Antioxidant activities of caffeic acid and its related hydroxycinnamic acid compounds

被引:779
作者
Chen, JH [1 ]
Ho, CT [1 ]
机构
[1] RUTGERS STATE UNIV, COOK COLL, DEPT FOOD SCI, NEW JERSEY AGR EXPT STN, NEW BRUNSWICK, NJ 08903 USA
关键词
antioxidants; caffeic acid; caffeic acid phenethyl ester; free radical scavenging activity; hydroxycinnamic acids;
D O I
10.1021/jf970055t
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Hydroxycinnamic acid compounds are an important source of antioxidants due to their ubiquitous occurrence in the plant kingdom and their characteristic activities. In this study, we compared the antioxidative and free radical scavenging activities of caffeic acid (CA), caffeic acid phenethyl ester (CAPE), ferulic acid (FA), ferulic acid phenethyl ester (FAPE), rosmarinic acid (RA), and chlorogenic acid (CHA) with those of alpha-tocopherol and BHT. In the Rancimat test, the addition of test compounds in lard significantly extended the induction time of lipid oxidation, and the activities in decreasing order were CA similar to alpha-tocopherol > CAPE similar to RA > CHA >> BHT > FA similar to FAPE. When the lipid substrate was changed to corn oil, the effectiveness of antioxidants on the induction time was obviously decreased, and the potency order of antioxidants was changed to RA > CA similar to CAPE similar to CHA > alpha-tocopherol > BHT; FA and FAPE had no significant antioxidative effect in the corn oil system. The 2,2-diphenyl-1-picrylhydrazyl radical (DPPH) scavenging activity of the test compounds was RA >> CAPE > CA > CHA > alpha-tocopherol > FA > FAPE > BHT. The effect on retarding oil-in-water emulsion oxidation was BHT > CA > CAPE > RA > FA > CHA > alpha-tocopherol > FAPE, and the incubation times to reach an absorbance of 0.4 by the ferric thiocyanate method were 14.4, 11.4, 8.6, 7.3, 6.4, 4.6, 4.2, and 2.8 days, respectively, with the value of the control around 1.3 days.
引用
收藏
页码:2374 / 2378
页数:5
相关论文
共 44 条
[1]  
BALTES W, 1976, ASIC S TU BERL, P91
[2]   ANTIOXIDANT DETERMINATIONS BY THE USE OF A STABLE FREE RADICAL [J].
BLOIS, MS .
NATURE, 1958, 181 (4617) :1199-1200
[3]  
BRAND-WILLIAMS W, 1995, FOOD SCI TECHNOL-LEB, V28, P25
[4]   MECHANISM OF INHIBITION OF N-METHYL-N'-NITRO-N-NITROSOGUANIDINE-INDUCED MUTAGENESIS BY PHENOLIC-COMPOUNDS [J].
CHAN, RIM ;
SAN, RHC ;
STICH, HF .
CANCER LETTERS, 1986, 31 (01) :27-34
[5]  
Chen C-W., 1995, J. Food Lipids, V2, P35, DOI [DOI 10.1111/J.1745-4522.1995.TB00028.X, 10.1111/j.1745-4522.1995.tb00028.x]
[6]   Antioxidant activity of designed peptides based on the antioxidative peptide isolated from digests of a soybean protein [J].
Chen, HM ;
Muramoto, K ;
Yamauchi, F ;
Nokihara, K .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1996, 44 (09) :2619-2623
[7]   Inhibitory effect of caffeic acid phenethyl ester on human leukemia HL-60 cells [J].
Chen, JH ;
Shao, Y ;
Huang, MT ;
Chin, CK ;
Ho, CT .
CANCER LETTERS, 1996, 108 (02) :211-214
[8]   Antioxidative activity and phenolic composition of pilot-plant and commercial extracts of sage and rosemary [J].
Cuvelier, ME ;
Richard, H ;
Berset, C .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1996, 73 (05) :645-652
[9]   COMPARISON OF THE ANTIOXIDATIVE ACTIVITY OF SOME ACID-PHENOLS - STRUCTURE ACTIVITY RELATIONSHIP [J].
CUVELIER, ME ;
RICHARD, H ;
BERSET, C .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1992, 56 (02) :324-325
[10]  
DESOTILLO DR, 1994, J FOOD SCI, V59, P649, DOI 10.1111/j.1365-2621.1994.tb05584.x