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Reactive oxygen species antioxidant mechanisms and serum cytokine levels in cancer patients: impact of an antioxidant treatment

机译:癌症患者的活性氧抗氧化剂机制和血清细胞因子水平:抗氧化剂治疗的影响

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Objective. So far, it is not well established whether oxidative stress found in cancer patients results from an increased production of oxidants in the body or from a failure of physiological antioxidant systems. To further investigate this question we have assessed the blood levels of reactive oxygen species as a marker of free radicals producing oxidative stress and the most relevant of the physiological body enzymes counteracting reactive oxygen species, namely glutathione peroxidase and superoxide dismutase. Serum levels of proinflammatory cytokines and IL‐2 were also investigated. All these parameters were studied in relation to the clinically most important index of disease progression, namely Performance Status (ECOG PS). We also tested the reducing ability of different antioxidant agents on reactive oxygen species levels by measuring the increase in glutathione peroxidase activity, and the reduction of serum levels of IL‐6 and TNF. Design, setting and subjects. We carried out an open non randomized study on 28 advanced stage cancer patients (stage III, 10.7%, and stage IV, 89.3%) with tumours at different (8) sites: all were hospitalized in the Medical Oncology Dept, University of Cagliari Interventions. The patients were divided into 5 groups and a different antioxidant treatment was administered to each group. The selected antioxidants were: alpha lipoic acid 200 mg/day orally, N‐acetylcysteine 1800 mg/day i.v. or carboxycysteine‐lysine salt 2.7 g/day orally, amifostine 375 mg/day i.v., reduced glutathione 600 mg/day i.v., vitamin A 30000 IU/day orally plus vitamin E 70 mg/day orally plus Vitamin C 500 mg/day orally. The antioxidant treatment was administered for 10 consecutive days. Results. Our results show that all but one of the antioxidants tested were effective in reducing reactive oxygen species levels and 2 of them (cysteine‐containing compounds and amifostine) had the additional effect of increasing glutathione peroxidase activity. Comprehensively, the “antioxidant treatment” was found to have an effect both on reactive oxygen species levels and glutathione peroxidase activity. The antioxidant treatment also reduced serum levels of IL‐6 and TNF. Patients in both ECOG PS 0‐1 and ECOG PS 2‐3 responded to antioxidant treatment.
机译:目的。迄今为止,尚不清楚癌症患者中发现的氧化应激是由于体内氧化剂产生的增加还是由于生理抗氧化剂系统的失效而引起的。为了进一步研究这个问题,我们评估了血液中的活性氧水平,这些自由基是产生氧化应激的自由基的标志,是与活性氧最相关的生理酶,即谷胱甘肽过氧化物酶和超氧化物歧化酶。还研究了血清促炎细胞因子和IL-2水平。所有这些参数均与疾病进展的临床最重要指标即表现状态(ECOG PS)进行了研究。我们还通过测量谷胱甘肽过氧化物酶活性的增加以及血清IL-6和TNF的降低来测试不同抗氧化剂对活性氧水平的还原能力。设计,设置和主题。我们对28名不同(8)部位肿瘤的晚期癌症患者(III期10.7%和IV期89.3%)进行了一项开放性非随机研究:所有患者均在卡利亚里大学干预医院的肿瘤科住院。将患者分为5组,每组给予不同的抗氧化剂治疗。选定的抗氧化剂为:口服α硫辛酸200毫克/天,静脉注射N-乙酰半胱氨酸1800毫克/天。或口服2.7g /天的羧半胱氨酸-赖氨酸盐,腹腔注射375 mg /天的氨磷汀,口服i-v。减少的谷胱甘肽600 mg /天,口服维生素A 30000 IU /天,口服维生素E 70 mg /天,口服维生素C 500 mg /天。连续10天进行抗氧化剂治疗。结果。我们的结果表明,除一种抗氧化剂外,所有抗氧化剂均可有效降低活性氧水平,其中两种(含半胱氨酸的化合物和氨磷汀)具有增加谷胱甘肽过氧化物酶活性的附加作用。全面地,发现“抗氧化剂处理”对活性氧水平和谷胱甘肽过氧化物酶活性都有影响。抗氧化剂治疗还降低了血清IL-6和TNF的水平。 ECOG PS 0-1和ECOG PS 2-3的患者均对抗氧化剂治疗有反应。

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