1985
DOI: 10.2337/diab.34.1.15
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Reversal of Diabetic Cataract by Sorbinil, an Aldose Reductase Inhibitor

Abstract: Aldose reductase is implicated in the pathogenesis of diabetic cataracts; therefore, inhibition of this enzyme subsequent to cataractogenesis may represent a therapeutic approach for restoration of lens physiology. In the present study, the effect of aldose reductase inhibition subsequent to stage I cataract formation was investigated in the streptozocin-induced diabetic rat. Our results indicated that the aldose reductase inhibitor sorbinil, a spirohydantoin, arrested further progression and promoted a repara… Show more

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Cited by 70 publications
(41 citation statements)
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“…Nine anthraquinones, aurantio-obtusin (1), chryso-obtusin (2), obtusin (3), chryso-obtusin-2-O-b-D-glucoside (4), physcion (5), emodin (6), chrysophanol (7), obtusifolin (8), and obtusifolin-2-O-b-D-glucoside (9) were isolated from an EtOAc-soluble extract of the seeds of Cassia tora. The structures of the known compounds were identified by physical and spectroscopic data (mp, 1 H-, 13 C-NMR, and MS) measurement and by comparison with published values.…”
Section: Resultsmentioning
confidence: 99%
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“…Nine anthraquinones, aurantio-obtusin (1), chryso-obtusin (2), obtusin (3), chryso-obtusin-2-O-b-D-glucoside (4), physcion (5), emodin (6), chrysophanol (7), obtusifolin (8), and obtusifolin-2-O-b-D-glucoside (9) were isolated from an EtOAc-soluble extract of the seeds of Cassia tora. The structures of the known compounds were identified by physical and spectroscopic data (mp, 1 H-, 13 C-NMR, and MS) measurement and by comparison with published values.…”
Section: Resultsmentioning
confidence: 99%
“…18) Previous phytochemical investigation on the seeds of C. tora have resulted in the isolation of several anthraquinone and naphthopyrone derivatives. 13,[16][17][18][19][20] In the present study, further fractionation of the EtOAc-soluble extract of the seeds of C. tora led to the purification of nine anthraquinones (1)(2)(3)(4)(5)(6)(7)(8)(9). The structures of 1-9 were determined by spectroscopic data interpretation and they were subjected to in vitro bioassays to evaluate their inhibitory activity against AGEs and RLAR.…”
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confidence: 99%
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“…25) Therefore, the EPS-stimulated Nrf2 activation is most likely achieved by altering Keap1 structure. Unlike EPS, other aldose reductase inhibitors, such as sorbinil and alrestatin, 26,27) failed to increase HO-1 levels (data not shown). This result indicates that sorbinil and alrestatin, which do not have an α,β-unsaturated aldehyde or ketone, have no influence on the Nrf2 pathway.…”
Section: )mentioning
confidence: 99%
“…3) Evidence suggests that compounds that inhibit AR could be effective in the prevention of diabetic complications. A number of structurally diverse naturally occurring and synthetic AR inhibitors have been studied in vivo to clarify their effectiveness in the prevention of diabetic complications in experimental animals, 4) as well as in clinical trials. 5) Specific inhibitors of the enzyme may be therapeutically attractive agents for the prevention and/or treatment of diabetic complications.…”
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confidence: 99%