Establishment of the New Zealand white rabbit animal model of fatty keratopathy associated with corneal neovascularization

被引:1
作者
Gao, Yikui [1 ]
Li, Cong [1 ]
Li, Xiaoyun [1 ]
Zhang, Minghong [2 ]
机构
[1] Eighth Peoples Hosp Qingdao, Ophthalmol Dept, Qingdao 266000, Peoples R China
[2] Qingdao Aier Eye Hosp, Refract Dept, Qingdao 266400, Peoples R China
来源
OPEN LIFE SCIENCES | 2021年 / 16卷 / 01期
关键词
neovascularization; cornea; animal modeling; keratopathy; rabbit; LYMPHATIC VESSELS; BLOOD; ANGIOGENESIS; PERMEABILITY;
D O I
10.1515/biol-2021-0111
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The term fatty keratopathy is used to describe the phenomenon of fat deposition caused by corneal neovascularization, which will severely affect the eye's beauty and vision. The purpose of this study was to establish a New Zealand white rabbit animal model of fatty keratopathy, that is, the establishment of an animal model of fatty keratopathy. The goal was achieved by the combination of a corneal neovascularization animal model and a hyperlipidemia animal model. Two groups were created according to the experimental sequence. The first group initially induced a corneal neovascularization pattern and later induced a hyperlipidemia pattern, and the second group followed the opposite sequence. The results of the two groups showed that all the significant crystalline deposits of the cornea were visible. So the animal models of fatty keratopathy were successfully established in both groups.
引用
收藏
页码:1261 / 1267
页数:7
相关论文
共 24 条
[1]   Regression of mature lymphatic vessels in the cornea by photodynamic therapy [J].
Bucher, F. ;
Bi, Y. ;
Gehlsen, U. ;
Hos, D. ;
Cursiefen, C. ;
Bock, F. .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2014, 98 (03) :391-395
[2]   Matrix metalloproteinase 14 modulates signal transduction and angiogenesis in the cornea [J].
Chang, Jin-Hong ;
Huang, Yu-Hui ;
Cunningham, Christy M. ;
Han, Kyu-Yeon ;
Chang, Michael ;
Seiki, Motoharu ;
Zhou, Zhongjun ;
Azar, Dimitri T. .
SURVEY OF OPHTHALMOLOGY, 2016, 61 (04) :478-497
[3]   Inflammatory Corneal Neovascularization: Etiopathogenesis [J].
Clements, John L. ;
Dana, Reza .
SEMINARS IN OPHTHALMOLOGY, 2011, 26 (4-5) :235-245
[4]  
COGAN DG, 1959, ARCH OPHTHALMOL-CHIC, V61, P219
[5]  
Colby KA, 1996, INVEST OPHTH VIS SCI, V37, P2734
[6]   Pericyte recruitment in human corneal angiogenesis:: an ultrastructural study with clinicopathological correlation [J].
Cursiefen, C ;
Hofmann-Rummelt, C ;
Küchle, M ;
Schlötzer-Schrehardt, U .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2003, 87 (01) :101-106
[7]   Differential Distribution of Blood and Lymphatic Vessels in the Murine Cornea [J].
Ecoiffier, Tatiana ;
Yuen, Don ;
Chen, Lu .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (05) :2436-2440
[8]   Nanotechnology in Corneal Neovascularization Therapy-A Review [J].
Gonzalez, Lilian ;
Loza, Raymond J. ;
Han, Kyu-Yeon ;
Sunoqrot, Suhair ;
Cunningham, Christy ;
Purta, Patryk ;
Drake, James ;
Jain, Sandeep ;
Hong, Seungpyo ;
Chang, Jin-Hong .
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2013, 29 (02) :124-134
[9]   VEGFR3 Modulates Vascular Permeability by Controlling VEGF/VEGFR2 Signaling [J].
Heinolainen, Krista ;
Karaman, Sinem ;
D'Amico, Gabriela ;
Tammela, Tuomas ;
Sormunen, Raija ;
Eklund, Lauri ;
Alitalo, Kari ;
Zarkada, Georgia .
CIRCULATION RESEARCH, 2017, 120 (09) :1414-+
[10]   Frequency of dendritiform inflammatory cells in the cornea in herpetic anterior uveitis without clinical keratitis and Fuchs uveitis [J].
Knoll A.B. ;
Postole A.S. ;
Auffarth G.U. ;
Mackensen F. .
Journal of Ophthalmic Inflammation and Infection, 4 (1) :1-6