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Novel pharmacological strategies for motor complications in Parkinson's disease

机译:帕金森氏病运动并发症的新药理策略

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In advanced Parkinson's disease,the combination of disease progression and levodopa therapy leads to the development of motor problems complicating the therapeutic response,known as motor response complications.The non-physiological,pulsatile stimulation produced by most currently available dopaminergic therapies triggers a complicated series of responses resulting in the dysregulation of glutamate receptors and many other neurotransmitter systems on striatal neurons.Although a number of novel compounds that provide a more continuous dopaminergic stimulation are becoming available,no practical way to accomplish this in a truly physiological manner currently exists.Novel strategies for pharmacological intervention with the use of non-dopaminergic treatments,with drugs targeting selected transmitter receptors expressed on striatal neurons appear more promising.These include NMDA or AMPA antagonists,or drugs acting on 5-hydroxytryptamine subtype 2A,alpha_2-adrenergic,adenosine A_(2A) and cannabinoid CB_1 receptors.Future strategies may also target pre- and postsynaptic components that regulate firing pattern,like synaptic vesicle proteins,or nonsynaptic gap junction communication mechanisms,or drugs with actions at the signal transduction systems that modulate the phosphorylation state of NMDA receptors.These new therapeutic strategies,alone or in combination,hold the promise of providing effective control or reversal of motor response complications.
机译:在晚期帕金森氏病中,疾病进展和左旋多巴疗法的结合导致运动问题的发展,使运动反应复杂化,称为运动反应并发症。目前大多数多巴胺能疗法产生的非生理性,脉冲刺激会触发一系列复杂的导致谷氨酸受体和纹状体神经元上许多其他神经递质系统失调的反应。尽管有许多提供更连续多巴胺能刺激的新型化合物可供使用,但目前尚不存在以真正的生理学方式实现这一目标的实用方法。对于使用非多巴胺能疗法的药物干预,针对纹状体神经元上表达的选定递质受体的药物似乎更有希望。这些药物包括NMDA或AMPA拮抗剂,或作用于5-羟色胺2A亚型,α_2-肾上腺素,腺苷A_( 2A)和大麻策略还可能针对突触前和突触后成分,这些成分调节着火模式,例如突触小泡蛋白或非突触间隙连接通讯机制,或在信号转导系统中起作用的药物,这些药物可调节NMDA受体的磷酸化状态。单独或组合使用的新治疗策略有望有效控制或逆转运动反应并发症。

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