trans-Resveratrol Reduces Precancerous Colonic Lesions in Dimethylhydrazine-Treated Rats

被引:32
作者
Alfaras, Irene
Emilia Juan, M. [1 ]
Planas, Joana M.
机构
[1] Univ Barcelona, Dept Fisiol Farm, E-08007 Barcelona, Spain
关键词
Aberrant crypt foci; colon cancer; dihydroresveratrol; mucin-depleted foci; trans-resveratrol; ABERRANT CRYPT FOCI; DIETARY RESVERATROL; INTESTINAL TUMORIGENESIS; CANCER-CELLS; APOPTOSIS; ABSORPTION; PREVENTION; IDENTIFICATION; INHIBITION; EXPRESSION;
D O I
10.1021/jf100702x
中图分类号
S [农业科学];
学科分类号
082806 [农业信息与电气工程];
摘要
trans-Resveratrol, a natural occurring polyphenol, has been described as an antiproliferative and proapoptotic agent in vitro. Here, we studied the effect of trans-resveratrol administered orally at a dose of 60 mg/kg for 49 days on early preneoplastic markers induced by the intraperitoneal injection of 1,2-dimethylhydrazine (20 mg/kg). We measured trans-resveratrol and its derivates by liquid-liquid extraction followed by high-performance liquid chromatography diode array detection analysis in colon contents. Dihydroresveratrol was the most abundant compound in the colon, followed by trans-resveratrol glucuronide and small amounts of trans-resveratrol and its sulfate. The administration of trans-resveratrol decreased aberrant crypt foci by 52%, and mucin depleted foci by 45% in colon. In conclusion, the correlation between the reduction of precancerous colonic lesions and the availability of trans-resveratrol in the colon provides a new insight into the therapeutical potential of this polyphenol and its metabolites.
引用
收藏
页码:8104 / 8110
页数:7
相关论文
共 37 条
[1]
Key elements of bioanalytical method validation for small molecules [J].
Bansal, Surendra ;
DeStefano, Anthony .
AAPS JOURNAL, 2007, 9 (01) :E109-E114
[2]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[3]
OBSERVATION AND QUANTIFICATION OF ABERRANT CRYPTS IN THE MURINE COLON TREATED WITH A COLON CARCINOGEN - PRELIMINARY FINDINGS [J].
BIRD, RP .
CANCER LETTERS, 1987, 37 (02) :147-151
[5]
Caderni G, 2003, CANCER RES, V63, P2388
[6]
Chemo-enzymatic synthesis and cell-growth inhibition activity of resveratrol analogues [J].
Cardile, V ;
Lombardo, L ;
Spatafora, C ;
Tringali, C .
BIOORGANIC CHEMISTRY, 2005, 33 (01) :22-33
[7]
Effects of resveratrol analogs on cell cycle progression, cell cycle associated proteins and 5fluoro-uracil sensitivity in human derived colon cancer cells [J].
Colin, Didier ;
Gimazane, Amandine ;
Lizard, Gerard ;
Izard, Jean-Claude ;
Solary, Eric ;
Latruffe, Norbert ;
Delmas, Dominique .
INTERNATIONAL JOURNAL OF CANCER, 2009, 124 (12) :2780-2788
[8]
Fortnightly review - Diet and the prevention of cancer [J].
Cummings, JH ;
Bingham, SA .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 317 (7173) :1636-1640
[9]
Resveratrol induces apoptosis through ROS-dependent mitochondria pathway in HT-29 human colorectal carcinoma cells [J].
Emilia Juan, M. ;
Wenzel, Uwe ;
Daniel, Hannelore ;
Planas, Joana M. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (12) :4813-4818
[10]
Multidrug Resistance Proteins Restrain the Intestinal Absorption of trans-Resveratrol in Rats [J].
Emilia Juan, M. ;
Gonzalez-Pons, Eulalia ;
Planas, Joana M. .
JOURNAL OF NUTRITION, 2010, 140 (03) :489-495