Castillo Rodrigo L, Zepeda Andrea B, Short Stefania E, Figueroa Elías, Bustos-Obregon Eduardo, Farías Jorge G
Pathophysiology Program, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile, Santiago, Chile.
Departamento de Ingeniería Química, Facultad de Ingeniería y Ciencias, Universidad de La Frontera, Casilla 54-D, Temuco, Chile.
J Biomed Sci. 2015 Jan 23;22(1):8. doi: 10.1186/s12929-015-0112-8.
Intermittent hypobaric hypoxia (IHH) induces changes in the redox status and structure in rat testis. These effects may be present in people at high altitudes, such as athletes and miners. Polyunsaturated fatty acids (PUFA) can be effective in counteracting these oxidative modifications due to their antioxidants properties. The aim of the work was to test whether PUFA supplementation attenuates oxidative damage in testis by reinforcing the antioxidant defense system. The animals were divided into four groups (7 rats per group): normobaric normoxia (750 tor; pO2 156 mmHg; Nx); Nx + PUFA, supplemented with PUFA (DHA: EPA = 3:1; 0.3 g kg(-1) of body weight per day); hypoxic hypoxia (428 tor; pO2 90 mmHg; Hx) and, Hx + PUFA. The hypoxic groups were exposed in 4 cycles to 96 h of HH followed by 96 h of normobaric normoxia for 32 days. Total antioxidant capacity (FRAP) and lipid peroxidation (malondialdehyde, MDA) in plasma and reduced (GSH)/oxidized glutathione (GSSG) ratio, tissue lipid peroxidation (TBARS) and antioxidant enzymes activity were assessed at the end of the study in testis. Also, SIRTUIN 1 and HIF-1 protein expression in testis were determined.
IHH increased lipid peroxidation in plasma and HIF-1 protein levels in testis. In addition, IHH reduced FRAP levels in plasma, antioxidant enzymes activities and SIRTUIN 1 protein levels in testis. PUFA supplementation attenuated these effects, inducing the increases in FRAP, in the antioxidant enzymes activity and HIF-1 levels.
These results suggest that the IHH model induces a prooxidant status in plasma and testis. The molecular protective effect of PUFA may involve the induction of an antioxidant mechanism.
间歇性低压缺氧(IHH)可引起大鼠睾丸氧化还原状态及结构的改变。这些影响可能存在于高海拔人群中,如运动员和矿工。多不饱和脂肪酸(PUFA)因其抗氧化特性,可有效对抗这些氧化修饰。本研究旨在测试补充PUFA是否通过增强抗氧化防御系统来减轻睾丸的氧化损伤。将动物分为四组(每组7只大鼠):常压常氧组(750托;pO2 156 mmHg;Nx);Nx + PUFA组,补充PUFA(DHA:EPA = 3:1;每天0.3 g/kg体重);低氧缺氧组(428托;pO2 90 mmHg;Hx)和Hx + PUFA组。低氧组在32天内经历4个周期,每次96小时的HH暴露,随后96小时的常压常氧暴露。在研究结束时,评估睾丸组织中血浆总抗氧化能力(FRAP)、脂质过氧化(丙二醛,MDA)、还原型(GSH)/氧化型谷胱甘肽(GSSG)比值、组织脂质过氧化(TBARS)及抗氧化酶活性。此外,还测定了睾丸组织中SIRTUIN 1和HIF-1蛋白表达。
IHH增加了血浆中的脂质过氧化及睾丸组织中的HIF-1蛋白水平。此外,IHH降低了血浆中的FRAP水平、睾丸组织中的抗氧化酶活性及SIRTUIN 1蛋白水平。补充PUFA减轻了这些影响,使FRAP、抗氧化酶活性及HIF-1水平升高。
这些结果表明,IHH模型可诱导血浆和睾丸的促氧化状态。PUFA的分子保护作用可能涉及诱导抗氧化机制。