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作 者:罗文婷[1] 张晓元[2] 张中宇[3] 张雪[3] 闫朝岐[4] 谢芳[5] 付红梅[1] 李丹丹[1] 赵兴鹃[1] 孙大卫[3]
机构地区:[1]哈尔滨医科大学第二附属医院体检中心,黑龙江哈尔滨150086 [2]哈尔滨医科大学第二附属医院心内科,黑龙江哈尔滨150086 [3]哈尔滨医科大学第二附属医院眼科,黑龙江哈尔滨150086 [4]哈尔滨医科大学第二附属医院乳腺外科,黑龙江哈尔滨150086 [5]哈尔滨医科大学第一附属医院眼科,黑龙江哈尔滨150001
出 处:《现代生物医学进展》2016年第34期6610-6613,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(81171381)
摘 要:目的:研究早期糖尿病大鼠视网膜和脉络膜血管中VEGFR-2的表达。方法:24只雄性Wistar大鼠,随机分为两组:正常对照组和糖尿病组。实验组给予一次性静脉注射60 mg/kg STZ建立糖尿病模型。STZ注射后24 h,血糖水平超过250 mg/dL被认为是糖尿病模型。WB技术检测VEGFR-2在视网膜和脉络膜的表达水平,免疫组化法用来定位VEGFR-2。结果:STZ注射14天后,糖尿病组的平均体重较对照组显著降低(糖尿病组:177±10 g,对照组:243±19 g,P<0.05),糖尿病组的平均血糖水平较对照组显著增高(糖尿病组的血糖为498±36 mg/m L,对照组的血糖为90±10 mg/m L,P<0.05)。VEGFR-2在糖尿病鼠的视网膜和脉络膜中表达较对照组增加,其差异有统计学意义(P<0.05)。免疫组化分析显示:VEGFR-2在糖尿病组的视网膜和脉络膜血管中表达显著增加,而在正常对照组中少量表达(P<0.05)。结论:VEGFR-2在试验诱导的糖尿病模型的视网膜和脉络膜血管中的表达增加,VEGFR-2可能成为糖尿病视网膜病变新的诊断靶点。Objective: To research the expression of VEGFR-2 in the retinal and choroidal vessels of diabetic rats in early stage. Methods: 24 male Wistar rats were divided into two groups randomly: normal control group and diabetic group. The experimental group was given a one-time intravenous injection of STZ (60 mg/kg) to establish diabetic model. Animals with blood glucose levels higher than 250 mg/dL 24 h after STZ injection were considered diabetic model. Western Blot was used to detect the expression of VEGFR-2 in the retina and choroid. Immunohistochemical staining method was used to localize VEGFR2. Results: 14 days after STZ-injection average body weight of diabetic rats showed significantly lower compared with the normal controls (diabetic rats: 177±10 g, normal controls: 243± 19 g, P〈0.05 ); average blood glucose of diabetic rats showed significantly higher compared with the normal controls (diabetic rats: 498±36 mg/mL, normal controls: 90± 10 mg/mL,P〈0.05 ). Compared with the control group, the expression of VEGFR-2 in the retinal and choroidal vessels of diabetic rats was increased, and the difference was statistically significant (P〈0.05). The immunohistochemical analysis showed significantly increased VEGFR-2 expression in the retinal and choroidal vessels of the diabetic group, whereas the VEGFR-2 of the retina and choroid in the control group was little (P〈0.05). Conclusions: The findings suggest that VEGFR-2 expression is increased in retinal and choroidal vessels in experimentally induced diabetes. VEGFR-2 may be a target for the diagnosis of diabetic retinopathy.
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