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Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment

PURPOSE: Rhegmatogenous retinal detachment (RRD) is a vision-threatening event that benefits from surgical intervention. While awaiting surgical reattachment, irreversible hypoxic and inflammatory damage to the retina often occurs. An interim therapy protecting photoreceptors could improve functiona...

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Autores principales: Huang, Peirong, Thomas, Claire C., Ambati, Kameshwari, Dholkawala, Roshni, Nagasaka, Ayami, Yerramothu, Praveen, Narendran, Siddharth, Pereira, Felipe, Nagasaka, Yosuke, Apicella, Ivana, Cai, Xiaoyu, Makin, Ryan D., Magagnoli, Joseph, Stains, Cliff I., Yin, Ruwen, Wang, Shao-bin, Gelfand, Bradley D., Ambati, Jayakrishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158986/
https://www.ncbi.nlm.nih.gov/pubmed/37129905
http://dx.doi.org/10.1167/iovs.64.5.3
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author Huang, Peirong
Thomas, Claire C.
Ambati, Kameshwari
Dholkawala, Roshni
Nagasaka, Ayami
Yerramothu, Praveen
Narendran, Siddharth
Pereira, Felipe
Nagasaka, Yosuke
Apicella, Ivana
Cai, Xiaoyu
Makin, Ryan D.
Magagnoli, Joseph
Stains, Cliff I.
Yin, Ruwen
Wang, Shao-bin
Gelfand, Bradley D.
Ambati, Jayakrishna
author_facet Huang, Peirong
Thomas, Claire C.
Ambati, Kameshwari
Dholkawala, Roshni
Nagasaka, Ayami
Yerramothu, Praveen
Narendran, Siddharth
Pereira, Felipe
Nagasaka, Yosuke
Apicella, Ivana
Cai, Xiaoyu
Makin, Ryan D.
Magagnoli, Joseph
Stains, Cliff I.
Yin, Ruwen
Wang, Shao-bin
Gelfand, Bradley D.
Ambati, Jayakrishna
author_sort Huang, Peirong
collection PubMed
description PURPOSE: Rhegmatogenous retinal detachment (RRD) is a vision-threatening event that benefits from surgical intervention. While awaiting surgical reattachment, irreversible hypoxic and inflammatory damage to the retina often occurs. An interim therapy protecting photoreceptors could improve functional outcomes. We sought to determine whether Kamuvudine-9 (K-9), a derivative of nucleoside reverse transcriptase inhibitors (NRTIs) that inhibits inflammasome activation, and the NRTIs lamivudine (3TC) and azidothymidine (AZT) could protect the retina following RRD. METHODS: RRD was induced in mice via subretinal injection (SRI) of 1% carboxymethylcellulose (CMC). To simulate outcomes following the clinical management of RRD, we determined the optimal conditions by which SRI of CMC induced spontaneous retinal reattachment (SRR) occurs over 10 days (RRD/SRR). K-9, 3TC, or AZT was administered via intraperitoneal injection. Inflammasome activation pathways were monitored by abundance of cleaved caspase-1, IL-18, and cleaved caspase-8, and photoreceptor death was assessed by TUNEL staining. Retinal function was assessed by full-field scotopic electroretinography. RESULTS: RRD induced retinal inflammasome activation and photoreceptor death in mice. Systemic administration of K-9, 3TC, or AZT inhibited retinal inflammasome activation and photoreceptor death. In the RRD/SRR model, K-9 protected retinal electrical function during the time of RRD and induced an improvement following retinal reattachment. CONCLUSIONS: K-9 and NRTIs exhibit anti-inflammatory and neuroprotective activities in experimental RRD. Given its capacity to protect photoreceptor function during the period of RRD and enhance retinal function following reattachment, K-9 shows promise as a retinal neuroprotectant and warrants study in RRD. Further, this novel RRD/SRR model may facilitate experimental evaluation of functional outcomes relevant to RRD.
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spelling pubmed-101589862023-05-05 Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment Huang, Peirong Thomas, Claire C. Ambati, Kameshwari Dholkawala, Roshni Nagasaka, Ayami Yerramothu, Praveen Narendran, Siddharth Pereira, Felipe Nagasaka, Yosuke Apicella, Ivana Cai, Xiaoyu Makin, Ryan D. Magagnoli, Joseph Stains, Cliff I. Yin, Ruwen Wang, Shao-bin Gelfand, Bradley D. Ambati, Jayakrishna Invest Ophthalmol Vis Sci Retina PURPOSE: Rhegmatogenous retinal detachment (RRD) is a vision-threatening event that benefits from surgical intervention. While awaiting surgical reattachment, irreversible hypoxic and inflammatory damage to the retina often occurs. An interim therapy protecting photoreceptors could improve functional outcomes. We sought to determine whether Kamuvudine-9 (K-9), a derivative of nucleoside reverse transcriptase inhibitors (NRTIs) that inhibits inflammasome activation, and the NRTIs lamivudine (3TC) and azidothymidine (AZT) could protect the retina following RRD. METHODS: RRD was induced in mice via subretinal injection (SRI) of 1% carboxymethylcellulose (CMC). To simulate outcomes following the clinical management of RRD, we determined the optimal conditions by which SRI of CMC induced spontaneous retinal reattachment (SRR) occurs over 10 days (RRD/SRR). K-9, 3TC, or AZT was administered via intraperitoneal injection. Inflammasome activation pathways were monitored by abundance of cleaved caspase-1, IL-18, and cleaved caspase-8, and photoreceptor death was assessed by TUNEL staining. Retinal function was assessed by full-field scotopic electroretinography. RESULTS: RRD induced retinal inflammasome activation and photoreceptor death in mice. Systemic administration of K-9, 3TC, or AZT inhibited retinal inflammasome activation and photoreceptor death. In the RRD/SRR model, K-9 protected retinal electrical function during the time of RRD and induced an improvement following retinal reattachment. CONCLUSIONS: K-9 and NRTIs exhibit anti-inflammatory and neuroprotective activities in experimental RRD. Given its capacity to protect photoreceptor function during the period of RRD and enhance retinal function following reattachment, K-9 shows promise as a retinal neuroprotectant and warrants study in RRD. Further, this novel RRD/SRR model may facilitate experimental evaluation of functional outcomes relevant to RRD. The Association for Research in Vision and Ophthalmology 2023-05-02 /pmc/articles/PMC10158986/ /pubmed/37129905 http://dx.doi.org/10.1167/iovs.64.5.3 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Huang, Peirong
Thomas, Claire C.
Ambati, Kameshwari
Dholkawala, Roshni
Nagasaka, Ayami
Yerramothu, Praveen
Narendran, Siddharth
Pereira, Felipe
Nagasaka, Yosuke
Apicella, Ivana
Cai, Xiaoyu
Makin, Ryan D.
Magagnoli, Joseph
Stains, Cliff I.
Yin, Ruwen
Wang, Shao-bin
Gelfand, Bradley D.
Ambati, Jayakrishna
Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title_full Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title_fullStr Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title_full_unstemmed Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title_short Kamuvudine-9 Protects Retinal Structure and Function in a Novel Model of Experimental Rhegmatogenous Retinal Detachment
title_sort kamuvudine-9 protects retinal structure and function in a novel model of experimental rhegmatogenous retinal detachment
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158986/
https://www.ncbi.nlm.nih.gov/pubmed/37129905
http://dx.doi.org/10.1167/iovs.64.5.3
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