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白细胞与早期糖尿病视网膜病变关系的研究 被引量:4

Study on Relationship between Leukocytes and Early Diabetic Retinopathy
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摘要 目的:探讨白细胞在早期糖尿病大鼠视网膜微血管中粘附、堆积,以致引起微循环障碍的作用。方法:健康成年雄性Wistar大鼠16只,随机分成正常对照组和链尿佐菌素(Streptozotocin,STZ)糖尿病3个月组各8只;对其视网膜消化铺片进行形态学观察及白细胞共有抗原(CD45)单克隆抗体免疫组织化学研究。结果:发现3个月病程的STZ诱导的糖尿病大鼠视网膜毛细血管已出现毛细血管管径不规则,呈节段性膨大或囊样扩张等形态学改变;视网膜毛细血管中CD45的表达明显增加,白细胞呈串珠样粘附和堆积。结论:3个月病程的STZ糖尿病大鼠可出现视网膜微血管改变;白细胞在糖尿病视网膜病变的发生发展中起着重要作用。 Purpose: To explore the leukocytic functions in adhesion, stacking and causingmicrocirculatory disorder in retinal microvessels in early diabetic rats.Methods: Sixteen healthy adult male Wistar rats were randomly divided into normalcontrol group and 3 months group of diabetes (STZ) . We carried out morphologicalobservations and CD45(Leukocyte Common Antigen) monoclonal antibody immunohist-ochemical studies of the retinal digest preparations.Results: Morphological changes including capillary varix, irregularity of capillarycaliber, was found in the retinal blood capillaries in diabetic rats at 3 months. Furthermore, the expression of CD45 was significantly increased in the diabetic retinalmicrovessels, which were found leukocytes adhering and stacking.Conclusion: Changes of retinal microvessels can be found in STZ diabetic rats at 3months. The leukocytes were important in the onset and development of diabeticretinopathy(DR).
出处 《眼科学报》 2002年第2期71-75,共5页 Eye Science
基金 本研究受"广东省眼科视觉科学重点实验室"专项基金资助(B60105)
关键词 糖尿病视网膜病 白细胞 大鼠 链尿佐菌素 diabetic retinopathy, leukocyte, rat, streptozotocin
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参考文献11

  • 1[1]Davis MD: Diabetic retinopathy: a clinical overview.Diabetes Care 1993; 15:1844 - 1873.
  • 2[2]Kohner EM, Chibber R: Diabetic retinopathy. In Diabetic Angiopathy. Tooke JE, Ed. New York, Oxford University Press 1999; P. 233 - 247.
  • 3[3]Miyamoto K, Khosrof S, Bursell S-E, et al: Prevention of leukostasis and vascular leakage in streptozotocin-induced diabetic retinopathy via intercellular adhesion molecule-linhibition. Proc Natl Acad Sci USA 1999, 96: 10836-10841.
  • 4[5]Kuwabara T, Cogan DG: Studies of retinal vascular patterns, part I: normal architecture. Arch Ophthalmol 1960; 64:904 - 911.
  • 5[6]Tang S, Scheiffarth OF, Thurau SR, et al: Cells of the immune system and their cytokines in epiretinal membranes and in the vitreous of patients with proliferative diabetic retinopathy (PDR). Ophthalmic Res 1993, 25:177 - 185.
  • 6[7]Dougherty GJ, Murdoch S, Hogg N: The function of human intercellular adhesion molecules-1 (ICAM-1) in the generation of an immune response. Eur J Immunol 1988;18:35 - 39.
  • 7[8]Scott M, Lefer DJ, Merges C, et al: Enhanced expression of intercellular adhesion molecule-1 and P-selectin in the diabetic human retina and choroids. Am J Pathol 1995;147:642 - 653.
  • 8[9]Mcleod DS, Lefer DJ, Merges C, et al: Enhanced expression of intracellular adhesion molecule-1 and P-selection in the diabetic human retina and choroid. Am J Pathol 1995;147:642 - 653.
  • 9[10]Schroder S, Palinki W, Schmid-Schonbein GW: Activated monocytes and granulocytes, capillary nonperfusion, and neovascularization in diabetic retinopathy. Am J Pathol 1991; 139:81 - 100.
  • 10[11]Tang S, Le-Ruppert KC: Activated T-lymphocytes in epiretinal membranes from patient with PDR. Graefe's Arch Clin Exp Ophthalmol 1995; 233:21 -25.

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