The inhibitory effects of 2,3,5,4'-tetrahydroxystilbene-2-O-beta-d-glucoside (THSG), extracted from the roots of Polygonum multiflorum Thunb, on inflammatory activity in animal models and cyclooxygenase-2 (COX-2) activity in lipopolysaccharide (LPS)-induced mouse RAW264.7 macrophage cells were investigated. The carrageenin (CGN)-induced rat paw oedema model and dimethylbenzene-induced mouse ear oedema model were prepared; MTT assay, semi-quantitative RT-PCR, Western blot and ELISA were adopted. THSG 2.3, 4.6 and 9.2 mg kg(- 1) by oral administration inhibited mouse ear oedema and the percentage of inhibition of THSG 9.2 mg kg(- 1) is 87%. THSG 3.2, 6.4 and 12.8 mg kg(- 1) by oral administration dose-dependently inhibited rat paw oedema and the percentage of inhibition of THSG 12.8 mg kg(- 1) is 56% at 6 h. Indomethacin 13 and 9 mg kg(- 1) showed 90% and 57% inhibition in the same animal models, respectively. LPS 1 microg ml(- 1) significantly up-regulated prostaglandin E(2) (PGE(2)) production (inducing COX-2 activity) by 35% (exogenous arachidonic acid, AA), which was dose-dependently decreased by THSG 1, 10, and 100 micromol L(- 1) and the percentage of inhibition of THSG 10 micromol L(- 1) was 40%. NS-398 10 micromol L(- 1) decreased PGE(2) production by 42%. THSG 1, 10, 100 micromol L(- 1) was shown to markedly inhibit the LPS-induced COX-2 protein and mRNA expression in RAW264.7 cells (P < 0.05) but had no effect on COX-1 protein and mRNA (P>0.05). In summary, the data showed that THSG possessed an anti-inflammatory effect, which was perhaps related to the inhibition of COX-2 enzyme activity and expression in RAW264.7 macrophage cells.

译文

:从何首乌根中提取的2,3,5,4'-四羟基O-2-O-β-d-葡萄糖苷(THSG)对动物模型和环氧合酶2(COX)的炎性活性有抑制作用-2)研究了脂多糖(LPS)诱导的小鼠RAW264.7巨噬细胞的活性。制备了角叉菜胶(CGN)诱导的大鼠爪水肿模型和二甲基苯诱导的小鼠耳水肿模型;采用MTT法,半定量RT-PCR,Western blot和ELISA。口服THSG 2.3、4.6和9.2 mg kg(-1)抑制了小鼠耳部水肿,THSG 9.2 mg kg(-1)的抑制百分比为87%。口服THSG 3.2、6.4和12.8 mg kg(-1)剂量依赖性抑制大鼠足水肿,在6 h时THSG 12.8 mg kg(-1)的抑制百分比为56%。吲哚美辛13和9 m​​g kg(-1)在同一动物模型中分别显示90%和57%的抑制作用。 LPS 1 microg ml(-1)显着上调前列腺素E(2)(PGE(2))的产生(诱导COX-2活性)35%(外源花生四烯酸,AA),THSG剂量依赖性降低1,10和100 micromol L(-1)和THSG 10 micromol L(-1)的抑制率为40%。 NS-398 10 micromol L(-1)使PGE(2)产量降低了42%。 THSG 1、10、100 micromol L(-1)可显着抑制LPS诱导的RAW264.7细胞中COX-2蛋白和mRNA表达(P <0.05),但对COX-1蛋白和mRNA没有影响( P> 0.05)。总之,数据显示THSG具有抗炎作用,这可能与抑制COX-2酶活性和在RAW264.7巨噬细胞中的表达有关。

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