Blebea John, Vu Jonathan-Hien, Assadnia Shahin, McLaughlin Patricia J, Atnip Robert G, Zagon Ian S
Department of Surgery, The Pennsylvania State University College of Medicine, Hershey 17033-0850, USA.
J Vasc Surg. 2002 Mar;35(3):532-8. doi: 10.1067/mva.2002.120042.
Angiogenesis, the development of new blood vessels, has become an area of increased interest for both scientific and clinical application purposes. Proangiogenic agents, such as vascular endothelial growth factor (VEGF) and naltrexone, have been shown to effectively induce new blood vessel growth. Other growth factors, such as the endogenous opioid growth factor (OGF; [Met(5)]-enkephalin) and retinoic acid, are inhibitors of angiogenesis. The differential effects on veins and arteries, however, by any vascular growth factor, have not previously been investigated.
The chick chorioallantoic membrane (CAM) assay was used for the in vivo quantitation of angiogenesis. After 3 days of incubation, fertilized chick embryos were explanted, and a 3.2-mm methylcellulose disk containing either the known angiogenic stimulators VEGF (0.2 microg, 1.0 microg) or naltrexone (0.1 microg, 5.0 microg), or the angiogenic inhibitors OGF (1.0 microg, 5.0 microg) or retinoic acid (1.0 microg) was placed onto the CAM surface. An equal volume of distilled water served as a control. After 2 days of growth, the CAM arteries and veins were identified, and images were obtained with a digital camera. Quantitative analysis of angiogenesis was performed on a 100-mm(2) area surrounding the applied disk, and the number and length of the veins and arteries were measured.
The angiogenic stimulators VEGF and naltrexone markedly increased both the total number and length of all blood vessels as compared with control values. The mean length of blood vessels decreased, suggesting the induction of new vessel growth. VEGF and naltrexone proportionately increased vein and arterial angiogenesis, maintaining artery/vein ratios for vessel number and length that were unchanged compared with controls. The angiogenic inhibitors, OGF and retinoic acid, notably decreased the total number and length of blood vessels in the CAM preparations. However, these compounds had a disproportionately greater inhibitory effect on arterial angiogenesis as reflected in decreased artery/vein ratios for vessel number and length.
The angiogenic stimulators VEGF and naltrexone induce development of veins and arteries in a proportional manner. In contrast, the angiogenic inhibitors OGF and retinoic acid demonstrated a greater inhibitory effect on arterial as compared with venous angiogenesis. Such differential effects on angiogenesis may be important in both defining mechanisms of action and designing therapeutic interventions.
血管生成,即新血管的形成,已成为科学研究和临床应用中日益受关注的领域。促血管生成剂,如血管内皮生长因子(VEGF)和纳曲酮,已被证明能有效诱导新血管生长。其他生长因子,如内源性阿片生长因子(OGF;[Met(5)]-脑啡肽)和视黄酸,则是血管生成的抑制剂。然而,此前尚未研究过任何血管生长因子对静脉和动脉的不同影响。
采用鸡胚绒毛尿囊膜(CAM)试验对血管生成进行体内定量研究。孵化3天后,取出受精鸡胚,将含有已知血管生成刺激剂VEGF(0.2微克、1.0微克)或纳曲酮(0.1微克、5.0微克),或血管生成抑制剂OGF(1.0微克、5.0微克)或视黄酸(1.0微克)的3.2毫米甲基纤维素圆盘置于CAM表面。等体积的蒸馏水作为对照。生长2天后,识别CAM的动脉和静脉,并用数码相机获取图像。在应用圆盘周围100平方毫米的区域进行血管生成的定量分析,测量静脉和动脉的数量及长度。
与对照值相比,血管生成刺激剂VEGF和纳曲酮显著增加了所有血管的总数和总长度。血管的平均长度减少,提示诱导了新血管生长。VEGF和纳曲酮按比例增加静脉和动脉的血管生成,血管数量和长度的动脉/静脉比率与对照相比保持不变。血管生成抑制剂OGF和视黄酸显著减少了CAM制剂中血管的总数和总长度。然而,这些化合物对动脉血管生成的抑制作用不成比例地更大,这反映在血管数量和长度的动脉/静脉比率降低。
血管生成刺激剂VEGF和纳曲酮以成比例的方式诱导静脉和动脉的发育。相比之下,血管生成抑制剂OGF和视黄酸对动脉血管生成的抑制作用比对静脉血管生成的抑制作用更大。这种对血管生成的不同影响在确定作用机制和设计治疗干预措施方面可能都很重要。