Rezai K A, Heimann K, Wiedemann P
University Eye Hospital, Cologne, Germany.
J Ocul Pharmacol Ther. 1995 Spring;11(1):65-71. doi: 10.1089/jop.1995.11.65.
Proliferative vitreoretinopathy (PVR) is the most severe complication of retinal detachment surgery, occurring approximately in one out of ten operated eyes. The proliferation of retinal pigment epithelial (RPE) cells and fibroblasts is a cornerstone in the pathogenesis of PVR. Since inhibitory peptides may take a part in the feedback mechanism underlying this proliferation, we assessed the effect of synthesized epidermal dipeptide, pyroglu-glyOH (EDP), on the proliferation of RPE cells and fibroblasts in vitro. The maximum inhibitory effect of EDP on the RPE cells was reached at concentrations ranging from 1.0710(-13) to 1.0710(-15) M. Its inhibitory effect on fibroblasts followed a similar pattern at all concentrations applied, 1.0710(-6) to 1.0710(-15) M. These results enhance the possibility that PVR may be due to an imbalance of inhibition/disinhibition mechanism under participation of several regulatory molecules like EDP. EDP might have the potential for reducing the risk of PVR.
增殖性玻璃体视网膜病变(PVR)是视网膜脱离手术最严重的并发症,约每十只接受手术的眼睛中就有一只发生。视网膜色素上皮(RPE)细胞和成纤维细胞的增殖是PVR发病机制的基石。由于抑制性肽可能参与这种增殖的反馈机制,我们评估了合成的表皮二肽焦谷氨酸-甘氨酸(EDP)对体外RPE细胞和成纤维细胞增殖的影响。EDP对RPE细胞的最大抑制作用在浓度范围为1.07×10^(-13)至1.07×10^(-15) M时达到。在所有应用浓度(1.07×10^(-6)至1.07×10^(-15) M)下,其对成纤维细胞的抑制作用遵循类似模式。这些结果增加了PVR可能是由于在EDP等几种调节分子参与下抑制/去抑制机制失衡的可能性。EDP可能具有降低PVR风险的潜力。