Beneficial health effects of lupeol triterpene: A review of preclinical studies

被引:246
作者
Siddique, Hifzur Rahman [1 ]
Saleem, Mohammad [1 ]
机构
[1] Univ Minnesota, Hormel Inst, Sect Mol Chemoprevent & Therapeut, Austin, MN 55912 USA
关键词
Diseases; Lupeol; Triterpene; Pharmacological; Clinical trial; ADJUVANT-INDUCED ARTHRITIS; NURVALA STEM BARK; PENTACYCLIC TRITERPENE; ALLANBLACKIA-MONTICOLA; CHEMICAL-CONSTITUENTS; ERYTHROCYTE-MEMBRANE; INHIBITORY-ACTIVITY; DIETARY TRITERPENE; LIPID-PEROXIDATION; LYSOSOMAL-ENZYMES;
D O I
10.1016/j.lfs.2010.11.020
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Since ancient times, natural products have been used as remedies to treat human diseases. Lupeol, a phytosterol and triterpene, is widely found in edible fruits, and vegetables. Extensive research over the last three decades has revealed several important pharmacological activities of lupeol. Various in vitro and preclinical animal studies suggest that lupeol has a potential to act as an anti-inflammatory, anti-microbial, anti-protozoal, anti-proliferative, anti-invasive, anti-angiogenic and cholesterol lowering agent. Employing various in vitro and in vivo models, lupeol has also been tested for its therapeutic efficiency against conditions including wound healing, diabetes, cardiovascular disease, kidney disease, and arthritis. Lupeol has been found to be pharmacologically effective in treating various diseases under preclinical settings (in animal models) irrespective of varying routes of administration viz; topical, oral, intra-peritoneal and intravenous. It is noteworthy that lupeol has been reported to selectively target diseased and unhealthy human cells, while sparing normal and healthy cells. Published studies provide evidence that lupeol modulates the expression or activity of several molecules such as cytokines IL-2, IL4,IL5, IL beta, proteases, alpha-glucosidase, cFLIP, Bcl-2 and NF kappa B. This minireview discusses in detail the preclinical studies conducted with lupeol and provides an insight into its mechanisms of action. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 293
页数:9
相关论文
共 86 条
[11]   Suppression of T lymphocyte activity by lupeol isolated from Crataeva religiosa [J].
Bani, S ;
Kaul, A ;
Khan, B ;
Ahmad, SF ;
Suri, KA ;
Gupta, BD ;
Satti, NK ;
Qazi, GN .
PHYTOTHERAPY RESEARCH, 2006, 20 (04) :279-287
[12]   Boswellia frereana (Frankincense) Suppresses Cytokine-Induced Matrix Metalloproteinase Expression and Production of Pro-Inflammatory Molecules in Articular Cartilage [J].
Blain, Emma J. ;
Ali, Ahmed Y. ;
Duance, Victor C. .
PHYTOTHERAPY RESEARCH, 2010, 24 (06) :905-912
[13]   Lupeol: Connotations for chemoprevention [J].
Chaturvedi, Pranav K. ;
Bhui, Kulpreet ;
Shukla, Yogeshwer .
CANCER LETTERS, 2008, 263 (01) :1-13
[14]   ALOE VERA, HYDROCORTISONE, AND STEROL INFLUENCE ON WOUND TENSILE-STRENGTH AND ANTI-INFLAMMATION [J].
DAVIS, RH ;
DIDONATO, JJ ;
JOHNSON, RWS ;
STEWART, CB .
JOURNAL OF THE AMERICAN PODIATRIC MEDICAL ASSOCIATION, 1994, 84 (12) :614-621
[15]   The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris [J].
Ding, Yan ;
Nguyen, Huu Tung ;
Kim, Sung In ;
Kim, Ha Won ;
Kim, Young Ho .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (13) :3607-3610
[16]  
Erazo S, 2008, Z NATURFORSCH C, V63, P492
[17]  
Rodrigues JCF, 2008, CURR PHARM DESIGN, V14, P925, DOI 10.2174/138161208784041033
[18]   Anti-inflammatory effect of Pimenta racemosa var. ozua and isolation of the triterpene lupeol [J].
Fernández, A ;
Alvarez, A ;
García, MD ;
Sáenz, MT .
FARMACO, 2001, 56 (04) :335-338
[19]   New insights into the mechanism of action of the anti-inflammatory triterpene lupeol [J].
Fernández, MA ;
de las Heras, B ;
García, MD ;
Sáenz, MT ;
Villar, A .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (11) :1533-1539
[20]   BIOLOGICAL AND CHEMICAL STUDIES OF PERA-BENENSIS, A BOLIVIAN PLANT USED IN FOLK MEDICINE AS A TREATMENT OF CUTANEOUS LEISHMANIASIS [J].
FOURNET, A ;
ANGELO, A ;
MUNOZ, V ;
ROBLOT, F ;
HOCQUEMILLER, R ;
CAVE, A .
JOURNAL OF ETHNOPHARMACOLOGY, 1992, 37 (02) :159-164