首页> 外文期刊>International journal of immunopathology and pharmacology. >Ibuprofen and lipoic acid diamide as co-drug with neuroprotective activity: Pharmacological properties and effects in β-amyloid (1-40) infused Alzheimer's disease rat model
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Ibuprofen and lipoic acid diamide as co-drug with neuroprotective activity: Pharmacological properties and effects in β-amyloid (1-40) infused Alzheimer's disease rat model

机译:布洛芬和硫辛酸二酰胺作为具有神经保护活性的辅助药物:输注阿尔茨海默氏病大鼠模型的药理学性质和对β-淀粉样蛋白(1-40)的影响

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摘要

Both oxidative stress and inflammation are elevated in brains of Alzheimer's disease patients, but their pathogenic significance still remains unclear. Current evidence support the hypothesis that non-steroidal anti-inflammatory drugs (NSAIDs) and antioxidant therapy might protect against the development of Alzheimer's disease, and Ibuprofen has the strongest epidemiological support. In the present work our attention was focused on (R)-α-lipoic acid considered as a potential neuroprotective agent in Alzheimer's disease therapy. In particular, we investigated a new co-drug (1) obtained by joining (R)-α-lipoic acid and Ibuprofen via a diamide bond, for evaluating its potential to antagonize the deleterious structural and cognitive effects of β-amyloid (1-40) in an infused Alzheimer's disease rat model. Our results indicated that infusion of β-amyloid (1-40) impairs memory performance through a progressive cognitive deterioration; however, Ibuprofen and co-drug 1 seemed to protect against behavioural detriment induced by simultaneous administration of β-amyloid (1-40) protein. The obtained data were supported by the histochemical findings of the present study: β-amyloid protein was less expressed in 1-treated than in Ibuprofen and (R)-α-lipoic acid alone-treated cerebral cortex. Taken together, the present findings suggest that co-drug 1 treatment may protect against the cognitive dysfunction induced by intracerebroventricular infusion of β-amyloid (1-40) in rats. Thus, co-drug 1 could prove useful as a tool for controlling Alzheimer's disease-induced cerebral amyloid deposits and behavioural deterioration.
机译:阿尔茨海默氏病患者的大脑中氧化应激和炎症均升高,但其致病意义仍不清楚。当前证据支持以下假设:非甾体抗炎药(NSAID)和抗氧化剂疗法可预防阿尔茨海默氏病的发展,布洛芬具有最强的流行病学支持。在目前的工作中,我们的注意力集中在(R)-α-硫辛酸上,该化合物被认为是阿尔茨海默氏病治疗中潜在的神经保护剂。特别是,我们研究了通过(R)-α-硫辛酸和布洛芬通过二酰胺键连接而获得的新的共用药物(1),以评估其拮抗β-淀粉样蛋白(1- 40)在输注的阿尔茨海默氏病大鼠模型中。我们的结果表明,β-淀粉样蛋白(1-40)的输注会通过进行性认知减退来损害记忆性能。然而,布洛芬和联合用药1似乎可以防止同时服用β-淀粉样蛋白(1-40)引起的行为损害。获得的数据得到本研究的组织化学发现的支持:与单独使用布洛芬和(R)-α-硫辛酸处理过的大脑皮层相比,在1种处理过的过程中β-淀粉样蛋白的表达较少。综上所述,本研究结果表明,联合用药1治疗可预防大鼠脑室内输注β-淀粉样蛋白(1-40)引起的认知功能障碍。因此,联合药物1可以证明是控制阿尔茨海默氏病引起的脑淀粉样蛋白沉积和行为恶化的工具。

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