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烯丙基甲基硫醚下调C57/BL6小鼠肾脏中X射线照射诱导的核因子-κB信号通路

Allylmethylsulfide Down-Regulates X-Ray Irradiation-Induced Nuclear Factor-kappaB Signaling in C57/BL6 Mouse Kidney.

作者信息

Lee Eun Kyeong, Chung Sang Woon, Kim Ji Young, Kim Ji Min, Heo Hyoung-Sam, Lim Hyun Ae, Kim Mi Kyung, Anton Stephen, Yokozawa Takako, Chung Hae Young

机构信息

Department of Pharmacy, Pusan National University, Busan, Republic of Korea.

出版信息

J Med Food. 2009 Jun;12(3):542-51. doi: 10.1089/jmf.2008.1073.

Abstract

Allylmethylsulfide (AMS), a volatile organosulfur derivative from garlic, has been shown to have radioprotective effects in radiation-challenged cell and animal models, but the mechanism of radioprotection is not well understood. To determine the mechanism of radioprotection in an in vivo model, we first verified the antioxidant capacity of AMS using 2,2'-azobis(2-amidinopropane) dihydrochloride-induced human embryonic kidney 293T cells by measuring reactive oxygen species generation, reduced glutathione, protein tyrosine kinase/protein tyrosine phosphatase balance, and nuclear factor-kappaB (NF-kappaB) protein levels. We then investigated the protective effects of AMS (55 and 275 micromol/kg, intraperitoneal treatment) on 15 Gy X-ray-irradiated mouse kidney. The results showed that AMS decreased the free radical-induced lipid peroxidation in mice exposed to X-rays. Moreover, the antioxidative AMS suppressed the activation of NF-kappaB and its dependent genes such as vascular cell adhesion molecule-1, inducible nitric oxide synthase, and cyclooxygenase-2 through inhibition of IkappaBalpha phosphorylation and activation of IkappaB kinase alpha/beta and mitogen-activated protein kinases (MAPKs). Based on these results, AMS may be a useful radioprotective agent by down-regulating the MAPKs and NF-kappaB signaling pathway that can be induced via X-ray irradiation.

摘要

烯丙基甲基硫醚(AMS)是一种源自大蒜的挥发性有机硫衍生物,已被证明在受辐射挑战的细胞和动物模型中具有辐射防护作用,但其辐射防护机制尚不清楚。为了确定体内模型中的辐射防护机制,我们首先通过测量活性氧生成、还原型谷胱甘肽、蛋白酪氨酸激酶/蛋白酪氨酸磷酸酶平衡以及核因子-κB(NF-κB)蛋白水平,使用2,2'-偶氮二(2-脒基丙烷)二盐酸盐诱导的人胚肾293T细胞验证了AMS的抗氧化能力。然后,我们研究了AMS(55和275微摩尔/千克,腹腔注射)对15 Gy X射线照射的小鼠肾脏的保护作用。结果表明,AMS降低了受X射线照射小鼠体内自由基诱导的脂质过氧化。此外,抗氧化性的AMS通过抑制IκBα磷酸化以及激活IκB激酶α/β和丝裂原活化蛋白激酶(MAPKs),抑制了NF-κB及其依赖性基因如血管细胞黏附分子-1、诱导型一氧化氮合酶和环氧化酶-2的激活。基于这些结果,AMS可能是一种有用的辐射防护剂,通过下调可由X射线照射诱导的MAPKs和NF-κB信号通路发挥作用。

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