Wang Hong-yun, Niu Ying-jun, Wang Pei-song, Zhou Zhan-yu, Liu Fu-ling, Yang Wen-yi, Zhang Yue-hong
Department of Ophthalmology, the Affiliated Hospital, the Medical School of Qingdao University, Qingdao 266003, China.
Zhonghua Yan Ke Za Zhi. 2005 May;41(5):434-8.
To study whether recombinant human erythropoietin can pass through mice blood-retina barrier and the protective role in light-induced damage in retina.
After the injection of rHEPO, the content of rHEPO in 24 BALB/c mice retina was examined by enzyme linked immunosorbent assay (ELISA). 24 BALB/c mice were used to establish a light-induced damaged model, the difference of retina in rHEPO group and control group was compared using light microscope and TdT-mediated dUTP nick end labeling (TUNEL).
The amount of retinal rHEPO in four deferent time points was (0.68 +/- 0.24) mU, (1.87 +/- 0.37) mU, (0.96 +/- 0.24) mU, (0.47 +/- 0.13) mU in 100 microg retinal total protein respectively by ELISA assay, there were statistical significances among groups. The density of rHEPO in the retina reached its peak at 4th hour after injection. Histology analysis: rHEPO group, at the 12th hour after light exposure the inner segment became condensed and disorganized. At the 36th hour the retina disorganized and vesiculated were seen in outer segments. At the 72nd hour the inner and outer segments were damaged more seriously and the outer nuclear layer became thinner and denser. On the 7th day, the retinal outer nuclear layer became thinner and condenses. rHEPO group showed a minimal damage in every time points but outer nuclear layer disorganized and vesiculated in inner and outer segments. No obvious changes in retinal thickness. The apoptotic cells were detected by TUNEL. At the 12th hour after light exposure, there were the apoptotic cells in outer nuclear layer near outer plexiform layer. At 36th hour the numbers of apoptotic cells were increased, however at the 72nd it was decreased obviously, only a few scattering apoptotic cells were revealed in the outer nuclear layer. Numbers of apoptotic cells between the rHEPO group and control group in outer nuclear layer were statistical significance (P < 0.01).
rHEPO can pass through the mice blood-retina barrier and rHEPO has neuroprotective effect on mice retina. rHEPO may be used to treat degenerative retinal diseases.
研究重组人促红细胞生成素是否能穿过小鼠血视网膜屏障及其对视网膜光损伤的保护作用。
注射重组人促红细胞生成素(rHEPO)后,采用酶联免疫吸附测定法(ELISA)检测24只BALB/c小鼠视网膜中rHEPO的含量。采用24只BALB/c小鼠建立视网膜光损伤模型,用光镜和TdT介导的dUTP缺口末端标记法(TUNEL)比较rHEPO组和对照组视网膜的差异。
ELISA法检测显示,在四个不同时间点,每100μg视网膜总蛋白中视网膜rHEPO含量分别为(0.68±0.24)mU、(1.87±0.37)mU、(0.96±0.24)mU、(0.47±0.13)mU,组间差异有统计学意义。注射后第4小时视网膜中rHEPO密度达到峰值。组织学分析:rHEPO组,光照后第12小时内节段变得浓缩且排列紊乱。第36小时视网膜排列紊乱,外节段可见空泡形成。第72小时内、外节段损伤更严重,外核层变薄且致密。第7天,视网膜外核层变薄并浓缩。rHEPO组在各时间点损伤均最小,但内、外节段外核层排列紊乱且有空泡形成。视网膜厚度无明显变化。用TUNEL法检测凋亡细胞。光照后第12小时,外丛状层附近的外核层有凋亡细胞。第36小时凋亡细胞数量增加,但第72小时明显减少,外核层仅见少数散在凋亡细胞。rHEPO组和对照组外核层凋亡细胞数量差异有统计学意义(P<0.01)。
rHEPO能穿过小鼠血视网膜屏障,对小鼠视网膜具有神经保护作用。rHEPO可能用于治疗视网膜退行性疾病。