Garweg Justus G, Wegmann-Burns Maria, Goldblum David
Department of Ophthalmology, Inselspital, University of Bern, 3010, Berne, Switzerland.
Graefes Arch Clin Exp Ophthalmol. 2006 Mar;244(3):382-9. doi: 10.1007/s00417-005-0017-4. Epub 2005 Aug 10.
We wished to investigate the toxicity of four immunosuppressant and antimetabolic drugs, which are known to influence postoperative wound healing, on three different human ocular cell lines.
Acute toxicity to cyclosporin A, azathioprine, mitomicyn C and daunorubicin was assessed in Chang cells by monitoring their uptake of propidium iodide during a 3-h period. Chronic toxicity was assessed by monitoring the proliferation and viability of subconfluent cultures of Chang cells, human corneal endothelial cells (HCECs) and retinal pigmented epithelial (RPE) cells after continuous exposure to the drugs for 7 days.
Acute toxicity testing revealed no obvious effects. However, the chronic toxicity tests disclosed a narrow concentration range over which cell proliferation decreased dramatically but calcein metabolism was sustained. Although the three lines reacted similarly to each agent, HCECs were the most vulnerable to daunorubicin and mitomycin. At a daunorubicin concentration of 0.05 microg/ml, a 75% decrease in calcein metabolism (P < 0.001) and a > or = 95% cell loss (P < 0.001) were observed. At a mitomycin concentration of 0.01 mug/ml, cell density decreased by 61% (P < 0.001) without a change in calcein metabolism, but at 0.1 microg/ml, the latter parameter decreased to 12% (P = 0.00014). At this concentration the proliferation of Chang and RPE cells decreased by more than 50%, whilst calcein metabolism was largely sustained. Cyclosporin inhibited cell proliferation moderately at lower concentrations (< 5 microg/ml; P=0.05) and substantially at higher ones, with a corresponding decline in calcein metabolism. Azathioprine induced a profound decrease in both parameters at concentrations above 5 microg/ml.
Daunorubicin, cyclosporin and azathioprine could be used to inhibit excessive intraocular scarring after glaucoma and vitreoretinal surgery without overly reducing cell viability. The attributes of immunosuppressants lie in their combined antiproliferative and immunomodulatory effects.
我们希望研究四种已知会影响术后伤口愈合的免疫抑制剂和抗代谢药物对三种不同人类眼细胞系的毒性。
通过监测3小时内碘化丙啶的摄取来评估环孢素A、硫唑嘌呤、丝裂霉素C和柔红霉素对Chang细胞的急性毒性。通过监测Chang细胞、人角膜内皮细胞(HCECs)和视网膜色素上皮(RPE)细胞亚汇合培养物在连续暴露于药物7天后的增殖和活力来评估慢性毒性。
急性毒性测试未显示明显影响。然而,慢性毒性测试揭示了一个狭窄的浓度范围,在此范围内细胞增殖急剧下降,但钙黄绿素代谢得以维持。尽管这三种细胞系对每种药物的反应相似,但HCECs对柔红霉素和丝裂霉素最为敏感。在柔红霉素浓度为0.05微克/毫升时,观察到钙黄绿素代谢下降75%(P<0.001),细胞损失≥95%(P<0.001)。在丝裂霉素浓度为0.01微克/毫升时,细胞密度下降61%(P<0.001),钙黄绿素代谢无变化,但在0.1微克/毫升时,后一参数降至12%(P=0.00014)。在此浓度下,Chang细胞和RPE细胞的增殖下降超过50%,而钙黄绿素代谢基本维持。环孢素在较低浓度(<5微克/毫升;P=0.05)时适度抑制细胞增殖,在较高浓度时显著抑制,同时钙黄绿素代谢相应下降。硫唑嘌呤在浓度高于5微克/毫升时导致这两个参数显著下降。
柔红霉素、环孢素和硫唑嘌呤可用于抑制青光眼和玻璃体视网膜手术后的过度眼内瘢痕形成,而不会过度降低细胞活力。免疫抑制剂的特性在于其联合的抗增殖和免疫调节作用。