Zhang Zhi-Hua, Jiang Li, Qiao Li-Xing
Medical College of Southeast University, Nanjing 210009, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2007 Aug;9(4):371-4.
To examine the expression of mRNA of vascular endothelial growth factor (VEGF) in a rat model of hyperoxia-induced retinopathy and to investigate the role of VEGF in the process of neovascularization in retinopathy.
One hundred fifty one-day-old neonatal Sprague-Dawley rats were randomly divided into hyperoxia-induced retinopathy and normal control groups. The rats in the retinopathy group were exposed to (80 +/- 2)% oxygen for 7 days and then replaced by room air. The rats in the control group were exposed to room air all the time of the experiment. The morphologic changes of retinal vessels were estimated by observing the vascular pattern in adenosine diphosphate ase (ADPase) stained retina flat mounts. The newborn vessels were quantified by haematoxylin and eosin staining. Reversal transcription-polymerase chain reaction (RT-PCR) was used to detect the VEGF mRNA expression.
In the retinopathy group at 7 days of age, most of central radial vessels became constricted and blocked, and central perfusion decreased obviously. After switching to room air exposure for 7 days (14 days of age), noticeable retinal neovascularization appeared. The expression of VEGF mRNA in the retinopathy group at 7 days of hyperoxia exposure was noticeably lower than in the control group, and increased gradually after switching to room air exposure. At 9 and 14 days of age, the expression of VEGF mRNA in the retinopathy group was noticeably higher than in the control group. The expression of retinal VEGF mRNA in the retinopathy group increased before neovascularization occurred, and decreased with regression of new vessels.
Hyperoxia exposure may decrease the transcription of VEGF mRNA and the growth of retinal blood vessels. The relative hypoxia after hyperxia withdrawal can up-regulate the transcription of VEGF mRNA, resulting in a significant retinal neovascularization. The abnormal expression of VEGF in the retina may play an important role in the development of neovascularization in retinopathy.
检测高氧诱导性视网膜病变大鼠模型中血管内皮生长因子(VEGF)mRNA的表达,探讨VEGF在视网膜病变新生血管形成过程中的作用。
将150只1日龄新生Sprague-Dawley大鼠随机分为高氧诱导性视网膜病变组和正常对照组。视网膜病变组大鼠置于(80±2)%氧环境中7天,然后换为空气。对照组大鼠在实验全程均置于空气中。通过观察二磷酸腺苷酶(ADPase)染色视网膜铺片的血管形态评估视网膜血管的形态学变化。用苏木精-伊红染色对新生血管进行定量。采用逆转录-聚合酶链反应(RT-PCR)检测VEGF mRNA表达。
在7日龄的视网膜病变组,多数中央放射状血管变窄并阻塞,中央灌注明显减少。换为空气暴露7天(14日龄)后,出现明显的视网膜新生血管形成。高氧暴露7天时,视网膜病变组VEGF mRNA表达明显低于对照组,换为空气暴露后逐渐升高。在9日龄和14日龄时,视网膜病变组VEGF mRNA表达明显高于对照组。视网膜病变组视网膜VEGF mRNA表达在新生血管形成前升高,随新生血管消退而降低。
高氧暴露可能降低VEGF mRNA转录及视网膜血管生长。高氧撤除后的相对低氧可上调VEGF mRNA转录,导致明显的视网膜新生血管形成。视网膜中VEGF的异常表达可能在视网膜病变新生血管形成发展中起重要作用。