Literature DB >> 15277465

Structural and elemental evidence for edema in the retina, retinal pigment epithelium, and choroid during recovery from experimentally induced myopia.

Helena Liang1, Sheila G Crewther, David P Crewther, Barbara M Junghans.   

Abstract

PURPOSE: The purpose of this study was to monitor temporal changes in the retina, retinal pigment epithelium (RPE), and choroid of chick eyes using biometric, ultrastructural, and elemental microanalysis techniques as a means of visualizing more detailed signs of the physiological processes underlying choroidal expansion and refractive normalization during recovery from form deprivation.
METHODS: Axial dimensions and refractions were measured on form-deprived and fellow eyes of 117 experimental chickens reared with monocular translucent occlusion from days 1 to 15 and given different lengths of visual experience (T = 0-144 hours) before death. Tissue was analyzed ultrastructurally by electron microscopy and relative sodium (Na) and chloride (Cl) ion abundances, by using x-ray microanalysis to determine changes in the presence of these indicators of tissue hydration.
RESULTS: Refractive error decreased from more than 20 D of myopia almost linearly over the first 144 hours after occlusion. Concurrent changes in thickness in the retina, RPE, and choroid were seen as a series of thickness increases and edema, which returned to normal thickness, first in the retina, and did not reach maximum until 3 days after occluder removal in the choroid. In freeze-dried tissue, Na and Cl ion concentrations were greatest in the RPE photoreceptor outer segments and extravascular choroid at T = 0, decreasing toward fellow eye levels by T = 48 in the RPE and choroid. Na and Cl ion abundances in the frozen lymph of choroidal lymphatics were nearly at control levels (T = 0) and increased later as the vessels became more distended after the extravascular edema became significant.
CONCLUSIONS: The results suggest that occluder removal induces edema across the retina and choroid and that this fluid may be the vector eliciting choroidal expansion during recovery from form deprivation possibly driven by the hyperosmolarity in the choroid, RPE, and photoreceptor outer segments that accompanies deprivation.

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Year:  2004        PMID: 15277465     DOI: 10.1167/iovs.03-1009

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  29 in total

Review 1.  RPE and Choroid Mechanisms Underlying Ocular Growth and Myopia.

Authors:  Yan Zhang; Christine F Wildsoet
Journal:  Prog Mol Biol Transl Sci       Date:  2015-07-23       Impact factor: 3.622

2.  Light modulation, not choroidal vasomotor action, is a regulator of refractive compensation to signed optical blur.

Authors:  Melanie J Murphy; David P Crewther; Melinda J Goodyear; Sheila G Crewther
Journal:  Br J Pharmacol       Date:  2011-11       Impact factor: 8.739

3.  The role of temporal contrast and blue light in emmetropization.

Authors:  Frances Rucker; Mark Henriksen; Tiffany Yanase; Christopher Taylor
Journal:  Vision Res       Date:  2017-08-01       Impact factor: 1.886

Review 4.  Fixation strategies for retinal immunohistochemistry.

Authors:  Tyler W Stradleigh; Andrew T Ishida
Journal:  Prog Retin Eye Res       Date:  2015-04-17       Impact factor: 21.198

5.  Ionic control of ocular growth and refractive change.

Authors:  Sheila G Crewther; Helena Liang; Barbara M Junghans; David P Crewther
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-05       Impact factor: 11.205

6.  Parasympathetic influences on emmetropization in chicks: evidence for different mechanisms in form deprivation vs negative lens-induced myopia.

Authors:  Debora L Nickla; Falk Schroedl
Journal:  Exp Eye Res       Date:  2012-07-22       Impact factor: 3.467

Review 7.  IMI - Report on Experimental Models of Emmetropization and Myopia.

Authors:  David Troilo; Earl L Smith; Debora L Nickla; Regan Ashby; Andrei V Tkatchenko; Lisa A Ostrin; Timothy J Gawne; Machelle T Pardue; Jody A Summers; Chea-Su Kee; Falk Schroedl; Siegfried Wahl; Lyndon Jones
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-02-28       Impact factor: 4.799

8.  Spatial and temporal dissociation of AQP4 and Kir4.1 expression during induction of refractive errors.

Authors:  Melinda J Goodyear; Sheila G Crewther; Melanie J Murphy; Loretta Giummarra; Agnes Hazi; Barbara M Junghans; David P Crewther
Journal:  Mol Vis       Date:  2010-08-14       Impact factor: 2.367

9.  Opposing effects of atropine and timolol on the color and luminance emmetropization mechanisms in chicks.

Authors:  Laura A Goldberg; Frances J Rucker
Journal:  Vision Res       Date:  2016-03-19       Impact factor: 1.886

Review 10.  The multifunctional choroid.

Authors:  Debora L Nickla; Josh Wallman
Journal:  Prog Retin Eye Res       Date:  2009-12-29       Impact factor: 21.198

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