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Direct visualization of peptide uptake activity in the central nervous system of the rat.

机译:直接观察大鼠中枢神经系统中的肽摄取活性。

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摘要

Carrier-mediated transport of small peptides and peptidomimetics offers the opportunity for a targeted drug delivery across cell membranes in the central nervous system (CNS). This process is mediated by the proton-coupled transporter PEPT2 which is expressed in glial and choroid plexus cells. In the present studies, an uptake assay was established to visualize directly peptide uptake in intact rat brain slices. Accumulation of a reporter molecule, the fluorophore-labeled dipeptide derivative D-Ala-L-Lys-AMCA, was found in plexus choroideus and glial cells and uptake was inhibited by prototypical PEPT2 substrates, such as glycyl-L-glutamine and cefadroxil. The presence of PEPT2 was confirmed by RT-PCR and Northern blot analysis. This first CNS peptide and drug transport-visualizing assay may be used to examine new compounds which are carried by the proton-driven CNS peptide transporter.
机译:载体介导的小肽和拟肽的运输为跨中枢神经系统(CNS)细胞膜的靶向药物递送提供了机会。该过程由质子偶联的转运蛋白PEPT2介导,其在神经胶质和脉络丛神经细胞中表达。在本研究中,建立了摄取测定法以直接可视化完整大鼠脑切片中的肽摄取。在脉络膜和神经胶质细胞中发现了报告分子(荧光团标记的二肽衍生物D-Ala-L-Lys-AMCA)的积累,原型PEPT2底物(如甘氨酰-L-谷氨酰胺和头孢他罗尔)抑制了摄取。通过RT-PCR和Northern印迹分析证实了PEPT2的存在。该第一CNS肽和药物转运可视化测定可用于检查由质子驱动的CNS肽转运蛋白携带的新化合物。

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