Shila Samuel, Subathra Marimuthu, Devi Muthuswamy Anusuya, Panneerselvam Chinnakkannu
Department of Medical Biochemistry, Dr ALM Post Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, 600 113, Chennai, India.
Arch Toxicol. 2005 Mar;79(3):140-6. doi: 10.1007/s00204-004-0614-8. Epub 2004 Nov 11.
The purpose of this study was to examine the effects of DL: -alpha-lipoic acid (LA) on arsenic (As) induced alteration of glutathione (GSH) level and of the activity of glutathione-related enzymes-glutathione peroxidase (GSH-Px), glutathione reductase (GR), and glucose-6-phosphate dehydrogenase (G6PDH)-in rat brain regions (cortex, hypothalamus, striatum, cerebellum and hippocampus). Male Wistar rats of 150+/-10 g weight were divided into four groups: control and three experimental groups supplemented with arsenic (sodium arsenite) alone (100 ppm mixed in drinking water), lipoic acid alone (70 mg kg(-1) body weight), arsenic plus lipoic acid (100 ppm arsenic in drinking water plus 70 mg lipoic acid kg(-1) body weight). The arsenic content of brain regions was found to increase with the administration of sodium arsenite. Arsenic exposure elicited a significant decline in glutathione content and in the activity of related enzymes, with the greatest decreases seen in the cortex, striatum, and hippocampus, whereas there were no significant differences between control rats and the group treated with lipoic acid alone. Highly elevated content of the thiobarbituric acid-reactive substance malondialdehyde (MDA) in the brain regions of arsenic-exposed rats reflected extensive lipid peroxidation (LPO) processes. Simultaneous lipoic acid treatment was effective in reducing brain regional arsenic levels and lipid peroxidation and in increasing the glutathione content and the activity of its related enzymes. Lipoic acid, by acting as an alternative sulfhydryl nucleophile to glutathione, prevents its oxidation to glutathione disulfide in detoxifying reactions against reactive oxygen species and consequently increases the activity of glutathione-related enzymes.
本研究的目的是检测右旋-α-硫辛酸(LA)对大鼠脑区(皮层、下丘脑、纹状体、小脑和海马体)中砷(As)诱导的谷胱甘肽(GSH)水平改变以及谷胱甘肽相关酶——谷胱甘肽过氧化物酶(GSH-Px)、谷胱甘肽还原酶(GR)和葡萄糖-6-磷酸脱氢酶(G6PDH)活性的影响。体重为150±10 g的雄性Wistar大鼠被分为四组:对照组和三个实验组,分别单独补充砷(亚砷酸钠,100 ppm混合于饮用水中)、单独补充硫辛酸(70 mg/kg体重)、砷加硫辛酸(饮用水中100 ppm砷加70 mg硫辛酸/kg体重)。发现随着亚砷酸钠的给药,脑区的砷含量增加。砷暴露导致谷胱甘肽含量和相关酶活性显著下降,在皮层、纹状体和海马体中下降最为明显,而单独用硫辛酸处理的组与对照大鼠之间没有显著差异。砷暴露大鼠脑区中硫代巴比妥酸反应性物质丙二醛(MDA)含量的高度升高反映了广泛的脂质过氧化(LPO)过程。同时进行硫辛酸处理可有效降低脑区砷水平和脂质过氧化,并增加谷胱甘肽含量及其相关酶的活性。硫辛酸作为谷胱甘肽的替代巯基亲核试剂,在针对活性氧的解毒反应中防止其氧化为谷胱甘肽二硫化物,从而提高谷胱甘肽相关酶的活性。