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The Effects and Mechanisms of Periplaneta americana Extract Reversal of Multi-Drug Resistance in BEL-7402/5-FU Cells

机译:美洲大plane提取物逆转BEL-7402 / 5-FU细胞多药耐药性的作用及其机制

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摘要

The present study reports the reversing effects of extracts from P. americana on multidrug resistance of BEL-7402/5-FU cells, as well as a preliminary investigation on their mechanism of action. A methylthiazolyl tetrazolium (MTT) method was applied to determine the multidrug resistance of BEL-7402/5-FU, while an intracellular drug accumulation assay was used to evaluate the effects of a column chromatography extract (PACC) and defatted extract (PADF) from P. americana on reversing multi-drug resistance. BEL-7402/5-FU reflected high resistance to 5-FU; PACC and PADF could promote drug accumulation in BEL-7402/5-FU cells, among which PADF was more effective than PACC. Moreover, results from the immunocytochemical method showed that PACC and PADF could downregulate the expression of drug resistance-associated proteins (P-gp, MRP, LRP); PACC and PADF had no effects on the expression of multidrug resistance-associated enzymes (GST-π), but PACC could increase the expression of multidrug resistance-associated enzymes (PKC). Results of real-time fluorescence quantitative PCR revealed that PACC and PADF were able to markedly inhibit the expression of multidrug resistance-associated genes (MDR1, LRP and MRP1); PACC presented a significant impact on the gene expression of multidrug resistance-associated enzymes, which increased the gene expression of GST-π and PKC. However, PADF had little impact on the expression of multidrug resistance-associated enzymes. These results demonstrated that PACC and PADF extracted from P. americana could effectively reverse MDR in BEL-7402/5-FU cells, whose mechanism was to inhibit the expression of P-gp, MRP, and LRP, and that PADF was more effective in the reversal of MDR than did PACC. In addition, some of extracts from P. americana altered (sometimes increasing) the expression of multidrug resistance-associated enzymes.
机译:本研究报告了美洲假单胞菌提取物对BEL-7402 / 5-FU细胞多药耐药性的逆转作用,并对其作用机理进行了初步研究。甲基噻唑基四唑鎓(MTT)方法用于确定BEL-7402 / 5-FU的多药耐药性,而细胞内药物累积测定用于评估柱层析提取物(PACC)和脱脂提取物(PADF)的效果。 P. americana逆转多重耐药性。 BEL-7402 / 5-FU表现出对5-FU的高抵抗力; PACC和PADF可以促进BEL-7402 / 5-FU细胞中的药物蓄积,其中PADF比PACC更有效。此外,免疫细胞化学方法的结果表明,PACC和PADF可以下调与药物相关的蛋白质(P-gp,MRP,LRP)的表达; PACC和PADF对多药耐药相关酶(GST-π)的表达没有影响,但是PACC可以增加多药耐药相关酶(PKC)的表达。实时荧光定量PCR结果表明,PACC和PADF能够显着抑制多药耐药相关基因(MDR1,LRP和MRP1)的表达。 PACC对多药耐药相关酶的基因表达有显着影响,增加了GST-π和PKC的基因表达。但是,PADF对多药耐药相关酶的表达影响很小。这些结果表明,从美洲假单胞菌中提取的PACC和PADF可以有效逆转BEL-7402 / 5-FU细胞中的MDR,其机制是抑制P-gp,MRP和LRP的表达,而PADF可以更有效地逆转BEL-7402 / 5-FU细胞。 MDR的逆转比PACC大。此外,美洲P.的一些提取物改变(有时增加)与多药耐药性相关的酶的表达。

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