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口服酪氨酸激酶抑制剂CM082对大鼠实验性脉络膜新生血管形成的影响。

The Effect of CM082, an Oral Tyrosine Kinase Inhibitor, on Experimental Choroidal Neovascularization in Rats.

作者信息

Ren Chengda, Shi Hui, Jiang Juanjuan, Liu Qingyu, Du Yaru, He Mengmei, Cai Wenting, Wei Qingquan, Yu Jing

机构信息

Department of Ophthalmology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, China.

Department of Cardiac Surgery, Institute of Cardiovascular Diseases of Fudan University, Affiliated Zhongshan Hospital of Fudan University, Shanghai, China.

出版信息

J Ophthalmol. 2017;2017:6145651. doi: 10.1155/2017/6145651. Epub 2017 Oct 22.

DOI:10.1155/2017/6145651
PMID:29201457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5671735/
Abstract

The aims of this study were to evaluate the effects of CM082 on the development of choroidal neovascularization (CNV) in a laser-induced CNV rat model and to determine the drug concentration in the ocular tissues. After the laser-induced CNV model was established in rats, CM082 was orally administered. The effects of CM082 on the CNV lesions were assessed using fundus fluorescein angiography (FFA), CNV histology, and retinal pigment epithelium- (RPE-) choroid-sclera eyecup analysis. The concentrations of CM082 in the plasma and eye tissues were determined using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Results of FFA, histology, and RPE-choroid-sclera eyecup analysis demonstrated that the CM082-treated (10 mg/kg/d or 30 mg/kg/d) rats exhibited significantly less neovascularization than did the control group. The total concentration of CM082 in the eyes (172.86 ± 57.11 ng/g) was similar to that in the plasma (196.87 ± 73.13 ng/ml). Within the eye, the concentrations of CM082 and its metabolites were highest in the retina-sclera. The orally administered CM082 thus effectively passed through the blood-retina barrier (BRB) to reach the retina in the Brown Norway rats. Therefore, at both 10 mg/kg/d and 30 mg/kg/d, CM082 was able to reduce CNV lesions in the laser-induced CNV rat model.

摘要

本研究的目的是评估CM082对激光诱导的脉络膜新生血管(CNV)大鼠模型中脉络膜新生血管形成的影响,并确定眼组织中的药物浓度。在大鼠中建立激光诱导的CNV模型后,口服给予CM082。使用眼底荧光血管造影(FFA)、CNV组织学和视网膜色素上皮-(RPE)-脉络膜-巩膜眼杯分析评估CM082对CNV病变的影响。使用液相色谱-串联质谱(LC-MS/MS)测定血浆和眼组织中CM082的浓度。FFA、组织学和RPE-脉络膜-巩膜眼杯分析结果表明,CM082治疗组(10mg/kg/d或30mg/kg/d)大鼠的新生血管形成明显少于对照组。眼中CM082的总浓度(172.86±57.11ng/g)与血浆中的总浓度(196.87±73.13ng/ml)相似。在眼内,CM082及其代谢产物的浓度在视网膜-巩膜中最高。因此,口服给予的CM082能有效穿过血视网膜屏障(BRB)到达挪威棕色大鼠的视网膜。所以,在10mg/kg/d和30mg/kg/d这两个剂量下,CM082都能够减少激光诱导的CNV大鼠模型中的CNV病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/8ed2e0ae7ee3/JOPH2017-6145651.008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/171e52afdc14/JOPH2017-6145651.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/8ed2e0ae7ee3/JOPH2017-6145651.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/7f8a4c4b4231/JOPH2017-6145651.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/deaa544600d3/JOPH2017-6145651.002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/cc91d11e0ad6/JOPH2017-6145651.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/171e52afdc14/JOPH2017-6145651.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/655a/5671735/8ed2e0ae7ee3/JOPH2017-6145651.008.jpg

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