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Cardiac effects of advanced glycation end products inhibitor (pyridoxamine) in type 1 diabetic female rats

Grant number: 17/22670-9
Support Opportunities:Scholarships in Brazil - Scientific Initiation
Start date: January 01, 2018
End date: July 22, 2019
Field of knowledge:Biological Sciences - Physiology - Physiology of Organs and Systems
Principal Investigator:Maria Andréia Delbin
Grantee:Matheus Pena Passos
Host Institution: Instituto de Biologia (IB). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil

Abstract

The pharmacologic approaches currently in clinical use have remained unsatisfactory in preventing the cardiac complications associated with diabetes and more innovative therapies are needed. The advanced glycation products (AGEs) formation is an important pathway involved in diabetic cardiomyopathy. In addition, the epicardial adipose tissue (EAT) secretes and expresses adipokines, which have pro- and anti-inflammatory role, and, due to its anatomic characteristics, can modulate cardiac muscle and coronary arteries. Therefore, the aim of this study will be to investigate important proteins involved in cardiac morphological alterations in type 1 diabetic female rats and the effects of co-treatment with insulin + pyridoxamine (inhibitor of AGEs). Additionally, we are going to evaluate the pro- and anti-inflammatory alterations of EAT. Female Wistar rats will be divided in four groups: control (CTR), type 1 DM (DM1, alloxan 170 mg/kg IP), DM1 treated with insulin (DM+INS, 2U morning + 4U evening) and DM1 treated with insulin + pyridoxamine (DM+INS+PDX, 180 mg/kg oral gavage). Circulating factors such as glucose, total cholesterol, triglycerides, glycated A1c hemoglobin, insulin, estradiol and advanced glycation end products-Nµ-carboxymethyllysine (CML), as well as, the protein expressions of AGE, RAGE, Cu/Zn-SOD, Mn-SOD, NOX2, NOX4, NF-kB, GPER (in left ventricle), UCP-1, PGC1-±, adiponectin, leptin, IL-1² and TNF-± (in EAT) will be analyzed. The histological and morphological analyses of heart will be conducted. Tissue reactive oxygen species (ROS) generation will be evaluated. (AU)

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Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
SOUSA, ANDRESSA S.; PASSOS, MATHEUS P.; RUBERTI, OLIVIA M.; JARRETE, ALINE P.; DELBIN, MARIA A.. Evaluation of coronary function in female rats with severe type 1 diabetes: Effects of combined treatment with insulin and pyridoxamine. MICROVASCULAR RESEARCH, v. 146, p. 10-pg., . (16/16351-5, 17/22670-9)
DELBIN, MARIA A.; PASSOS, MATHEUS P.; RUBERTI, OLIVIA M.; JARRETE, ALINE P.; SOUSA, ANDRESSA S.. Cardiovascular Effects of Pyridoxamine in Type 1 Diabetic Female Rats. FASEB JOURNAL, v. 33, p. 2-pg., . (17/22670-9, 16/16351-5)