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Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms

Myopia affects well over 30% of adult humans globally. However, the underlying physiological mechanism is little understood. This study tested the hypothesis that ocular growth and refractive compensation to optical defocus can be controlled by manipulation of potassium and chloride ion-driven trans...

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Autores principales: Crewther, Sheila G., Murphy, Melanie J., Crewther, David P.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481396/
https://www.ncbi.nlm.nih.gov/pubmed/18665233
http://dx.doi.org/10.1371/journal.pone.0002839
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author Crewther, Sheila G.
Murphy, Melanie J.
Crewther, David P.
author_facet Crewther, Sheila G.
Murphy, Melanie J.
Crewther, David P.
author_sort Crewther, Sheila G.
collection PubMed
description Myopia affects well over 30% of adult humans globally. However, the underlying physiological mechanism is little understood. This study tested the hypothesis that ocular growth and refractive compensation to optical defocus can be controlled by manipulation of potassium and chloride ion-driven transretinal fluid movements to the choroid. Chicks were raised with +/−10D or zero power optical defocus rendering the focal plane of the eye in front of, behind, or at the level of the retinal photoreceptors respectively. Intravitreal injections of barium chloride, a non-specific inhibitor of potassium channels in the retina and RPE or bumetanide, a selective inhibitor of the sodium-potassium-chloride cotransporter were made, targeting fluid control mechanisms. Comparison of refractive compensation to 5mM Ba(2+) and 10(−5) M bumetanide compared with control saline injected eyes shows significant change for both positive and negative lens defocus for Ba(2+) but significant change only for negative lens defocus with bumetanide [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]). Vitreous chamber depths showed a main effect for drug conditions with less depth change in response to defocus shown for Ba(2+) relative to Saline, while bumetanide injected eyes showed a trend to increased depth without a significant interaction with applied defocus. The results indicate that both K channels and the NKCC cotransporter play a role in refractive compensation with NKCC blockade showing far more specificity for negative, compared with positive, lens defocus. Probable sites of action relevant to refractive control include the apical retinal pigment epithelium membrane and the photoreceptor/ON bipolar synapse. The similarities between the biometric effects of NKCC inhibition and biometric reports of the blockade of the retinal ON response, suggest a possible common mechanism. The selective inhibition of refractive compensation to negative lens in chick by loop diuretics such as bumetanide suggests that these drugs may be effective in the therapeutic management of human myopia.
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spelling pubmed-24813962008-07-30 Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms Crewther, Sheila G. Murphy, Melanie J. Crewther, David P. PLoS One Research Article Myopia affects well over 30% of adult humans globally. However, the underlying physiological mechanism is little understood. This study tested the hypothesis that ocular growth and refractive compensation to optical defocus can be controlled by manipulation of potassium and chloride ion-driven transretinal fluid movements to the choroid. Chicks were raised with +/−10D or zero power optical defocus rendering the focal plane of the eye in front of, behind, or at the level of the retinal photoreceptors respectively. Intravitreal injections of barium chloride, a non-specific inhibitor of potassium channels in the retina and RPE or bumetanide, a selective inhibitor of the sodium-potassium-chloride cotransporter were made, targeting fluid control mechanisms. Comparison of refractive compensation to 5mM Ba(2+) and 10(−5) M bumetanide compared with control saline injected eyes shows significant change for both positive and negative lens defocus for Ba(2+) but significant change only for negative lens defocus with bumetanide [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]; [Image: see text]). Vitreous chamber depths showed a main effect for drug conditions with less depth change in response to defocus shown for Ba(2+) relative to Saline, while bumetanide injected eyes showed a trend to increased depth without a significant interaction with applied defocus. The results indicate that both K channels and the NKCC cotransporter play a role in refractive compensation with NKCC blockade showing far more specificity for negative, compared with positive, lens defocus. Probable sites of action relevant to refractive control include the apical retinal pigment epithelium membrane and the photoreceptor/ON bipolar synapse. The similarities between the biometric effects of NKCC inhibition and biometric reports of the blockade of the retinal ON response, suggest a possible common mechanism. The selective inhibition of refractive compensation to negative lens in chick by loop diuretics such as bumetanide suggests that these drugs may be effective in the therapeutic management of human myopia. Public Library of Science 2008-07-30 /pmc/articles/PMC2481396/ /pubmed/18665233 http://dx.doi.org/10.1371/journal.pone.0002839 Text en Crewther et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Crewther, Sheila G.
Murphy, Melanie J.
Crewther, David P.
Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title_full Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title_fullStr Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title_full_unstemmed Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title_short Potassium Channel and NKCC Cotransporter Involvement in Ocular Refractive Control Mechanisms
title_sort potassium channel and nkcc cotransporter involvement in ocular refractive control mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481396/
https://www.ncbi.nlm.nih.gov/pubmed/18665233
http://dx.doi.org/10.1371/journal.pone.0002839
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