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Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model

PURPOSE: To study the long-term photoreceptor changes and to evaluate the effects of topical application of a carbonic anhydrase inhibitor (CAI) in a mouse model of X-linked retinoschisis (XLRS). METHODS: Conventional electroretinograms (ERGs) and dark-adapted 10-Hz flicker ERGs were recorded in con...

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Autores principales: Liu, Meng, Liu, Jingyang, Wang, Weiping, Liu, Guangming, Jin, Xiuxiu, Lei, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273824/
https://www.ncbi.nlm.nih.gov/pubmed/35836954
http://dx.doi.org/10.3389/fmed.2022.886947
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author Liu, Meng
Liu, Jingyang
Wang, Weiping
Liu, Guangming
Jin, Xiuxiu
Lei, Bo
author_facet Liu, Meng
Liu, Jingyang
Wang, Weiping
Liu, Guangming
Jin, Xiuxiu
Lei, Bo
author_sort Liu, Meng
collection PubMed
description PURPOSE: To study the long-term photoreceptor changes and to evaluate the effects of topical application of a carbonic anhydrase inhibitor (CAI) in a mouse model of X-linked retinoschisis (XLRS). METHODS: Conventional electroretinograms (ERGs) and dark-adapted 10-Hz flicker ERGs were recorded in control and Rs1(−/Y) mice generated with CRISPR/Cas9. ON-pathway blocker 2-amino-4-phosphobutyric acid (APB) was injected intravitreally. Morphology was evaluated with histology and optical coherence tomography (OCT). Mice were treated with a CAI inhibitor brinzolamide eye drops (10 mg/ml) three times a day for 3 months. OCT and ERG findings at 1, 4, and 10 months were analyzed. RESULTS: Negative ERGs and retinal cavities were evident in Rs1(−/Y) mice. Both a-wave and b-wave amplitudes decreased with age when compared with age-matched controls. The APB-isolated a-wave (a′) amplitudes of Rs1(−/Y) mice were reduced in all age groups. In dark-adapted 10-Hz flicker ERG, the amplitude-intensity curve of Rs1(−/Y) mice shifted down. The thickness of ONL and IS/OS decreased in Rs1(−/Y) mice. CAI reduced the splitting retinal cavities but didn't affect the ERG. CONCLUSIONS: In addition to post receptoral impairments, photoreceptor cells underwent progressive dysfunction since early age in Rs1(−/Y) mice. Long-term CAI treatment improved the shrinkage of the splitting retinal cavity, while no functional improvement was observed.
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spelling pubmed-92738242022-07-13 Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model Liu, Meng Liu, Jingyang Wang, Weiping Liu, Guangming Jin, Xiuxiu Lei, Bo Front Med (Lausanne) Medicine PURPOSE: To study the long-term photoreceptor changes and to evaluate the effects of topical application of a carbonic anhydrase inhibitor (CAI) in a mouse model of X-linked retinoschisis (XLRS). METHODS: Conventional electroretinograms (ERGs) and dark-adapted 10-Hz flicker ERGs were recorded in control and Rs1(−/Y) mice generated with CRISPR/Cas9. ON-pathway blocker 2-amino-4-phosphobutyric acid (APB) was injected intravitreally. Morphology was evaluated with histology and optical coherence tomography (OCT). Mice were treated with a CAI inhibitor brinzolamide eye drops (10 mg/ml) three times a day for 3 months. OCT and ERG findings at 1, 4, and 10 months were analyzed. RESULTS: Negative ERGs and retinal cavities were evident in Rs1(−/Y) mice. Both a-wave and b-wave amplitudes decreased with age when compared with age-matched controls. The APB-isolated a-wave (a′) amplitudes of Rs1(−/Y) mice were reduced in all age groups. In dark-adapted 10-Hz flicker ERG, the amplitude-intensity curve of Rs1(−/Y) mice shifted down. The thickness of ONL and IS/OS decreased in Rs1(−/Y) mice. CAI reduced the splitting retinal cavities but didn't affect the ERG. CONCLUSIONS: In addition to post receptoral impairments, photoreceptor cells underwent progressive dysfunction since early age in Rs1(−/Y) mice. Long-term CAI treatment improved the shrinkage of the splitting retinal cavity, while no functional improvement was observed. Frontiers Media S.A. 2022-06-28 /pmc/articles/PMC9273824/ /pubmed/35836954 http://dx.doi.org/10.3389/fmed.2022.886947 Text en Copyright © 2022 Liu, Liu, Wang, Liu, Jin and Lei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Liu, Meng
Liu, Jingyang
Wang, Weiping
Liu, Guangming
Jin, Xiuxiu
Lei, Bo
Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title_full Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title_fullStr Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title_full_unstemmed Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title_short Longitudinal Photoreceptor Phenotype Observation and Therapeutic Evaluation of a Carbonic Anhydrase Inhibitor in a X-Linked Retinoschisis Mouse Model
title_sort longitudinal photoreceptor phenotype observation and therapeutic evaluation of a carbonic anhydrase inhibitor in a x-linked retinoschisis mouse model
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273824/
https://www.ncbi.nlm.nih.gov/pubmed/35836954
http://dx.doi.org/10.3389/fmed.2022.886947
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