摘要
目的测定帕金森病(PD)患者尿中8-异前列腺素F2α(8-iso-PGF2α)和血中低密度脂蛋白体外氧化延迟时间的变化。方法运用病例一对照观察,根据Calne标准选取31例男性PD患者、同时选取31例年龄、影响因素等相当的健康男性为对照。通过铜氧化共轭双烯法在波长234nm测定血中低密度脂蛋白体外氧化延迟时间以及酶联免疫法测定尿中8-iso-PGF2α浓度。结果PD患者组尿中8-iso-PGF2α含量比对照组明显增高[(81.1±1.6)ng/mmol肌酐vs(46.9±1.1)ng/mmol肌酐],差异有统计学意义(P〈0.05);而血中低密度脂蛋白体外氧化延迟时间明显减低[(63.5±6.0)min vs(84.4±8.8)min],差异有统计学意义(P〈0.05)。结论增高的氧化压力与降低的抗氧化能力在PD的病理过程中具有一定的作用,提示有效的抗氧化治疗可能对控制疾病的发展具有一定的意义。
Objective To measure the changes in urinary 8-iso-prostaglandin-F2α(8-iso-PGF2α) and oxidized low-density lipoprotein (ox-LDL) lag time in patients with Parkinson's disease (PD). Methods A case-control study was performed involving 31 male patients with PD (mean age of 59.7 years) diagnosed according to the Calne criteria and 31 age-matched healthy male subjects with comparable status of smoking and life style. For each subject, urinary 8-iso-PGF2α was measured quantitatively using enzyme-linked immunosorbent assay, and LDL oxidizability was measured by determining LDL oxidation lag time in conjugated diene product at 234 nm using Cu-stimulated oxidation. Results Compared to the levels in the control subjects, the PD patients showed significantly increased urinary 8-iso-PGF2α (81.1±1.6 vs 46.9±1.1 ng/mmol creatinine, P〈0.05) and significantly reduced LDL oxidation lag time (63.5 ±6.0 vs 84.4±8.8 min, P〈0.05). Conclusion Increased 8-iso-PGF2α and decreased anti-oxidant ability are implicated in the pathogenesis of PD, suggesting the value of appropriate antioxidant therapy in controlling the progression of PD.
出处
《中华神经医学杂志》
CAS
CSCD
北大核心
2009年第1期54-56,共3页
Chinese Journal of Neuromedicine
关键词
帕金森病
氧化压力
低密度脂蛋白
Parkinson's disease
Oxidative stress
Low-density lipoprotein