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某些中性氨基酸对低渗溶血的保护作用。

Protective effects of some neutral amino acids against hypotonic hemolysis.

作者信息

Morimoto Y, Tanaka K, Iwakiri Y, Tokuhiro S, Fukushima S, Takeuchi Y

机构信息

Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kobe-Gakuin University, Japan.

出版信息

Biol Pharm Bull. 1995 Oct;18(10):1417-22. doi: 10.1248/bpb.18.1417.

Abstract

The protective effects of some neutral amino acids against hypotonic hemolysis were examined at various pHs. At pH 5.0, 7.0 and 8.0, 50% hemolysis was induced at 200, 160 and 140 mOsM, respectively, suggesting that erythrocyte membranes became more fragile to osmotic shock with decreasing pH. All amino acids tested reduced the hypotonic hemolysis at pH 5.0, but enhanced it at pH 8.0. It is therefore likely that these amino acids controlled the osmotic fragility of the cell membranes. At pH 7.0, glycine (Gly) reduced hypotonic hemolysis with increasing concentration. Phenylalanine (Phe) also reduced hypotonic hemolysis at low concentrations, but had an incrementally opposite effect at high concentrations. It was suggested that Phe interacted with erythrocyte membranes in a similar way to amphipathic drugs. Kinetic studies demonstrated that hypotonic hemolysis occurred immediately, according to osmotic shock, and that Gly and a low concentration of Phe decreased osmotic shock. Phe at a high concentration showed fast hemolysis with a short lag-time. Gly also showed fast hemolysis after the suppression of hypotonic hemolysis. Morphological observations demonstrated that these amino acids induced exvagination, exovesiculation and then invagination. It was suggested that with exvagination, the membrane expansion decreased the osmotic fragility, but the further shape change evoked membrane hole-formation.

摘要

在不同pH值条件下,研究了某些中性氨基酸对低渗溶血的保护作用。在pH 5.0、7.0和8.0时,分别在200、160和140 mOsM诱导50%的溶血,这表明随着pH值降低,红细胞膜对渗透压休克变得更加脆弱。所有测试的氨基酸在pH 5.0时均降低了低渗溶血,但在pH 8.0时则增强了低渗溶血。因此,这些氨基酸可能控制了细胞膜的渗透脆性。在pH 7.0时,甘氨酸(Gly)随着浓度增加降低了低渗溶血。苯丙氨酸(Phe)在低浓度时也降低了低渗溶血,但在高浓度时具有相反的作用。提示Phe与红细胞膜的相互作用方式类似于两亲性药物。动力学研究表明,根据渗透压休克,低渗溶血立即发生,并且Gly和低浓度的Phe降低了渗透压休克。高浓度的Phe表现出快速溶血且滞后时间短。Gly在抑制低渗溶血后也表现出快速溶血。形态学观察表明,这些氨基酸诱导外翻、外囊泡形成,然后内陷。提示随着外翻,膜扩张降低了渗透脆性,但进一步的形状变化引发了膜孔形成。

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