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安卡菲德®止血剂对人脐静脉内皮细胞中转录因子及红细胞蛋白质谱的影响。

The effects of Ankaferd® Blood Stopper on transcription factors in HUVEC and the erythrocyte protein profile.

作者信息

Yılmaz Erkan, Güleç Şükrü, Torun Didem, Haznedaroğlu İbrahim Celalettin, Akar Nejat

机构信息

Biotechnology Institute, Ankara University, 06100 Ankara, Turkey, Phone: +90 312 222 58 26 E-mail:

出版信息

Turk J Haematol. 2011 Dec 5;28(4):276-85. doi: 10.5152/tjh.2011.39.

Abstract

OBJECTIVE

Ankaferd® Blood Stopper (ABS) is an herbal extract that has historically been used as a hemostatic agent in traditional Turkish medicine. ABS is comprised of a standardized herbal mixture of T. vulgaris, G. glabra, V. vinifera, A. officinarum, and U. dioica. ABS's basic mechanism of action is the formation of an encapsulated protein web, which represents the focal point for vital erythrocyte masses. The hemostatic effects of ABS have been observed in vitro and in vivo. ABS was registered as a hemostatic agent for external hemorrhages and dental bleeding following phase I randomized, double-blind crossover placebo-controlled clinical research, and safety and efficacy reports. In terms of the potential use of ABS, transcription factors may be novel factors that play a role in the hemostatic and other pleiotropic effects of ABS.

METHODS

Hence, the present study aimed to investigate the effects of ABS on endothelium, and possible transcription factor changes in HUVEC (human umbilical vein endothelial cells) and the erythrocyte membrane profile. ABS (5 μL and 50 μL) was administered to HUVEC (in 75 cm2; ~75% fullness) for 5 min and 15 min.

RESULTS

ABS caused significant increases in the level of activation of the following transcription factors; AP2, AR, CRE/ATF1, CREB, E2F1-5, E2F6, EGR, GATA, HNF-1, ISRE, Myc-Max, NF-1, NFkB, p53, PPAR, SMAD 2/3, SP1, TRE/AP1, and YY1. Following erythrocyte membrane isolation, protein complexes were undissolved, but denatured. The protein complex formed was resistant to heat and detergent. Trypsin and sonication were used in order to break this complex; the complex dissolved and erythrocyte membrane proteins were released in SDS-PAGE.

CONCLUSION

ABS established a very fast and solid protein web, and increased the level of transcription factor activation. Therefore the cellular effects of ABS could be related to different intracellular biological pathways.

摘要

目的

安卡非德血液止血剂(ABS)是一种草药提取物,在传统土耳其医学中一直被用作止血剂。ABS由百里香、光果甘草、葡萄、高良姜和异株荨麻的标准化草药混合物组成。ABS的基本作用机制是形成一个包裹性的蛋白质网,这是重要红细胞团块的焦点。已在体外和体内观察到ABS的止血作用。在I期随机、双盲交叉安慰剂对照临床研究以及安全性和有效性报告之后,ABS被注册为用于外部出血和牙科出血的止血剂。就ABS的潜在用途而言,转录因子可能是在ABS的止血和其他多效性作用中发挥作用的新因素。

方法

因此,本研究旨在研究ABS对内皮细胞的影响,以及人脐静脉内皮细胞(HUVEC)中可能的转录因子变化和红细胞膜谱。将ABS(5微升和50微升)加入到HUVEC(培养于75平方厘米;约75%满)中,作用5分钟和15分钟。

结果

ABS导致以下转录因子的激活水平显著增加;AP2、AR、CRE/ATF1、CREB、E2F1 - 5、E2F6、EGR、GATA、HNF - 1、ISRE、Myc - Max、NF - 1、NFkB、p53、PPAR、SMAD 2/3、SP1、TRE/AP1和YY1。红细胞膜分离后,蛋白质复合物未溶解,但发生了变性。形成的蛋白质复合物耐热且耐去污剂。使用胰蛋白酶和超声处理来破坏这种复合物;复合物溶解,红细胞膜蛋白在SDS - PAGE中释放。

结论

ABS建立了非常快速且稳固的蛋白质网,并提高了转录因子的激活水平。因此,ABS的细胞效应可能与不同的细胞内生物学途径有关。

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