BIOACTIVITY OF SELENIUM FROM BRAZIL NUT FOR CANCER PREVENTION AND SELENOENZYME MAINTENANCE

被引:54
作者
IP, C [1 ]
LISK, DJ [1 ]
机构
[1] CORNELL UNIV, DEPT FRUIT & VEGETABLE SCI, ITHACA, NY 14853 USA
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 1994年 / 21卷 / 03期
关键词
D O I
10.1080/01635589409514319
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Brazil nut (Bertholletia excelsa) is one of very few consumable products with exceptionally high levels of selenium. The mean selenium concentrations of two shipments of Brazil nut used in the present study were determined to be 16 and 30 mu g/g. In contrast, most common foods contain much less selenium, from 0.01 to 1 mu g/g. previous research on selenium cancer chemoprevention invariably used a pure compound, whereas little information is available on the efficacy of selenium delivered naturally in a food form. This paper reports the results of two mammary cancer prevention experiments in the rat dimethylbenz[a]anthracene model by continuous feeding of selenium-rich Brazil nut (processed to a smooth-textured nut material for mixing in the diet). A dose-dependent inhibitory response was observed at dietary selenium concentrations of 1-3 mu g/g. Interestingly, Brazil nut was found to be just as powerful as sodium selenite, if not more so, at similar levels of dietary selenium intake. Mammary cancer protection by Brazil nut was associated with increased selenium retention in the liver, kidney, mammary gland, and plasma. The magnitude of tissue selenium accumulation was proportional to the amount of Brazil nut added to the diet. The nutritional biopotency of selenium in Brazil nut was also evaluated by the repletion of two selenoenzymes, glutathione peroxidase and type I 5'-deiodinase, in selenium-deficient rats. Supplementation with Brazil nut as the sole source of selenium produced an efficient gradient of enzyme restoration at 0.05-0.2 mu g/g of dietary selenium. A parallel comparison with sodium selenite indicated that the selenium in Brazil nut and selenite selenium were equally bioactive. Although at this point it can only be inferred that the above biologic effects are likely to be attributable to the high selenium content of Brazil nut, there is persuasive evidence to suggest that the models under investigation are responding to the selenium rather than to the other components of Brazil nut.
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页码:203 / 212
页数:10
相关论文
共 35 条
  • [1] SELENO-CYSTATHIONINE A PHARMACOLOGICALLY ACTIVE FACTOR IN SEEDS OF LECYTHIS OLLARIA
    ARONOW, L
    KERDELVE.F
    WAGNER, F
    RUSSELL, PB
    GRANT, NH
    ALBURN, HE
    CLARK, DE
    MILLER, JA
    [J]. NATURE, 1965, 205 (4977) : 1185 - &
  • [2] EFFECT OF SELENIUM DEFICIENCY ON HEPATIC TYPE-I 5-IODOTHYRONINE DEIODINASE ACTIVITY AND HEPATIC THYROID-HORMONE LEVELS IN THE RAT
    BECKETT, GJ
    RUSSELL, A
    NICOL, F
    SAHU, P
    WOLF, CR
    ARTHUR, JR
    [J]. BIOCHEMICAL JOURNAL, 1992, 282 : 483 - 486
  • [3] IDENTIFICATION OF TYPE-I IODOTHYRONINE 5'-DEIODINASE AS A SELENOENZYME
    BEHNE, D
    KYRIAKOPOULOS, A
    MEINHOLD, H
    KOHRLE, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) : 1143 - 1149
  • [4] MOLECULAR-BIOLOGY OF SELENIUM WITH IMPLICATIONS FOR ITS METABOLISM
    BURK, RF
    [J]. FASEB JOURNAL, 1991, 5 (09) : 2274 - 2279
  • [5] NUTRITIONAL BIOAVAILABILITY TO RATS OF SELENIUM IN BRAZIL NUTS AND MUSHROOMS
    CHANSLER, MW
    MUTANEN, M
    MORRIS, VC
    LEVANDER, OA
    [J]. NUTRITION RESEARCH, 1986, 6 (12) : 1419 - 1428
  • [6] NUTRITIONAL AVAILABILITY TO RATS OF SELENIUM IN TUNA, BEEF KIDNEY, AND WHEAT
    DOUGLASS, JS
    MORRIS, VC
    SOARES, JH
    LEVANDER, OA
    [J]. JOURNAL OF NUTRITION, 1981, 111 (12) : 2180 - 2187
  • [7] ELBAYOUMY K, 1991, CANCER PRINCIPLES PR, P1
  • [8] ELEMENTAL COMPOSITION OF TREE NUTS
    FURR, AK
    MACDANIELS, LH
    STJOHN, LE
    GUTENMANN, WH
    PAKKALA, IS
    LISK, DJ
    [J]. BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1979, 21 (03) : 392 - 396
  • [9] GANTHER HE, 1987, J AM COLL TOXICOL, V5, P1
  • [10] Goyer R.A., 1986, CASARETT DOULLS TOXI, P582