Panax notoginseng Attenuates Experimental Colitis in the Azoxymethane/Dextran Sulfate Sodium Mouse Model

被引:52
|
作者
Wen, Xiao-Dong [1 ,2 ,3 ]
Wang, Chong-Zhi [1 ,2 ]
Yu, Chunhao [1 ,2 ]
Zhao, Lei [4 ]
Zhang, Zhiyu [1 ,2 ]
Matin, Adiba [1 ,2 ]
Wang, Yunwei [5 ]
Li, Ping [3 ]
Xiao, Shu-Yuan [4 ]
Du, Wei [6 ]
He, Tong-Chuan [7 ]
Yuan, Chun-Su [1 ,2 ,8 ]
机构
[1] Univ Chicago, Tang Ctr Herbal Med Res, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Anesthesia & Crit Care, Chicago, IL 60637 USA
[3] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[4] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[6] Univ Chicago, Ben May Dept Canc Res, Chicago, IL 60637 USA
[7] Univ Chicago, Dept Orthoped Surg, Chicago, IL 60637 USA
[8] Univ Chicago, Comm Clin Pharmacol & Pharmacogen, Chicago, IL 60637 USA
关键词
Panax notoginseng; notoginseng; inflammatory bowel disease; colitis; AOM; DSS model; colorectal carcinogenesis; INFLAMMATORY-BOWEL-DISEASE; COLON CARCINOGENESIS; COLORECTAL-CANCER; LIQUID-CHROMATOGRAPHY; INHIBITS COLITIS; EXTRACT; TUMOR; SAPONIN; ROOTS;
D O I
10.1002/ptr.5066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Patients suffering from inflammatory bowel disease are at a high risk of developing colorectal cancer. To assess the anticancer potential of botanicals, in this study, we evaluated the effects of Panax notoginseng on azoxymethane/dextran sulfate sodium (DSS)-induced colitis. One week after A/J mice received azoxymethane, the animals received DSS for 8days or were supplemented with P.notoginseng extract, at 30 or 90mg/kg. DSS-induced colitis was scored with the disease activity index. The severity of the inflammatory lesions was evaluated by a colon tissue histological assessment. The expression of inducible nitric oxide synthase and cyclooxygenase-2 (COX-2) were also explored. We observed that the effects of P.notoginseng on the reduction of colon inflammation, expressed in disease activity index score, were in a dose-related manner (p<0.01). P.notoginseng inhibited the reduction of the colon length and the loss of bodyweight in dose-related manner (all p<0.05). The histological assessment of the colitis and inflammatory-related immunohistochemical data also supported the pharmacological observations. Our data suggest that P.notoginseng is a promising candidate in preventing and treating colitis and inflammation-associated colon carcinogenesis. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:892 / 898
页数:7
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