首页> 外文期刊>Iranian Journal of Basic Medical Sciences >EFFECT OF WR-1065 ON 6-HYDROXYDOPAMINE-INDUCED CATALEPSY AND IL-6 LEVEL IN RATS
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EFFECT OF WR-1065 ON 6-HYDROXYDOPAMINE-INDUCED CATALEPSY AND IL-6 LEVEL IN RATS

机译:WR-1065对6-羟多巴胺诱导的大鼠僵直和IL-6水平的影响

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Objective (s): Neuroinflammation and oxidative stress play a key role in pathogenesis of Parkinson’s disease (PD). In the present study we investigated the effect of reactive oxygen species (ROS) scavenger WR-1065 on catalepsy and cerebrospinal fluid (CSF) level of interleukin 6 (IL-6) and striatum superoxide dismutase (SOD) activity in 6-hydroxydopamine (6-OHDA) induced experimental model of PD.Materials and Methods: Seventy two male Wistar rats were divided into 9 equal groups and 6-OHDA (8 m g/2 m l/rat) was infused unilaterally into substantia nigra pars copmacta (SNc) to induce PD. Catalepsy was measured by standard bar test, CSF level of IL-6 was assessed by enzyme-linked immunosorbent assay (ELISA) method and SOD activity measured by spectrophotometric method. In pre-treatment groups WR-1065 (20, 40 and 80 m g/2 m l/rat/day, for 3 days) was infused into the SNc before 6-OHDA administration and 21 days later, as a recovery period, behavioral and molecular assay tests were done.Results: Our results showed that pre-treatment with WR-1065 improved (PConclusion: Our study indicated that pre-treatment with WR-1065 could modulate catalepsy and IL-6 level in 6-OHDA-lesioned rats. Also WR1065 could increase SOD activity up to normal range. It can be regarded as an anti-oxidative drug in prevention or adjunctive therapy of PD.
机译:目的:神经炎症和氧化应激在帕金森氏病(PD)的发病机理中起关键作用。在本研究中,我们研究了活性氧(ROS)清除剂WR-1065对6-羟基多巴胺(6)中的僵直症和脑脊髓液(CSF)白细胞介素6(IL-6)水平和纹状体超氧化物歧化酶(SOD)活性的影响。 -OHDA)诱导的PD实验模型。材料与方法:将72只雄性Wistar大鼠分成9组,将6-OHDA(8 mg / 2 ml /大鼠)单侧注入黑质铜斑病(SNc)中诱导。 PD。通过标准棒试验测量僵直症,通过酶联免疫吸附测定(ELISA)方法评估IL-6的CSF水平,并通过分光光度法测量SOD活性。在预处理组中,将WR-1065(20、40和80 mg / 2 ml /大鼠/天,连续3天)注入SNc中,然后施用6-OHDA,之后21天作为恢复期,行为和分子结果:我们的结果表明,WR-1065的预处理有所改善(PConclusion:我们的研究表明,WR-1065的预处理可以调节6-OHDA损伤大鼠的僵直和IL-6水平。 WR1065可使SOD活性增加至正常范围,可作为PD预防或辅助治疗中的抗氧化药物。

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