期刊文献+

大鼠糖尿病性白内障晶状体中NADPH的实验研究

Analysis of lens NADPH activity in rat diabetic cataract
下载PDF
导出
摘要 目的研究分析糖尿病大鼠晶状体内还原型辅酶Ⅱ(nicotinamide adenine dinucleotide 2'-phosphate reduced tetrasodium salt,NADPH)的变化及其原因。方法通过腹腔注射链脲佐菌素诱导1型糖尿病大鼠模型,待典型白内障形成时,检测晶状体内NADPH的含量以及6-磷酸葡萄糖脱氢酶(glucose-6-phosphate dehydrogenase,G6PD)的活性,并与对照组进行比较。结果同对照组透明晶状体相比,糖尿病性白内障(diabetic cataract,DC)晶状体内NADPH含量明显减少,G6PD活性显著降低。结论 G6PD活性的降低引起的NADPH含量减少以及伴随的氧化损伤加剧,与DC的发生密切相关。 Objective To identify lens nicotinamide adenine dinucleotide 2′-phosphate re-duced tetrasodium salt ( NADPH) activity changes in diabetic rats .Methods Type 1 diabetes was induced by abdominal streptozotocin injection in rats .When characteristic cataracts were present in the diabetic rats , the levels of NADPH and G6PD activity were measured and com-pared with those in controls .Results Lens NADPH was significantly decreased and G 6 PD ac-tivity was also decreased greatly in rat diabetic cataract ( DC) compared with those in transpar-ent lenses of controls .Conclusion The decreases of G6PD activity result in lower levels of NADPH and subsequent increase of oxidative damage , which is highly associated with DC formation.
出处 《哈尔滨医科大学学报》 CAS 北大核心 2014年第6期479-481,共3页 Journal of Harbin Medical University
关键词 糖尿病性白内障 还原型辅酶Ⅱ 6-磷酸葡萄糖脱氢酶 diabetic cataract NADPH glucose-6-phosphate dehydrogenase
  • 相关文献

参考文献10

  • 1Obrosova IG, Chung SS, Kador PF. Diabetic cataracts: mecha- nisms and management [ J ]. Diabetes Metab Res Rev, 2010,26 (3) :172-180.
  • 2Kametaka S, Kasahara T, Ueo M, et al. A novel high resolution in vivo digital imaging system for the evaluation of experimental cataract in diabetic rats [ J ]. J Pharmacol Sci, 2008,106 (1) :144- 151.
  • 3Giblin FJ, Reddy VN. Pyridine nucleotides in ocular tissues as determined by the cycling assay[J]. Exp Eye Res, 1980, 31 (5) :601-609.
  • 4Dovrat A, Gershon D. Rat lens superexide dismutase and glueose- 6-phosphate dehydrogenase: studies on the catalytic activity and the fate" of enzyme antigen as a function of age[J]. Exp Eye Res, 1981,33 ( 6 ) :651-661.
  • 5Hashim Z, Zarina S. Antioxidant markers in human senile and di- abetic cataractous lenses[ J]. J Coll Physicians Surg Pak, 2006, 16(10) :637-640.
  • 6Obrosova IG. Increased sorbitol pathway activity generates oxida- tive stress in tissue sites for diabetic complications [ J ]. Antioxid Redox Signal, 2005',7(11-12) :1543-1552.
  • 7Spector A. Oxidative stress-induced cataract: mechanism of action [J]. FASEB J, 1995,9(12) :1173-1182.
  • 8刘平,苏胜.白内障蛋白质组学研究的现状及未来研究方向[J].眼科新进展,2014,34(1):1-4. 被引量:11
  • 9Gul A, Rahman MA, Hasnain SN. Role of fructose concentration on cataractogenesis in senile diabetic and non-diabetic patients [ J ]. Graefes Arch Clin Exp Ophthalmol, 2009,247 ( 6 ) : 809- 814.
  • 10Zhang S, Chai FY, Yan H, et al. Effects of N-aeetyleysteine and glutathione ethyl ester drops on streptozotoein-indueed diabetic cataract in rats [ J ]. Mol Vis, 2008,14 : 862-870.

二级参考文献2

共引文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部