Nawata Hajime, Yanase Toshihiko, Goto Kiminobu, Okabe Taijiro, Nomura Masatoshi, Ashida Kenji, Watanabe Tetsuhiro
Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Horm Res. 2004;62 Suppl 3:110-4. doi: 10.1159/000080509.
Dehydroepiandrosterone(DHEA) and DHEA-S are steroids that are abundantly produced by the adrenal gland. Plasma concentrations of DHEA and DHEA-S increase during adrenarche but decrease steadily after puberty. Although DHEA and DHEA-S have few intrinsic androgenic actions, they have recently attracted widespread attention due to their beneficial anti-aging effects. We clarified the beneficial effects of DHEA as an anti-aging steroid with regard to its stimulation of the immune system and its anti-diabetes, anti-atherosclerosis, anti-dementia (neurosteroid), anti-obesity and anti-osteoporosis effects. There are two possible biochemical and molecular mechanisms: direct action via the DHEA receptor on the target gene; and indirect action. We identified a high affinity of DHEA binding in human T-lymphocytes by searching for the target genes that are induced in activated T-lymphocytes in the presence of DHEA, determined the gene sequence and named DHEA-induced dual p38-specific phosphatase (DDSP). DDSP transgenic mice have been created to identify the anti-aging effects of DDSP. The conversion of DHEA to estrone by cytochrome P450 aromatase in primary cultured human osteoblasts was clarified. We are currently undertaking an open trial of DHEA replacement therapy.
脱氢表雄酮(DHEA)和硫酸脱氢表雄酮(DHEA-S)是由肾上腺大量分泌的类固醇。DHEA和DHEA-S的血浆浓度在肾上腺初现时升高,但在青春期后稳步下降。尽管DHEA和DHEA-S几乎没有内在的雄激素作用,但它们最近因其有益的抗衰老作用而受到广泛关注。我们阐明了DHEA作为一种抗衰老类固醇在刺激免疫系统、抗糖尿病、抗动脉粥样硬化、抗痴呆(神经甾体)、抗肥胖和抗骨质疏松方面的有益作用。有两种可能的生化和分子机制:通过DHEA受体对靶基因的直接作用;以及间接作用。我们通过寻找在DHEA存在下在活化T淋巴细胞中诱导的靶基因,确定了DHEA在人T淋巴细胞中的高亲和力结合,确定了基因序列并将其命名为DHEA诱导的双p38特异性磷酸酶(DDSP)。已创建DDSP转基因小鼠以确定DDSP的抗衰老作用。阐明了原代培养的人成骨细胞中细胞色素P450芳香化酶将DHEA转化为雌酮的过程。我们目前正在进行DHEA替代疗法的开放试验。