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IKKβ Inhibitor IMD-0354 Attenuates Radiation Damage in Whole-body X-Irradiated Mice

机译:IKKβ抑制剂IMD-0354衰减全体X辐照的小鼠的辐射损伤

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Nuclear factor-kappa B (NF-κB) transcription factor plays a critical role in regulating radiation-induced inflammatory and immune responses. Intracellular reactive oxygen species generation induces the activation of NF-κB via the inhibitor of κB (IκB) kinase (IKK) complex signaling. Previous studies have reported that the inhibition of IKK-driven NF-κB activation offers a therapeutic strategy for managing inflammatory disorders and various cancers, but it has additionally been reported that treatment targeting NF-κB also shows a radioprotective effect. IMD-0354 is an IKKβ inhibitor that blocks IκBα phosphorylation in the NF-κB pathway. This compound is known to exert anti-inflammatory and antitumor effects, but its radioprotective effects are unclear. Therefore, in the present study, we examined whether or not IMD-0354 has a mitigative effect on radiation-induced damages in mice. IMD-0354 was dissolved in soybean oil and subcutaneously administered to C57BL/6J Jcl mice for 3 consecutive days after 7?Gy of whole-body X-irradiation. The survival rate on day 30 and the NF-κB p65 and IκBα in bone marrow and spleen cells based on flow cytometry were assessed. IMD-0354 administration significantly suppressed the lethality induced by whole-body X-irradiation, and the survival rate increased by 83%. The NF-κB p65 and IκBα in bone marrow and spleen cells were significantly lower in IMD-0354-treated mice than in irradiated mice, suggesting that the IKKβ inhibitor IMD-0354 exerts a radiomitigative effect by suppressing the NF-κB.
机译:核因子-Kappa B(NF-κB)转录因子在调节辐射诱导的炎症和免疫应答方面发挥着关键作用。细胞内反应性氧物种产生通过κB(IκB)激酶(IKK)复合信号传导的抑制剂诱导NF-κB的活化。以前的研究报道说,IKK驱动的NF-κB活化的抑制提供了管理炎症疾病和各种癌症的治疗策略,但另外据报道,靶向NF-κB的治疗也显示出辐射保护作用。 IMD-0354是一种IKKβ抑制剂,其阻断NF-κB途径中的IκBα磷酸化。已知该化合物施加抗炎和抗肿瘤作用,但其放射性保护作用尚不清楚。因此,在本研究中,我们检查了IMD-0354是否对小鼠辐射诱导的损伤具有缓解作用。将IMD-0354溶解在大豆油中,并将其皮下给予C57BL / 6J JCL小鼠,连续3天在7?GY的全体X辐射后3天。评估了第30天的存活率和基于流式细胞术的骨髓和脾细胞中的NF-κBP65和IκBα。 IMD-0354管理显着抑制了全体X辐射诱导的致命性,生存率增加了83%。在IMD-0354处理的小鼠中,骨髓和脾细胞中的NF-κBP65和IκBα显着低于照射小鼠,表明IKKβ抑制剂IMD-0354通过抑制NF-κB施加辐射效果。

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