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在体外,白蛋白和其他血浆成分可减弱去污剂硬化剂对红细胞、血小板、内皮细胞和微粒的溶解作用。

The lytic effects of detergent sclerosants on erythrocytes, platelets, endothelial cells and microparticles are attenuated by albumin and other plasma components in vitro.

作者信息

Parsi K, Exner T, Connor D E, Herbert A, Ma D D F, Joseph J E

机构信息

Haematology Research Laboratory, St Vincent's Hospital, Sydney, Australia; The University of New South Wales, Sydney, Australia.

Haematology Research Laboratory, St Vincent's Hospital, Sydney, Australia.

出版信息

Eur J Vasc Endovasc Surg. 2008 Aug;36(2):216-223. doi: 10.1016/j.ejvs.2008.03.001. Epub 2008 Apr 8.

Abstract

OBJECTIVE

To investigate the lytic effects of sodium tetradecyl sulphate (STS) and polidocanol (POL) on erythrocytes, platelets, endothelial cells and platelet-derived microparticle (PDMP) formation in vitro and the potential protective effects of serum albumin and agents such as procaine.

MATERIALS AND METHODS

The effects of sclerosants were studied in blood samples obtained from normal individuals. Absorbance densitometry was used to assess the lytic effects of sclerosants on blood cells and cultured human microvascular endothelial cells (HMEC) in plasma and in saline. PDMP were quantified by flow cytometry.

RESULTS

Haemolysis occurred in whole blood at sclerosant concentrations greater than 0.25% for STS and above 0.45% for POL. Similar concentrations of both agents caused platelet and endothelial cell lysis. Both sclerosants released PDMP at low concentrations but destroyed PDMP at higher concentrations. Albumin significantly reduced the lytic effect of both sclerosants on all cells but had a greater inhibitory effect on POL. Protamine at 0.01% had a neutralising effect on STS, whereas procaine and lignocaine showed no such activity.

CONCLUSIONS

Sclerosants at therapeutic concentrations lyse blood cells and endothelial cells in vitro. This effect is strongly reduced by serum albumin possibly contributing towards the low incidence of thromboembolic complications of sclerotherapy.

摘要

目的

研究十四烷基硫酸钠(STS)和聚多卡醇(POL)对红细胞、血小板、内皮细胞的溶解作用以及对体外血小板衍生微粒(PDMP)形成的影响,同时研究血清白蛋白和普鲁卡因等药物的潜在保护作用。

材料与方法

在从正常个体采集的血样中研究硬化剂的作用。采用吸光度密度测定法评估硬化剂在血浆和盐水中对血细胞及培养的人微血管内皮细胞(HMEC)的溶解作用。通过流式细胞术对PDMP进行定量分析。

结果

当STS浓度大于0.25%、POL浓度高于0.45%时,全血中出现溶血现象。两种药物的相似浓度均可导致血小板和内皮细胞溶解。两种硬化剂在低浓度时均可释放PDMP,但在高浓度时会破坏PDMP。白蛋白可显著降低两种硬化剂对所有细胞的溶解作用,且对POL的抑制作用更强。0.01%的鱼精蛋白对STS有中和作用,而普鲁卡因和利多卡因则无此活性。

结论

治疗浓度的硬化剂在体外可溶解血细胞和内皮细胞。血清白蛋白可显著减轻这种作用,这可能是硬化治疗血栓栓塞并发症发生率较低的原因之一。

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