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The bile acids, deoxycholic acid and ursodeoxycholic acid, regulate colonic epithelial wound healing.胆汁酸,脱氧胆酸和熊去氧胆酸,可调节结肠上皮的伤口愈合。
Am J Physiol Gastrointest Liver Physiol. 2018 Mar 1;314(3):G378-G387. doi: 10.1152/ajpgi.00435.2016. Epub 2018 Jan 11.
2
Diffuse-Type Caroli Disease with Characteristic Central Dot Sign Complicated by Multiple Intrahepatic and Common Bile Duct Stones.伴有特征性中心点征的弥漫型卡罗里病合并多发肝内胆管及胆总管结石
Clin Endosc. 2017 Jul;50(4):400-403. doi: 10.5946/ce.2016.150. Epub 2017 Jun 20.
3
Bile acids deoxycholic acid and ursodeoxycholic acid differentially regulate human β-defensin-1 and -2 secretion by colonic epithelial cells.胆汁酸脱氧胆酸和熊去氧胆酸对结肠上皮细胞分泌人β-防御素-1和-2有不同的调节作用。
FASEB J. 2017 Sep;31(9):3848-3857. doi: 10.1096/fj.201601365R. Epub 2017 May 9.
4
Rhubarb extract partially improves mucosal integrity in chemotherapy-induced intestinal mucositis.大黄提取物可部分改善化疗引起的肠道黏膜炎中的黏膜完整性。
World J Gastroenterol. 2016 Oct 7;22(37):8322-8333. doi: 10.3748/wjg.v22.i37.8322.
5
Ursodeoxycholic Acid Ameliorated Diabetic Nephropathy by Attenuating Hyperglycemia-Mediated Oxidative Stress.熊去氧胆酸通过减轻高血糖介导的氧化应激改善糖尿病肾病。
Biol Pharm Bull. 2016 Aug 1;39(8):1300-8. doi: 10.1248/bpb.b16-00094. Epub 2016 May 18.
6
Mechanisms of Biliary Plastic Stent Occlusion and Efforts at Prevention.胆道塑料支架阻塞的机制及预防措施
Clin Endosc. 2016 Mar;49(2):139-46. doi: 10.5946/ce.2016.024. Epub 2016 Mar 22.
7
Efficacy and safety of ursodeoxycholic acid composite on fatigued patients with elevated liver function and/or fatty liver: a multi-centre, randomised, double-blinded, placebo-controlled trial.熊去氧胆酸复合物对肝功能异常和/或脂肪肝疲劳患者的疗效及安全性:一项多中心、随机、双盲、安慰剂对照试验
Int J Clin Pract. 2016 Apr;70(4):302-11. doi: 10.1111/ijcp.12790. Epub 2016 Mar 20.
8
Saireito (TJ-114), a Japanese traditional herbal medicine, reduces 5-fluorouracil-induced intestinal mucositis in mice by inhibiting cytokine-mediated apoptosis in intestinal crypt cells.柴苓汤(TJ-114),一种日本传统草药,通过抑制细胞因子介导的肠隐窝细胞凋亡,减轻5-氟尿嘧啶诱导的小鼠肠道黏膜炎。
PLoS One. 2015 Jan 7;10(1):e0116213. doi: 10.1371/journal.pone.0116213. eCollection 2015.
9
Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice.用布拉酵母菌进行预处理不能预防瑞士小鼠的实验性粘膜炎。
J Negat Results Biomed. 2014 Apr 11;13:6. doi: 10.1186/1477-5751-13-6.
10
Systematic review of agents for the management of gastrointestinal mucositis in cancer patients.系统评价癌症患者胃肠道黏膜炎管理中的药物。
Support Care Cancer. 2013 Jan;21(1):313-26. doi: 10.1007/s00520-012-1644-z. Epub 2012 Nov 10.

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.

DOI:10.3892/ol.2018.8893
PMID:30008943
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6036549/
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。