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Effect of inflammasome inhibitor on rat kidneys after brain death: cold storage versus normothermic machine perfusion.

Grant number: 23/03915-1
Support Opportunities:Scholarships in Brazil - Doctorate
Start date: October 01, 2023
End date: February 29, 2028
Field of knowledge:Health Sciences - Medicine - Medical Clinics
Principal Investigator:Mario Abbud Filho
Grantee:Ludimila Leite Marzochi
Host Institution: Faculdade de Medicina de São José do Rio Preto (FAMERP). Secretaria de Desenvolvimento Econômico (São Paulo - Estado). São José do Rio Preto , SP, Brazil
Associated scholarship(s):23/17655-1 - Effect of inflammasome inhibitor on rat kidneys after brain death: cold storage versus normothermic machine perfusion., BE.EP.DR

Abstract

Introduction: The brain death process stimulates systemic inflammation with consequent activation of inflammatory pathways in organs donated for transplants. The combination of prolonged cold ischemia time and brain death-induced inflammation is crucial for activating kidneys' innate immunity and pro-inflammatory mechanisms. The inflammasome is one of the most expressed molecules during this process. Thus, its blockade could reduce the innate inflammatory response, minimizing sterile inflammation, improving the quality of "non-ideal" kidneys, and reducing the discard rates of these organs. Objective: Evaluate the effect of administration of the NLRP3 inflammasome inhibitor (MCC950) on gene and protein expression related to innate immunity and sterile inflammation, in rat kidneys, after the brain death process with in situ perfusion or normothermic machine perfusion (NMP). Methods. 56 male rats will be divided into 6 groups: 1) sham (n=7), 2) induction of brain death without treatment (n=10); 3) induction of brain death and in situ perfusion of the kidney without treatment; 4) induction of brain death and in situ perfusion with the administration of MCC950 (n=10); 5) induction of brain death and administration of MCC950 in the perfusion fluid in NMP (n=10), 6) induction of brain death without treatment using NMP (n=10). From the collected kidney samples, gene, and protein expression will be performed using the TaqMan Gene Expression Array Plates system and western blotting, in addition to histological analysis.

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