Ruberti J W, Klyce S D, Smolek M K, Karon M D
Department of Biomedical Engineering, Tulane University, New Orleans, USA.
Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2523-30.
To investigate the nature and cause of an acute, anomalous stromal edema after epithelial debridement in the rabbit cornea.
Series I: Adult New Zealand White rabbit corneas were mounted in perfusion chambers. The endothelium was bathed with Ringer's fluid, and the outer surface was covered with silicone oil. The epithelium of one eye was débrided with a scalpel before mounting, and the cornea of the fellow eye was débrided with a rotating brush after stabilization in the perfusion chamber. Using specular microscope tracking software, it was possible to measure total swelling and local swelling within the cornea. Series II: Diclofenac sodium ophthalmic solution 0.1% or a placebo was applied topically, 1 drop per 45 minutes for 3 hours before animals were euthanatized.
Series I: Corneas with their epithelium scraped with a scalpel before mounting were 37.5 +/- 17.5 microm (n = 6; P < 0.001) thicker in vitro than the stromas of perfused, intact fellow corneas. Epithelial débridement with a rotating brush after mounting resulted in an immediate (within 8 minutes) stromal swelling that plateaued in 1 hour at 31.0 +/- 5.3 microm (n = 6; P < 0.001). Curiously, in six of six corneas, the anterior stroma swelled more than the posterior stroma. In four of six corneas, the posterior stroma thinned. Analysis showed this pattern to be consistent with a sudden increase in anterior swelling pressure or osmotic pressure and to be inconsistent with a change in endothelial transport properties. Series II: Placebo-treated corneas swelled 30.6 +/- 7.7 microm (n = 5) 1 hour after débridement, whereas corneas pretreated with diclofenac sodium swelled only 19.2 +/- 3.1 microm (n = 6; P < 0.008).
The anterior stromal swelling occurs rapidly and near the site of epithelial injury suggesting messenger and/or enzymatic involvement with an effect parallel to apoptosis. Reduction of the swelling response with nonsteroidal anti-inflammatory drugs (NSAIDs) implicates the cyclooxygenase pathway. The swelling is similar to the unexplained acute edema that occurs during inflammation in the rat paw edema model, and may represent a general mechanism for mobilization of inflammatory cells.
研究兔角膜上皮清创术后急性异常基质水肿的性质和原因。
系列一:将成年新西兰白兔的角膜安装在灌注室中。内皮用林格氏液冲洗,外表面覆盖硅油。一只眼睛的上皮在安装前用手术刀清创,另一只眼睛的角膜在灌注室中稳定后用旋转刷清创。使用镜面显微镜跟踪软件,可以测量角膜内的总肿胀和局部肿胀。系列二:在动物安乐死之前,局部应用0.1%双氯芬酸钠眼药水或安慰剂,每45分钟滴1滴,共3小时。
系列一:在安装前用手术刀刮除上皮的角膜在体外比灌注的完整对侧角膜基质厚37.5±17.5微米(n = 6;P < 0.001)。安装后用旋转刷进行上皮清创导致立即(8分钟内)基质肿胀,1小时后达到平台期,为31.0±5.3微米(n = 6;P < 0.001)。奇怪的是,在六只角膜中的六只中,前基质比后基质肿胀更明显。在六只角膜中的四只中,后基质变薄。分析表明,这种模式与前肿胀压力或渗透压的突然增加一致,与内皮运输特性的变化不一致。系列二:安慰剂处理的角膜在清创后1小时肿胀30.6±7.7微米(n = 5),而用双氯芬酸钠预处理的角膜仅肿胀19.2±3.1微米(n = 6;P < 0.008)。
前基质肿胀迅速发生且靠近上皮损伤部位,提示信使和/或酶参与其中,其作用类似于细胞凋亡。用非甾体抗炎药(NSAIDs)减少肿胀反应表明环氧化酶途径参与其中。这种肿胀类似于大鼠足肿胀模型炎症期间发生的无法解释的急性水肿,可能代表炎症细胞动员的一般机制。