Autor(es)

de Jesus, Jessica Adriana ^[1] ; Laurenti, Marcia Dalastra ^[1] ; Antonangelo, Leila ^{[2, 3]} ; Faria, Caroline Silverio ^[3] ; Lago, Joao Henrique Ghilardi ^[4] ; Passero, Luiz Felipe Domingues ^{[5, 6]}

Afiliação do(s) autor(es)

^[1] Univ Sao Paulo, Dept Pathol, Lab Pathol Infect Dis LIM50, Med Sch, Av Dr Arnaldo, 455 Cerqueira Cesar, BR-01246903 Sao Paulo, SP - Brazil

^[2] Univ Sao Paulo, Hosp Clin, Dept Patol, Lab Patol Clin, Fac Med, Sao Paulo, SP - Brazil

^[3] Univ Sao Paulo, Hosp Clin, Lab Invest Med LIM03, Fac Med, Sao Paulo, SP - Brazil

^[4] Fed Univ ABC UFABC, Ctr Nat & Human Sci, BR-09210580 Santo Andre, SP - Brazil

^[5] Sao Paulo State Univ UNESP, Inst Biosci, Praca Infante Dom Henrique S-N, BR-11330900 Sao Vicente, SP - Brazil

^[6] Sao Paulo State Univ UNESP, Inst Adv Studies Ocean, Joao Francisco Bensdorp 1178, BR-11350011 Sao Vicente, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: JOURNAL OF IMMUNOLOGY RESEARCH; v. 2021, FEB 18 2021.
• Citações Web of Science: 0

Resumo

Leishmaniasis is a neglected tropical disease caused by the flagellated protozoa of the genus Leishmania that affects millions of people around the world. Drugs employed in the treatment of leishmaniasis have limited efficacy and induce local and systemic side effects to the patients. Natural products are an interesting alternative to treat leishmaniasis, because some purified molecules are selective toward parasites and not to the host cells. Thus, the aim of the present study was to compare the in vitro antileishmanial activity of the triterpenes betulin (Be), lupeol (Lu), and ursolic acid (UA); analyze the physiology and morphology of affected organelles; analyze the toxicity of selected triterpenes in golden hamsters; and study the therapeutic activity of triterpenes in hamsters infected with L. (L.) infantum as well as the cellular immunity induced by studied molecules. The triterpenes Lu and UA were active on promastigote (IC50=4.0 +/- 0.3 and 8.0 +/- 0.2 mu M, respectively) and amastigote forms (IC50=17.5 +/- 0.4 and 3.0 +/- 0.2 mu M, respectively) of L. (L.) infantum, and their selectivity indexes (SI) toward amastigote forms were higher (>= 13.4 and 14, respectively) than SI of miltefosine (2.7). L. (L.) infantum promastigotes treated with Lu and UA showed cytoplasmic degradation, and in some of these areas, cell debris were identified, resembling autophagic vacuoles, and parasite mitochondria were swelled, fragmented, and displayed membrane potential altered over time. Parasite cell membrane was not affected by studied triterpenes. Studies of toxicity in golden hamster showed that Lu did not alter blood biochemical parameters associated with liver and kidney functions; however, a slight increase of aspartate aminotransferase level in animals treated with 2.5 mg/kg of UA was detected. Lu and UA triterpenes eliminated amastigote forms in the spleen (87.5 and 95.9% of reduction, respectively) and liver of infected hamster (95.9 and 99.7% of reduction, respectively); and UA showed similar activity at eliminating amastigote forms in the spleen and liver than amphotericin B (99.2 and 99.8% of reduction). The therapeutic activity of both triterpenes was associated with the elevation of IFN-gamma and/or iNOS expression in infected treated animals. This is the first comparative work showing the in vitro activity, toxicity, and therapeutic activity of Lu and UA in the chronic model of visceral leishmaniasis caused by L. (L.) infantum; additionally, both triterpenes activated cellular immune response in the hamster model of visceral leishmaniasis. (AU)

• Processo FAPESP: 16/00468-0 - Uso do reposicionamento de fármacos e da bioprospecção de produtos naturais para caracterizar compostos com ação leishmanicida in vitro e in vivo
• Beneficiário: Luiz Felipe Domingues Passero
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 18/07885-1 - Biomoléculas oriundas de espécies vegetais de áreas remanescentes da Mata Atlântica e do Cerrado para tratamento de doenças tropicais negligenciadas - aspectos químicos e farmacológicos
• Beneficiário: João Henrique Ghilardi Lago
• Modalidade de apoio: Auxílio à Pesquisa - Programa BIOTA - Regular
• Processo FAPESP: 16/10324-6 - Nanopartículas lípidicas como carreadores de triterpenos para o tratamento da Leishmaniose Visceral Experimental
• Beneficiário: Jéssica Adriana de Jesus
• Modalidade de apoio: Bolsas no Brasil - Doutorado