Selective loss of orientation column maps in visual cortex during brief elevation of intraocular pressure

Investigative Ophthalmology and Visual Science

Volumn 44, Issue 1, 2003, Pages 435-441

  Chen, Xin ^a   Sun, Chao ^a   Huang, Luoxiu ^a   Shou, Tiande ^a,b  

^a FUDAN UNIVERSITY   (China)

^b INSTITUTE OF BIOPHYSICS   (China)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHLORIDE;

ANIMAL EXPERIMENT; ANTERIOR EYE CHAMBER; ARTICLE; BRAIN FUNCTION; BRAIN MAPPING; INTRAOCULAR HYPERTENSION; NONHUMAN; PERFUSION PRESSURE; PRIORITY JOURNAL; RETINA BLOOD FLOW; SPATIAL FREQUENCY DISCRIMINATION; VISUAL CORTEX; VISUAL IMPAIRMENT; VISUAL ORIENTATION; VISUAL STIMULATION; VISUAL SYSTEM;

ANIMALS; BLOOD PRESSURE; CATS; HYPERTENSION; INTRAOCULAR PRESSURE; OCULAR HYPERTENSION; ORIENTATION; PERCEPTUAL DISORDERS; RETINA; VISUAL CORTEX;

EID: 0037251295     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.02-0194     Document Type: Article

References (43)

1. Wulfing B. Clinical electroretino-dynamography. Doc Ophthalmol. 1964;18:419-429.
2. Fox WD, Black R, Bourne JR. Visual evoked cortical potentials during pressure-blinding. Vision Res. 1973;13:501-503.
3. Shou T, Yang G, Zhang KA. Comparative study of the effect of intraocular pressure elevation on ERG and VECP in the rabbit [in Chinese]. Acta Physiol Sinica. 1985;37:567-571.
4. Siliprandi R, Bucci MG, Canella, Carmignoto G. Flash and pattern electroretinograms during and after acute intraocular pressure elevation in cats. Invest Ophthalmol Vis Sci. 1988;29:558-565.
5. Hayreh SS, Revie IH, Edwards J. Vasogenic origin of visual field defects and optic nerve changes in glaucoma. Br J Ophthalmol. 1971;54:461-469.
6. Grehn F, Prost M. Function of retinal nerve fibers depends on perfusion pressure: neurophysiologic investigations during acute pressure elevation. Invest Ophthalmol Vis Sci. 1983;24:347-357.
7. Dondona L, Hendrickson A, Quigley HA. Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus. Invest Ophthalmol Vis Sci. 1991;32:1593-1599.
8. Ochoa J, Fowler TJ, Gilliatt RW. Anatomical change in peripheral nerves compressed by a pneumatic tourniquet. J Anat. 1972;113:433-455.
9. Hubel DH, Wiesel TN. Receptive fields, binocular interaction and functional architecture in the cat's visual cortex. J Physiol. 1962;160:106-154.
10. Hubel DH, Wiesel TN. Sequence regularity and geometry of orientation columns in the monkey striate cortex. J Comp Neurol. 1974;158:267-294.
11. Shou T, Zhou Y. Y cells in the cat retina are more tolerant than X cells to brief elevation of IOP. Invest Ophthalmol Vis Sci. 1989;30:2093-2098.
12. Zhou Y, Wang W, Ren B, Shou T. Receptive field properties of cat retinal ganglion cells during short-term elevation of IOP. Invest Ophthalmol Vis Sci. 1994;35:2758-2754.
13. Shou T, Zhou Y. Incremental IOP for abolishing the response of cat LGN Y cells and X cells to flash stimulation of the eye. Chin J Physiol Sci. 1990;6:95-99.
14. Enroth-Cugell C, Robson JG. The contrast sensitivity of retinal ganglion cells of the cat. J Physiol. 1966;187:517-552.
15. Cleland BG, Dubin MW, Levick WR. Sustained and transient neurons in cat's retina and lateral geniculate nucleus. J Physiol. 1971;217:473-496.
16. Cleland BG, Levick WR, Wässle H. Physiological identification of a morphological class of cat retinal ganglion cells. J Physiol. 1975;248:151-171.
17. Fukuda Y, Stone J. Retinal distribution and central projections of Y-, X-, and W-cells of the cat's retina. J Neurophysiol. 1974;38:749-772.
18. Grinvald A, Lieke E, Frostig RD, et al. Functional organization of primate visual cortex revealed by optical imaging of intrinsic signals. Nature. 1986;324:361-364.
19. Haglund MM, Ojemann GA, Hochman DW. Optical imaging of epileptic form and functional activity in human cerebral cortex. Nature. 1992;358:668-671.
20. Yu H, Shou T. The oblique effect revealed by optical imaging in primary visual cortex of cats [in Chinese]. Acta Physiol Sinica. 2000;52:431-434.
21. Bonhoeffer T, Grinvald A. Optical imaging based on intrinsic signals: the methodology. In: Toga AW, Mazziotta JC, eds, Brain Mapping: The Methods. London: Academic Press; 1996:55-97.
22. Fernald R, Chase R. An improved method for plotting retinal landmarks and focusing the eye. Vision Res. 1971;11:95-96.
23. Zhang K, Yu H, Shou T. The establishment of optical imaging system based on intrinsic signals [in Chinese]. Acta Biophys Sinica. 1999;15:597-604.
24. Ratzlaff HE, Grivald A. A tandem-lens epifluorescence microscope: hundred-fold brightness advantage for wide-field imaging. J Neurosci Methods. 1991;36:127-137.
25. Godecke I, Bonhoeffer T. Development of identical orientation maps for two eyes without common visual experience. Nature. 1996;379:251-254.
26. Movshon JA, Thompson ID, Tohurst DJ, Spatial and temporal contrast sensitivity of neurons in areas 17 and 18 of the cat's visual cortex. J Physiol. 1978;283:101-120.
27. Issa NP, Trepel C, Stryker MP. Spatial frequency maps in cat visual cortex. J Neurosci. 2000;20:8504-8514.
28. Shoham D, Hubener M, Schulze S, Grinvald A, Bonhoeffer T. Spatio-temporal frequency domains and their relation to cytochrome oxidase staining in cat visual cortex. Nature. 1997;385:529-532.
29. Hung CP, Ramsden BM, Chen LM, Roe AW. Building surface from borders in areas 17 and 18 of the cat. Vision Res. 2001;41:1389-1407.
30. Dreher B, Fukuda Y, Rodieck RM. Identification and anatomical segregation of cells with X-like and Y-like properties in the lateral geniculate nucleus of old-world primates. J Physiol. 1976;258:433-452.
31. Kirk DL, Cleland BG, Levick WR. Axonal conduction latencies of cat retinal ganglion cells. J Neurophysiol. 1975;38:1395-1402.
32. Sherman SM, Spear PD. Organization of visual pathways in normal and visually deprived cats. Physiol Rev. 1982;62:738-855.
33. Tusa RJ, Palman LA, Rosenquist AC. The retinotopic organization of area 17 (striate cortex) in the cat. J Comp Neurol. 1978;177:213-236.
34. Wässl H, Boycott BB, Illing RB. Morphology and lattice of on- and off- beta cells in the cat retina and some functional considerations. Proc R Soc Lond Biol Sci. 1981;212:177-195.
35. Zhan X, Troy JB. Modeling cat retinal beta-cell arrays. Vis Neurosci. 2000;17:23-39.
36. Chapman B, Styker MP, Bonhoeffer T. Development of orientation preference maps in ferret primary visual cortex. J Neurosci. 1996;16:6443-6453.
37. Levick WR, Thibos LN. Analysis of orientation bias in cat retina. J Physiol. 1982;329:243-261.
38. Shou T, Ruan D, Zhou Y. The orientation bias of LGN neurons shows topographic relation to area centralis in the cat retina. Exp Brain Res. 1986;64:233-236.
39. Shou T, Leventhal AG. Organized arrangement of orientation-sensitive relay cells in the cat's dorsal lateral geniculate nucleus. J Neurosci. 1989;9:4387-4302.
40. Soodak RE, Shapley, RM, Kaplan E. Linear mechanism of orientation tuning in the retina and lateral geniculate nucleus of the cat. J Neurophysiol. 1987;58:267-274.
41. Ferster D, Chung S, Weat H. Orientation selectivity of thalamic input of simple cells of cat visual cortex. Nature. 1996;380:249-252.
42. Zhou Y, Leventhal AG, Thompson KG. Visual deprivation does not affect the orientation and direction sensitivity of relay cells in the lateral geniculate nucleus of the cat. J Neurosci. 1995;15:189-198.
43. Chapman B, Godecke I. Cortical cell orientation selectivity fails to develop in the absence of on-center ganglion cell activity. J Neurosci. 2000;20:1922-1930.