Dipartimento di Medicina e Scienze dell'Invecchiamento, Università degli Studi "G. d'Annunzio" Chieti Pescara, 66100 Chieti, Italy; Laboratorio di Fisiopatologia dello Stress Ossidativo, CeSI-MeT, Center of Excellence on Aging, Università degli Studi "G. d'Annunzio" Chieti Pescara, 66100 Chieti, Italy.
Dipartimento di Medicina e Scienze dell'Invecchiamento, Università degli Studi "G. d'Annunzio" Chieti Pescara, 66100 Chieti, Italy; Laboratorio di Fisiopatologia dello Stress Ossidativo, CeSI-MeT, Center of Excellence on Aging, Università degli Studi "G. d'Annunzio" Chieti Pescara, 66100 Chieti, Italy.
Exp Gerontol. 2019 Feb;116:7-13. doi: 10.1016/j.exger.2018.11.013. Epub 2018 Nov 23.
It is not known whether aging alters the enzymatic reactive aldehyde- and lipid hydroperoxide-detoxifying capacity of the human arterial tissue favoring vascular oxidative stress. To address this issue, we studied the specific enzymatic activities of class 1, 2 and 3 aldehyde dehydrogenase (ALDH1, ALDH2 and ALDH3), glutathione S‑transferase (isozyme A4-4, GSTA4-4) and aldose reductase (AR), namely the major reactive aldehyde-scavenging enzymes, together with the activity of the lipid hydroperoxide-removing enzyme glutathione peroxidase (GSH-Px), in superior thyroid arteries (STA) specimens obtained in the thyroid surgery setting in aged subjects (age 72.3 ± 3.6 years) and young adult controls (age 31.9 ± 3.5 years). Vascular lipid peroxidation was also studied by assessing in STA fluorescent damage products of lipid peroxidation (FDPL), which reflect oxidant-induced 4‑hydroxynonenal and lipid hydroperoxide formation. Remarkably, the activities of ALDH1, ALDH2, ALDH3, GSTA4-4, AR and GSH-Px were significantly lower, and FDPL levels higher, in the arterial tissue of the aged subjects than in that of the young adult controls. Moreover, the enzymatic activities were inversely and significantly correlated with the levels of FDPL in the arterial tissue of both the aged and young subjects, highlighting their vascular antioxidant/antilipoperoxidative role in vivo. Thus, aging impairs the enzymatic reactive aldehyde-detoxifying capacity and GSH-Px activity of the human arterial tissue eventually favoring vascular oxidative stress.
目前尚不清楚衰老是否会改变人体动脉组织中酶促反应性醛类和脂质过氧化物解毒能力,从而有利于血管氧化应激。为了解决这个问题,我们研究了 1 类、2 类和 3 类醛脱氢酶(ALDH1、ALDH2 和 ALDH3)、谷胱甘肽 S-转移酶(同工酶 A4-4、GSTA4-4)和醛还原酶(AR)的特定酶活性,这些酶是主要的反应性醛清除酶,以及脂质过氧化物清除酶谷胱甘肽过氧化物酶(GSH-Px)的活性,研究对象为甲状腺手术中获得的老年(72.3±3.6 岁)和年轻成年(31.9±3.5 岁)受试者的甲状腺上动脉(STA)标本。通过评估 STA 中脂质过氧化的荧光损伤产物(FDPL)来研究血管脂质过氧化,FDPL 反映了氧化剂诱导的 4-羟基壬烯醛和脂质过氧化物的形成。值得注意的是,与年轻成年对照组相比,老年受试者的动脉组织中 ALDH1、ALDH2、ALDH3、GSTA4-4、AR 和 GSH-Px 的活性显著降低,FDPL 水平更高。此外,在老年和年轻受试者的动脉组织中,酶活性与 FDPL 水平呈负相关且显著相关,这突出了它们在体内的血管抗氧化/抗脂质过氧化作用。因此,衰老会损害人体动脉组织的酶促反应性醛解毒能力和 GSH-Px 活性,最终有利于血管氧化应激。