Yh. Cheng et al., Effects of aflatoxin and carotenoids on growth performance and immune response in mule ducklings, COMP BIOC C, 128(1), 2001, pp. 19-26
Citations number
39
Categorie Soggetti
Pharmacology & Toxicology
Journal title
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY
The purpose of this study was to investigate if carotenoids could alleviate
the adverse effects caused by aflatoxin with respect to growth performance
acid immune response. In two experiments, a total of 320 mule ducklings we
re assigned to 5 treatments, i.e. control, aflatoxin B-1 (AFB(1)) 200 ppb,
AFB(1) + beta -carotene (BC) 200 ppm, AFB(1) + BC 400 ppm, and AFB(1) + ast
axanthin (AS) 200 ppm. In experiment 1, the addition of beta -carotene or a
staxanthin in the diet containing AFB(1) 200 ppb resulted in a significant
decrease in average daily gain as compared with the control. AFB(1) 200 ppb
alone and the addition of BC or AS on top of AFB(1) resulted in a signific
antly lower daily feed intake than for the control group. There were no sig
nificant differences in relative organ weights among treatment groups. Both
treatments of BC 400 ppm and AS 200 ppm had significantly more macrophages
harvested per duck than the control and AFB(1) 200 ppb treatments. However
, there were no significant differences among treatments in percentages of
phagocytotic macrophages and number of Candida albican phagocytized by phag
ocytotic macrophages. In experiment 2, blood biochemical parameters and ant
ibody titers were evaluated. There were no significant differences among tr
eatments in total bilirubin content and alkaline phosphatase activity in th
e serum or in antibody titers against fowl cholera. However, AFB(1) treatme
nt had the highest activities of AST and ALT in the serum. The addition of
BC 400 ppm on top of AFB(1) significantly reduced ALT activity as compared
with the AFB(1) 200 ppb treatment. These results suggest that carotenoids c
ould provide a slightly toxic alleviating effect on growth performance, enh
ance the chemotaxis ability of macrophages, and reduce ALT activity elevate
d by AFB(1). (C) 2001 Elsevier Science Inc. All rights reserved.