RETINOIC ACID CAN BE PRODUCED FROM EXCENTRIC CLEAVAGE OF BETA-CAROTENE IN HUMAN INTESTINAL-MUCOSA

被引:79
作者
WANG, XD
KRINSKY, NI
TANG, G
RUSSELL, RM
机构
[1] TUFTS UNIV, USDA,HUMAN NUTR RES CTR,GASTROINTESTINAL LAB, 711 WASHINGTON ST, BOSTON, MA 02111 USA
[2] TUFTS UNIV, SCH NUTR, BOSTON, MA 02111 USA
[3] TUFTS UNIV, SCH MED, DEPT BIOCHEM, BOSTON, MA 02111 USA
关键词
D O I
10.1016/0003-9861(92)90399-H
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The hypothesis that retinoic acid (RA) is produced from the excentric cleavage of β-carotene was tested in human intestinal homogenates in vitro. Significant amounts of RA were identified by HPLC and derivatization after incubation of intestinal mucosal homogenates with retinal, β-carotene, or β-apocarotenals at 37 °C for 60 min. RA formation was inhibited, in a dose-dependent fashion, when retinal was incubated in the presence of 0.1-3.0 mm citral (3,7-dimethyl-2,6-octadienal) under identical experimental conditions. The formation of RA from both β-carotene and β-apocarotenals was dose and time dependent and RA was the major metabolite of both β-apo8′-carotenal and β-apo- 12′-carotenal after the incubation. However, citral (0.1 to 4 mm) did not inhibit the formation of β-apocarotenals and RA from 2 μm β-carotene (P > 0.05), which proves the existence of an excentric cleavage mechanism for β-carotene conversion into retinoids. Furthermore, RA formation from both β-apo-8′-carotenal and β-apo-12′-carotenal in human intestinal homogenate occurred in the presence of citral, which demonstrates that RA can be produced from excentric cleavage of β-carotene via a series of β-apocarotenals as intermediates. © 1992.
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页码:298 / 304
页数:7
相关论文
共 36 条
[21]  
LEACH EH, 1956, P NUTR SOC, V15, pR15
[22]   A PATHWAY FOR OXIDATIVE DEGRADATION OF PHYTANIC ACID IN MAMMALS [J].
MIZE, CE ;
STEINBERG, D ;
AVIGAN, J ;
FALES, HM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1966, 25 (03) :359-+
[24]  
NAPOLI JL, 1988, J BIOL CHEM, V263, P17372
[25]   ENZYMATIC CLEAVAGE OF BETA-CAROTENE INTO VITAMIN A BY SOLUBLE ENZYMES OF RAT LIVER AND INTESTINE [J].
OLSON, JA ;
HAYAISHI, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1965, 54 (05) :1364-&
[26]  
OLSON JA, 1990, METHOD ENZYMOL, V189, P425
[27]   CAN DIETARY BETA-CAROTENE MATERIALLY REDUCE HUMAN CANCER RATES [J].
PETO, R ;
DOLL, R ;
BUCKLEY, JD ;
SPORN, MB .
NATURE, 1981, 290 (5803) :201-208
[28]   STUDIES ON RELATIVE BIOPOTENCIES AND INTESTINAL-ABSORPTION OF DIFFERENT APO-BETA-CAROTENOIDS IN RATS AND CHICKENS [J].
SHARMA, RV ;
MATHUR, SN ;
GANGULY, J .
BIOCHEMICAL JOURNAL, 1976, 158 (02) :377-383
[29]   STUDIES ON METABOLISM OF BETA-CAROTENE AND APO-BETA-CAROTENOIDS IN RATS AND CHICKENS [J].
SHARMA, RV ;
MATHUR, SN ;
DMITROVSKII, AA ;
DAS, RC ;
GANGULY, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 486 (01) :183-194
[30]   ENZYMATIC CLEAVAGE OF CAROTENOIDS [J].
SINGH, H ;
CAMA, HR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1974, 370 (01) :49-61