METFORMIN REGULATES INFLAMMATORY RESPONSE OF T. CRUZI-INFECTED PERITONEAL MACROPHAGES IN AN EX VIVO TREATMENT MODEL

BAIGORRÍ, RE; ANA, Y; BRUGO, MB; VOLPINI, X; MOTRAN, CC; STEMPIN, CC; CERBAN, FM

Congreso; REUNIÓN DE SOCIEDADES DE BIOCIENCIAS 2020; 2020

During the acute phase of T. cruzi infection, high replication of the parasite is controlled by a strong inflammatory response with activation of the innate immune cells due to increase of Th1proinflammatory cytokines. Macrophages (Mø) have been described to control intracellular parasite replication when iNOS expression and ON production are induced in vitro. We previouslyreported that pretreatment of bone marrow derived Mø with Metformin (Metf) leads these cellsto control parasite replication presumably by modulating inflammasome activation without increase of iNOS expression. However, it has been demonstrated that high and continuous ONrelease by Mø and other cells, is involved in Th1 T cell suppression. In this context, Metf was associated to reduce inflammatory-related ischemic cardiovascular events, prolong lifespan and decrease aged-related inflammation. To determine the Mø activation profile during in vivo T. cruzi infection and the possibles effects of Metf treatment, we tested iNOS expression by FACS in Peritoneal Mø (Pe-Mø) subsets, LPM (Large Pe-Mø) and SPM (Small Pe-Mø). We observed increased iNOS expression (p