Savagian Caitlin A, Dubielzig Richard R, Nork T Michael
Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53792-3220, USA.
Am J Vet Res. 2008 Feb;69(2):265-72. doi: 10.2460/ajvr.69.2.265.
To determine the effect of acute (clinical history of glaucoma for <or= 2 days) and chronic (clinical history of glaucoma for 7 days) goniodysgenesis-related glaucoma on various stress-inducible proteins in canine retinas.
15 canine retinas (5 from control eyes, 5 from eyes with acute glaucoma, and 5 from eyes with chronic glaucoma).
Globes were obtained from the Comparative Ocular Pathology Laboratory of Wisconsin. Eyes were characterized on the basis of clinical history. The distribution of glial fibrillary acidic protein (GFAP), heat shock protein (HSP) 60, and hypoxia-inducible factor (HIF)-1alpha was determined by use of immunohistochemical analysis.
Intensity of GFAP staining increased with temporal progression of glaucoma. In specimens from eyes with acute glaucoma, staining for HSP 60 was more variable among eyes, compared with that of the control eyes, whereas specimens from eyes with chronic glaucoma typically had less HSP 60 staining than was evident in the control eyes. Neither the control eyes nor specimens from the eyes with acute glaucoma had nuclear staining for HIF-1alpha in the retinas. Four of 5 specimens from eyes with chronic glaucoma had nuclear staining for HIF-1alpha in cells of the outer nuclear layer. Staining for HIF-1alpha was distributed segmentally in regions of more severe atrophy and disorganization.
Results of the study reported here supported a clinically evident, rapidly progressive disease with a shift in cell regulation between acute and chronic glaucoma and also supported ischemia as a mechanism of retinal injury in this disease.
确定急性(青光眼临床病史≤2天)和慢性(青光眼临床病史7天)与前房角发育异常相关的青光眼对犬视网膜中各种应激诱导蛋白的影响。
15个犬视网膜(5个来自对照眼,5个来自急性青光眼眼,5个来自慢性青光眼眼)。
从威斯康星比较眼病理实验室获取眼球。根据临床病史对眼睛进行特征描述。通过免疫组织化学分析确定胶质纤维酸性蛋白(GFAP)、热休克蛋白(HSP)60和缺氧诱导因子(HIF)-1α的分布。
GFAP染色强度随青光眼的时间进展而增加。与对照眼相比,急性青光眼眼标本中HSP 60的染色在不同眼睛之间变化更大,而慢性青光眼眼标本中HSP 60的染色通常比对照眼中明显更少。对照眼和急性青光眼眼的标本在视网膜中均未检测到HIF-1α的核染色。慢性青光眼眼的5个标本中有4个在外核层细胞中检测到HIF-1α的核染色。HIF-1α的染色在更严重萎缩和结构紊乱的区域呈节段性分布。
本研究结果支持一种临床上明显的、快速进展的疾病,急性和慢性青光眼之间存在细胞调节的转变,也支持缺血是该疾病视网膜损伤的一种机制。