TY - JOUR
T1 - Effect of vitamin C depletion on UVR-B induced cataract in SMP30/GNL knockout mice
AU - Ishikawa, Yohei
AU - Hashizume, Kouhei
AU - Kishimoto, Seishi
AU - Tezuka, Yu
AU - Nishigori, Hideo
AU - Yamamoto, Naoki
AU - Kondo, Yoshitaka
AU - Maruyama, Naoki
AU - Ishigami, Akihito
AU - Kurosaka, Daijiro
PY - 2012/1
Y1 - 2012/1
N2 - We investigated whether decreased vitamin C (VC) in a mouse model increases lens opacity (cataract) induced by invivo exposure to ultraviolet radiation type B (UVR-B).Senescence marker protein-30 (SMP30) knockout (KO) mice, which cannot synthesize VC due to genetic disruption of the gluconolactonase (GNL) gene, were divided into 2 groups: VC sufficient (VC (+)) and VC deficient (VC (-)). Starting at 1 month of age, these groups had free access to water containing 0.0375 and 1.5g/L of VC, respectively. SMP30 KO VC (-), SMP30 KO VC (+), and wild-type (WT) mice, all 14 weeks of age, were unilaterally exposed invivo to UVR-B (200mW/cm 2) for 100s twice a week for 3 weeks (total: 1200mJ/cm 2). At 48h after the last UVR-B exposure, cataract morphology was documented, and the ratio of cataract induction was quantified as the cataract area ratio (opacity area/anterior capsule).UVR-B exposure induced cataract mainly at anterior sub-capsular in SMP30 KO VC (-), SMP30 KO VC (+), and WT mice. In SMP30 KO VC (-) lenses the opacities were more extensive than in SMP30 KO VC (+) or WT lenses (cataract area ratios: 59.3%±10% vs. 32.2%±11.7% or 29.0%±9.0%; P<0.01).In conclusion, VC depletion may increase the susceptibility to develop UVR-B induced cataracts in mice unable to endogenously produce VC.
AB - We investigated whether decreased vitamin C (VC) in a mouse model increases lens opacity (cataract) induced by invivo exposure to ultraviolet radiation type B (UVR-B).Senescence marker protein-30 (SMP30) knockout (KO) mice, which cannot synthesize VC due to genetic disruption of the gluconolactonase (GNL) gene, were divided into 2 groups: VC sufficient (VC (+)) and VC deficient (VC (-)). Starting at 1 month of age, these groups had free access to water containing 0.0375 and 1.5g/L of VC, respectively. SMP30 KO VC (-), SMP30 KO VC (+), and wild-type (WT) mice, all 14 weeks of age, were unilaterally exposed invivo to UVR-B (200mW/cm 2) for 100s twice a week for 3 weeks (total: 1200mJ/cm 2). At 48h after the last UVR-B exposure, cataract morphology was documented, and the ratio of cataract induction was quantified as the cataract area ratio (opacity area/anterior capsule).UVR-B exposure induced cataract mainly at anterior sub-capsular in SMP30 KO VC (-), SMP30 KO VC (+), and WT mice. In SMP30 KO VC (-) lenses the opacities were more extensive than in SMP30 KO VC (+) or WT lenses (cataract area ratios: 59.3%±10% vs. 32.2%±11.7% or 29.0%±9.0%; P<0.01).In conclusion, VC depletion may increase the susceptibility to develop UVR-B induced cataracts in mice unable to endogenously produce VC.
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U2 - 10.1016/j.exer.2011.11.010
DO - 10.1016/j.exer.2011.11.010
M3 - Article
C2 - 22155581
AN - SCOPUS:84855846986
SN - 0014-4835
VL - 94
SP - 85
EP - 89
JO - Experimental Eye Research
JF - Experimental Eye Research
IS - 1
ER -