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Publication : The influence of genetic background on conventional outflow facility in mice.

First Author  Boussommier-Calleja A Year  2013
Journal  Invest Ophthalmol Vis Sci Volume  54
Issue  13 Pages  8251-8
PubMed ID  24235015 Mgi Jnum  J:215286
Mgi Id  MGI:5604993 Doi  10.1167/iovs.13-13025
Citation  Boussommier-Calleja A, et al. (2013) The influence of genetic background on conventional outflow facility in mice. Invest Ophthalmol Vis Sci 54(13):8251-8
abstractText  PURPOSE: Intraocular pressure (IOP) varies between genetically distinct strains of mice. The purpose was to test the hypothesis that strain-dependent differences in IOP are attributable to differences in conventional outflow facility (C). METHODS: The IOP was measured by rebound tonometry in conscious or anesthetized BALB/cJ, C57BL/6J, and CBA/J mice (N = 6-10 per strain). Conventional outflow facility was measured by ex vivo perfusion of enucleated eyes (N = 9-10 per strain). RESULTS: Conscious IOP varied between strains, being highest in CBA/J (14.5 +/- 0.9 mm Hg, mean +/- SD), intermediate in C57BL/6J (12.3 +/- 1.0 mm Hg), and lowest in BALB/cJ (10.6 +/- 1.8 mm Hg) mice. Anesthesia reduced IOP and eliminated any detectable differences between strains. Conventional outflow facility also varied between strains, but, in contrast to IOP, C was lowest in CBA/J (0.0113 +/- 0.0031 muL/min/mm Hg) and highest in BALB/cJ (0.0164 +/- 0.0059 muL/min/mm Hg). Like IOP, C was intermediate in C57BL/6J (0.0147 +/- 0.0029 muL/min/mm Hg). There was a strong correlation between conscious IOP and outflow resistance (1/C) from individual eyes across all three strains, revealing that 70% of the variation in IOP was attributable to variation in outflow resistance. CONCLUSIONS: Differences in IOP among three genetically distinct murine strains are attributable largely to differences in conventional outflow facility. These results motivate further studies using mice to identify the morphologic and genetic factors that underlie IOP regulation within the conventional outflow pathway.
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