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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >A pharmacological MRI assessment of dizocilpine (MK-801) in the 3-nitroproprionic acid-lesioned rat.
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A pharmacological MRI assessment of dizocilpine (MK-801) in the 3-nitroproprionic acid-lesioned rat.

机译:在3-硝基丙酸损伤的大鼠中进行地佐西平(MK-801)的药理MRI评估。

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摘要

The NMDA-antagonist dizocilpine (MK-801) is known to have dissociative, neurotoxic and neuroprotective properties. Although its neuroprotective properties are well documented, at present only ex vivo autoradiography has demonstrated its activity in lesioned brains. We report here the use of pharmacological magnetic resonance imaging (phMRI) to visualise the neural substrates of MK-801 in normal control rats and in animals that received systemic 3-nitroproprionic acid (3-NPA) 2 weeks earlier. In control animals, this NMDA-antagonist resulted in activity in the hippocampus, retrospinal (RS) cortex, anterior cingulate and the medial prefrontal cortex (MPFC). Activity in the MPFC has been associated with the dissociative properties of this agent and has been suggested to be the neurological substrate of positive psychotic symptoms, whereas RS and hippocampus have been the main sites of neurotoxic actions of MK-801. In contrast, in animals with 3-NPA-lesions affecting the striatum, no activity in the MPFC was observed, but a positive BOLD signal in the striatum was apparent. Lesioned animals injected with saline did not show this pattern of activity indicating that it is not merely an artefact of the ongoing neurodegeneration. This striatal activity could therefore be a site of MK-801-mediated neuroprotection. phMRI therefore sheds further light on the in vivo activity of MK-801 which, in turn, may allow us to more fully understand the different actions of NMDA-antagonists.
机译:已知NMDA-拮抗剂二唑西平(MK-801)具有解离,神经毒性和神经保护特性。尽管其神经保护特性已得到充分证明,但目前仅离体放射自显影已证明其在病变脑中具有活性。我们在这里报告使用药理磁共振成像(phMRI)可视化正常对照大鼠和2周前接受全身性3-硝基丙酸(3-NPA)的动物中MK-801的神经基质。在对照动物中,这种NMDA拮抗剂在海马,后脊髓(RS)皮层,前扣带回和内侧前额叶皮层(MPFC)中产生活性。 MPFC中的活性与该药物的解离特性有关,并被认为是精神病性症状阳性的神经系统底物,而RS和海马已成为MK-801神经毒性作用的主要部位。相反,在具有3-NPA损伤的动物影响纹状体的动物中,未观察到MPFC中的活性,但是在纹状体中出现了明显的BOLD信号。注射生理盐水的病变动物没有显示出这种活动模式,这表明它不仅仅是正在进行的神经变性的假象。因此,这种纹状体活动可能是MK-801介导的神经保护的位点。 phMRI因此进一步揭示了MK-801的体内活性,这反过来又可以使我们更加全面地了解NMDA拮抗剂的不同作用。

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