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大鼠外分泌胰腺中的氨基酸转运。II. 镧和丁卡因的抑制作用。

Amino acid transport in the rat exocrine pancreas. II. Inhibition by lanthanum and tetracaine.

作者信息

Bieger W, Peter S, Völkl A, Kern H F

出版信息

Cell Tissue Res. 1977 May 10;180(1):45-62. doi: 10.1007/BF00227029.

Abstract

The two calcium antagonistic agents lanthanum and tetracaine cause severe disturbances in the secretory process of the exocrine pancreas, including inhibition of the rate of protein synthesis and exocytosis. The former effect resulted mainly from the inhibition of amino acid transport. Lanthanum in a concentration up to 1 mM inhibited transport of different species of amino acids in an unspecific way whereas tetracaine interfered specifically with the Na+ -dependent transport system for neutral amino acids (14C-alpha-amino-isobutyric acid). Na+ -dependent transport of neutral amino acids (3H-leucine) was not affected. Transport inhibition was correlated to the acitvity of the Na+, K+ -ATPase system which was measured in isolated plasma membrane fractions. At higher concentrations (5-10 mM) some uptake of lanthanum into the cells by limited endocytosis was observed. At lower concentrations lanthanum seemed to bind exclusively to certain components of the plasms membrane, mainly at the lateral and basal cell surface. Even at a concentration of 5-10 mM no binding to the apical surface occurred. Similarly no binding of lanthanum was observed to the limiting membrane of isolated zymogen granules, while mitochondria, contained in the same fraction showed considerable binding affinity. The action of lanthanum and tetracaine on membrane carrier systems did not affect the interior organization of the plasma membrane. Particle density and distribution in freeze-fracture replicas as well as the submembrane microfilamentous=microtubular system and the junctional elements remained unaffected.

摘要

两种钙拮抗剂镧和丁卡因会严重干扰外分泌胰腺的分泌过程,包括抑制蛋白质合成速率和胞吐作用。前一种效应主要是由于氨基酸转运受到抑制。浓度高达1 mM的镧以非特异性方式抑制不同种类氨基酸的转运,而丁卡因则特异性地干扰中性氨基酸(14C-α-氨基异丁酸)的钠依赖性转运系统。中性氨基酸(3H-亮氨酸)的钠依赖性转运不受影响。转运抑制与在分离的质膜组分中测量的钠钾ATP酶系统的活性相关。在较高浓度(5-10 mM)下,观察到镧通过有限的内吞作用进入细胞。在较低浓度下,镧似乎仅与质膜的某些成分结合,主要是在细胞的侧面和基底表面。即使在5-10 mM的浓度下,也未观察到与顶端表面的结合。同样,未观察到镧与分离的酶原颗粒的限制膜结合,而同一组分中的线粒体显示出相当大的结合亲和力。镧和丁卡因对膜载体系统的作用并未影响质膜的内部组织结构。冷冻蚀刻复制品中的颗粒密度和分布以及膜下微丝-微管系统和连接元件均未受影响。

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