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首页> 外文期刊>Journal of Pharmacopuncture >Stimulative Effects of Hominis Placental Pharmacopuncture Solution Combined with Zinc-oxide Nanoparticles on RAW 264.7 Cells - ZnO HPPS more easily stimulates RAW 264.7 cells -
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Stimulative Effects of Hominis Placental Pharmacopuncture Solution Combined with Zinc-oxide Nanoparticles on RAW 264.7 Cells - ZnO HPPS more easily stimulates RAW 264.7 cells -

机译:人参胎盘药物穿刺溶液结合氧化锌纳米粒子对RAW 264.7细胞的刺激作用-ZnO HPPS更容易刺激RAW 264.7细胞-

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Objectives: The purpose of this study is to examine whether Hominis Placental pharmacopuncture solution (HPPS) combined with zinc-oxide nanoparticles (ZnO NP) activates RAW 264.7 cells. Methods: We soaked ZnO nanoparticles in the Hominis Placenta pharmacopuncture solution, thereby making a combined form (ZnO NP HPPS). The effect of ZnO NP HPPS on the intracellular reactive oxygen species (ROS) production was measured by 2', 7'-dichlorofluorescin diacetate (DCFH-DA) assay. The effect of ZnO NP HPPS on NF- was measured by using a luciferase assay. The effect of ZnO NP HPPS on the cytokine expression was assessed by semi-quantitative reverse transcriptase polymerase chain reaction (RT-PCR). The cellular uptake of ZnO NP HPPS was measured by using a flow cytometric analysis, and cellular structural alterations were analyzed by using transmission electron microscopy (TEM). Results: Neither the HPPS nor the ZnO NPs induced intracellular ROS production in RAW 264.7 cells. Neither of the materials activated NF- or it's dependent genes, such as TNF- , IL-1, and MCP-1. However, ZnO NP HPPS, the combined form of ZnO NPs and HPPS, did induce the intracellular ROS production, as well as prominently activating NF- and it's dependent genes. Also, compared to ZnO NPs, it effectively increa-sed the uptake by RAW 264.7 cells. In addition, cellular structural alterations were observed in groups treated with ZnO NP HPPS. Conclusions: Neither ZnO NP nor HPPS activated RAW 264.7 cells, which is likely due to a low cellular uptake. The ZnO NP HPPS, however, significantly activated NF- and up-regulated its dependent genes such as TNF- , IL-1, and MCP-1. ZnO NP HPPS was also more easily taken into the RAW 264.7 cells than either ZnO NP or HPPS.
机译:目的:本研究的目的是检查人参胎盘药物穿刺溶液(HPPS)与氧化锌纳米颗粒(ZnO NP)的结合是否能激活RAW 264.7细胞。方法:将ZnO纳米颗粒浸泡在Hominis胎盘药物穿刺溶液中,制成复合形式(ZnO NP HPPS)。 ZnO NP HPPS通过2',7'-dichlorofluorescin diacetate(DCFH-DA)检测来测量细胞内活性氧(ROS)产生的影响。 ZnO NP HPPS对NF-的影响通过荧光素酶测定法进行了测定。 ZnO NP HPPS对细胞因子表达的影响通过半定量逆转录酶聚合酶链反应(RT-PCR)进行了评估。 ZnO NP HPPS的细胞吸收率通过流式细胞仪分析,并通过透射电子显微镜(TEM)分析细胞结构变化。结果:HPPS和ZnO NP均未诱导RAW 264.7细胞中细胞内ROS的产生。两种材料均未激活NF-或它的依赖基因,例如TNF-,IL-1和MCP-1。然而,ZnO NP HPPS(ZnO NP和HPPS的组合形式)确实诱导了细胞内ROS的产生,并显着激活了NF-及其依赖基因。而且,与ZnO NP相比,它可以有效地增加RAW 264.7细胞的摄取。另外,在用ZnO NP HPPS处理的组中观察到细胞结构改变。结论:ZnO NP和HPPS均未激活RAW 264.7细胞,这很可能是由于细胞摄取低所致。但是,ZnO NP HPPS可以显着激活NF-并上调其依赖性基因,例如TNF-,IL-1和MCP-1。与ZnO NP或HPPS相比,ZnO NP HPPS也更容易进入RAW 264.7细胞。

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