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Dietary intake of probiotic kimchi ameliorated IL-6-driven cancer cachexia

机译:饮食中益生菌泡菜的饮食摄入改善了IL-6驱动的癌症恶病质

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摘要

Cancer cachexia is a syndrome accompanying weight loss, skeletal muscle atrophy, and loss of adipose tissue in patients with advanced cancer. Since interleukin-6 (IL-6) is one of core mediators causing cancer cachexia and kimchi can modulate IL-6 response, we hypothesized dietary intake of kimchi can ameliorate cancer cachexia. In this study, we studied preemptive administration of kimchi can ameliorate mouse colon carcinoma cells colon (C26) adenocarcinoma-induced cancer cachexia and explored anti-cachexic mechanisms of kimchi focused on the changes of muscle atrophy, cachexic inflammation, and catabolic catastrophe. As results, dietary intake of kimchi significantly attenuated the development of cancer cachexia, presented with lesser weight loss, higher muscle preservation as well as higher survival from cancer cachexia in mice. Starting from significant inhibition of IL-6 and its signaling, kimchi afforded significant inhibition of muscle specific ubiquitin-proteasome system including inhibition of atrogin-1 and muscle ring finger protein-1 (MuRF-1) with other muscle related genes including mitofusin-2 (Mfn-2) and PGC-1α. Significant inhibition of lipolysis gene such as adipose triglyceride lipase (ATGL) and hormone-sensitive ligase (HSL) accompanied with significant induction of fatty acid synthase (FAS) and sterol response element binding protein 1 (SREBP1) was achieved with kimchi. As gene regulation, IL-6 and their receptor as well as Janus kinase 2 (JAK2) and signal transducer and activator of transcription 3 (STAT3) were significantly attenuated with kimchi. In conclusion, dietary intake of cancer preventive kimchi can be an anticipating option to ameliorate cancer cachexia via suppressive action of IL-6 accompanied with decreased muscle atrophy and lipolysis.
机译:癌症恶病质是伴随晚期癌症患者的体重减轻,骨骼肌萎缩和脂肪组织减少的综合征。由于白介素6(IL-6)是引起癌症恶病质的核心介质之一,泡菜可以调节IL-6反应,因此我们假设饮食中摄入的泡菜可以改善癌症恶病质。在这项研究中,我们研究了泡菜的预先服用可以改善小鼠结肠癌细胞结肠(C26)腺癌引起的癌症恶病质,并探讨了泡菜的抗恶病质机制,重点在于肌肉萎缩,恶病质炎症和分解代谢性巨灾的变化。结果,饮食中摄入的泡菜显着减弱了癌症恶病质的发展,表现出体重减轻较少,肌肉保留更高,小鼠恶病质的存活率更高。从显着抑制IL-6及其信号转导开始,泡菜提供了对肌肉特异性泛素-蛋白酶体系统的显着抑制,包括对atrogin-1和肌肉无名指蛋白1(MuRF-1)以及其他与肌相关的基因的抑制,包括线粒体2 (Mfn-2)和PGC-1α。使用泡菜可以显着抑制脂解基因,例如甘油三酸酯脂肪酶(ATGL)和激素敏感性连接酶(HSL),并显着诱导脂肪酸合酶(FAS)和固醇响应元件结合蛋白1(SREBP1)。作为基因调控,泡菜大大减弱了IL-6及其受体以及Janus激酶2(JAK2)以及信号转导和转录激活因子3(STAT3)的功能。总之,饮食中摄入预防癌的泡菜可以通过IL-6的抑制作用以及减少的肌肉萎缩和脂解作用来改善癌症恶病质。

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