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4-羟基苯甲醇的抗血管生成作用的体内外评价。

In vitro and in vivo evaluation of the anti-angiogenic actions of 4-hydroxybenzyl alcohol.

机构信息

Institute for Clinical & Experimental Surgery, University of Saarland, Homburg/Saar, Germany.

出版信息

Br J Pharmacol. 2011 Jun;163(4):835-44. doi: 10.1111/j.1476-5381.2011.01292.x.

Abstract

BACKGROUND AND PURPOSE

4-Hydroxybenzyl alcohol (HBA) is a phenolic plant compound, which has been shown to influence many cellular mechanisms. In the present study, we analysed in vitro and in vivo the anti-angiogenic actions of this pleiotropic agent.

EXPERIMENTAL APPROACH

Migration and protein expression of HBA- and vehicle-treated endothelial-like eEND2 cells was assessed by cell migration assay and Western blot analyses. HBA action on vascular sprouting was analysed in an aortic ring assay. In vivo anti-angiogenic actions of HBA were studied in the dorsal skinfold chamber model of endometriosis in mice.

KEY RESULTS

Western blot analyses demonstrated that HBA inhibited proliferation of eEND2 cells, as indicated by down-regulation of proliferating cell nuclear antigen expression, and reduced expression of vascular endothelial growth factor and matrix metalloproteinase 9. HBA suppressed the migration of eEND2 cells, accompanied by inhibition of actin filament reorganization, revealed by fluorescence staining of the cytoskeleton. In addition, HBA reduced vascular sprouting in the aortic ring assay. Finally, we found, in the dorsal skinfold chamber model in vivo using intravital fluorescence microscopy, that HBA inhibited the vascularization of developing endometriotic lesions, as indicated by a decreased functional capillary density of lesions in HBA-treated mice and a reduced lesion size, compared with control animals.

CONCLUSIONS AND IMPLICATIONS

HBA targets several angiogenic mechanisms and therefore represents a promising anti-angiogenic agent for the treatment of angiogenic diseases, such as endometriosis.

摘要

背景与目的

4-羟基苯甲醇(HBA)是一种酚类植物化合物,已被证明能影响多种细胞机制。在本研究中,我们分析了该多效性药物的体外和体内抗血管生成作用。

实验方法

通过细胞迁移实验和 Western blot 分析评估 HBA 和载体处理的类内皮细胞 eEND2 的迁移和蛋白表达。在主动脉环实验中分析 HBA 对血管发芽的作用。在小鼠子宫内膜异位症的背部皮肤囊模型中研究 HBA 的体内抗血管生成作用。

主要结果

Western blot 分析表明,HBA 通过下调增殖细胞核抗原的表达和降低血管内皮生长因子和基质金属蛋白酶 9 的表达来抑制 eEND2 细胞的增殖。HBA 抑制 eEND2 细胞的迁移,并通过细胞骨架的荧光染色显示肌动蛋白丝重组的抑制。此外,HBA 减少了主动脉环实验中的血管发芽。最后,我们通过体内活体荧光显微镜在背部皮肤囊模型中发现,与对照组动物相比,HBA 处理的小鼠中病变的功能性毛细血管密度降低,病变体积减小,表明 HBA 抑制了正在发育的子宫内膜异位症病变的血管生成。

结论和意义

HBA 靶向几种血管生成机制,因此是治疗血管生成疾病(如子宫内膜异位症)的有前途的抗血管生成药物。

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