Felinski Edward A, Antonetti David A
Department of Cellular and Molecular Physiology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Curr Eye Res. 2005 Nov;30(11):949-57. doi: 10.1080/02713680500263598.
Loss of blood-retinal barrier (BRB) integrity and vascular permeability characterizes diabetic retinopathy, and new therapies to reverse or prevent vascular permeability are needed to treat this debilitating disease. Glucocorticoids are currently under investigation for use as a local therapeutic treatment for diabetic retinopathy. This review examines the changes that occur to barrier properties in diabetic retinopathy and the potential to use glucocorticoids to restore vascular barrier properties in the retina. Glucocorticoids are useful in preserving the integrity of the blood-brain barrier in the treatment of brain tumors, and these steroids show similar effects on the retinal vasculature suggesting their potential usefulness in treating diabetic retinopathy. Recent progress has been made toward the goal of elucidating the precise mechanism underlying the protective effects of glucocorticoids on the retinal vasculature. Glucocorticoids may act by both suppressing inflammation and by directly affecting the endothelial cells by regulating phosphorylation, organization, and content of tight junction proteins. Further work will advance our understanding of glucocorticoid regulation of barrier properties allowing the ultimate goal of developing a specific and safe therapy to treat or prevent loss of the blood-neural barrier in a number of diseases, including brain tumors and diabetic retinopathy.
血视网膜屏障(BRB)完整性丧失和血管通透性增加是糖尿病视网膜病变的特征,因此需要新的疗法来逆转或预防血管通透性,以治疗这种使人衰弱的疾病。目前正在研究将糖皮质激素用作糖尿病视网膜病变的局部治疗方法。本综述探讨了糖尿病视网膜病变中屏障特性的变化,以及使用糖皮质激素恢复视网膜血管屏障特性的潜力。糖皮质激素在治疗脑肿瘤时有助于维持血脑屏障的完整性,并且这些类固醇对视网膜血管系统显示出类似的作用,表明它们在治疗糖尿病视网膜病变方面具有潜在用途。在阐明糖皮质激素对视网膜血管系统保护作用的确切机制这一目标上,最近已取得进展。糖皮质激素可能通过抑制炎症以及通过调节紧密连接蛋白的磷酸化、组织和含量直接影响内皮细胞来发挥作用。进一步的研究将增进我们对糖皮质激素对屏障特性调节的理解,从而实现开发一种特定且安全的疗法这一最终目标,以治疗或预防包括脑肿瘤和糖尿病视网膜病变在内的多种疾病中的血神经屏障丧失。