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Evaluation of pharmacological and molecular inhibition of NLRP3 inflammasome and its consequences in an in vitro model of preeclampsia

Grant number: 20/14610-9
Support Opportunities:Scholarships in Brazil - Post-Doctoral
Start date: July 01, 2021
End date: August 31, 2024
Field of knowledge:Health Sciences - Medicine - Maternal and Child Health
Principal Investigator:Valeria Cristina Sandrim
Grantee:Priscila Rezeck Nunes
Host Institution: Instituto de Biociências (IBB). Universidade Estadual Paulista (UNESP). Campus de Botucatu. Botucatu , SP, Brazil
Associated scholarship(s):22/07226-3 - IDENTIFICATION OF METABOLIC PATHWAYS RELATED TO ENDOTHELIAL DYSFUNCTION OF PRE-ECLAMPSIA IN VITRO MODEL, BE.EP.PD

Abstract

Preeclampsia (PE) is a specific syndrome of a human pregnancy, being one of the main causes of maternal death in Brazil. The pathophysiology of PE has not been fully clarified, but it is known that placental ischemia is of fundamental importance to the process, since the release of products resulting from malperfusion in maternal circulation can lead to systemic endothelial dysfunction. A persistent endothelial inflammation stimulates the secretion of various inflammatory mediators, which triggers an important process in inflammatory conditions due to the activation of various signalization patterns. Considering that the causes related to endothelial dysfunction, oxidative stress, and inflammation in PE still remain a challenge for clinical practice, the use of drugs and the use of molecular approaches related to the inhibition of NLRP3 inflammasome could be a good choice for future treatments. The objective of this project is: to assess the pharmacological and molecular action of NLRP3 inflammation inhibitors in an in vitro model of PE and the relationships with biomarkers of endothelial dysfunction, oxidative stress and inflammation. To achieve this objective, the following experiments will be carried out: 1- Assess the effect of plasma from pregnant women with PE and normotensive (NT) pregnant women in the activation of the NLRP3 inflammassome via NF-ºB in endothelial cell line, 2- Comparison of the activation of the inflammation in primary endothelial cells of pregnant women with PE and NT subjected to treatment with pharmacological inhibitors and small interfering RNA, 3- Validate the effect the pharmacological and molecular inhibition on the function of endothelial cells incubated with plasma through tests of tube formation, permeability, markers of endothelial dysfunction, oxidative stress, autophagy and pyroptose, 4- Observe the effect of two inhibitors of NLRP3 inflammassome on contraction and relaxation of vessels from pregnant women by vascular reativity test. The results will be validated by parametric or non-parametric tests, depending on the variability, considering significance level <0.05. Studies on endothelial dysfunction and its relationship with inflammation in PE still remain an objective to be further explored and elucidated, and the molecular mechanisms associated with the interactions between inflammation and endothelial dysfunction can be favorable to develop new treatments and more effective therapies.

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Scientific publications (8)
(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.)
NUNES, PRISCILA REZECK; PINHEIRO, LUCAS CEZAR; MARTINS, LAISLA ZANETONI; DIAS-JUNIOR, CARLOS ALAN; PALEI, ANA CAROLINA TAVEIROS; SANDRIM, VALERIA CRISTINA. A new look at the role of nitric oxide in preeclampsia: Protein S-nitrosylation. PREGNANCY HYPERTENSION-AN INTERNATIONAL JOURNAL OF WOMENS CARDIOVASCULAR HEALTH, v. 29, p. 7-pg., . (20/14610-9, 17/07570-8, 18/24484-0, 19/07230-8)
ZAMPIERI, GABRIELA MORELLI; NUNES, PRISCILA REZECK; ABBADE, JOELCIO FRANCISCO; DIAS, CARLOS ALAN; SANDRIM, VALERIA CRISTINA. Vascular contraction of umbilical arteries of pregnant women with preeclampsia. Revista Brasileira de Ginecologia e Obstetrícia, v. 46, p. 7-pg., . (20/14610-9, 19/07230-8)
BUENO-PEREIRA, THAINA OMIA; BERTOZZI-MATHEUS, MARIANA; ZAMPIERI, GABRIELA MORELLI; ABBADE, JOELCIO FRANCISCO; CAVALLI, RICARDO C.; NUNES, PRISCILA REZECK; SANDRIM, VALERIA CRISTINA. Markers of Endothelial Dysfunction Are Attenuated by Resveratrol in Preeclampsia. ANTIOXIDANTS, v. 11, n. 11, p. 12-pg., . (21/01945-5, 20/14610-9, 19/07230-8)
NUNES, PRISCILA R.; CERON, CARLA S.; LUIZON, MARCELO R.; SANDRIM, VALERIA C.. Interaction among extracellular nicotinamide phosphoribosyltransferase, toll-like receptor-4, and inflammatory cytokines in pre-eclampsia. American Journal of Reproductive Immunology, v. 87, n. 1, . (19/07230-8, 20/14610-9)
NUNES, PRISCILA REZECK; BUENO PEREIRA, THAINA OMIA; BERTOZZI MATHEUS, MARIANA; GRANDINI, NUBIA ALVES; SIQUEIRA, JULIANA SILVA; CORREA, CAMILA RENATA; ABBADE, JOELCIO FRANCISCO; SANDRIM, VALERIA CRISTINA. Glibenclamide Increases Nitric Oxide Levels and Decreases Oxidative Stress in an In Vitro Model of Preeclampsia. ANTIOXIDANTS, v. 11, n. 8, p. 12-pg., . (20/14610-9, 19/07230-8)
NUNES, PRISCILA REZECK; MATTIOLI, SARAH VIANA; SANDRIM, VALERIA CRISTINA. NLRP3 Activation and Its Relationship to Endothelial Dysfunction and Oxidative Stress: Implications for Preeclampsia and Pharmacological Interventions. CELLS, v. 10, n. 11, p. 14-pg., . (20/14610-9, 19/07230-8)
NUNES, PRISCILA REZECK; PEREIRA, DANIELA ALVES; PASSETI, LUIS FERNANDO PEREIRA; GOMES, KARINA BRAGA; SANDRIM, VALERIA CRISTINA; LUIZON, MARCELO RIZZATTI. The interplay between extracellular NAMPT and inflammatory cytokines in preeclampsia. JOURNAL OF REPRODUCTIVE IMMUNOLOGY, v. 163, p. 9-pg., . (20/14610-9, 19/07230-8)
SANTOS, KAROLINY NUNE; BIZZOTTO, JULIANA Q.; BUENO-PEREIRA, THAINA O.; ROMAO-VEIGA, MARIANA; RIBEIRO-VASQUES, VANESSA R.; OLIVEIRA, LARISSA RAGOZO CARDOSO; SANDRIM, VALERIA C.; NUNES, PRISCILA R.. Preeclamptic plasma disrupts endothelial function and promotes inflammation in endothelial cells: beneficial effects of glibenclamide and MCC950 in this scenario. JOURNAL OF RECEPTORS AND SIGNAL TRANSDUCTION, v. 45, n. 4, p. 13-pg., . (24/01935-8, 20/14610-9)