期刊论文详细信息
Journal of Pharmacological Sciences
Effect of a Dihydrobenzofuran Derivative on Lipid Hydroperoxide-Induced Rabbit Corneal Neovascularization
Seiichi Uchida3  Yoko Taguchi1  Yuta Saito1  Ryohei Koide1  Shinichi Iwai2  Donald Armstrong1  Takako Nakanishi-Ueda2  Hajime Yasuhara2  Hirotsugu Ogura1  Toshihiko Ueda1  Katsuji Oguchi2 
[1] Department of Ophthalmology, School of Medicine, Showa University, Japan;Department of Pharmacology, School of Medicine, Showa University, Japan;Department of Biological Research, Division 2, Odawara Research Center, Nippon Soda, Co., Ltd., Japan
关键词: neovascularization;    lipid hydroperoxide;    dihydrobenzofuran derivative;    vascular endothelial growth factor (VEGF);    matrix metalloproteinase (MMP);   
DOI  :  10.1254/jphs.FP0061301
学科分类:药学
来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society
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【 摘 要 】

References(37)Cited-By(5)The aim of this study was to investigate the effect of A-3922, a dihydrobenzofuran derivative, on linoleic acid hydroperoxide (LHP)-induced corneal neovascularization (NV) in a rabbit model. Male New Zealand rabbits received intraperitoneal (i.p.) injections of 10 or 30 mg/kg per day A-3922 or its vehicle as control for 3 days. One day after i.p. injections, LHP was injected with a 30-gauge needle into the corneal stroma of the superior quadrant 4.5-mm below the limbus. Photographs of the vessels were taken for digital analysis with a surgical microscope. Vascular endothelial growth factor (VEGF) was measured using an immunoassay kit, and matrix metalloproteinase (MMP)-9 was measured by gelatin zymography in corneal samples. At 7 days post-LHP injection, the total vessel length was 26.7 ± 3.8 mm in the control animals (n = 8), 16.1 ± 0.8 mm in the A-3922 (10 mg/kg)-treated group (n = 5), and 11.4 ± 2.1 mm in the 30 mg/kg group (n = 8, P<0.01 vs control), respectively. After LHP injection, the content of VEGF and MMP-9 activity were increased in the superior cornea, but these were not influenced by A-3922 treatments. These results indicate that LHP-induced corneal NV is inhibited by treatment with A-3922 and therefore may represent a potential pharmacological intervention for ocular neovascularization disorders.

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