Dietary beta-carotene and ultraviolet-induced immunosuppression

被引:11
作者
Noonan, FP
Webber, LJ
DeFabo, EC
Hoffman, HA
Bendich, A
MathewsRoth, M
机构
[1] HOFFMANN LA ROCHE INC,PARAMUS,NJ
[2] HARVARD UNIV,SCH MED,CHANNING LAB,BOSTON,MA 02115
关键词
ultraviolet B; immunosuppression; beta-carotene; contact hypersensitivity;
D O I
10.1046/j.1365-2249.1996.905595.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ultraviolet (UV)-induced immunosuppression is a critical step in UV carcinogenesis, permitting tumour outgrowth. We investigated the effect of dietary beta-carotene on UV suppression of contact hypersensitivity (CHS) to trinitrochlorobenzene (TNCB) in BALB/c mice. Mice were fed for 10-16 weeks chow alone or supplemented with 1% beta-carotene or placebo as beadlets. Serum beta-carotene was detectable by high performance liquid chromatography (HPLC) analysis only in beta-carotene-fed mice (206 +/- 0.15 mu g/ml). Serum retinol was 0.22-0.27 mu g/ml in all three groups. Mice (n=41/dietary group) were irradiated with 0, 4.5, 9 or 18 kJ/m(2) of UVB and the CHS response was measured. Decreased CHS responses were observed in all UV-irradiated groups compared with unirradiated controls. UV dose-responses for suppression of CHS derived by first-order regression analyses of plots of percentage suppression of CHS as a function of log(10)UV dose showed significant slopes (P < 0.02) for all three dietary groups and similar residual variances between groups, P > 0.05. The UV pose for 50% suppression of CHS was 6.3 kJ/m(2) for control, 6.4 kJ/m(2) for placebo, and 5.5 kJ/m(2) for beta-carotene-fed mice. No significant differences in slopes or elevations between UV dose-responses were observed, P > 0.05. Skin levels of the initiator of UV-induced immunosuppression, cis urocanic acid, were determined by HPLC in mice given 0 or 9 kJ/m(2) of UV (n = 28/dietary group). No significant differences were observed between dietary groups (range 35.2-41.1 ng/mg skin, P > 0.15) We conclude feeding beta-carotene to BALB/c mice does not alter susceptibility to UV immune suppression, in contrast to human studies.
引用
收藏
页码:54 / 60
页数:7
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