首页> 外文会议>Nanoelectronics Conference (INEC), 2010 >Minocycline nano-liposome inhibit the production of TNF-α in LPS-stimulated macrophages
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Minocycline nano-liposome inhibit the production of TNF-α in LPS-stimulated macrophages

机译:米诺环素纳米脂质体抑制LPS刺激的巨噬细胞中TNF-α的产生

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To evaluate the effects of minocycline nano-liposome on regulating endotoxin-induced upregulation of inflammatory molecules were elucidated. Murine macrophages (ANA-1 cells) were prepared and treated with lipopolysaccharide (LPS, 10 ¿g/ ml), LPS plus minocycline nano-liposome (10, 20, 40, 50 and 70 ¿g/ ml), LPS plus minocycline (50 ¿g/ ml). MTT assay was used to evaluate the in vitro cytoxicity. The levels of TNF-¿ mRNA were measured by fluorescent RT-PCR. Minocycline nano-liposome showed dose- and ratio-dependent inhibition. LPS-stimulated inflammatory cytokine TNF-¿ secretion in the macrophages and reduced LPS-induced TNF-¿ mRNA expression on macrophages. It shows statistically significance when compared minocycline nano-liposome (10, 20, 40, 50 and 70 ¿g/ ml) to the vehicle control group; Statistic difference (P>0.05) was not found between minocycline nano-liposome (10, 20, 40 ¿g/ ml) and minocycline (50 ¿g/ ml). It indicated that the minocycline nano-liposome can provide a potential therapeutic tool to reduce the amount of drug that is required to treat a inflammation or immune diseases of periodontitis associated with the production of TNF-a, and have less side effect.
机译:为了评估米诺环素纳米脂质体在调节内毒素诱导的炎症分子上调中的作用。制备鼠巨噬细胞(ANA-1细胞),并用脂多糖(LPS,10μg/ ml),LPS和米诺环素纳米脂质体(10、20、40、50和70μs处理)克/毫升),LPS加美满霉素(50克/毫升)。使用MTT测定法评估体外细胞毒性。荧光RT-PCR测定了TNF-α,mRNA的水平。米诺环素纳米脂质体显示出剂量和比例依赖性抑制作用。 LPS刺激巨噬细胞中的炎性细胞因子TNF-γ的分泌和减少巨噬细胞上LPS诱导的TNF-γ的mRNA表达。当将米诺环素纳米脂质体(10、20、40、50和70μg/ ml)与车辆对照组进行比较时,它显示出统计学意义;米诺环素纳米脂质体(10、20、40μg/ ml)和米诺环素(50μg/ ml)之间未发现统计差异(P> 0.05)。这表明,米诺环素纳米脂质体可以提供一种潜在的治疗工具,以减少治疗与产生TNF-α有关的牙周炎的炎症或免疫疾病所需的药物量,并且副作用较小。

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