Efficacy of Osthole in Management of Hypoperfused Retina

Purpose. To determine the effect of osthole on the retina in a chronic cerebral hypoperfusion (CCH) rat model and to investigate its therapeutic activity. Methods. Seventy-two rats were randomly allocated into 6 groups. CCH was induced by permanent bilateral common carotid artery occlusion (BCCAO) i...

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Main Authors: Ran Du, Zhao-yang Meng, Jia-lin Wang, Yan-ling Wang
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Ophthalmology
Online Access:http://dx.doi.org/10.1155/2018/6178347
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author Ran Du
Zhao-yang Meng
Jia-lin Wang
Yan-ling Wang
author_facet Ran Du
Zhao-yang Meng
Jia-lin Wang
Yan-ling Wang
author_sort Ran Du
collection DOAJ
description Purpose. To determine the effect of osthole on the retina in a chronic cerebral hypoperfusion (CCH) rat model and to investigate its therapeutic activity. Methods. Seventy-two rats were randomly allocated into 6 groups. CCH was induced by permanent bilateral common carotid artery occlusion (BCCAO) in five groups. Sham surgery was performed without occlusion of the artery in the sixth group (control group). Animals were administered with saline (model group), osthole (osthole-IG group), aspirin (aspirin group), or ginaton (ginaton group); the osthole-PI group was performed with peribulbar injection of osthole. Four rats in each group were sacrificed every 5 days after drug administration, and histopathology along with morphology of retina were observed. Fundus fluorescein angiography was performed before the animals were sacrificed at day 15. Retinal Akt, NF-κB, Bax, and Bcl-2 levels were assessed using immunohistochemistry, immunofluorescence, and reverse-transcription PCR; retinal injury was assessed using TUNEL in situ; retinal levels of superoxide dismutase (SOD) and malondialdehyde (MDA) were measured. Results. Fundus fluorescein angiography revealed the retinal vascular diameter in the osthole-IG group rats to be wider than that in the model, osthole-PI, aspirin, or ginaton group rats. Histological analysis of retinal tissue revealed an increase in retinal thickness in all treatment groups, and significant improvement was noticed in the osthole-IG group. TUNEL staining revealed fewer apoptotic cells in the osthole-IG and osthole-PI groups than in the other groups. For immunohistochemistry results, in the osthole-IG group, levels of NF-κB and Akt were lower than those in the other treated groups, while levels of the ratio Bcl-2/Bax were higher. Levels of MDA were lower and levels of SOD were higher in the osthole-IG group than in the other groups. Conclusions. Osthole protects the retina from ischemia injury secondary to CCH induced by BCCAO, mainly through anti-inflammatory, antioxidant, and antiapoptotic effects.
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spelling doaj-art-52f9f60d7a9c4d3ead78640cf546d80f2025-02-03T07:26:04ZengWileyJournal of Ophthalmology2090-004X2090-00582018-01-01201810.1155/2018/61783476178347Efficacy of Osthole in Management of Hypoperfused RetinaRan Du0Zhao-yang Meng1Jia-lin Wang2Yan-ling Wang3Department of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaDepartment of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaDepartment of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaDepartment of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaPurpose. To determine the effect of osthole on the retina in a chronic cerebral hypoperfusion (CCH) rat model and to investigate its therapeutic activity. Methods. Seventy-two rats were randomly allocated into 6 groups. CCH was induced by permanent bilateral common carotid artery occlusion (BCCAO) in five groups. Sham surgery was performed without occlusion of the artery in the sixth group (control group). Animals were administered with saline (model group), osthole (osthole-IG group), aspirin (aspirin group), or ginaton (ginaton group); the osthole-PI group was performed with peribulbar injection of osthole. Four rats in each group were sacrificed every 5 days after drug administration, and histopathology along with morphology of retina were observed. Fundus fluorescein angiography was performed before the animals were sacrificed at day 15. Retinal Akt, NF-κB, Bax, and Bcl-2 levels were assessed using immunohistochemistry, immunofluorescence, and reverse-transcription PCR; retinal injury was assessed using TUNEL in situ; retinal levels of superoxide dismutase (SOD) and malondialdehyde (MDA) were measured. Results. Fundus fluorescein angiography revealed the retinal vascular diameter in the osthole-IG group rats to be wider than that in the model, osthole-PI, aspirin, or ginaton group rats. Histological analysis of retinal tissue revealed an increase in retinal thickness in all treatment groups, and significant improvement was noticed in the osthole-IG group. TUNEL staining revealed fewer apoptotic cells in the osthole-IG and osthole-PI groups than in the other groups. For immunohistochemistry results, in the osthole-IG group, levels of NF-κB and Akt were lower than those in the other treated groups, while levels of the ratio Bcl-2/Bax were higher. Levels of MDA were lower and levels of SOD were higher in the osthole-IG group than in the other groups. Conclusions. Osthole protects the retina from ischemia injury secondary to CCH induced by BCCAO, mainly through anti-inflammatory, antioxidant, and antiapoptotic effects.http://dx.doi.org/10.1155/2018/6178347
spellingShingle Ran Du
Zhao-yang Meng
Jia-lin Wang
Yan-ling Wang
Efficacy of Osthole in Management of Hypoperfused Retina
Journal of Ophthalmology
title Efficacy of Osthole in Management of Hypoperfused Retina
title_full Efficacy of Osthole in Management of Hypoperfused Retina
title_fullStr Efficacy of Osthole in Management of Hypoperfused Retina
title_full_unstemmed Efficacy of Osthole in Management of Hypoperfused Retina
title_short Efficacy of Osthole in Management of Hypoperfused Retina
title_sort efficacy of osthole in management of hypoperfused retina
url http://dx.doi.org/10.1155/2018/6178347
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