INBIAS   27338
INSTITUTO DE BIOTECNOLOGIA AMBIENTAL Y SALUD
Unidad Ejecutora - UE
artículos
Título:
Prevention of tubulin/aldose reductase association delays the development of pathological complications in diabetic rats
Autor/es:
SANTANDER, VERÓNICA S.; PREVITALI, GABRIELA; CASALE, CÉSAR H.; NIGRA, AYELEN D.; PRIMO, EMILIANAO; RIVELLI ANTONELLI, JUAN F.; MONESTEROLO, NOELIA E.; OTERO, LISANDRO H.
Revista:
JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY
Editorial:
SERVICIO PUBLICACIONES UNIVERSIDAD NAVARRA
Referencias:
Lugar: Navarra; Año: 2021 vol. 77 p. 565 - 576
ISSN:
1138-7548
Resumen:
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 tubulindependent 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.