Chen T S, Richie J P, Lang C A
Department of Pharmacology, University of Louisville, Kentucky 40292.
Proc Soc Exp Biol Med. 1989 Apr;190(4):399-402. doi: 10.3181/00379727-190-42879.
A general glutathione (GSH) deficiency occurs in many tissues of the aging mouse. However, there is no information on GSH in the aging brain even though it has been involved in a number of neurobiologic reactions. To this end, C57BL/6 mice, 3-31 months old, representing the growth, maturation, and aging periods of the life-span were studied. Brain cortex, hippocampus, and stem samples were dissected, processed, and analyzed specifically for reduced and oxidized glutathione (GSH, GSSG) and cyst(e)ine using high performance liquid chromatography with dual electrochemical detection. The GSH content of each brain region varied in the order brain cortex greater than brain hippocampus greater than brainstem. However, the GSH profiles of all regions were the same through the life-span, namely, high values during growth dropping to a maturation plateau and then decreasing 30% during aging. In contrast to GSH, the order of cysteine levels was brain cortex less than brain hippocampus less than brainstem and no life-span changes occurred in any region. In addition, the brain GSSG and cystine contents of all regions were very low and did not change during the life-span. Thus, the GSH loss was not accountable by oxidation to GSSG or degradation to cyst(e)ine. Altogether these results demonstrated a GSH deficiency in brain tissues of aging mice like that found previously in other tissues. These findings suggest an increased susceptibility of the aging brain to oxidative damage.
衰老小鼠的许多组织中普遍存在谷胱甘肽(GSH)缺乏的情况。然而,尽管GSH参与了多种神经生物学反应,但关于衰老大脑中GSH的情况却尚无相关信息。为此,研究了3至31月龄的C57BL/6小鼠,它们分别代表了生命周期中的生长、成熟和衰老阶段。解剖、处理并分析了大脑皮质、海马体和脑干样本,使用具有双电化学检测功能的高效液相色谱法专门检测还原型和氧化型谷胱甘肽(GSH、GSSG)以及半胱氨酸。每个脑区的GSH含量按大脑皮质>脑海马体>脑干的顺序变化。然而,所有区域的GSH分布在整个生命周期中都是相同的,即在生长期间含量较高,降至成熟平台期,然后在衰老期间下降30%。与GSH相反,半胱氨酸水平的顺序是大脑皮质<脑海马体<脑干,且任何区域在生命周期中都没有变化。此外,所有区域的大脑GSSG和胱氨酸含量都非常低,并且在生命周期中没有变化。因此,GSH的损失不能归因于氧化为GSSG或降解为半胱氨酸。总之,这些结果表明衰老小鼠的脑组织中存在GSH缺乏,就像之前在其他组织中发现的那样。这些发现表明衰老大脑对氧化损伤的易感性增加。