Pelissier Marie-Agnès, Trap Catherine, Malewiak Marie-Irène, Morfin Robert
Laboratoire de Biologie, EA-3199, Conservatoire National des Arts et Métiers, 2 rue Conté, 75003 Paris, France.
Steroids. 2004 Feb;69(2):137-44. doi: 10.1016/j.steroids.2003.12.006.
This study examined in healthy male Wistar rats the in vivo antioxidant effect of dehydroepiandrosterone (DHEA) and 7alpha-hydroxy-DHEA administered by intraperitoneal injections (50 mg/kg body weight) for 2 or 7 days. Markers of oxidative damage to lipids (thiobarbituric acid-reacting substances, TBARS) and to proteins (protein carbonyls) were assessed in colon, small intestine, and liver homogenates. DHEA and 7alpha-hydroxy-DHEA caused a decrease in body weight. DHEA treatment significantly increased liver, colon, and small intestine cell weights. After 7 days, DHEA exerted an antioxidant effect in all organs studied. In the colon, oxidative damage protection was accompanied by a goblet cell proliferation and increase in acidic mucus production. After 2 days, the antioxidant effect of 7alpha-hydroxy-DHEA was mainly observed in the liver. Nonprotein sulfhydryl groups (mostly glutathione levels) were altered by DHEA in the liver whereas they remained unchanged after 7alpha-hydroxy-DHEA treatment. The results indicate that in healthy animals, DHEA exerts a protective effect, particularly in the colon, by reducing the tissue susceptibility to oxidation of both lipids and proteins. This effect was not limited to a specific tissue, whereas the metabolite 7alpha-hydroxy-DHEA exerted its antioxidant effect towards the two markers of oxidative damage earlier than DHEA, and mainly in the liver.
本研究在健康雄性Wistar大鼠中,检测了通过腹腔注射(50毫克/千克体重)给予脱氢表雄酮(DHEA)和7α-羟基-DHEA 2天或7天的体内抗氧化作用。在结肠、小肠和肝脏匀浆中评估了脂质氧化损伤标志物(硫代巴比妥酸反应物质,TBARS)和蛋白质氧化损伤标志物(蛋白质羰基)。DHEA和7α-羟基-DHEA导致体重下降。DHEA处理显著增加了肝脏、结肠和小肠的细胞重量。7天后,DHEA在所有研究器官中发挥抗氧化作用。在结肠中,氧化损伤保护伴随着杯状细胞增殖和酸性黏液分泌增加。2天后,7α-羟基-DHEA的抗氧化作用主要在肝脏中观察到。DHEA改变了肝脏中的非蛋白巯基(主要是谷胱甘肽水平),而7α-羟基-DHEA处理后它们保持不变。结果表明,在健康动物中,DHEA通过降低组织对脂质和蛋白质氧化的易感性发挥保护作用,尤其是在结肠中。这种作用不限于特定组织,而代谢物7α-羟基-DHEA比DHEA更早地对氧化损伤的两个标志物发挥抗氧化作用,且主要在肝脏中。