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多巴胺信号在癫痫发生中的作用。

The role of dopamine signaling in epileptogenesis.

机构信息

Laboratory of Molecular Neuropathology, Centre for Integrative Biology, University of Trento Trento, Italy ; Neuroscience Institute, National Research Council Pisa, Italy.

出版信息

Front Cell Neurosci. 2013 Sep 17;7:157. doi: 10.3389/fncel.2013.00157.

Abstract

Clinical and experimental studies implicate most neuromodulatory systems in epileptogenesis. The dopaminergic system has a seizure-modulating effect that crucially depends on the different subtypes of dopamine (DA) receptors involved and the brain regions in which they are activated. Specifically, DA plays a major role in the control of seizures arising in the limbic system. Studies performed in a wide variety of animal models contributed to illustrate the opposite actions of D1-like and D2-like receptor signaling in limbic epileptogenesis. Indeed, signaling from D1-like receptors is generally pro-epileptogenic, whereas D2-like receptor signaling exerts an anti-epileptogenic effect. However, this view might appear quite simplistic as the complex neuromodulatory action of DA in the control of epileptogenesis likely requires a physiological balance in the activation of circuits modulated by these two major DA receptor subtypes, which determines the response to seizure-promoting stimuli. Here we will review recent evidences on the identification of molecules activated by DA transduction pathways in the generation and spread of seizures in the limbic system. We will discuss the intracellular signaling pathways triggered by activation of different DA receptors in relation to their role in limbic epileptogenesis, which lead to the activation of neuronal death/survival cascades. A deep understanding of the signaling pathways involved in epileptogenesis is crucial for the identification of novel targets for the treatment of epilepsy.

摘要

临床和实验研究表明,大多数神经调节系统都参与了癫痫发生。多巴胺能系统具有调节癫痫发作的作用,这主要取决于涉及的不同多巴胺 (DA) 受体亚型以及它们在其中被激活的脑区。具体来说,DA 在控制边缘系统起源的癫痫发作中起着重要作用。在各种动物模型中进行的研究有助于说明 D1 样和 D2 样受体信号在边缘性癫痫发生中的相反作用。事实上,D1 样受体的信号通常是致痫性的,而 D2 样受体信号则产生抗癫痫作用。然而,这种观点可能显得过于简单化,因为 DA 在控制癫痫发生中的复杂神经调节作用可能需要这些两种主要的 DA 受体亚型调节的电路的激活中的生理平衡,这决定了对促痫刺激的反应。在这里,我们将回顾最近关于在边缘系统中癫痫发作的产生和传播中被 DA 转导途径激活的分子的鉴定的证据。我们将讨论不同 DA 受体激活引发的细胞内信号通路与它们在边缘性癫痫发生中的作用之间的关系,这导致神经元死亡/存活级联的激活。深入了解癫痫发生中的信号通路对于确定治疗癫痫的新靶标至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bea/3774988/4adf750593eb/fncel-07-00157-g001.jpg

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