Literature DB >> 34097242

Prevention of tubulin/aldose reductase association delays the development of pathological complications in diabetic rats.

Juan F Rivelli Antonelli1,2, Verónica S Santander1,2, Ayelen D Nigra1,2, Noelia E Monesterolo1,2, Gabriela Previtali1,2, Emilianao Primo1,2, Lisandro H Otero3, César H Casale4,5.   

Abstract

In recent studies, we found that compounds derived from phenolic acids (CAFs) prevent the formation of the tubulin/aldose reductase complex and, consequently, may decrease the occurrence or delay the development of secondary pathologies associated with aldose reductase activation in diabetes mellitus. To verify this hypothesis, we determined the effect of CAFs on Na+,K+-ATPase tubulin-dependent activity in COS cells, ex vivo cataract formation in rat lenses and finally, to evaluate the antidiabetic effect of CAFs, diabetes mellitus was induced in Wistar rats, they were treated with different CAFs and four parameters were determinates: cataract formation, erythrocyte deformability, nephropathy and blood pressure. After confirming that CAFs are able to prevent the association between aldose reductase and tubulin, we found that treatment of diabetic rats with these compounds decreased membrane-associated acetylated tubulin, increased NKA activity, and thus reversed the development of four AR-activated complications of diabetes mellitus determined in this work. Based on these results, the existence of a new physiological mechanism is proposed, in which tubulin is a key regulator of aldose reductase activity. This mechanism can explain the incorrect functioning of aldose reductase and Na+,K+-ATPase, two key enzymes in the pathogenesis of diabetes mellitus. Moreover, we found that such alterations can be prevented by CAFs, which are able to dissociate tubulin/aldose reductase complex.
© 2021. University of Navarra.

Entities:  

Keywords:  Aldose reductase; Diabetes; Phenolic acids; Tubulin

Mesh:

Substances:

Year:  2021        PMID: 34097242     DOI: 10.1007/s13105-021-00820-1

Source DB:  PubMed          Journal:  J Physiol Biochem        ISSN: 1138-7548            Impact factor:   4.158


  35 in total

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Authors:  C H Casale; A D Alonso; H S Barra
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

2.  Erythrocyte Na(+)-K(+)-ATPase activity, metabolic control, and neuropathy in IDDM patients.

Authors:  D Raccah; C Fabreguetts; J P Azulay; P Vague
Journal:  Diabetes Care       Date:  1996-06       Impact factor: 19.112

3.  Decreased Na/K ATPase ouabain binding sites in red blood cells of patients with insulin-dependent diabetes and healthy north African control subjects: relationship with diabetic neuropathy.

Authors:  D Raccah; F Dadoun; T Coste; P Vague
Journal:  Horm Metab Res       Date:  1996-03       Impact factor: 2.936

4.  Effect of antioxidant treatment of streptozotocin-induced diabetic rats on endoneurial blood flow, motor nerve conduction velocity, and vascular reactivity of epineurial arterioles of the sciatic nerve.

Authors:  L J Coppey; J S Gellett; E P Davidson; J A Dunlap; D D Lund; M A Yorek
Journal:  Diabetes       Date:  2001-08       Impact factor: 9.461

5.  Synthesis and rat lens aldose reductase inhibitory activity of some benzopyran-2-ones.

Authors:  A N Brubaker; J DeRuiter; W L Whitmer
Journal:  J Med Chem       Date:  1986-06       Impact factor: 7.446

6.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

7.  Purification of the synaptosomal plasma membrane (Ca(2+) + Mg(2+))-ATPase from pig brain.

Authors:  J M Salvador; A M Mata
Journal:  Biochem J       Date:  1996-04-01       Impact factor: 3.857

8.  Glomerular Na+-K+-ATPase activity in acute and chronic diabetes and with aldose reductase inhibition.

Authors:  M P Cohen; H Klepser
Journal:  Diabetes       Date:  1988-05       Impact factor: 9.461

9.  High glucose levels induce inhibition of Na,K-ATPase via stimulation of aldose reductase, formation of microtubules and formation of an acetylated tubulin/Na,K-ATPase complex.

Authors:  Juan F Rivelli; Marina R Amaiden; Noelia E Monesterolo; Gabriela Previtali; Verónica S Santander; Adriana Fernandez; Carlos A Arce; Cesar H Casale
Journal:  Int J Biochem Cell Biol       Date:  2012-04-27       Impact factor: 5.085

Review 10.  C-peptide, Na+,K(+)-ATPase, and diabetes.

Authors:  P Vague; T C Coste; M F Jannot; D Raccah; M Tsimaratos
Journal:  Exp Diabesity Res       Date:  2004 Jan-Mar
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