Quantitative correlation of optic nerve pathology with ocular pressure and corneal thickness in the DBA/2 mouse model of glaucoma

被引:109
作者
Inman, DM
Sappington, RM
Horner, PJ
Calkins, DJ
机构
[1] Univ Washington, Dept Neurosurg, Harborview Res & Training, Seattle, WA 98104 USA
[2] Vanderbilt Univ, Med Ctr, Dept Ophthalmol & Visual Sci, Nashville, TN USA
关键词
D O I
10.1167/iovs.05-0925
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To investigate quantitatively the relationships between elevated intraocular pressure (IOP), axonal loss, and corneal thickness in the DBA/2 mouse model of glaucoma, to understand better how these factors contribute to disease progression. METHODS. IOP was measured with a handheld tonometer (Tono-Pen; Medtronic Solan, Jacksonville, FL) in 195 to 446 eyes of mice 2 to 10 months of age sampled from a colony of 400 DBA/2 mice. From a group of 24 eyes at 4, 9, and 10 months of age, correlations were determined between the density and number of RGC axons, corneal thickness, and IOP. RESULTS. Mean IOP levels in the colony were 15 to 16 turn Hg at 2 months of age and rose almost linearly at a rate of 0.9 mm Hg/mo before reaching 22 to 23 mm Hg at 10 months. Both the density and number of axons decreased with increasing average lifetime IOP. IOP variation within age groups strongly correlated with density. Age-matched mice with lower mean IOP had greater preservation of axons in the optic nerve. Elevated IOP was accompanied by increased corneal thickness at the limbus. Surprisingly, corneal thickness was a strong predictor of axonal density (r(2) = -0.75), regardless of age. CONCLUSIONS. IOP increased with age in most, but not all, DBA/2 mice. In age-matched mice, differences in IOP corresponded to differences in axonal density and number. In young mice with elevated IOP, the loss of axons resembled that of older animals with similar IOP. Whether corneal thickness is a byproduct of elevated IOP remains unknown, but it may be useful as an index of optic nerve degeneration.
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页码:986 / 996
页数:11
相关论文
共 36 条
[1]  
ANDERSON DR, 1983, OPHTHALMOLOGY, V90, P766
[2]   Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice [J].
Anderson, MG ;
Smith, RS ;
Hawes, NL ;
Zabaleta, A ;
Chang, B ;
Wiggs, JL ;
John, SWM .
NATURE GENETICS, 2002, 30 (01) :81-85
[3]  
Avila MY, 2001, INVEST OPHTH VIS SCI, V42, P1841
[4]   The influence of corneal thickness on the diagnosis and management of glaucoma [J].
Brandt, JD .
JOURNAL OF GLAUCOMA, 2001, 10 (05) :S65-S67
[5]   Morphological identification of ganglion cells expressing the a subunit of type II calmodulin-dependent protein kinase in the macaque retina [J].
Calkins, DJ ;
Sappington, RM ;
Hendry, SHC .
JOURNAL OF COMPARATIVE NEUROLOGY, 2005, 481 (02) :194-209
[6]   Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice [J].
Chang, B ;
Smith, RS ;
Hawes, NL ;
Anderson, MG ;
Zabaleta, A ;
Savinova, O ;
Roderick, TH ;
Heckenlively, JR ;
Davisson, MT ;
John, SWM .
NATURE GENETICS, 1999, 21 (04) :405-409
[7]  
Cohan BE, 2001, INVEST OPHTH VIS SCI, V42, P2560
[8]  
Copt RP, 1999, ARCH OPHTHALMOL-CHIC, V117, P14
[9]   Quantitative analysis of retinal ganglion cell (RGC) loss in aging DBA/2NNia glaucomatous mice: Comparison with RGC loss in aging C57/BL6 mice [J].
Danias, J ;
Lee, KC ;
Zamora, MF ;
Chen, B ;
Shen, F ;
Filippopoulos, T ;
Su, YL ;
Goldblum, D ;
Podos, SM ;
Mittag, T .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (12) :5151-5162
[10]   Method for the noninvasive measurement of intraocular pressure in mice [J].
Danias, J ;
Kontiola, AI ;
Filippopoulos, T ;
Mittag, T .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (03) :1138-1141