Literature DB >> 3100473

Immunohistochemical localization for aldose reductase in diabetic lenses.

Y Akagi, P F Kador, J H Kinoshita.   

Abstract

Sugar cataract formation has been demonstrated to result from lenticular sorbitol accumulation. In the lens, the activity of aldose reductase has been observed to increase with the onset of diabetes, while the activity of sorbitol dehydrogenase decreases. This shift in activities of these two Sorbitol Pathway enzymes favors the increased accumulation of sorbitol. Immunohistochemical studies with antibodies prepared against purified rat lens aldose reductase reveal a striking increase in immunoreactive positive staining for aldose reductase in lenses from diabetic rats. Two weeks after the onset of diabetes, increased immunohistochemical staining for aldose reductase appears beneath the epithelial region where water cleft formation occurs, and the intensity of this staining increases with the formation of vacuoles. By 6-8 weeks, the presence of large vacuoles and areas of liquifaction containing dense immunoreactive stain can be observed. Examination of human cataractous lenses with antibodies prepared against purified human placenta aldose reductase suggest similar increases in immunoreactive staining in the human diabetic lens. Cataractous lenses from diabetic patients revealed increased immunoreactive staining for aldose reductase, which was associated with the presence of vacuoles in both the anterior or posterior superficial cortical layers. Examination of similar vacuole containing regions from non-diabetic cataractous lenses revealed no increase in immunoreactive staining for aldose reductase. These results suggest that the enhanced activity of aldose reductase observed in diabetes is due to an increased amount of enzyme, rather than enzyme activation.

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Year:  1987        PMID: 3100473

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  8 in total

1.  Osmotic stress, not aldose reductase activity, directly induces growth factors and MAPK signaling changes during sugar cataract formation.

Authors:  Peng Zhang; Kuiyi Xing; James Randazzo; Karen Blessing; Marjorie F Lou; Peter F Kador
Journal:  Exp Eye Res       Date:  2012-06-15       Impact factor: 3.467

2.  In vitro expression of rat lens aldose reductase in Escherichia coli.

Authors:  S E Old; S Sato; P F Kador; D A Carper
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

Review 3.  Sorbitol, osmoregulation, and the complications of diabetes.

Authors:  M B Burg; P F Kador
Journal:  J Clin Invest       Date:  1988-03       Impact factor: 14.808

4.  Effect of an aldose reductase inhibitor on type IV collagen production by human endothelial cells cultured in high glucose.

Authors:  A Bakillah; A M Grigorova-Borsos; R Guillot; P Urios; M Sternberg
Journal:  Diabetologia       Date:  1996-06       Impact factor: 10.122

5.  Demonstration that polyol accumulation is responsible for diabetic cataract by the use of transgenic mice expressing the aldose reductase gene in the lens.

Authors:  A Y Lee; S K Chung; S S Chung
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

6.  Effects of galactose feeding on aldose reductase gene expression.

Authors:  R R Wu; P A Lyons; A Wang; A J Sainsbury; S Chung; T N Palmer
Journal:  J Clin Invest       Date:  1993-07       Impact factor: 14.808

7.  Transient elevation of aldose reductase mRNA in lens of rats developing galactose cataracts.

Authors:  S Shi; N J Unakar; Y Wen; J Tsui; I Bekhor
Journal:  Mol Cell Biochem       Date:  1992-09-22       Impact factor: 3.396

8.  A simple and stable galactosemic cataract model for rats.

Authors:  Lixia Ji; Caina Li; Ning Shen; Yi Huan; Quan Liu; Shuainan Liu; Zhufang Shen
Journal:  Int J Clin Exp Med       Date:  2015-08-15
  8 in total

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