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Are insulin-resistance and oxidative stress cause or consequence of aging

机译:是胰岛素抵抗和氧化应激原因或老化的结果

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Insulin resistance (IR) may be associated with oxidative stress and leads to cardiovascular disorders. Current research focuses on interplay between insulin-resistance indices and oxidant-antioxidant markers in elderly individuals with or without insulin-resistance. The assessment involved anthropometric data (weight, height, BMI, percentage of body fat (FAT)) and biochemical tests (glucose, lipids, serum insulin and plasma oxidant-antioxidant markers: Thiobarbituric Acid-Reacting Substances (TBARS), Cu,Zn-superoxide dismutase (SOD-1) and total antioxidant status). Insulin resistance index (IR) assuming a cut-off point of 0.3 allows to divides groups into: insulin sensitive group (InsS) IR < 0,3 (n = 35, median age 69.0 years) and insulin-resistant group (InsR) IR ≥ 0.3 (n = 51, median age 71.0 years). Lipids and antioxidant defense system markers did not differentiate the investigated groups. In the InsR elderly group, the FAT was increased (P < 0.000003) and TBARS (P = 0.008) concentration decreased in comparison with InsS group. A positive correlation for SOD-1 and total antioxidant status (P < 0.05; r =  0.434) and a negative correlation for TBARS and age (P < 0.05 with r = −0.421) were calculated in InsR individuals. In elderly individuals, oxidative stress persists irrespective of insulin-resistance status. We suggest that increased oxidative stress may be consequence of old age. An insulin action identifies those at high risk for atherosclerosis, via congruent associations with oxidative stress and extra- and intra-cellular antioxidant defense systems. Thus, we maintain that insulin-resistance is not the cause of aging.
机译:胰岛素抵抗(IR)可以与氧化应激相关并导致心血管障碍。目前的研究侧重于胰岛素抵抗指数和氧化剂 - 抗氧化标志物在具有或没有胰岛素抗性的老年人中的相互作用。评估涉及人体测量数据(体重,高度,BMI,体脂(脂肪)的百分比)和生化试验(葡萄糖,脂质,血清胰岛素和血浆氧化剂 - 抗氧化标记:硫氨基吡啶酸反应物质(TBAR),Cu,Zn-超氧化物歧化酶(SOD-1)和总抗氧化剂状态)。假设截止点为0.3的胰岛素抵抗指数(IR)允许将组分成:胰岛素敏感组(INSS)IR <0.3(n = 35,中位数69.0岁)和胰岛素抗性组(INSR)IR ≥0.3(n = 51,中位数年龄71.0岁)。脂质和抗氧化剂防御系统标记没有区分所研究的群体。在Insr老年群中,脂肪增加(P <0.000003),与INSS组相比,TBARS(P = 0.008)浓度降低。对SOD-1和总抗氧化剂状态的正相关(P <0.05; r = 0.434)和TBAR和年龄的负相关(P <0.05与r = -0.421)进行了计算。在老年人身上,无论胰岛素抵抗状态如何都存在氧化应激。我们建议增加氧化压力可能是老年的结果。胰岛素作用鉴定了动脉粥样硬化的高风险,通过与氧化应激和细胞内和细胞内抗氧化剂防御系统的联系。因此,我们认为胰岛素抵抗不是老化的原因。

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