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Mechanisms of excentric remodeling associated with vascular calcification in obesity and insulin resistance

Grant number: 13/09652-0
Support type:Scholarships in Brazil - Doctorate
Effective date (Start): January 01, 2014
Effective date (End): June 30, 2017
Field of knowledge:Health Sciences - Medicine - Medical Clinics
Principal Investigator:Emmanuel de Almeida Burdmann
Grantee:Luciana Simao Do Carmo
Home Institution: Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE). Sociedade Beneficente Israelita Brasileira Albert Einstein (SBIBAE). São Paulo , SP, Brazil

Abstract

Vascular calcification is an important clinical disease which increases cardiovascular morbidity and mortality, occurring frequently in both diabetes and in chronic renal failure. Previously considered a passive and chronic degenerative condition of ageing, recently it is understood as an active and complex process, with definite pathophysiology that recapitulates osteogenesis. Vascular calcification usually occurs concomitantly with bone loss and bone remodeling such as in osteoporosis and in renal osteodystrophy. Vascular remodeling is an adaptive response of the vessel to specific stimuli, which participates in pathophysiology of various cardiovascular conditions such as aneurism and dissection, atherosclerosis, vascular stiffness, systemic hypertension and arteriovenous fistula. Focusing on cardiovascular risk factors that are common to both vascular calcification and vascular remodeling, we will investigate the mechanisms and pathways that may connect and explain these conditions together. We hypothesized that ob/ob mice, which are obese and have insulin resistance, demonstrate increased excentric vascular remodeling and vascular calcification response to a calcifying stimulus with Vitamin D3 in vivo compared to C57BL/6 mice. Furthermore, we will assess the role of vascular calcification in excentric vascular remodeling and also the association of these conditions with bone loss and bone architecture in this model. More importantly, we will investigate vascular calcifying proteins gene/protein expression change that may activate vascular remodeling mediators such as metalloproteinases, tissue inhibitors of metalloproteinases and increased oxidative stress that may connect vascular calcification to vascular remodeling mechanisms after Vitamin D3 stimulation in vivo in ob/ob compared to C57BL/6 mice. We will assess the role of MSX2, a potent osteogenic transcription factor, in excentric vascular remodeling and in calcification, through investigating the vascular response in MSX2 siRNA transfected obob and C57BL/6 after Vitamin D3 stimulation in vivo. In conclusion, we will pursue novel mechanisms and potential therapeutic targets, through understanding the pathophysiological relationship between excentric remodeling and vascular calcification in obesity and insulin resistant background.

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)
ALMEIDA, YOURI E.; FESSEL, MELISSA R.; DO CARMO, LUCIANA SIMAO; JORGETTI, VANDA; FARIAS-SILVA, ELISANGELA; PESCATORE, LUCIANA ALVES; GAMARRA, LIONEL F.; ANDRADE, MARIA CLAUDINA; SIMPLICIO-FILHO, ANTONIO; PITANGUEIRAS MANGUEIRA, CRISTOVAO LUIS; RANGEL, ERIKA B.; LIBERMAN, MARCEL. Excessive cholecalciferol supplementation increases kidney dysfunction associated with intrarenal artery calcification in obese insulin-resistant mice. SCIENTIFIC REPORTS, v. 10, n. 1 JAN 9 2020. Web of Science Citations: 0.
CARMO, LUCIANA S.; BURDMANN, EMMANUEL A.; FESSEL, MELISSA R.; ALMEIDA, YOURI E.; PESCATORE, LUCIANA A.; FARIAS-SILVA, ELISANGELA; GAMARRA, LIONEL F.; LOPES, GABRIEL H.; ALOIA, THIAGO P. A.; LIBERMAN, MARCEL. Expansive Vascular Remodeling and Increased Vascular Calcification Response to Cholecalciferol in a Murine Model of Obesity and Insulin Resistance. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, v. 39, n. 2, p. 200-211, FEB 2019. Web of Science Citations: 4.
ANDRADE, MARIA CLAUDINA; CARMO, LUCIANA S.; FARIAS-SILVA, ELISANGELA; LIBERMAN, MARCEL. Msx2 is required for vascular smooth muscle cells osteoblastic differentiation but not calcification in insulin-resistant ob/ob mice. ATHEROSCLEROSIS, v. 265, p. 14-21, OCT 2017. Web of Science Citations: 5.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.