Aldose reductase (AR; AKR1B1) a member of aldo-keto reductase super family, that we had shown earlier mediates cytotoxic signals induced by high glucose, cytokines and growth factors, also mediates the inflammatory signals induced by Gram-negative bacterial endotoxin, lipopolysaccharide (LPS). Inhibition of AR by three distinct AR inhibitors sorbinil, tolrestat or zopolrestat suppressed the LPS-induced production of inflammatory cytokines such as TNF-alpha, IL-6, IL-1beta, IFN-gamma, and chemokine MCP-1 in murine peritoneal macrophages. Inhibition of AR also prevented the production of nitric oxide, and prostaglandin E2 and expression of iNOS and Cox-2 proteins. The LPS-induced DNA binding activity of NF-kappaB and AP1 were significantly inhibited by AR inhibitors, and this effect was mediated through the inhibition of phosphorylation of IkappaB-alpha, IKK alpha/beta and PKC. These results suggest the therapeutic use of AR inhibitors as anti-inflammatory drugs.

译文

醛糖还原酶 (AR; AKR1B1) 是aldo-酮还原酶超级家族的成员,我们已经显示出较早的介导高糖,细胞因子和生长因子诱导的细胞毒性信号,也介导革兰氏阴性细菌内毒素,脂多糖 (LPS) 诱导的炎症信号。三种不同的AR抑制剂sorbinil,tolrestat或zopolrestat对AR的抑制作用抑制了LPS诱导的炎症细胞因子的产生,例如TNF-α,IL-6,IL-1beta,IFN-γ 和小鼠腹膜巨噬细胞中的趋化因子MCP-1。抑制AR还阻止了一氧化氮和前列腺素E2的产生以及iNOS和Cox-2蛋白的表达。AR抑制剂显著抑制了LPS诱导的NF-κ b和AP1的DNA结合活性,并且这种作用是通过抑制IkappaB-α,IKK α/β 和PKC的磷酸化来介导的。这些结果表明AR抑制剂作为抗炎药的治疗用途。

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