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首页> 外文期刊>Neuropharmacology >Effect of amphetamine on extracellular concentrations of amino acids in striatum in neurotensin subtype 1 and 2 receptor null mice: a possible interaction between neurotensin receptors and amino acid systems for study of schizophrenia.
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Effect of amphetamine on extracellular concentrations of amino acids in striatum in neurotensin subtype 1 and 2 receptor null mice: a possible interaction between neurotensin receptors and amino acid systems for study of schizophrenia.

机译:苯丙胺对神经降压素亚型1和2受体缺失小鼠纹状体中氨基酸的细胞外浓度的影响:神经降压素受体和氨基酸系统之间的可能相互作用,用于研究精神分裂症。

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摘要

Neurotensin (NT) is a tridecapeptide that acts as a neuromodulator in the central nervous system mainly through two NT receptors: NTS1 and NTS2. The present study was done to determine the roles of NTS1 and NTS2 on amino acid release in striatum with the use of NTS1 or NTS2 knockout ((-/-)) mice given d-amphetamine. Both NTS1(-/-) and NTS2(-/-) mice had lower extracellular concentrations of D-serine in striatum than did wild type (WT) mice. NTS2(-/-) but not NTS1(-/-) mice also had significantly lower basal concentrations of glutamate in striatum as compared to that for WT mice. Systemic administration of d-amphetamine (4 mg/kg, ip) increased glutamate release by 500% in WT mice, as compared to 300% in NTS2(-/-) mice, and 250% in NTS1(-/-) mice. Additionally, d-amphetamine injection caused a 4-fold increase in GABA release in both WT and NTS2(-/-) mice, but only a 2-fold increase in NTS1(-/-) mice. Therefore, NTS1 and NTS2 modulate basal release of D-serine and glutamate, and also d-amphetamine-induced GABA and glutamate release in striatum. These results provide further support for the involvement of NT receptors in the pathogenesis of schizophrenia and provide a better understanding of the imbalance of amino acid systems through investigation of a DA-based animal model.
机译:神经降压素(NT)是一种三肽,主要通过两个NT受体NTS1和NTS2在中枢神经系统中充当神经调节剂。通过使用给予d-苯异丙胺的NTS1或NTS2敲除((-/-))小鼠,完成本研究以确定NTS1和NTS2对纹状体氨基酸释放的作用。 NTS1(-/-)和NTS2(-/-)小鼠的纹状体中D-丝氨酸的细胞外浓度均低于野生型(WT)小鼠。与野生型小鼠相比,NTS2(-/-)小鼠而不是NTS1(-/-)小鼠纹状体中谷氨酸的基础浓度也显着降低。全身给药d-苯异丙胺(4 mg / kg,ip)在WT小鼠中谷氨酸释放增加500%,而在NTS2(-/-)小鼠中为300%,在NTS1(-/-)小鼠中为250%。此外,d-苯丙胺注射液在WT和NTS2(-/-)小鼠中导致GABA释放增加4倍,而在NTS1(-/-)小鼠中仅引起2倍增加。因此,NTS1和NTS2调节D-丝氨酸和谷氨酸的基础释放,以及d-苯异丙胺诱导的纹状体中GABA和谷氨酸的释放。这些结果为NT受体参与精神分裂症的发病机理提供了进一步的支持,并通过对基于DA的动物模型的研究,对氨基酸系统的失衡有了更好的理解。

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