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Bisbenzoxazole derivatives had an antiinflammatory effect on in vitro stimulated macrophages

机译:双苯并恶唑衍生物对体外刺激的巨噬细胞具有抗炎作用

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摘要

Benzoxazoles are DNA base bioisosteres and studies suggest that their derivatives have antiproliferative activities. Based on their antiproliferative activities they have been mostly studied as new generation anticancer drugs. In our study we exploited their antiproliferative effect, aiming to delineate bisbenzoxazole derivatives' (RHE 231 and RHE 238) potential antiinflammatory effect on mouse macrophages that are activated in vitro through danger signal LPS stimulation. RAW 267.4 mammalian macrophages were activated in the presence of our derivatives with or without danger mimic E. coli derived LPS. We present data that support the strong antiinflammatory activity of the bisbenzoxazole derivatives RHE 231 and RHE 238 on stimulated mammalian macrophages. There was a significant and substantial decrease in the production levels of TNF-$lpha $, IL-1$eta $, and IL-6 proinflammatory cytokines in the presence of RHE 231 and RHE 238. These molecules had an antiproliferative effect on the macrophages and, probably, this was their mechanism of action on the cells to alter their inflammatory functions. Our results show that bisbenzoxazole structures RHE 231 and RHE 238 have potential to be used as antiinflammatory drug agents.
机译:苯并恶唑是DNA的生物等排体,研究表明它们的衍生物具有抗增殖活性。基于它们的抗增殖活性,它们主要被研究为新一代抗癌药。在我们的研究中,我们利用了它们的抗增殖作用,旨在描述双苯并恶唑衍生物(RHE 231和RHE 238)对通过危险信号LPS刺激体外激活的小鼠巨噬细胞的潜在抗炎作用。在存在或不存在模拟危险的危险的情况下,在存在我们衍生物的情况下将RAW 267.4哺乳动物巨噬细胞激活。大肠杆菌衍生的LPS。我们目前的数据支持双苯并恶唑衍生物RHE 231和RHE 238对受刺激的哺乳动物巨噬细胞的强抗炎活性。在存在RHE 231和RHE 238的情况下,TNF-α,IL-1,β和IL-6促炎细胞因子的产生水平显着且显着降低。这些分子具有抗增殖作用巨噬细胞,可能是它们对细胞改变炎症功能的作用机制。我们的结果表明,双苯并恶唑结构RHE 231和RHE 238具有用作抗炎药的潜力。

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