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Behavioral consequences of co-administration of MTEP and the COX-2 inhibitor NS398 in mice. Part 1

机译:MTEP和COX-2抑制剂NS398在小鼠中的行为后果。 第1部分

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Background: The immunologic modulation of glutamate (Glu) neurotransmission is a topic of great interest. Neuroinflammation is an intrinsic component of neurodegenerative diseases, as well as a factor responsible for cognitive and behavioral changes. Cyclooxygenase-2 (COX-2) expression in the brain was shown to be associated with inflammation. COX-2 is also widely expressed in the brain including neurons and glia and participates in fundamental brain functions, e.g. in synaptic plasticity or memory consolidation. Furthermore, COX-2/Glu interplay has been reported, while metabotropic glutamate receptors (mGluRs) are known to contribute to plastic changes and to behavior. The primary goal of this study was to explain the behavioral consequences of the modulation of the glutamatergic pathway via the interaction of the mGlu5 receptor and COX-2, utilizing a panel of behavioral tests.
机译:背景:谷氨酸(Glu)神经递质的免疫调节是一种极其兴趣的主题。 神经引发是神经变性疾病的内在成分,以及负责认知和行为变化的因素。 显示脑中的环氧氧酶-2(COX-2)表达式表达与炎症有关。 COX-2也广泛表达在包括神经元和峡谷的大脑中,并参与基本脑功能,例如基本脑功能。 在突触可塑性或记忆整合中。 此外,已经报道了COX-2 / Glu相互作用,而已知代谢谷氨酸受体(MGLURA)有助于塑性变化和行为。 本研究的主要目标是通过MGLU5受体和COX-2的相互作用来解释通过MGLU5受体和COX-2的相互作用来解释谷氨酸宫途径的行为后果。

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