首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Montelukast potentiates the protective effect of rofecoxib against kainic acid-induced cognitive dysfunction in rats
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Montelukast potentiates the protective effect of rofecoxib against kainic acid-induced cognitive dysfunction in rats

机译:孟鲁司特增强罗非昔布对海藻酸诱导的大鼠认知功能障碍的保护作用

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摘要

There is an evolving consensus that mild cognitive impairment (MCI) serves as a prodrome to Alzheimer's disease. Antioxidants and COX-2 (cyclo-oxygenase-2) inhibitors have also been reported to have beneficial effects against conditions of memory impairment. Newer drugs like cysteinyl leukotriene inhibitors have shown neuroprotective effect in animal models of ischemia. Thus, the present study purports to explore the potential role of montelukast (a cysteinyl leukotriene inhibitor) in concert with rofecoxib (COX-2 inhibitor) and caffeic acid (a 5-LOX inhibitor and potent antioxidant) against kainic acid induced cognitive dysfunction in rats. In the experimental protocol, kainic acid (0.4 μg/2 μl) in artificial cerebrospinal fluid (ACSF) was given intrahippocampally (CA3 region) to induce a condition similar to MCI. Memory performance was measured on days 10-14 and the locomotor activity was measured on days 1, 7 and 14. For estimation of biochemical, mitochondrial and histopathological parameters, animals were sacrificed on day 14, stored at - 80 °C and the estimation was done on the 15th day. The treatment groups consisting of montelukast (0.5 and 1 mg/kg), rofecoxib (5 and 10 mg/kg) and caffeic acid (5 and 10 mg/kg) showed significant improvement in memory performance, oxidative stress parameters and mitochondrial function as compared to that of control (kainic acid treated), however, combination of montelukast with rofecoxib showed significant improvement in their protective effect. Thus the present study emphasizes the positive modulation of cysteinyl leukotriene receptor inhibition on COX (cyclooxygenase) and LOX (lipoxygenase) pathways in the control of the neuroinflammation in kainic acid induced cognitive dysfunction in rats.
机译:逐渐形成的共识是,轻度认知障碍(MCI)是阿尔茨海默氏病的前兆。抗氧化剂和COX-2(环加氧酶2)抑制剂也据报道对记忆障碍有有益作用。半胱氨酸白三烯抑制剂等新型药物在缺血动物模型中显示出神经保护作用。因此,本研究旨在探讨孟鲁司特(半胱氨酰白三烯抑制剂)与罗非考昔(COX-2抑制剂)和咖啡酸(5-LOX抑制剂和强效抗氧化剂)协同作用对海藻酸诱导的大鼠认知功能障碍的潜在作用。 。在实验方案中,在海马内(CA3区)给予人工脑脊液(ACSF)中的海藻酸(0.4μg/ 2μl),以诱发类似于MCI的疾病。在第10-14天测量记忆力,在第1、7和14天测量运动能力。为评估生化,线粒体和组织病理学参数,在第14天处死动物,储存在-80°C,在第15天完成。由孟鲁司特(0.5和1 mg / kg),罗非昔布(5和10 mg / kg)和咖啡酸(5和10 mg / kg)组成的治疗组与记忆疗法,氧化应激参数和线粒体功能相比有显着改善与对照(经海藻酸处理)相比,孟鲁司特与罗非昔布的组合显示出明显的保护作用。因此,本研究强调了半胱氨酰白三烯受体抑制对COX(环加氧酶)和LOX(脂加氧酶)途径的正调控,以控制海藻酸诱导的大鼠认知功能障碍的神经炎症。

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