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小分子诱导的红细胞聚集的抑制与加速

Inhibition and acceleration of erythrocyte aggregation induced by small macromolecules.

作者信息

Maeda N, Shiga T

出版信息

Biochim Biophys Acta. 1985 Nov 22;843(1-2):128-36. doi: 10.1016/0304-4165(85)90059-5.

Abstract

The aggregation (especially the 'rouleau' formation) of human erythrocytes induced by polysaccharide and polyglutamic acid was quantitatively examined by using a low-shear rheoscope combined with a television image analyzer and a computer. (1) The morphological characteristics of rouleaux induced by these macromolecules are presented. (2) Polysaccharides with high molecular weights of 70 400 and 494 000 and poly(glutamic acids) with weights of 50 000 and 66 000 formed the rouleaux (then the three-dimensional aggregates). But polysaccharides with the low molecular weights of 10 300 and 42 500 and poly(glutamic acids) with weights of 8000 and 20 000 did not. The dependences of the velocity of rouleau formation on the macromolecule concentration and on the shear rate are shown. (3) The erythrocyte aggregation induced by high-molecular-weight polysaccharides was inhibited by low-molecular-weight polysaccharides and glucose, but was not affected by low-molecular-weight poly(glutamic acids). (4) The aggregation induced by high-molecular-weight poly(glutamic acids) was inhibited by poly(glutamic acid) with a molecular weight of 8000, but was accelerated by that of 20 000. The poly(glutamic acid)-induced aggregation was not affected by low-molecular-weight polysaccharides. (5) The stereochemical structure-dependent interaction (or the mode of bridging) of macromolecules with erythrocytes was stressed for the mechanism of erythrocyte aggregation.

摘要

使用结合了电视图像分析仪和计算机的低剪切流变仪,对多糖和聚谷氨酸诱导的人红细胞聚集(尤其是“缗钱状”形成)进行了定量检测。(1)呈现了这些大分子诱导形成的缗钱状的形态特征。(2)分子量为70400和494000的多糖以及分子量为50000和66000的聚谷氨酸形成了缗钱状(进而形成三维聚集体)。但分子量为10300和42500的多糖以及分子量为8000和20000的聚谷氨酸则未形成。展示了缗钱状形成速度对大分子浓度和剪切速率的依赖性。(3)高分子量多糖诱导的红细胞聚集受到低分子量多糖和葡萄糖的抑制,但不受低分子量聚谷氨酸的影响。(4)高分子量聚谷氨酸诱导的聚集受到分子量为8000的聚谷氨酸的抑制,但受到分子量为20000的聚谷氨酸的促进。聚谷氨酸诱导的聚集不受低分子量多糖的影响。(5)强调了大分子与红细胞之间立体化学结构依赖性相互作用(或桥联模式)在红细胞聚集机制中的作用。

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