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纹状体多巴胺释放逆转帕金森病模型中的病理性运动行为。

Reversal of pathological motor behavior in a model of Parkinson's disease by striatal dopamine uncaging.

机构信息

Facultad de Ciencias, Universidad Autónoma de San Luis Potosi, San Luis Potosi, Mexico.

Instituto de Neurobiologia, Universidad Nacional Autónoma de Mexico, Juriquilla, Queretaro, Mexico.

出版信息

PLoS One. 2023 Aug 18;18(8):e0290317. doi: 10.1371/journal.pone.0290317. eCollection 2023.

Abstract

Motor deficits observed in Parkinson's disease (PD) are caused by the loss of dopaminergic neurons and the subsequent dopamine depletion in different brain areas. The most common therapy to treat motor symptoms for patients with this disorder is the systemic intake of L-DOPA that increases dopamine levels in all the brain, making it difficult to discern the main locus of dopaminergic action in the alleviation of motor control. Caged compounds are molecules with the ability to release neuromodulators locally in temporary controlled conditions using light. In the present study, we measured the turning behavior of unilateral dopamine-depleted mice before and after dopamine uncaging. The optical delivery of dopamine in the striatum of lesioned mice produced contralateral turning behavior that resembled, to a lesser extent, the contralateral turning behavior evoked by a systemic injection of apomorphine. Contralateral turning behavior induced by dopamine uncaging was temporarily tied to the transient elevation of dopamine concentration and was reversed when dopamine decreased to pathological levels. Remarkably, contralateral turning behavior was tuned by changing the power and frequency of light stimulation, opening the possibility to modulate dopamine fluctuations using different light stimulation protocols. Moreover, striatal dopamine uncaging recapitulated the motor effects of a low concentration of systemic L-DOPA, but with better temporal control of dopamine levels. Finally, dopamine uncaging reduced the pathological synchronization of striatal neuronal ensembles that characterize unilateral dopamine-depleted mice. We conclude that optical delivery of dopamine in the striatum resembles the motor effects induced by systemic injection of dopaminergic agonists in unilateral dopamine-depleted mice. Future experiments using this approach could help to elucidate the role of dopamine in different brain nuclei in normal and pathological conditions.

摘要

帕金森病(PD)中观察到的运动缺陷是由多巴胺能神经元的丧失和随后不同脑区的多巴胺耗竭引起的。治疗这种疾病患者运动症状的最常见疗法是系统摄入左旋多巴,它会增加大脑中所有部位的多巴胺水平,使得难以辨别多巴胺能作用在缓解运动控制中的主要作用部位。笼状化合物是一类能够在暂时受控条件下局部释放神经调质的分子,使用光。在本研究中,我们在单侧多巴胺耗竭的小鼠之前和之后测量了未笼状多巴胺的旋转行为。光在损伤小鼠纹状体中的多巴胺传递产生了对侧旋转行为,在较小程度上类似于全身注射阿扑吗啡引起的对侧旋转行为。由多巴胺去笼引起的对侧旋转行为暂时与多巴胺浓度的短暂升高有关,当多巴胺降低到病理水平时,对侧旋转行为会逆转。值得注意的是,通过改变光刺激的功率和频率来调节对侧旋转行为,为使用不同的光刺激方案来调节多巴胺波动打开了可能性。此外,纹状体多巴胺去笼重现了低浓度全身 L-DOPA 的运动效应,但对多巴胺水平的时间控制更好。最后,多巴胺去笼减少了单侧多巴胺耗竭小鼠特征性的纹状体神经元集合的病理性同步。我们得出结论,纹状体中多巴胺的光传递类似于系统注射多巴胺激动剂在单侧多巴胺耗竭小鼠中引起的运动效应。使用这种方法的未来实验可以帮助阐明多巴胺在正常和病理条件下不同脑核中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b587/10437883/996447ad30d7/pone.0290317.g001.jpg

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