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Cognitive effects of NSAIDs in cerebral ischemia: A hypothesis exploring mechanical action mediated pharmacotherapy

机译:NSAIDs在脑缺血中的认知作用:一种假设探讨机械作用介导的药物治疗

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摘要

Cerebral ischemia is associated with altered neuronal mechanics leading to dynamic reshaping of neuronal structures, giving rise to a cascade of biological pathways leading to many deleterious consequences and cognitive deficits. Memory and learning specifically are mediated by neurotransmitter release from vesicles clustered at the synapse. Mechanical tension is an important factor governing the amount of vesicular neurotransmitter release in response to an action potential. Neuroinflammation in cerebral ischemia leads to altered mechanical/physical forces on neurons which gives rise to abnormal mechanical tension along the neuron resulting in neurotransmitter imbalance leading to cognitive dysfunction. We consider the possibility that modulation of mechanical forces on neurons may be a therapeutic strategy to help prevent cognitive deficit in cerebral ischemia. Here we show how NSAIDs may act as candidate pharmacological molecules which have the ability to inhibit neuroinflammation and which can alter neuronal mechanics by their COX-2 inhibiting property.
机译:脑缺血与神经元力学改变相关,导致神经元结构的动态重塑,从而导致一系列生物途径,导致许多有害后果和认知缺陷。记忆和学习是通过神经递质从突触中聚集的囊泡释放介导的。机械张力是控制响应动作电位的水泡神经递质释放量的重要因素。脑缺血中的神经炎症导致神经元上机械/物理力的改变,从而引起沿神经元的异常机械张力,从而导致神经递质失衡,从而导致认知功能障碍。我们认为对神经元的机械力进行调节可能是一种有助于预防脑缺血的认知缺陷的治疗策略。在这里,我们显示了NSAIDs如何充当候选药理分子,它们具有抑制神经炎症的能力,并可以通过其COX-2抑制特性改变神经元力学。

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