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大鼠中枢神经系统中肽摄取活性的直接可视化。

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

作者信息

Groneberg David A, Rubio-Aliaga Isabel, Nickolaus Monika, Döring Frank, Fischer Axel, Daniel Hannelore

机构信息

Biomedical Research Center, Otto-Heubner-Centre, Charité School of Medicine, Free University Berlin and Humboldt-University, Augustenburger Platz 1 OR1, D-13353 Berlin, Germany.

出版信息

Neurosci Lett. 2004 Jun 24;364(1):32-6. doi: 10.1016/j.neulet.2004.04.013.

Abstract

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.

摘要

载体介导的小肽和拟肽转运为中枢神经系统(CNS)中跨细胞膜的靶向药物递送提供了机会。这个过程由质子偶联转运体PEPT2介导,它在神经胶质细胞和脉络丛细胞中表达。在本研究中,建立了一种摄取测定法,以直接观察完整大鼠脑片中的肽摄取情况。在脉络丛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,并且摄取受到典型PEPT2底物(如甘氨酰-L-谷氨酰胺和头孢羟氨苄)的抑制。通过RT-PCR和Northern印迹分析证实了PEPT2的存在。这种首个中枢神经系统肽和药物转运可视化测定法可用于检测由质子驱动的中枢神经系统肽转运体携带的新化合物。

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