Absorption and biological activity of phytochemical-rich extracts from acai (Euterpe oleracea Mart.) pulp and oil in vitro

被引:58
作者
Pacheco-Palencia, Lisbeth A. [1 ]
Talcott, Stephen T. [1 ]
Safe, Stephen [2 ]
Mertens-Talcott, Susanne [1 ,2 ]
机构
[1] Texas A&M Univ, Dept Nutr & Food Sci, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Vet Physiol & Pharmacol, College Stn, TX 77843 USA
关键词
acai; polyphenolic; absorption; cell proliferation; in vitro;
D O I
10.1021/jf8001608
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Polyphenolic extracts from various fruits and vegetables have been shown to exert growth inhibitory effects in cell culture studies. Whereas individual polyphenolic compounds have been extensively evaluated, understanding of the biological activity of polyphenolic extracts from natural sources is limited and critical to the understanding of their potential effects on the human body. This study investigated the absorption and antiproliferative effects of phytochemical extracts from acai pulp and a polyphenolic-enriched acai oil obtained from the fruit pulp of the acai berry (Euterpe oleracea Mart.). Chemical composition, antioxidant properties, and polyphenolic absorption of phytochemical fractions in a Caco-2 monolayer were determined, along with their cytotoxicity in HT-29 human colon adenocarcinoma cells. Standardized extracts were characterized by their predominance of hydroxybenzoic acids, monomeric flavan-3-ols, and procyanidin dimers and trimers. Polyphenolic mixtures (0-12 mu g of gallic acid equiv/mL) from both acai pulp and acai oil extracts inhibited cell proliferation by up to 90.7%, which was accompanied by an increase of up to 2.1-fold in reactive oxygen species. Absorption experiments using a Caco-2 intestinal cell monolayer demonstrated that phenolic acids such as p-hydroxybenzoic, vanillic, syringic, and ferulic acids, in the presence of DMSO, were readily transported from the apical to the basolateral side along with monomeric flavanols such as (+)-catechin and (-)-epicatechin. Results from this study provide further evidence for the bioactive properties of acai polyphenolics and offer new insight on their composition and cellular absorption.
引用
收藏
页码:3593 / 3600
页数:8
相关论文
共 38 条
[1]   Current methodologies used for evaluation of intestinal permeability and absorption [J].
Balimane, PV ;
Chong, SH ;
Morrison, RA .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2000, 44 (01) :301-312
[2]   Red wine polyphenols inhibit the growth of colon carcinoma cells and modulate the activation pattern of mitogen-activated protein kinases [J].
Briviba, K ;
Pan, L ;
Rechkemmer, G .
JOURNAL OF NUTRITION, 2002, 132 (09) :2814-2818
[3]   Hibiscus anthocyanins rich extract-induced apoptotic cell death in human promyelocytic leukemia cells [J].
Chang, YC ;
Huang, HP ;
Hsu, JD ;
Yang, SF ;
Wang, CJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 205 (03) :201-212
[4]   Grapefruit juice-drug interactions: Grapefruit juice and its components inhibit p-glycoprotein (ABCB1) mediated transport of talinolol in caco-2 cells [J].
De Castro, Whocely Victor ;
Mertens-Talcott, Susanne ;
Derendorf, Hartmut ;
Butterweck, Veronika .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (10) :2808-2817
[5]   Acai (Euterpe oleracea mart.) polyphenolics in their glycoside and aglycone forms induce apoptosis of HL-60 leukemia cells [J].
Del Pozo-Insfran, D ;
Percival, SS ;
Talcott, ST .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (04) :1222-1229
[6]   Transport of proanthocyanidin dimer, trimer, and polymer across monolayers of human intestinal epithelial Caco-2 cells [J].
Deprez, S ;
Mila, I ;
Huneau, JF ;
Tome, D ;
Scalbert, A .
ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (06) :957-967
[7]  
ElAttar TMA, 1999, ANTICANCER RES, V19, P5407
[8]   A flavonoid fraction from cranberry extract inhibits proliferation of human tumor cell lines [J].
Ferguson, PJ ;
Kurowska, E ;
Freeman, DJ ;
Chambers, AF ;
Koropatnick, DJ .
JOURNAL OF NUTRITION, 2004, 134 (06) :1529-1535
[9]  
HIDALGO IJ, 1989, GASTROENTEROLOGY, V96, P736
[10]   Potential mechanisms of cancer chemoprevention by anthocyanins [J].
Hou, DX .
CURRENT MOLECULAR MEDICINE, 2003, 3 (02) :149-159