Literature DB >> 11311787

Progressive visual sensitivity loss in the Royal College of Surgeons rat: perimetric study in the superior colliculus.

Y Sauvé1, S V Girman, S Wang, J M Lawrence, R D Lund.   

Abstract

The Royal College of Surgeons rat has a retinal pigment epithelial cell defect which causes a progressive loss of rods occurring primarily over the first few months of life. We have studied the consequences of this degenerative process on visual sensitivity across the visual field. Sensitivities were determined in the superior colliculus for unit responses recorded from 22 days up to one year of age from sites encompassing the whole visual field representation. Following visual sensitivity assessment, retinae were examined anatomically at the light and electron microscopic level. At 22 days of age, sensitivities in dystrophic rats were comparable to those of non-dystrophics at any age (40+/-1 and 41+/-1dB, respectively), despite the fact that signs of degenerative events were clear at the electron microscopic level, including presence of pyknotic photoreceptor nuclei, disorganised outer segments and accumulation of debris. However, loss in sensitivity was first detected only at 28-36 days of age (27+/-4dB). From then on, sensitivities progressively decreased to reach a plateau by 180-240 days (4+/-2dB). Starting around 90 days and onward, there was a positive gradient of sensitivities from temporal to nasal field. Drops in visual sensitivity were parallelled by several changes in visual response properties, including prolonged latency, inconsistent responsiveness, appearance of bursting spontaneous activity and activation of units by stimuli presented outside their classical receptive fields. The measure of visual sensitivities by recording visual responses at specific sites in the superior colliculus provides a reliable point-to-point assessment of retinal function comparable to visual perimetry testing in humans. This experimental approach provides the background for answering questions arising during the development of potential experimental therapies for retinal degeneration using animal models like the Royal College of Surgeons rat.

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Year:  2001        PMID: 11311787     DOI: 10.1016/s0306-4522(00)00557-1

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  17 in total

1.  A new immunodeficient retinal dystrophic rat model for transplantation studies using human-derived cells.

Authors:  Biju B Thomas; Danhong Zhu; Tai-Chi Lin; Young Chang Kim; Magdalene J Seiler; Juan Carlos Martinez-Camarillo; Bin Lin; Yousuf Shad; David R Hinton; Mark S Humayun
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2018-09-13       Impact factor: 3.117

2.  Spatiotemporal characteristics of retinal response to network-mediated photovoltaic stimulation.

Authors:  Elton Ho; Richard Smith; Georges Goetz; Xin Lei; Ludwig Galambos; Theodore I Kamins; James Harris; Keith Mathieson; Daniel Palanker; Alexander Sher
Journal:  J Neurophysiol       Date:  2017-10-18       Impact factor: 2.714

3.  Discordant anatomical, electrophysiological, and visual behavioral profiles of retinal degeneration in rat models of retinal degenerative disease.

Authors:  Trevor J McGill; Glen T Prusky; Robert M Douglas; Douglas Yasumura; Michael T Matthes; Robert J Lowe; Jacque L Duncan; Haidong Yang; Kelly Ahern; Kate M Daniello; Byron Silver; Matthew M LaVail
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-09-14       Impact factor: 4.799

4.  Subretinal transplantation of genetically modified human cell lines attenuates loss of visual function in dystrophic rats.

Authors:  R D Lund; P Adamson; Y Sauvé; D J Keegan; S V Girman; S Wang; H Winton; N Kanuga; A S Kwan; L Beauchène; A Zerbib; L Hetherington; P O Couraud; P Coffey; J Greenwood
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

5.  Changes in physiological properties of rat ganglion cells during retinal degeneration.

Authors:  Chris Sekirnjak; Lauren H Jepson; Pawel Hottowy; Alexander Sher; Wladyslaw Dabrowski; A M Litke; E J Chichilnisky
Journal:  J Neurophysiol       Date:  2011-03-09       Impact factor: 2.714

6.  Cellular origin of spontaneous ganglion cell spike activity in animal models of retinitis pigmentosa.

Authors:  David J Margolis; Peter B Detwiler
Journal:  J Ophthalmol       Date:  2010-09-29       Impact factor: 1.909

7.  Loss of responses to visual but not electrical stimulation in ganglion cells of rats with severe photoreceptor degeneration.

Authors:  Chris Sekirnjak; Clare Hulse; Lauren H Jepson; Pawel Hottowy; Alexander Sher; Wladyslaw Dabrowski; A M Litke; E J Chichilnisky
Journal:  J Neurophysiol       Date:  2009-09-02       Impact factor: 2.714

8.  Protection of visual functions by human neural progenitors in a rat model of retinal disease.

Authors:  David M Gamm; Shaomei Wang; Bin Lu; Sergei Girman; Toby Holmes; Nicholas Bischoff; Rebecca L Shearer; Yves Sauvé; Elizabeth Capowski; Clive N Svendsen; Raymond D Lund
Journal:  PLoS One       Date:  2007-03-28       Impact factor: 3.240

9.  Functional changes in Tg P23H-1 rat retinal responses: differences between ON and OFF pathway transmission to the superior colliculus.

Authors:  James W Fransen; Gobinda Pangeni; Ian S Pyle; Maureen A McCall
Journal:  J Neurophysiol       Date:  2015-08-05       Impact factor: 2.714

Review 10.  Origins of spontaneous activity in the degenerating retina.

Authors:  Stuart Trenholm; Gautam B Awatramani
Journal:  Front Cell Neurosci       Date:  2015-07-29       Impact factor: 5.505

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