Ohbuchi Katsuya, Nishiumi Shin, Fujitsuka Naoki, Hattori Tomohisa, Yamamoto Masahiro, Inui Akio, Azuma Takeshi, Yoshida Masaru
Division of Metabolomics Research, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-Cho, Chuo-ku, Kobe, Hyogo 650-0017, Japan ; Tsumura Research Laboratories, Tsumura and Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, Japan.
Division of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-Cho, Chuo-ku, Kobe, Hyogo 650-0017, Japan.
Evid Based Complement Alternat Med. 2015;2015:871832. doi: 10.1155/2015/871832. Epub 2015 Sep 15.
Cancer cachexia, which is characterized by decreased food intake, weight loss and systemic inflammation, increases patient's morbidity and mortality. We previously showed that rikkunshito (RKT), a Japanese traditional herbal medicine (Kampo), ameliorated the symptoms of cancer cachexia through ghrelin signaling-dependent and independent pathways. To investigate other mechanisms of RKT action in cancer cachexia, we performed metabolome analysis of plasma in a rat model bearing the Yoshida AH-130 hepatoma. A total of 110 metabolites were detected in plasma and RKT treatment significantly altered levels of 23 of those metabolites in cachexia model rats. Among them, glucarate, which is known to have anticarcinogenic activity through detoxification of carcinogens via inhibition of β-glucuronidase, was increased in plasma following administration of RKT. In our AH-130 ascites-induced cachexia rat model, administration of glucarate delayed onset of weight loss, improved muscle atrophy, and reduced ascites content. Additionally, glucarate reduced levels of plasma interferon-γ (IFN-γ) in tumor-bearing rats and was also found to suppress LPS-induced IFN-γ expression in splenocytes in vitro. These results suggest that glucarate has anti-inflammatory activity via a direct effect on immune host cells and suggest that RKT may also ameliorate inflammation partly through the elevation of glucarate in plasma.
癌症恶病质以食物摄入减少、体重减轻和全身炎症为特征,会增加患者的发病率和死亡率。我们之前表明,日本传统草药(汉方)六君子汤(RKT)通过胃饥饿素信号依赖和非依赖途径改善了癌症恶病质的症状。为了研究RKT在癌症恶病质中的其他作用机制,我们对携带吉田AH-130肝癌的大鼠模型血浆进行了代谢组分析。血浆中共检测到110种代谢物,RKT治疗显著改变了恶病质模型大鼠中23种代谢物的水平。其中,已知通过抑制β-葡萄糖醛酸酶对致癌物进行解毒而具有抗癌活性的葡萄糖醛酸,在给予RKT后血浆中含量增加。在我们的AH-130腹水诱导的恶病质大鼠模型中,给予葡萄糖醛酸可延迟体重减轻的发生,改善肌肉萎缩,并减少腹水含量。此外,葡萄糖醛酸降低了荷瘤大鼠血浆中干扰素-γ(IFN-γ)的水平,并且还发现在体外可抑制脂多糖诱导的脾细胞中IFN-γ的表达。这些结果表明,葡萄糖醛酸通过对免疫宿主细胞的直接作用具有抗炎活性,并表明RKT也可能部分通过提高血浆中葡萄糖醛酸的水平来改善炎症。