首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Bethanechol versus selegiline in amelioration of spinal cord injury in a rat model: A potential therapeutic option in spinal cord injury treatment
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Bethanechol versus selegiline in amelioration of spinal cord injury in a rat model: A potential therapeutic option in spinal cord injury treatment

机译:Bethanechol与Selegiline在大鼠模型中的脊髓损伤的改善:脊髓损伤治疗中的潜在治疗选择

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Purpose: To compare the effect of bethanechol versus selegiline in ameliorating spinal cord injury (SCI) in a rat model. Methods: Male adult Wistar rats (200 – 250 g) were equally divided into 3 groups: test (SCI rats treated with bethanechol), and control reference (SCI rats treated with selegiline) and control (SCI rats treated with vehicle). SCI was induced in the rats using the clipping method. Thereafter, motor function was assessed in the rats using a rotarod. Each rat was sacrificed by decapitation, and the cortex was excised for use in the study of the involvement of cholinergic and monoaminergic transmission in SCI rats using real-time quantitative polymerase chain reaction and western blot analysis. Results: Retention time was numerically greater in rats treated with acetyl choline agonist at all rotations (10, 15 and 25 rpm) when compared to MAO A inhibitor group, but the difference was not statistically significant (p 0.05). Both bethanechol and selegiline improved motor function by increasing cholinergic and monoaminergic transmission. Both drugs (bethanechol and selegiline) were effective in ameliorating the motor function deficit caused by spinal cord injury. A significant upregulation in acetylcholine esterase (AChE) was observed in the cortex of the SCI rats, relative to non-SCI rats (p 0.005). Results from cholinergic receptor binding studies revealed significantly decreased Bmax and kd values for muscarinic receptors in SCI rats, when compared to non-SCI rats. Moreover, the reduction in the intensity of cholinergic receptors was significantly higher in the cerebral cortex of SCI rats than in non-SCI rats. Conclusion: Bethanechol and selegiline are effective in ameliorating motor function deficit caused by spinal cord injury in rats. Both drugs also improve motor function in SCI rats. Therefore, the drugs have potentials for use in the therapeutical management of spinal cord injury.
机译:目的:比较伯亚替金属对大鼠模型改善脊髓损伤(SCI)的影响。方法:雄性成人Wistar大鼠(200 - 250g)平均分为3组:试验(用伯替替替替替苯甲醚处理的SCI大鼠),对照参考(用烯嘧啶处理的SCI大鼠)和对照(用载体处理的SCI大鼠)。使用剪切方法在大鼠中诱导SCI。此后,使用滚子在大鼠中评估电机功能。通过斩波处死每只大鼠,并且切除皮质用于研究使用实时定量聚合酶链反应和Western印迹分析的SCI大鼠中胆碱能和单氨基能速率的参与研究。结果:与MAO A抑制剂组相比,用乙酰胆碱激动剂(10,15和25rpm)处理的大鼠在数值较大,但差异在统计学上没有统计学意义(P> 0.05),保持时间更大。通过增加胆碱能和单氨基能传输,伯尼奥和索尔尼林均改善电机功能。药物(Bethanechol和Selegiline)都有效地改善由脊髓损伤引起的运动功能缺陷。相对于非SCI大鼠在SCI大鼠的皮质中观察到乙酰胆碱酯酶(疼痛)中的显着上调(P <0.005)。与非SCI大鼠相比,胆碱能受体结合研究的结果显着降低了SCI大鼠肌肉蛋白受体的BMAX和KD值。此外,SCI大鼠脑皮层的胆碱能受体强度的降低显着高于非SCI大鼠。结论:贝替金洛琳和莱基林在大鼠脊髓损伤引起的改善电动机功能缺陷方面是有效的。两种药物还改善了SCI大鼠的运动功能。因此,药物具有用于脊髓损伤的治疗管理的潜力。

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