TY - JOUR
T1 - Dehydroepiandrosterone synergizes with antioxidant supplements for immune restoration in old as well as retrovirus-infected mice
AU - Jiang, Shuguang
AU - Lee, Jeongmin
AU - Zhang, Zhen
AU - Inserra, Paula
AU - Solkoff, David
AU - Watson, Ronald R.
N1 - Funding Information:
This article was supported as model for human aging by grants from Wallace Genetic Foundation, Inc. and immune modulation in AIDS by NIH HL 59794. We wish to thank Bailin Liang PhD, for participating and helping in the experiment, and Sherry Chow, PhD, for providing HPLC and technical assistance.
PY - 1998/7
Y1 - 1998/7
N2 - Production of the antioxidant hormone dehydroepiandrosterone (DHEA) declines as immunosenescence develops in the elderly. Very old C57BL/6 female mice, survivors after 71% had died due to aging, were evaluated after DHEA supplementation for 6 weeks. DHEA significantly increased their T-cell proliferation, restored secretion of Th1 cytokines [interleukin (IL)-2], decreased interferon-γ (IFN-γ) production, and normalized secretion of Th2 cytokine (IL-4 and IL-6) by lowered production. Survival was significantly increased in the 29-month-old mice treated by DHEA. Dehydroepiandrosterone sulfate (DHEAS), the storage form of DHEA, has lowered immune dysfunction caused by increased oxidation during LP-BM5 murine retrovirus infection. To assert the synergistic effect of DHEA + antioxidant nutrients, 17-month-old mice were fed with antioxidants or antioxidants + DHEAS for 16 weeks. DHEAS + antioxidants significantly increased B-cell proliferation and IL-2 secretion, and maintained Th2 cytokine secretion and hepatic vitamin E levels nearer to that of old, uninfected mice than antioxidant supplementation alone. Our study suggests that DHEA alone, and especially DHEAS plus antioxidant nutrients, can prevent immune dysfunction in very old and in old, retrovirus-infected mice. Copyright (C) 1998 Elsevier Science Inc.
AB - Production of the antioxidant hormone dehydroepiandrosterone (DHEA) declines as immunosenescence develops in the elderly. Very old C57BL/6 female mice, survivors after 71% had died due to aging, were evaluated after DHEA supplementation for 6 weeks. DHEA significantly increased their T-cell proliferation, restored secretion of Th1 cytokines [interleukin (IL)-2], decreased interferon-γ (IFN-γ) production, and normalized secretion of Th2 cytokine (IL-4 and IL-6) by lowered production. Survival was significantly increased in the 29-month-old mice treated by DHEA. Dehydroepiandrosterone sulfate (DHEAS), the storage form of DHEA, has lowered immune dysfunction caused by increased oxidation during LP-BM5 murine retrovirus infection. To assert the synergistic effect of DHEA + antioxidant nutrients, 17-month-old mice were fed with antioxidants or antioxidants + DHEAS for 16 weeks. DHEAS + antioxidants significantly increased B-cell proliferation and IL-2 secretion, and maintained Th2 cytokine secretion and hepatic vitamin E levels nearer to that of old, uninfected mice than antioxidant supplementation alone. Our study suggests that DHEA alone, and especially DHEAS plus antioxidant nutrients, can prevent immune dysfunction in very old and in old, retrovirus-infected mice. Copyright (C) 1998 Elsevier Science Inc.
KW - Aging
KW - B-cell proliferation
KW - DHEA
KW - Immunosenescence
KW - T-cell proliferation
KW - cytokine
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U2 - 10.1016/S0955-2863(98)00041-2
DO - 10.1016/S0955-2863(98)00041-2
M3 - Review article
AN - SCOPUS:0032125405
SN - 0955-2863
VL - 9
SP - 362
EP - 369
JO - Journal of Nutritional Biochemistry
JF - Journal of Nutritional Biochemistry
IS - 7
ER -