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脱氢表雄酮(DHEA)对氧化应激外周标志物的年龄相关影响。

Age-related effects of DHEA on peripheral markers of oxidative stress.

机构信息

Departamento de Fisiologia, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

出版信息

Cell Biochem Funct. 2010 Jan;28(1):52-7. doi: 10.1002/cbf.1619.

DOI:10.1002/cbf.1619
PMID:19924683
Abstract

Ageing is an inevitable biological process characterized by a general decline in various physiological functions. DHEA and DHEAS levels are maximal between the second and third life decades, then start to decline 2% per year, leaving a residual of 10-20% of the peak production by the eighth decade. Erythrocytes are exposed to frequent oxidative stress due to the oxygen radicals continuously generated by haemoglobin auto-oxidation. We investigated DHEA chronic (10 mg/kg, subcutaneously, for 5 weeks) effects over oxidative stress markers in erythrocytes of male Wistar rats of 3, 13 and 18 month-old. In the 13 month-old group, we found increased lipid peroxidation (LPO), superoxide dismutase (SOD), glutathione-S-transferase and catalase activities when compared to the other age groups. DHEA produced a marked increase in LPO of 13 month-old group when compared to its control. DHEA exerted this pro-oxidant effects in all ages studied, especially in age 13 month-old. It seems that at 13 month-old there would be an important depletion of some specific anti-oxidant in order to determine such susceptibility to DHEA effects. Since this approach allows a minimally invasive assessment, it would be useful as a routine method in human clinical studies investigating DHEA effects during the ageing process.

摘要

衰老是一种不可避免的生物过程,其特征是各种生理功能普遍下降。DHEA 和 DHEAS 的水平在第二和第三个生命十年之间达到最大值,然后开始每年下降 2%,到第八个十年时,剩余的产量为峰值的 10-20%。由于血红蛋白自动氧化不断产生自由基,红细胞经常受到氧化应激。我们研究了 DHEA 慢性(10mg/kg,皮下,5 周)对雄性 Wistar 大鼠红细胞氧化应激标志物的影响,这些大鼠分别为 3、13 和 18 个月大。在 13 个月大的组中,与其他年龄组相比,发现脂质过氧化(LPO)、超氧化物歧化酶(SOD)、谷胱甘肽-S-转移酶和过氧化氢酶活性增加。与对照组相比,DHEA 使 13 个月大的组的 LPO 明显增加。DHEA 在所有研究的年龄组中都产生了明显的促氧化作用,尤其是在 13 个月大的年龄组。似乎在 13 个月大时,某些特定的抗氧化剂会大量消耗,从而导致对 DHEA 作用的敏感性。由于这种方法可以进行微创评估,因此在研究衰老过程中 DHEA 作用的人类临床研究中作为常规方法可能很有用。

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