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Drinking water supplementation with ascorbate is not protective against UVR-B-induced cataract in the guinea pig

机译:补充抗坏血酸的饮用水不能预防UVR-B诱导的豚鼠白内障

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Purpose: To study if ascorbate supplementation decreases ultraviolet radiation (UVR)-induced cataract development in the guinea pig.Methods: Sixty 6-9-week-old pigmented guinea pigs received drinking water supplemented with or without 5.5 mm L-ascorbate for 4 weeks. After supplementation, 40 animals were exposed unilaterally in vivo under anaesthesia to 80 kJ/m2 UVR-B. One day later, the animals were killed and lenses were extracted. Degree of cataract was quantified by measurement of intensity of forward lens light scattering. Lens ascorbate concentration was determined with high-performance liquid chromatography (HPLC) with UVR detection at 254 nm. Twenty animals were used as non-exposed control.Results: Supplementation increased lens ascorbate concentration significantly. In UVR-exposed animals, mean 95% confidence intervals (CIs) for animal-averaged lens ascorbate concentration (mumol/g wet weight lens) were 0.54 +-0.07 (no ascorbate) and 0.83 +-0.05 (5.5 mM ascorbate). In non-exposed control animals, mean 95% CIs for animal-averaged lens ascorbate concentration (mumol/g wet weight lens) were 0.72 +-0.12 (0 mM ascorbate) and 0.90 +-0.15 (5.5 mM ascorbate). All non-exposed lenses were devoid of cataract. Superficial anterior cataract developed in all UVR-exposed lenses. The lens light scattering was 39.2 +-14.1 milli transformed equivalent diazepam concentration (m(tEDC)) without and 35.9 +-14.0 m(tEDC) with ascorbate supplementation. Conclusion: Superficial anterior cataract develops in lenses exposed to UVR-B. Ascorbate supplementation is non-toxic to both UVR-B-exposed lenses and non-exposed control lenses. Ascorbate supplementation does not reduce in vivo lens forward light scattering secondary to UVR-B exposure in the guinea pig.
机译:目的:研究补充抗坏血酸是否会降低豚鼠紫外线(UVR)诱发的白内障发展。方法:60只6-9周龄的有色豚鼠接受饮用水补充或不添加5.5mm L-抗坏血酸4周。 。补充后,将40只动物在麻醉下体内单侧暴露于80kJ / m 2 UVR-B。一天后,将动物处死并取出晶状体。白内障的程度通过测量前向透镜光散射的强度来量化。镜头抗坏血酸浓度通过高效液相色谱(HPLC)在254 nm处进行UVR检测来确定。 20只动物作为未暴露的对照组。结果:补充物显着增加了晶状体抗坏血酸的浓度。在暴露于UVR的动物中,动物平均晶状体抗坏血酸浓度(mumol / g湿重晶状体)的平均95%置信区间(CIs)为0.54 + -0.07(无抗坏血酸)和0.83 + -0.05(5.5 mM抗坏血酸)。在未暴露的对照动物中,动物平均晶状体抗坏血酸浓度(mumol / g湿重晶状体)的平均95%CI为0.72 + -0.12(0 mM抗坏血酸)和0.90 + -0.15(5.5 mM抗坏血酸)。所有未曝光的镜片都没有白内障。所有暴露于UVR的晶状体均出现浅表性白内障。透镜光散射为无添加时为39.2 + -14.1毫安换算当量地西epa浓度(m(tEDC))和补充抗坏血酸时为35.9 + -14.0 m(tEDC)。结论:暴露于UVR-B的晶状体表面浅表白内障发生。抗坏血酸补充剂对暴露于UVR-B的镜片和未暴露的对照镜片均无毒。补充抗坏血酸不会减少豚鼠体内继UVR-B暴露后的体内晶状体前向光散射。

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