Clear Evidence of Carcinogenic Activity by a Whole-Leaf Extract of Aloe barbadensis Miller (Aloe vera) in F344/N Rats

被引:56
作者
Boudreau, Mary D. [1 ]
Mellick, Paul W. [2 ]
Olson, Greg R. [2 ]
Felton, Robert P. [3 ]
Thorn, Brett T. [3 ]
Beland, Frederick A. [1 ]
机构
[1] US FDA, Div Biochem Toxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[2] US FDA, Toxicol Pathol Associates, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[3] US FDA, Div Bioinformat & Biostatist, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
关键词
natural products; metabolism; histopathology; chronic; gastrointestinal; carcinogenesis; dietary supplement; Aloe vera; Aloe barbadensis Miller; colon cancer; rodents; VAR. NATALENSIS BERGER; TRANSFORMING BARBALOIN; GASTROINTESTINAL-TRACT; ANTHRANOID LAXATIVES; CHRONIC TOXICITY; CROHNS-DISEASE; COLON-CANCER; METABOLISM; POLYSACCHARIDES; INGESTION;
D O I
10.1093/toxsci/kfs275
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Aloe barbadensis Miller (Aloe vera) is an herbal remedy promoted to treat a variety of illnesses; however, only limited data are available on the safety of this dietary supplement. Drinking water exposure of F344/N rats and B6C3F1 mice to an Aloe vera whole-leaf extract (1, 2, and 3%) for 13 weeks resulted in goblet cell hyperplasia of the large intestine in both species. Based upon this observation, 2-year drinking water studies were conducted to assess the carcinogenic potential of an Aloe vera whole-leaf extract when administered to F344/N rats (48 per sex per group) at 0.5, 1, and 1.5%, and B6C3F1 mice (48 per sex per group) at 1, 2, and 3%. Compared with controls, survival was decreased in the 1.5% dose group of female rats. Treatment-related neoplasms and nonneoplastic lesions in both species were confined primarily to the large intestine. Incidences of adenomas and/or carcinomas of the ileo-cecal and cecal-colic junction, cecum, and ascending and transverse colon were significantly higher than controls in male and female rats in the 1 and 1.5% dose groups. There were no neoplasms of the large intestine in mice or in the 0 or 0.5% dose groups of rats. Increased incidences of mucosa hyperplasia of the large intestine were observed in F344/N rats, and increased incidences of goblet cell hyperplasia of the large intestine occurred in B6C3F1 mice. These results indicate that Aloe vera whole-leaf extract is an intestinal irritant in F344/N rats and B6C3F1 mice and a carcinogen of the large intestine in F344/N rats.
引用
收藏
页码:26 / 39
页数:14
相关论文
共 91 条
[1]  
Akao T, 1996, BIOL PHARM BULL, V19, P136
[2]  
Atherton P, 1998, Nurs Stand, V12, P49
[3]  
Atherton P., 1998, NURS STAND, V12, P54
[4]  
Ayushveda, 2010, AL DRINK BEN AL JUIC
[5]   AN ILLUSTRATION OF DANGERS OF IGNORING SURVIVAL DIFFERENCES IN CARCINOGENIC DATA [J].
BAILER, AJ ;
PORTIER, CJ .
JOURNAL OF APPLIED TOXICOLOGY, 1988, 8 (03) :185-189
[6]   RATIO ESTIMATES, THE DELTA METHOD, AND QUANTAL RESPONSE TESTS FOR INCREASED CARCINOGENICITY [J].
BIELER, GS ;
WILLIAMS, RL .
BIOMETRICS, 1993, 49 (03) :793-801
[7]   BARBALOIN .1. SOME OBSERVATIONS ON ITS STRUCTURE [J].
BIRCH, AJ ;
DONOVAN, FW .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1955, 8 (04) :523-528
[8]   PRECHRONIC TOXICITY OF ORTHO-BENZYL-PARA-CHLOROPHENOL IN RATS AND MICE [J].
BIRNBAUM, LS ;
DESKIN, R ;
GRUMBEIN, SL ;
KURTZ, P ;
FOWLER, KL ;
PETERS, AC .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1986, 7 (04) :615-625
[9]   Evaluation of the antibacterial and anticancer activities of some South African medicinal plants [J].
Bisi-Johnson, Mary A. ;
Obi, Chikwelu L. ;
Hattori, Toshio ;
Oshima, Yoshiteru ;
Li, Shenwei ;
Kambizi, Learnmore ;
Eloff, Jacobus N. ;
Vasaikar, Sandeep D. .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2011, 11
[10]  
BOORMAN GA, 1986, MANAGING CONDUCT DAT, P271