首页> 美国卫生研究院文献>Parkinsons Disease >Pentoxifylline Neuroprotective Effects Are Possibly Related to Its Anti-Inflammatory and TNF-Alpha Inhibitory Properties in the 6-OHDA Model of Parkinsons Disease
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Pentoxifylline Neuroprotective Effects Are Possibly Related to Its Anti-Inflammatory and TNF-Alpha Inhibitory Properties in the 6-OHDA Model of Parkinsons Disease

机译:在帕金森氏病的6-OHDA模型中己酮可可碱的神经保护作用可能与其抗炎和TNF-α抑制特性有关。

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摘要

Pentoxifylline (PTX) is a phosphodiesterase inhibitor with anti-TNF-alpha activity, associated with its anti-inflammatory action. Considering Parkinson's disease (PD) as a neuroinflammatory disorder, the objectives were to evaluate PTX neuroprotective properties, in a model of PD. Male Wistar rats, divided into sham-operated (SO), untreated 6-OHDA, and 6-OHDA treated with PTX (10, 25, and 50 mg/kg) groups, received a unilateral 6-OHDA injection, except the SO group administered with saline. Treatments started 24 h after surgery and continued for 15 days when the animals were submitted to apomorphine-induced rotations, open field, and forced swimming tests. At the next day, they were euthanized and their striata processed for neurochemical (DA and DOPAC determinations), histological, and immunohistochemical (Fluoro-Jade, TH, DAT, OX-42, TNF-alpha, COX-2, and iNOS) studies. PTX reversed the behavioral changes observed in the untreated 6-OHDA animals. Furthermore, PTX partially reversed the decrease in DA contents and improved neuronal viability. In addition, decreases in immunostaining for TH and dopamine transporter (DAT) were reversed. The untreated 6-OHDA group showed intense OX-42, TNF-alpha, COX-2, and iNOS immunoreactivities, which were attenuated by PTX. In conclusion, we demonstrated a neuroprotective effect of PTX, possibly related to its anti-inflammatory and antioxidant actions, indicating its potential as an adjunct treatment for PD.
机译:己酮可可碱(PTX)是一种具有抗TNF-α活性的磷酸二酯酶抑制剂,具有抗炎作用。将帕金森氏病(PD)视为一种神经炎性疾病,目的是在PD模型中评估PTX的神经保护特性。将Wistar雄性大鼠分为假手术(SO),未经治疗的6-OHDA和经PTX(10、25和50μmg/ kg)组治疗的6-OHDA,除SO组外,均接受单侧6-OHDA注射。给予生理盐水。手术后24小时开始治疗,并持续15天(当动物接受阿扑吗啡诱导的旋转,旷野和强迫游泳测试时)。第二天,对它们实施安乐死并对其纹状体进行处理,以进行神经化学(DA和DOPAC测定),组织学和免疫组织化学(Fluoro-Jade,TH,DAT,OX-42,TNF-alpha,COX-2和iNOS)研究。 PTX逆转了在未经治疗的6-OHDA动物中观察到的行为变化。此外,PTX部分逆转了DA含量的下降并改善了神经元的生存能力。此外,TH和多巴胺转运蛋白(DAT)的免疫染色减少被逆转。未经处理的6-OHDA组显示出强烈的OX-42,TNF-α,COX-2和iNOS免疫反应性,这些反应被PTX减弱。总之,我们证明了PTX的神经保护作用,可能与其抗炎和抗氧化作用有关,表明其作为PD的辅助治疗的潜力。

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