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[苯酚及相关化合物对大鼠红细胞、肝细胞和二棕榈酰磷脂酰胆碱脂质体的影响]

[Effects of phenol and related compounds on erythrocytes and hepatocytes from rats and dipalmitoyl phosphatidylcholine-liposomes].

作者信息

Usami K, Manabe A, Nakayama S, Sakamoto K

出版信息

Nihon Yakurigaku Zasshi. 1987 Apr;89(4):235-41. doi: 10.1254/fpj.89.235.

Abstract

The effects of phenol, guaiacol and m-cresol on erythrocytes, hepatocytes, dipalmitoyl phosphatidylcholine (DPPC)-liposomes and surface tension were studied at various concentrations. Phenol at 10 mM caused a slight inhibition of hypotonic hemolysis in rat erythrocytes. Guaiacol at 4 and 10 mM and m-cresol at 0.6 to 10 mM caused a significant inhibition of hypotonic hemolysis. In the enzyme leakage from isolated rat hepatocytes, phenol at 0.001 to 0.4 mM and 2 to 10 mM, guaiacol at 2 to 10 mM and m-cresol at 0.001 to 4 mM caused an inhibition in GOT leakage. The leakage of GPT from hepatocytes was inhibited by phenol at 0.4 to 10 mM, guaiacol at 2 to 10 mM, and m-cresol at 0.001 to 4 mM. m-Cresol at 10 mM caused increases in GOT and GPT leakage. The inhibition of phenol and m-cresol on the LDH leakage in hepatocytes were observed at a concentration of 0.001 mM and 0.1 to 1 mM, respectively. Guaiacol or m-cresol at 10 mM caused an increase in LDH leakage. Phase-transition temperature of DPPC-liposomes was depressed by phenol and m-cresol at 1 to 10 mM and by guaiacol at 5 and 10 mM. Guaiacol at 1 and 10 mM and m-cresol at 10 mM caused a depression of surface tension, but phenol caused no change in surface tension. The order of effects on erythrocyte, hepatocyte and DPPC-liposome membranes was m-cresol greater than phenol greater than or equal to guaiacol. In the present study, phenol and its related compound showed a positive correlation between their effects on various membranes and germicidal effects as evaluated by the phenol coefficient, but the effects were not related to a depression of surface tension.

摘要

研究了不同浓度的苯酚、愈创木酚和间甲酚对红细胞、肝细胞、二棕榈酰磷脂酰胆碱(DPPC)脂质体及表面张力的影响。10 mM的苯酚对大鼠红细胞低渗溶血有轻微抑制作用。4 mM和10 mM的愈创木酚以及0.6至10 mM的间甲酚对低渗溶血有显著抑制作用。在离体大鼠肝细胞的酶泄漏实验中,0.001至0.4 mM和2至10 mM的苯酚、2至10 mM的愈创木酚以及0.001至4 mM的间甲酚对谷草转氨酶(GOT)泄漏有抑制作用。0.4至10 mM的苯酚、2至10 mM的愈创木酚以及0.001至4 mM的间甲酚对肝细胞谷丙转氨酶(GPT)泄漏有抑制作用。10 mM的间甲酚导致GOT和GPT泄漏增加。分别在0.001 mM和0.1至1 mM浓度下观察到苯酚和间甲酚对肝细胞乳酸脱氢酶(LDH)泄漏有抑制作用。10 mM的愈创木酚或间甲酚导致LDH泄漏增加。1至10 mM的苯酚和间甲酚以及5 mM和10 mM的愈创木酚使DPPC脂质体的相变温度降低。1 mM和10 mM的愈创木酚以及10 mM的间甲酚导致表面张力降低,但苯酚对表面张力无影响。对红细胞、肝细胞和DPPC脂质体膜的作用顺序为:间甲酚>苯酚≥愈创木酚。在本研究中,苯酚及其相关化合物对各种膜的作用与通过苯酚系数评估的杀菌作用之间呈正相关,但这些作用与表面张力降低无关。

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