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[采用薄层色谱法和反相高效液相色谱法从蟾酥中分离纯化钠泵内源性抑制剂]

[Separation and purification of an endogenous inhibitor of sodium pump from chansu by thin-layer chromatography and reversed-phase high performance liquid chromatography].

作者信息

Li S Q

机构信息

Department of Biochemistry, Institute of Experimental Medicine, Hebei Academy of Medical Sciences, Shijiazhuang 050021, China.

出版信息

Se Pu. 2001 Nov;19(6):555-7.

PMID:12545474
Abstract

An endogenous inhibitor of the sodium pump from the Chinese medication Chansu was purified. The dry substance Chansu was extracted with methanol. The dry residue dissolved in water and filtered subsequently through membrane filters with the exclusion size of 1000 Da, 3000 Da and 10000 Da in a Filtron Pro Vario-3-System and applied to thin-layer chromatographic plate made of Silica gel 60 F254 + 366 developed with a mixture of CHCl3-MeOH-H2O(75:20:5, volume ratio). The fractions with Rf 0.55 inhibiting the sodium pump were purified on an HPLC C18-RP column using a linear H2O-methanol gradient with 220 nm and 300 nm DAD detection. The bioactivity was measured by 86Rb-uptake into human red blood cells. The results showed that a low molecular weight, water soluble compound, which inhibited the sodium pump activity in the red blood cells and had a maximum absorbance at 250 nm was isolated from the Chinese medication Chansu. Several mg of the compound in pure state could be obtained from 1 kg Chansu. It was different from ouabain and proscillaridin A in chemical structure, because ouabain and proscillaridin A show a UV maximum absorption at 220 nm and 300 nm, while the new inhibitor at 250 nm.

摘要

从中国药物蟾酥中纯化出一种钠泵的内源性抑制剂。将干燥的蟾酥用甲醇提取。将干燥残渣溶于水,随后在Filtron Pro Vario - 3系统中通过截留分子量为1000 Da、3000 Da和10000 Da的膜过滤器过滤,并应用于由硅胶60 F254 + 366制成的薄层色谱板上,用CHCl3 - MeOH - H2O(体积比75:20:5)的混合物展开。在HPLC C18 - RP柱上,使用线性水 - 甲醇梯度,在220 nm和300 nm进行二极管阵列检测(DAD),对Rf为0.55的抑制钠泵的馏分进行纯化。通过测量86Rb进入人红细胞的量来测定生物活性。结果表明,从中国药物蟾酥中分离出一种低分子量、水溶性化合物,它抑制红细胞中的钠泵活性,在250 nm处有最大吸收峰。从1 kg蟾酥中可获得几毫克纯态的该化合物。它在化学结构上与哇巴因和海葱苷A不同,因为哇巴因和海葱苷A在220 nm和300 nm处有最大紫外吸收,而这种新抑制剂在250 nm处有最大吸收。

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