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Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits

PURPOSE: Ripasudil is a novel Rho-associated protein kinase inhibitor that is used to treat ocular hypertension. However, the comparison of the intraocular pressure (IOP)-lowering effects between ripasudil alone and other ocular hypotensive drugs has not been studied thoroughly. The purpose of this...

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Autores principales: Kamaruddin, Muhammad Irfan, Nakamura-Shibasaki, Momoko, Mizuno, Yu, Kiuchi, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383069/
https://www.ncbi.nlm.nih.gov/pubmed/28408797
http://dx.doi.org/10.2147/OPTH.S131416
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author Kamaruddin, Muhammad Irfan
Nakamura-Shibasaki, Momoko
Mizuno, Yu
Kiuchi, Yoshiaki
author_facet Kamaruddin, Muhammad Irfan
Nakamura-Shibasaki, Momoko
Mizuno, Yu
Kiuchi, Yoshiaki
author_sort Kamaruddin, Muhammad Irfan
collection PubMed
description PURPOSE: Ripasudil is a novel Rho-associated protein kinase inhibitor that is used to treat ocular hypertension. However, the comparison of the intraocular pressure (IOP)-lowering effects between ripasudil alone and other ocular hypotensive drugs has not been studied thoroughly. The purpose of this study is to examine the ocular hypotensive effects of 0.4% ripasudil, 2% pilocarpine, 0.5% timolol and 0.1% dorzolamide in rabbits. We also studied the IOP changes when 0.4% ripasudil was combined with 2% pilocarpine, 0.5% timolol or 0.1% dorzolamide. METHODS: One drop of saline solution, 0.4% ripasudil, 0.5% timolol, 2% pilocarpine or 1% dorzolamide or a combination of these agents was applied topically to the left eyes of eight healthy albino rabbits. Posttreatment changes in the IOP of albino rabbits were monitored using a rebound tonometer over a 5-h time course. Changes in IOP after application of saline served as the control. One-way analysis of variance and Dunnett’s post hoc tests were used for statistical analyses. RESULTS: After topical instillation, 0.4% ripasudil resulted in significant decreases in IOP at 0.5 and 1 h compared with the control group. Treatment with timolol, pilocarpine or dorzolamide had no significant effect on IOP. Treatment with timolol, pilocarpine or dorzolamide in combination with ripasudil resulted in significant reductions in IOP at 1 h. However, none of these agents enhanced the IOP-lowering effects of ripasudil. CONCLUSION: Ripasudil has stronger IOP-lowering effects than timolol, pilocarpine or dorzolamide hypotensive agents in our rabbit model. Addition of timolol, pilocarpine or dorzolamide did not enhance the IOP-lowering effects of ripasudil alone.
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spelling pubmed-53830692017-04-13 Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits Kamaruddin, Muhammad Irfan Nakamura-Shibasaki, Momoko Mizuno, Yu Kiuchi, Yoshiaki Clin Ophthalmol Original Research PURPOSE: Ripasudil is a novel Rho-associated protein kinase inhibitor that is used to treat ocular hypertension. However, the comparison of the intraocular pressure (IOP)-lowering effects between ripasudil alone and other ocular hypotensive drugs has not been studied thoroughly. The purpose of this study is to examine the ocular hypotensive effects of 0.4% ripasudil, 2% pilocarpine, 0.5% timolol and 0.1% dorzolamide in rabbits. We also studied the IOP changes when 0.4% ripasudil was combined with 2% pilocarpine, 0.5% timolol or 0.1% dorzolamide. METHODS: One drop of saline solution, 0.4% ripasudil, 0.5% timolol, 2% pilocarpine or 1% dorzolamide or a combination of these agents was applied topically to the left eyes of eight healthy albino rabbits. Posttreatment changes in the IOP of albino rabbits were monitored using a rebound tonometer over a 5-h time course. Changes in IOP after application of saline served as the control. One-way analysis of variance and Dunnett’s post hoc tests were used for statistical analyses. RESULTS: After topical instillation, 0.4% ripasudil resulted in significant decreases in IOP at 0.5 and 1 h compared with the control group. Treatment with timolol, pilocarpine or dorzolamide had no significant effect on IOP. Treatment with timolol, pilocarpine or dorzolamide in combination with ripasudil resulted in significant reductions in IOP at 1 h. However, none of these agents enhanced the IOP-lowering effects of ripasudil. CONCLUSION: Ripasudil has stronger IOP-lowering effects than timolol, pilocarpine or dorzolamide hypotensive agents in our rabbit model. Addition of timolol, pilocarpine or dorzolamide did not enhance the IOP-lowering effects of ripasudil alone. Dove Medical Press 2017-03-31 /pmc/articles/PMC5383069/ /pubmed/28408797 http://dx.doi.org/10.2147/OPTH.S131416 Text en © 2017 Kamaruddin et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Kamaruddin, Muhammad Irfan
Nakamura-Shibasaki, Momoko
Mizuno, Yu
Kiuchi, Yoshiaki
Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title_full Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title_fullStr Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title_full_unstemmed Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title_short Ocular hypotensive effects of a Rho-associated protein kinase inhibitor in rabbits
title_sort ocular hypotensive effects of a rho-associated protein kinase inhibitor in rabbits
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383069/
https://www.ncbi.nlm.nih.gov/pubmed/28408797
http://dx.doi.org/10.2147/OPTH.S131416
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