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Protective effect of Bu-Zhong-Yi-Qi decoction, the water extract of Chinese traditional herbal medicine, on 5-fluorouracil-induced intestinal mucositis in mice

机译:中草药水提取物补中益气汤对5-氟尿嘧啶致小鼠肠黏膜炎的保护作用

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摘要

Intestinal mucositis is a serious toxic side effect of 5-fluorouracil (5-FU) treatment. Bu-Zhong-Yi-Qi decoction (BZYQD), a water extract of Chinese traditional herbal medicine, is widely used in chemotherapy in Asia as an alternative treatment to reduce the side effects of chemotherapy. However, the mechanism is unknown. To evaluate its mechanism, we investigated the effect of BZYQD on 5-FU-induced intestinal mucositis in mice, especially with regard to apoptosis in the intestinal mucosal epithelia. In the present study, mice were divided into three groups: control, 5-FU, and 5-FU + BZYQD. Mice in the 5-FU and 5-FU + BZYQD groups were administered 5-FU (100 mg/kg/day, intraperitoneally) for 6 days, and the mice in the latter group were given BZYQD (8 g/kg/day, intragastrically) beginning 4 days before 5-FU and continuing until the termination of the experiment. Loss in body weight and diarrhea during the 5-FU treatment were significantly attenuated by administration of BZYQD. The morphological signs of intestinal damage, including shortened villi height, crypt destruction, apoptosis, and necrosis, in intestinal mucosal epithelia were also reversed, accompanied by reduced neutrophil infiltration, nitrite levels, and inflammatory factors (tumor necrosis factor a and interleukin 1 beta) and increased levels of reduced glutathione. These results suggest that BZYQD inhibits 5-FU-induced intestinal mucositis, and this effect may be due to the reduction in apoptosis and necrosis in intestinal mucosal epithelia via the suppression of inflammatory cytokine upregulation. In conclusion, inhibiting cytokine-mediated apoptosis or necrosis can be the molecular mechanism by which BZYQD reduces the gastrointestinal side effects of cancer chemotherapy.
机译:肠粘膜炎是5-氟尿嘧啶(5-FU)治疗的严重毒副作用。补中益气汤(BZYQD)是中草药的水提取物,在亚洲广泛用于化疗,作为减少化疗副作用的替代疗法。但是,该机制是未知的。为了评估其机制,我们研究了BZYQD对5-FU诱导的小鼠肠黏膜炎的影响,特别是在肠黏膜上皮细胞凋亡方面。在本研究中,小鼠分为三组:对照组,5-FU和5-FU + BZYQD。对5-FU和5-FU + BZYQD组的小鼠进行5-FU(100 mg / kg /天,腹膜内)给药6天,对后者的小鼠给予BZYQD(8 g / kg /天,胃内)从5-FU开始前4天开始,一直持续到实验终止。通过服用BZYQD,5-FU治疗期间的体重减轻和腹泻明显减轻。肠粘膜上皮中肠损害的形态学特征(包括绒毛高度缩短,隐窝破坏,凋亡和坏死)也被逆转,并伴有中性粒细胞浸润,亚硝酸盐水平和炎性因子减少(肿瘤坏死因子a和白介素1 beta)和增加的还原型谷胱甘肽水平。这些结果表明BZYQD抑制5-FU诱导的肠道粘膜炎,并且这种作用可能是由于通过抑制炎性细胞因子上调抑制了肠黏膜上皮的凋亡和坏死。总之,抑制细胞因子介导的细胞凋亡或坏死可能是BZYQD降低癌症化学疗法的胃肠道副作用的分子机制。

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