Carolina Davies
National Scientific and Technical Research Council
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Featured researches published by Carolina Davies.
PLOS Neglected Tropical Diseases | 2014
Carolina Davies; Nilay Dey; Olga Sánchez Negrette; Luis Antonio Parada; Miguel A. Basombrío; Nisha Jain Garg
Background Treatment of Chagas disease, caused by Trypanosoma cruzi, relies on nifurtimox and benznidazole (BZL), which present side effects in adult patients, and natural resistance in some parasite strains. Hydroxymethylnitrofurazone (NFOH) is a new drug candidate with demonstrated trypanocidal activity; however, its safety is not known. Methods HepG2 cells dose response to NFOH and BZL (5–100 µM) was assessed by measurement of ROS, DNA damage and survival. Swiss mice were treated with NFOH or BZL for short-term (ST, 21 d) or long-term (LT, 60 d) periods. Sera levels of cellular injury markers, liver inflammatory and oxidative stress, and fibrotic remodeling were monitored. Results HepG2 cells exhibited mild stress, evidenced by increased ROS and DNA damage, in response to NFOH, while BZL at 100 µM concentration induced >33% cell death in 24 h. In mice, NFOH ST treatment resulted in mild-to-no increase in the liver injury biomarkers (GOT, GPT), and liver levels of inflammatory (myeloperoxidase, TNF-α), oxidative (lipid peroxides) and nitrosative (3-nitrotyrosine) stress. These stress responses in NFOH LT treated mice were normalized to control levels. BZL-treated mice exhibited a >5-fold increase in GOT, GPT and TNF-α (LT) and a 20–40% increase in liver levels of MPO activity (ST and LT) in comparison with NFOH-treated mice. The liver inflammatory infiltrate was noted in the order of BZL>vehicle≥NFOH and BZL>NFOH≥vehicle, respectively, after ST and LT treatments. Liver fibrotic remodeling, identified after ST treatment, was in the order of BZL>vehicle>NFOH; lipid deposits, indicative of mitochondrial dysfunction and in the order of NFOH>vehicle>BZL were evidenced after LT treatment. Conclusions NFOH induces mild ST hepatotoxicity that is normalized during LT treatment in mice. Our results suggest that additional studies to determine the efficacy and toxicity of NFOH are warranted.
Acta Tropica | 2016
José Maria Bermudez; Carolina Davies; Analía Simonazzi; Juan Pablo Real; Santiago D. Palma
Journal of Medicinal Chemistry | 2007
Williams Porcal; Paola Hernández; Mariana Boiani; Gabriela Aguirre; Lucía Boiani; Agustina Chidichimo; Juan José Cazzulo; Nuria E. Campillo; Juan A. Páez; Ana Castro; R. Luise Krauth-Siegel; Carolina Davies; Miguel A. Basombrío; Mercedes González; Hugo Cerecetto
Antimicrobial Agents and Chemotherapy | 2010
Carolina Davies; Rubén M. Cardozo; Olga Sánchez Negrette; María Celia Mora; Man Chin Chung; Miguel A. Basombrío
European Journal of Medicinal Chemistry | 2008
Lucía Boiani; Carolina Davies; Carolina Arredondo; Williams Porcal; Alicia Merlino; Alejandra Gerpe; Mariana Boiani; José Pedro Pacheco; Miguel A. Basombrío; Hugo Cerecetto; Mercedes González
Revista Argentina De Microbiologia | 2012
Hugo Ramiro Poma; Carolina Davies; Dolores Gutiérrez Cacciabue; María Celia Mora; Miguel A. Basombrío; Verónica Beatriz Rajal
Journal of Pharmaceutical Sciences | 2018
Analía Simonazzi; Carolina Davies; Alicia Graciela Cid; Elio E. Gonzo; Luis Antonio Parada; José Maria Bermudez
Archive | 2014
Carolina Davies; Ramiro Poma; Rubén M. Cardozo; María Celia Mora; Federico Ramos; Verónica Beatriz Rajal; Miguel A. Basombrío
Acta Bioquimica Clinica Latinoamericana | 2014
Carolina Davies; Ramiro Poma; Rubén M. Cardozo; María Celia Mora; Federico Ramos; Verónica Beatriz Rajal; Miguel A. Basombrío
Archive | 2013
Olga Sánchez Negrette; María Concepción Monteros; Carolina Davies; Mario Oscar Zaidenberg