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首页> 外文期刊>Journal of Ophthalmology >The Role of Intravitreal Anti-VEGF Agents in Rabbit Eye Model of Open-Globe Injury
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The Role of Intravitreal Anti-VEGF Agents in Rabbit Eye Model of Open-Globe Injury

机译:玻璃体内抗VEGF代理在开放全球损伤兔眼模型中的作用

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Purpose . To evaluate the effects of intravitreal anti-VEGF agents in a rabbit model of open-globe injury (OGI). Methods . OGI was induced in the right eyes of 75 Belgian rabbits by making 5?mm circumferential incision placed 6?mm behind the limbus. The rabbits were divided into 4 groups: control ( n ?=?5), OGI group ( n ?=?40), and intravitreal Ranibizumab and Conbercept ( n ?=?15 each). Ranibizumab or Conbercept was injected into the vitreous at 0.5?hours, 3 days, or 7?days. Vitreous fluid was collected, and levels of growth factors and cytokines were measured by enzyme-linked immunosorbent assay (ELISA). On day 28 after OGI, B scan examination and histological examination were performed to evaluate intravitreal proliferation and formation of epiretinal fibrosis. Results . Vitreous levels of vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), transforming growth factor-beta (TGF- β ), and plasminogen activator inhibitor-1 (PAI-1) were significantly increased in rabbit eyes after OGI. Compared to eyes in OGI group, anti-VEGF treatments significantly reduced these growth factors and cytokines. Among the 7 eyes examined from each group for intravitreal proliferative changes, they were found in 7 of 7 (100%) in OGI group and were decreased by Ranibizumab and Conbercept to 5 of 7 (71.4%) and 4 of 7 (57.1%), respectively. Both Ranibizumab and Conbercept inhibited epiretinal scar formation at the wound site, with Conbercept showing the greatest effect (maximal length of scar ( L ), L OGI ?=?503?±?82.44? μ m, L Ranibizumab ?=?355?±?43.66? μ m, and L Conbercept ?=?250.33?±?36.02? μ m). Conclusion . Anti-VEGF treatments after OGI significantly attenuated the upregulation of growth factors and cytokines in the vitreous and prevented intravitreal proliferation and epiretinal scar formation and thus may protect against the development of posttraumatic complications such as proliferative vitreoretinopathy (PVR).
机译:目的 。评价玻璃体内抗VEGF剂在开放综合损伤(OGI)兔模型中的影响。方法 。通过制作5?mm的周向切口,在林山上落后6米,在比利时兔的右眼诱导ogi。兔子分为4组:控制(n?=?5),ogi组(n?=?40),intraviteal ranibizumab和conbercept(n?=?每个)。 Ranibizumab或Conbercept在0.5?小时,3天或7天内注射到玻璃体中。收集玻璃体流体,通过酶联免疫吸附试验(ELISA)测量生长因子和细胞因子水平。在ogi,B扫描检查和组织学检查后的第28天进行评估玻璃体内增殖和表位纤维化的形成。结果 。在OGI之后,玻璃体血管内皮生长因子(VEGF),血小板衍生的生长因子(PDGF),转化生长因子-β(TGF-β)和纤溶酶原激活剂抑制剂-1(PAI-1)显着增加。与OGI集团的眼睛相比,抗VEGF治疗显着降低了这些生长因子和细胞因子。在从每组检查的7只眼中进行纤维体增殖性变化,它们在ogi组中的7个(100%)中被发现,Ranibizumab的7个(100%)下降,并且Conbercept到7个(71.4%)和4个(57.1%) , 分别。 ranibizumab和conbercept都抑制了伤口部位的血肿疤痕形成,显示了效果的最大效果(最大长度(l),l ogi?= 503?±82.44?μm,l ranibizumab?=?355?± ?43.66?μm,和l conbercept?=?250.33?±36.02?μm)。结论 。 OGI后的抗VEGF治疗显着减弱了玻璃体中的生长因子和细胞因子的上调,并防止了玻璃体内增殖和表骨瘢痕形成,因此可能会用于保护错误培养物(PVR)的发育性并发症(PVR)。

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