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熊去氧胆酸减轻大鼠模型中5-氟尿嘧啶诱导的粘膜炎。

Ursodeoxycholic acid attenuates 5-fluorouracil-induced mucositis in a rat model.

作者信息

Kim Seung Han, Chun Hoon Jai, Choi Hyuk Soon, Kim Eun Sun, Keum Bora, Seo Yeon Seok, Jeen Yoon Tae, Lee Hong Sik, Um Soon Ho, Kim Chang Duck

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Institute of Gastrointestinal Medical Instrument Research, Korea University College of Medicine, Seoul 02841, Republic of Korea.

出版信息

Oncol Lett. 2018 Aug;16(2):2585-2590. doi: 10.3892/ol.2018.8893. Epub 2018 Jun 4.

Abstract

Intestinal mucositis is a commonly encountered complication of chemotherapy. However, there are few effective treatments or preventive methods. Ursodeoxycholic acid (UDCA) stabilizes cell membranes, acts as an antioxidant and inhibits apoptosis, thereby exerting cytoprotective effects. The aim of the present study was to examine the ability of UDCA to protecting against chemotherapy-associated mucositis. Sprague-Dawley rats were randomly assigned to five groups: Control, vehicle + 5-fluorouracil (5-FU), 5-FU + UDCA (10 mg/kg/day), 5-FU + UDCA (100 mg/kg/day) and 5-FU + UDCA (500 mg/kg/day). Following randomization, a single dose of 5-FU was injected and varying amounts of UDCA was administered to each group. UDCA was administered orally to rats for 6 days, beginning 1 day prior to 5-FU administration. The rats were sacrificed 1 day following the last UDCA administration and intestinal tissue specimens were prepared for analysis. UDCA administration attenuated body weight loss, decreased inflammatory cytokine levels and curbed intestinal villus damage in the 10 and 100 mg/kg/day groups. When compared with the jejunal villi lengths in the vehicle+5-FU group (212.8±58.0 µm), those in the 5-FU + UDCA (10 mg/kg/day) and 5-FU + UDCA (100 mg/kg/day) groups were significantly greater [331.3±18.0 µm (P=0.001) and 310.0±112.6 µm (P=0.046), respectively]. Tumor necrosis factor-α and interleukin-6 levels were reduced in the 10 and 100 mg/kg/day UDCA groups (P<0.05). UDCA considerably attenuated the elevation in inflammatory cytokines and intestinal villus damage. The results of the study suggest that UDCA may be used as a protective agent against chemotherapy-associated intestinal mucositis.

摘要

肠道黏膜炎是化疗常见的并发症。然而,有效的治疗方法或预防措施却很少。熊去氧胆酸(UDCA)可稳定细胞膜,作为抗氧化剂并抑制细胞凋亡,从而发挥细胞保护作用。本研究的目的是检验UDCA预防化疗相关性黏膜炎的能力。将Sprague-Dawley大鼠随机分为五组:对照组、赋形剂+5-氟尿嘧啶(5-FU)组、5-FU+UDCA(10毫克/千克/天)组、5-FU+UDCA(100毫克/千克/天)组和5-FU+UDCA(500毫克/千克/天)组。随机分组后,给每组注射单剂量的5-FU,并给予不同剂量的UDCA。在5-FU给药前1天开始,给大鼠口服UDCA,持续6天。在最后一次给予UDCA后1天处死大鼠,并制备肠道组织标本用于分析。在10毫克/千克/天和100毫克/千克/天剂量组中,给予UDCA可减轻体重减轻,降低炎性细胞因子水平并抑制肠道绒毛损伤。与赋形剂+5-FU组的空肠绒毛长度(212.8±58.0微米)相比,5-FU+UDCA(10毫克/千克/天)组和5-FU+UDCA(100毫克/千克/天)组的空肠绒毛长度明显更长[分别为331.3±18.0微米(P=0.001)和310.0±112.6微米(P=0.046)]。在10毫克/千克/天和100毫克/千克/天UDCA组中,肿瘤坏死因子-α和白细胞介素-6水平降低(P<0.05)。UDCA可显著减轻炎性细胞因子的升高和肠道绒毛损伤。研究结果表明,UDCA可用作预防化疗相关性肠道黏膜炎的保护剂。

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