南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2010年
3期
552-554
,共3页
王建明%宋艳萍%孙乃学%惠娜%赵世平%胡凯
王建明%宋豔萍%孫迺學%惠娜%趙世平%鬍凱
왕건명%송염평%손내학%혜나%조세평%호개
促红细胞生成素%bcl-2蛋白%视网膜%神经保护
促紅細胞生成素%bcl-2蛋白%視網膜%神經保護
촉홍세포생성소%bcl-2단백%시망막%신경보호
erythropoietin%bcl-2 protein%retina%neuroprotection
目的 探讨全身应用重组人促红细胞生成索(rhEPO)对急性高眼压兔眼视网膜bcl-2蛋白表达的影响及意义.方法 在设立正常对照、急性高眼压模型对照的情况下,日本大耳白兔皮下注射rhEPO,分别于造模后第1、3、7、14天免疫组化法观察视网膜bcl-2蛋白表达.结果 正常视网膜组织可见bcl-2蛋白表达,染色阳性细胞数为每高倍视野(10.5±1.2)个.模型组和EPO组兔眼视网膜bcl-2蛋白表达阳性细胞数均较正常对照组减少(P<0.05,P<0.01).EPO组第7天、14天视网膜bcl-2蛋白表达阳性细胞数较模型组增加(P<0.05,P<0.01).结论 rhEPO可以上调视网膜bcl-2蛋白表达,这可能是rhEPO保护急性高眼压引起的兔眼视网膜神经功能损害的机制之一.
目的 探討全身應用重組人促紅細胞生成索(rhEPO)對急性高眼壓兔眼視網膜bcl-2蛋白錶達的影響及意義.方法 在設立正常對照、急性高眼壓模型對照的情況下,日本大耳白兔皮下註射rhEPO,分彆于造模後第1、3、7、14天免疫組化法觀察視網膜bcl-2蛋白錶達.結果 正常視網膜組織可見bcl-2蛋白錶達,染色暘性細胞數為每高倍視野(10.5±1.2)箇.模型組和EPO組兔眼視網膜bcl-2蛋白錶達暘性細胞數均較正常對照組減少(P<0.05,P<0.01).EPO組第7天、14天視網膜bcl-2蛋白錶達暘性細胞數較模型組增加(P<0.05,P<0.01).結論 rhEPO可以上調視網膜bcl-2蛋白錶達,這可能是rhEPO保護急性高眼壓引起的兔眼視網膜神經功能損害的機製之一.
목적 탐토전신응용중조인촉홍세포생성색(rhEPO)대급성고안압토안시망막bcl-2단백표체적영향급의의.방법 재설립정상대조、급성고안압모형대조적정황하,일본대이백토피하주사rhEPO,분별우조모후제1、3、7、14천면역조화법관찰시망막bcl-2단백표체.결과 정상시망막조직가견bcl-2단백표체,염색양성세포수위매고배시야(10.5±1.2)개.모형조화EPO조토안시망막bcl-2단백표체양성세포수균교정상대조조감소(P<0.05,P<0.01).EPO조제7천、14천시망막bcl-2단백표체양성세포수교모형조증가(P<0.05,P<0.01).결론 rhEPO가이상조시망막bcl-2단백표체,저가능시rhEPO보호급성고안압인기적토안시망막신경공능손해적궤제지일.
Objective To investigate the effect of recombinant human erythropoietin (rhEPO) on the expression of bcl-2 protein in the retina of rabbits with acute high intraocular pressure and explore the mechanism underlying the protective effect of rhEPO on the retina against ischemia-reperfusion injury. Methods rhEPO was injected subcutaneously in the ear of a rabbit model of acute high intraocular pressure induced by physiological saline perfusion into the anterior chamber. Bcl-2 protein expression in the retina of the rabbits was observed by immunohistochemical staining on days 1, 3, 7, and 14 after retinal ischemia-reperfusion and compared with that in normal rabbits and untreated rabbit models. Results bcl-2-positive cells were observed in the retina of normal rabbits with a mean positive cell number of 10.5 ±1.2 in each high-power visual field. Compared with that in the normal control group, the number of the positive cells decreased significantly in both the model group and EPO group (P<0.05, P<0.01), but the latter group showed a significantly greater number than the former (P<0.05 at day 7 and P<0.01 at day 14). Conclusion Systemic administration of rhEPO can up-regulate the expression ofbcl-2 protein in the retina of rabbits with acute high intraocular pressure, which is probably one of the mechanisms for the protective effect of rhEPO on the retina against ischemia-repeffusion injury.