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DOI 10.1016/j.exer.2019.02.017

Медицинская библиотека · Experimental eye research · 2019

In vivo detecting mouse persistent hyperplastic primary vitreous by Spectralis Optical Coherence Tomography.

Lian Qing, Zhao Minglei, Li Tianzhong, Wu Keling, Zhu Deliang, Shang Bizhi, Mei Tingfang, Li Weihua, Lin Ying, Mao Fuxiang, Liu Yizhi, Liu Chujun, Lu Lin, Zhao Ling

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

To identify imaging characteristics of mouse persistent hyperplastic primary vitreous (PHPV) by Spectralis Optical Coherence Tomography (OCT), as well as to assess and compare the sensitivity and precision of OCT with color photography (CP) and Fundus Fluorescein Angiography (FFA) imaging in detecting mouse PHPV. Notch4-/- C57BL/6J mice (224 eyes) aged from 3 months to 7 months were examined in this study. CP, FFA and OCT imaging were utilized to examine vitreous cavity and retina of mouse eyes. Horizontal and radial OCT scan volume was centered on the optic nerve head. Hematoxylin and eosin (H&E) staining was performed to validate PHPV. For color photography and FFA imaging, retrolental irregular fibrovascular membrane-like tissues were found in 33 eyes with/without blood vessels in vitreous cavity. Among them, 31 eyes were visualized with lateral and oblique linear hyperreflective opacities in vitreous cavity using Spectralis OCT. Position of PHPV in posterior segment of eyes was also measured via OCT. Mouse PHPV was validated by H&E staining. Typical hyperreflective opacities in vitreous cavity were detected in PHPV mouse using Spectralis OCT. Spectralis OCT imaging can effectively detect mouse PHPV as color photography and FFA.

Для цитирования: Lian Qing, Zhao Minglei, Li Tianzhong, Wu Keling, Zhu Deliang, Shang Bizhi, Mei Tingfang, Li Weihua, Lin Ying, Mao Fuxiang, Liu Yizhi, Liu Chujun, Lu Lin, Zhao Ling. In vivo detecting mouse persistent hyperplastic primary vitreous by Spectralis Optical Coherence Tomography.. Experimental eye research. 2019. DOI: 10.1016/j.exer.2019.02.017.

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