Effect of Glycated Albumin in the expression of glucose transporter GLUT4 in adipose cell: potencial participation of transcription factor NFKB

• Grant number: 16/17002-4
• Support Opportunities: Scholarships in Brazil - Master
• Start date: December 01, 2016
• End date: July 31, 2018
• Field of knowledge: Biological Sciences - Physiology - Physiology of Organs and Systems
• Principal Investigator: Ubiratan Fabres Machado
• Grantee: Maria Luiza Estimo Michalani Toledo
• Host Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil

Abstract

Diabetes mellitus (DM) is a chronic disease characterized by the loss of glycemic homeostasis. With the progression of the disease, there is an establishment of a chronic hyperglycemia condition, which results in accelerated formation of advanced glycated end products (AGEs), that may compromise the uptake glucose ability by muscle and adipose tissues, contributing to the loss of glycemic homeostasis.The interaction between the RAGE receptor with AGE generates an oxidative stress capable of activates the NFKB pathway, a transcriptional factor that can either stimulate gene transcriptional (for example, Ager and Nfkb1 genes) or inhibit the gene transcriptional (for example, Slc2a4 gene). The Slc2a4 gene expressed in musle and adipose cells and it encodes the GLUT4 transporter, which is translocated to the plasma membrane, under stimulation of insulin, increasing glucose uptake, and, thereby regulating glycemic homeostasis.Although AGEs are studied in the pathogenesis of diabetes complication, little or nothing is known about its potential contribution to the impairment of glucose uptake by muscle and adipose tissue characteristic of the diabetes state. Preliminary studies by our group have shown that treatment with glycated albumin of normal rats reduces sensibility of insulin. However, it was not shown whether this effect involves a direct action of AGEs on the expression of Slc2a4 gene.This project, thus, proposes to analyze the effects of glycated albumin on the expression of Slc2a4 gene and protein GLUT4 in 3T3-L1 adipocytes lineage and verify whether this effect is mediated by the activation of NFKB pathway.

Scientific publications

(The scientific publications listed on this page originate from the Web of Science or SciELO databases. Their authors have cited FAPESP grant or fellowship project numbers awarded to Principal Investigators or Fellowship Recipients, whether or not they are among the authors. This information is collected automatically and retrieved directly from those bibliometric databases.)

MICHALANI, M. L. E.; PASSARELLI, M.; MACHADO, U. F.. Effect of glycated albumin in the expression of glucose transporter GLUT4 in adipocytes: potential participation of transcription factor NF-kB. Diabetologia, v. 61, p. 2-pg., 2018-10-01. (16/17002-4)

MICHALANI, MARIA LUIZA ESTIMO; PASSARELLI, MARISA; MACHADO, UBIRATAN FABRES. Nuclear Factor-Kappa-B Mediates the Advanced Glycation End Product-Induced Repression of Slc2a4 Gene Expression in 3T3-L1 Adipocytes. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v. 25, n. 15, p. 14-pg., 2024-08-01. (16/17002-4, 16/15603-0)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

TOLEDO, Maria Luiza Estimo Michalani. Glycated albumin modulates the expression of Slc2a4/GLUT4 in adipose cells in a hormetic manner with potential participation of the NFKB pathway.. 2019. Master's Dissertation - Universidade de São Paulo (USP). Instituto de Ciências Biomédicas (ICB/SDI) São Paulo.