中华眼底病杂志
中華眼底病雜誌
중화안저병잡지
CHINESE JOURNAL OF OCULAR FUNDUS DISEASES
2010年
1期
23-26
,共4页
脉络膜新生血管化/药物疗法%血管生成抑制剂%抗体,单克隆/治疗应用%抗体,单克隆/投药和剂量%疾病模型,动物
脈絡膜新生血管化/藥物療法%血管生成抑製劑%抗體,單剋隆/治療應用%抗體,單剋隆/投藥和劑量%疾病模型,動物
맥락막신생혈관화/약물요법%혈관생성억제제%항체,단극륭/치료응용%항체,단극륭/투약화제량%질병모형,동물
Choroidal neovascularization/drug therapy%Angiogenesis inhibitors/therapeutic use%Antibodies,monoclonal/therapeutic use%Antibodies,monoclonal/administration & dosage%Disease models,animal
目的 观察玻璃体腔注射抗血管内皮生长因子(VEGF)单克隆抗体bevacizumab(商品名Avastin)抑制激光诱导的实验性脉络膜新生血管(CNV)的效果及特点.方法 12只雄性棕色挪威(BN)大鼠平均分为bevacizumab组和对照组,每组6只.每一只大鼠随机选取1只眼为实验眼,采用半导体激光围绕其视盘激光光凝8点后,bevacizumab组和对照组玻璃体腔立即分别给予2.00 μl bevacizumab和乳酸林格注射液.激光光凝后7、14、21 d两组行荧光素跟底血管造影(FFA)和吲哚青绿血管造影(ICGA)动态观察CNV的形态及渗漏情况.激光光凝后21 d摘除实验眼作石蜡切片行苏木精-伊红染色,比较两组CNV的高度,同时行VEGF免疫组织化学染色,观察CNV斑块中VEGF的表达情况.结果 激光光凝后7 d,ICGA检查结果显示,bevacizumab组和对照组均有CNV生成.FFA检查结果显示,bevacizumab组的渗漏强度始终比对照组弱,但bevacizumab组渗漏强度随时间推移逐渐增强.bevacizumab组CNV平均厚度比对照组低.免疫组织化学检查结果显示,bevacizumab组VEGF表达阴性.结论 激光光凝后立即玻璃体腔注射2.00 μl bevacizumab可以降低CNV厚度并抑制其渗漏,但不能阻止CNV的生成,抑制CNV渗漏的效果不能长时间保持.
目的 觀察玻璃體腔註射抗血管內皮生長因子(VEGF)單剋隆抗體bevacizumab(商品名Avastin)抑製激光誘導的實驗性脈絡膜新生血管(CNV)的效果及特點.方法 12隻雄性棕色挪威(BN)大鼠平均分為bevacizumab組和對照組,每組6隻.每一隻大鼠隨機選取1隻眼為實驗眼,採用半導體激光圍繞其視盤激光光凝8點後,bevacizumab組和對照組玻璃體腔立即分彆給予2.00 μl bevacizumab和乳痠林格註射液.激光光凝後7、14、21 d兩組行熒光素跟底血管造影(FFA)和吲哚青綠血管造影(ICGA)動態觀察CNV的形態及滲漏情況.激光光凝後21 d摘除實驗眼作石蠟切片行囌木精-伊紅染色,比較兩組CNV的高度,同時行VEGF免疫組織化學染色,觀察CNV斑塊中VEGF的錶達情況.結果 激光光凝後7 d,ICGA檢查結果顯示,bevacizumab組和對照組均有CNV生成.FFA檢查結果顯示,bevacizumab組的滲漏彊度始終比對照組弱,但bevacizumab組滲漏彊度隨時間推移逐漸增彊.bevacizumab組CNV平均厚度比對照組低.免疫組織化學檢查結果顯示,bevacizumab組VEGF錶達陰性.結論 激光光凝後立即玻璃體腔註射2.00 μl bevacizumab可以降低CNV厚度併抑製其滲漏,但不能阻止CNV的生成,抑製CNV滲漏的效果不能長時間保持.
목적 관찰파리체강주사항혈관내피생장인자(VEGF)단극륭항체bevacizumab(상품명Avastin)억제격광유도적실험성맥락막신생혈관(CNV)적효과급특점.방법 12지웅성종색나위(BN)대서평균분위bevacizumab조화대조조,매조6지.매일지대서수궤선취1지안위실험안,채용반도체격광위요기시반격광광응8점후,bevacizumab조화대조조파리체강립즉분별급여2.00 μl bevacizumab화유산림격주사액.격광광응후7、14、21 d량조행형광소근저혈관조영(FFA)화신타청록혈관조영(ICGA)동태관찰CNV적형태급삼루정황.격광광응후21 d적제실험안작석사절편행소목정-이홍염색,비교량조CNV적고도,동시행VEGF면역조직화학염색,관찰CNV반괴중VEGF적표체정황.결과 격광광응후7 d,ICGA검사결과현시,bevacizumab조화대조조균유CNV생성.FFA검사결과현시,bevacizumab조적삼루강도시종비대조조약,단bevacizumab조삼루강도수시간추이축점증강.bevacizumab조CNV평균후도비대조조저.면역조직화학검사결과현시,bevacizumab조VEGF표체음성.결론 격광광응후립즉파리체강주사2.00 μl bevacizumab가이강저CNV후도병억제기삼루,단불능조지CNV적생성,억제CNV삼루적효과불능장시간보지.
Objective To observe the inhibitory effects and characteristics of intravitreal injection with bevacizumab on laser-induced choroidal neovascularization (CNV).Methods Twelve male brown norway (BN) rats were divided into the bevacizumab group and control group with six rats in each group.One eye of rats were received a series of 8 diode laser esions around optic disc to induce CNV,then the rats in bevacizumab group and control group underwent intravitreal injection with 2 μl bevacizumab and ringer's lactate.On days 7,14,and 21,the morphology and leakage of CNV were observed by fundus fluorescein angiography (FFA) and indocyanine green angiography (ICGA).On day 21 after photocoagulation,thephotocoagulated eyes were enucleated and processed for histopathologie examination,including hematoxylin and eosin (H&E) staining and immunohistochemistry staining for vascular endothelial growth factor (VEGF).Results On day 7 after photocoagulation,ICGA showed that CNV developed in the bevacizumab group and the control group.FFA showed that leakage intensity in the bevacizumab group was significantly lower than that in the control group,but the bevacizumab group gradually increased over time.The mean thickness of CNV significantly decreased in the bevacizumab group.The CNV in the bevacizumab group were negative for VEGF according to the result of immmuohistochemistry staining.Conclusions Early intravitreal injection with 2 μl bevacizumab can reduce the thickness of CNV and inhibit the leakage of CNV.However,bevacizumab could neither block the formation of CNV,nor suppress the permeability permanently.Combined other therapies with bevacizumab may be more potential to treat CNV effectively.