NUTRITIONAL-STATUS AND IMMUNE-RESPONSES IN MICE WITH MURINE AIDS ARE NORMALIZED BY VITAMIN-E SUPPLEMENTATION

被引:66
作者
WANG, YJ
HUANG, DS
LIANG, BL
WATSON, RR
机构
[1] UNIV ARIZONA, DEPT FAMILY & COMMUNITY MED, TUCSON, AZ 85724 USA
[2] UNIV ARIZONA, NUTR SCI PROGRAM, TUCSON, AZ 85724 USA
[3] UNIV ARIZONA, DEPT MICROBIOL & IMMUNOL, TUCSON, AZ 85724 USA
[4] UNIV ARIZONA, DEPT NUTR SCI, TUCSON, AZ 85724 USA
关键词
VITAMIN-E; CYTOKINE; MICE; MURINE AIDS; IMMUNE RESPONSE;
D O I
10.1093/jn/124.10.2024
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Female C57BL/6 mice were infected with LP-BM5 retrovirus, causing murine AIDS, which is functionally similar to human AIDS. Vitamin E effects on immune functions, cytokine production and nutritional concentrations in retrovirus-infected mice were determined. Retrovirus infection inhibited release of interleukin-2 (IL) and interferon-gamma (IFN) and some immune functions, whereas it stimulated secretion of IL-4, IL-5, IL-6 and tumor necrosis factor-alpha (TNF) and immunoglobulin (Ig) production. Furthermore, retrovirus infection induced some nutritional deficiencies in the tissues. A 15-fold increase in dietary vitamin E largely restored concentrations of some micronutrients (vitamins A and E, zinc and copper) in the liver, intestine, serum and thymus. It also partially restored production of IL-2 and IFN-gamma by splenocytes. Retrovirus-induced elevated production of IL-4, IL-5 and IL-6 by splenocytes in vitro was normalized by vitamin E. Elevated release of IL-6, TNF-alpha, IgA and IgG produced by splenocytes in vitro during murine AIDS were also completely or partially normalized by vitamin E. Vitamin E also prevented retrovirus-induced suppression of splenocyte proliferation and natural killer cell activity. These data indicate that vitamin E supplementation during murine AIDS can help to ameliorate the disorders during murine AIDS, suggesting vitamin E usefulness in treatment of AIDS in humans.
引用
收藏
页码:2024 / 2032
页数:9
相关论文
共 31 条
[1]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[2]   CHARACTERIZATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 STRAINS RECOVERED FROM THE BOWEL OF INFECTED INDIVIDUALS [J].
BARNETT, SW ;
BARBOZA, A ;
WILCOX, CM ;
FORSMARK, CE ;
LEVY, JA .
VIROLOGY, 1991, 182 (02) :802-809
[3]   THE ROLE OF OXIDATIVE STRESS IN DISEASE PROGRESSION IN INDIVIDUALS INFECTED BY THE HUMAN-IMMUNODEFICIENCY-VIRUS [J].
BARUCHEL, S ;
WAINBERG, MA .
JOURNAL OF LEUKOCYTE BIOLOGY, 1992, 52 (01) :111-114
[4]   INTERMITTENT, ALTERNATING, AND CONCURRENT REGIMENS OF ZIDOVUDINE AND 2'-3'DIDEOXYCYTIDINE IN THE LP-BM5 MURINE INDUCED IMMUNODEFICIENCY MODEL [J].
BASHAM, T ;
HOLDENER, T ;
MERIGAN, T .
JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (04) :869-872
[5]   EPIDEMIOLOGY OF HUMAN IMMUNODEFICIENCY VIRUS-INFECTION AND ACQUIRED IMMUNODEFICIENCY SYNDROME [J].
BERKELMAN, RL ;
HEYWARD, WL ;
STEHRGREEN, JK ;
CURRAN, JW .
AMERICAN JOURNAL OF MEDICINE, 1989, 86 (06) :761-770
[6]   MICRONUTRIENT STATUS AND HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) INFECTION [J].
BOGDEN, JD ;
BAKER, H ;
FRANK, O ;
PEREZ, G ;
KEMP, F ;
BRUENING, K ;
LOURIA, D .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1990, 587 :189-195
[7]  
BRAY RA, 1986, J IMMUNOL, V136, P1783
[8]  
BRUNDA MT, 1990, J IMMUNOL, V24, P2682
[9]   VITAMINS AND MINERALS IN HIV-INFECTION [J].
COODLEY, G ;
GIRARD, DE .
JOURNAL OF GENERAL INTERNAL MEDICINE, 1991, 6 (05) :472-479
[10]   CRYPTOSPORIDIOSIS FACILITATED BY MURINE RETROVIRAL INFECTION WITH LP-BM5 [J].
DARBAN, H ;
ENRIQUEZ, J ;
STERLING, CR ;
LOPEZ, MC ;
CHEN, G ;
ABBASZADEGAN, M ;
WATSON, RR .
JOURNAL OF INFECTIOUS DISEASES, 1991, 164 (04) :741-745