the fermentation broth of Chromobacterium violaceum No.968.Their structures were
Replacement of the native promoter of the global regulator LaeA-like gene of Daldinia eschscholzii by a strong gpdA promoter led to the generation of two novel cyclopentenone metabolites,named dalestones A and B,whose structures were assigned by a combina
Notopterygium incisum (QH) has been used for the treatment of rheumatoid arthritis (RA),and volatile oils may be its mainly bioactive constituents.The present study was designed to analyze the volatile compounds in QH and to determine the anti-arthritic c
Astragali Radix,the root of Astragalus membranaceus (Fisch.) Bge.var.mongholicus (Bge.) Hsiao or Astragalus membranaceus (Fisch.) Bge.,is widely used as a tonic decoction pieces in the clinic of traditional Chinese medicine (TCM).Astragali Radix has vario
Sophorae Flavescentis Radix (Sophora flavescens Ait.,SFR) and Sophorae Tonkinensis Radix et Rhizoma (S.tonkinensis Gapnep.,STR) are two commonly used traditional Chinese medicines from Sophora (Leguminosae) plants,which are believed to possess similar bio
Gnaphalium affine D. Don, a medicinal and edible plant, has been used to treat gout in traditional Chinese medicine and popularly consumed in China for a long time. A detailed phytochemical investigation on the aerial part of G. affine led to the isolatio
Catalpol, a major bioactive component from Rehmannia glutinosa, which has been used to treat diabetes. The present study was designed to elucidate the anti-diabetic effect and mechanism of action for catalpol in db/db mice. The db/db mice were randomly di
Analysis errors can occur in the desorbing process of ginkgo diterpene lactone meglumine injection (GDMI) by a conventional analysis method, due to several factors, such as easily crystallized samples, solvent volatility, time-consuming sample pre-process
The present study was designed to evaluate protective activity of an ethanol extract of the stems ofSchisandra chinensis (SCE) and explore its possible molecular mechanisms on acetaminophen (APAP) induced hepatotoxicity in a mouse model.The results of HPL