Literature DB >> 3098544

Aldose reductase inhibitors and late complications of diabetes.

P Benfield.   

Abstract

Neuropathy and retinopathy are two potentially serious late complications of diabetes. There is accumulating evidence that the development of these conditions is closely related to increased activity of the polyol pathway, which occurs in certain tissues as a consequence of long term hyperglycaemia. Symptomatic diabetic neuropathy may appear as one of many forms and is frequently accompanied by pain. Diabetic retinopathy is a progressive degeneration of the retina that represents one of the major causes of blindness in the developed world. A good prognosis for either of these conditions is believed to rely on early diagnosis and optimisation of glycaemic control as they become less reversible with progression of cellular damage. A new approach to the treatment of these and other late complications of diabetes may be offered by recently developed drugs, such as sorbinil, that inhibit the enzyme aldose reductase. In various animal models of late complications of diabetes sorbinil and other aldose reductase inhibitors have been shown to reverse some of the biochemical and physiological changes believed to underlie these complications. These include prevention or reversal of the accumulation of sorbitol and depletion of myo-inositol in nerve, lens and renal glomeruli. Sorbinil also counteracts the slowing of nerve conduction velocities, reverses the structural changes of Sipple stages I and II cataracts and prevents proteinuria in diabetic rats. Orally administered sorbinil is absorbed rapidly and reaches steady state plasma concentrations after 6 to 10 days' administration. Its elimination half-life is long (38-52 hours) and much greater than that of another aldose reductase inhibitor, tolrestat (10-12 hours). Within the dose range 50-250 mg about one-third of administered sorbinil appears in the urine as unchanged drug. In the small number of clinical studies of diabetic patients with neuropathies sorbinil has demonstrated limited therapeutic effects. There is now a requirement for studies of its prophylactic use and its therapeutic use in patients with diabetic neuropathy in the early stages of development.

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Year:  1986        PMID: 3098544     DOI: 10.2165/00003495-198600322-00010

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  42 in total

1.  Aldose reductase inhibition, glomerular metabolism, and diabetic nephropathy.

Authors:  M Cohen
Journal:  Diabet Med       Date:  1985-05       Impact factor: 4.359

2.  Tolrestat kinetics.

Authors:  D R Hicks; M Kraml; M N Cayen; J Dubuc; S Ryder; D Dvornik
Journal:  Clin Pharmacol Ther       Date:  1984-10       Impact factor: 6.875

3.  Assessment of cardiovascular effects in diabetic autonomic neuropathy and prognostic implications.

Authors:  D J Ewing; I W Campbell; B F Clarke
Journal:  Ann Intern Med       Date:  1980-02       Impact factor: 25.391

4.  Aldose reductase inhibition: studies with alrestatin.

Authors:  K H Gabbay; N Spack; S Loo; H J Hirsch; A A Ackil
Journal:  Metabolism       Date:  1979-04       Impact factor: 8.694

5.  Glomerular polyol accumulation in diabetes and its prevention by oral sorbinil.

Authors:  A Beyer-Mears; L Ku; M P Cohen
Journal:  Diabetes       Date:  1984-06       Impact factor: 9.461

6.  A controlled trial of sorbinil, an aldose reductase inhibitor, in chronic painful diabetic neuropathy.

Authors:  R J Young; D J Ewing; B F Clarke
Journal:  Diabetes       Date:  1983-10       Impact factor: 9.461

7.  Effects of a fructose-rich diet and the aldose reductase inhibitor, ONO-2235, on the development of diabetic neuropathy in streptozotocin-treated rats.

Authors:  N Hotta; H Kakuta; H Fukasawa; M Kimura; N Koh; M Iida; H Terashima; T Morimura; N Sakamoto
Journal:  Diabetologia       Date:  1985-03       Impact factor: 10.122

8.  The effects of an aldose reductase inhibitor upon the sorbitol pathway, fructose-1-phosphate and lactate in the retina and nerve of streptozotocin-diabetic rats.

Authors:  R Poulsom; D J Mirrlees; D C Earl; H Heath
Journal:  Exp Eye Res       Date:  1983-05       Impact factor: 3.467

9.  Inhibition of galactose-induced alterations in ocular lens with sorbinil.

Authors:  N J Unakar; J Y Tsui
Journal:  Exp Eye Res       Date:  1983-05       Impact factor: 3.467

10.  The effects of a new aldose reductase inhibitor (tolrestat) in galactosemic and diabetic rats.

Authors:  N Simard-Duquesne; E Greselin; J Dubuc; D Dvornik
Journal:  Metabolism       Date:  1985-10       Impact factor: 8.694

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  4 in total

1.  myo-Inositol oxygenase: molecular cloning and expression of a unique enzyme that oxidizes myo-inositol and D-chiro-inositol.

Authors:  R J Arner; K S Prabhu; J T Thompson; G R Hildenbrandt; A D Liken; C C Reddy
Journal:  Biochem J       Date:  2001-12-01       Impact factor: 3.857

2.  Proteomic changes associated with diabetes in the BB-DP rat.

Authors:  D Thor Johnson; Robert A Harris; Stephanie French; Angel Aponte; Robert S Balaban
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-11-04       Impact factor: 4.310

3.  Sorbitol metabolism in retina studied in vitro.

Authors:  P Naeser; S E Brolin; U J Eriksson
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1989       Impact factor: 3.117

4.  Sodium glucose cotransporter 2 in mesangial cells and retinal pericytes and its implications for diabetic nephropathy and retinopathy.

Authors:  Masarori Wakisaka; Tetsuhiko Nagao
Journal:  Glycobiology       Date:  2017-08-01       Impact factor: 4.313

  4 in total

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