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首页> 外文期刊>European review for medical and pharmacological sciences. >Nitric oxide and peroxynitrite serum levels in Parkinson’s disease: correlation of oxidative stress and the severity of the disease
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Nitric oxide and peroxynitrite serum levels in Parkinson’s disease: correlation of oxidative stress and the severity of the disease

机译:帕金森氏病中的一氧化氮和过氧亚硝酸盐血清水平:氧化应激与疾病严重程度的关系

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BACKGROUND: Nitric oxide (NO) and its toxic product peroxynitrite contribute to oxidative stress and neurodegeneration in Parkinson’s disease (PD). The relationship of serum levels of these oxidants with the severity of the disease [evaluated by the Unified Parkinson’s Disease Rating Scale (UPDRS)] is not established. AIM: This study was designed to evaluate whether patients with PD had higher NO and peroxynitrite serum level or not. PATIENTS AND METHODS: Fifty eight patients with PD and 15 healthy volunteers entered this study. The concentrations of serum NO and peroxynitrite were assayed and their correlation with the UPDRS score was assessed. RESULTS: Mean serum NO levels in patient group was 29.8 ± 21.631 versus 7.49 ± 2.573 in control group, which was significantly higher in patients (p ≤ 0.0001). Peroxynitrite levels in patient and control groups were 7.37±3.501 μmol/L and 3.94 ±1.389 μmol/L respectively. Patients had a significantly higher peroxynitrite level (p = 0.0004). CONCLUSIONS: Higher levels of NO and peroxynitrite leads to higher UPDRS scores. It seems since current PD treatments do not affect the pathology of the disease, using drugs that exert neuroprotective properties should be considered for the treatment of PD in order to prevent further neuronal cell loss.
机译:背景:一氧化氮(NO)及其有毒产物过氧亚硝酸盐有助于帕金森氏病(PD)的氧化应激和神经变性。这些氧化剂的血清水平与疾病的严重程度之间的关系尚未建立[由帕金森综合症评分量表(UPDRS)评估]。目的:本研究旨在评估PD患者是否具有较高的NO和过氧亚硝酸盐血清水平。患者与方法:58位PD患者和15位健康志愿者进入了这项研究。测定血清NO和过亚硝酸盐的浓度,并评估它们与UPDRS评分的相关性。结果:患者组的平均血清NO水平为29.8±21.631,而对照组为7.49±2.573,患者明显更高(p≤0.0001)。患者和对照组的过亚硝酸盐水平分别为7.37±3.501μmol/ L和3.94±1.389μmol/ L。患者的过亚硝酸盐水平明显更高(p = 0.0004)。结论:NO和过氧亚硝酸盐含量越高,UPDRS得分越高。似乎由于目前的PD治疗不影响疾病的病理,因此应考虑使用具有神经保护特性的药物治疗PD,以防止进一步的神经元细胞丢失。

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