Leishmanicidal and healing effects of 3β,6β,16β-trihydroxy lup-20 (29)-ene isolated from Combretum leprosum on Leishmania braziliensis infection in vitro and in vivo
Authors/Creators
- Aline Sombra Santos1
- Naya Lúcia de Castro Rodrigues1
- Francisco Rafael Marciano Fonseca1
- Nathalia Braga Fayão Oliveira1
- Bianca Oliveira Loucard2
- Fabíola Fernandes Heredia1
- Teresa Neuma Albuquerque Gomes Nogueira1
- Ticiana Monteiro Abreu1
- Hélcio Silva dos Santos3
- Edson Holanda Teixeira4
- et al. Show all 14 authors
- Aline Sombra Santos1
- Naya Lúcia de Castro Rodrigues1
- Francisco Rafael Marciano Fonseca1
- Nathalia Braga Fayão Oliveira1
- Bianca Oliveira Loucard2
- Fabíola Fernandes Heredia1
- Teresa Neuma Albuquerque Gomes Nogueira1
- Ticiana Monteiro Abreu1
- Hélcio Silva dos Santos3
- Edson Holanda Teixeira4
- Luzia Kalyne Almeida Moreira Leal2
- Regis Bernardo Brandim Gomes5
- Clarissa Romero Teixeira5
- Maria Jania Teixeira1
- 1. Parasitology Laboratory, Department of Pathology and Legal Medicine, Faculty of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil
- 2. Laboratory of Pharmacognosy and Pharmaceutical Technology, Department of Pharmacy, Faculty of Pharmacy Dentistry and Nursing, Federal University of Ceará, Fortaleza, Ceará, Brazil.
- 3. Universidade Estadual Vale do Acaraú, Sobral, Ceará, Brazil
- 4. Integrated Laboratory of Biomolecules, Department of Pathology and Legal Medicine, Faculty of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil
- 5. FIOCRUZ Ceará, Oswaldo Cruz Foundation, Eusébio, Fortaleza, Ceará, Brazil
Description
Treatment of cutaneous leishmaniasis depends on drugs that potentially cause serious side effects and resistance. Thus, topical therapies are attractive alternatives to the drugs currently used. 3β, 6β, 16β-trihydroxylup-20 (29)-ene is a lupane triterpene isolated from Combretum leprosum Mart. leaves (CLF-1), with reports of in vitro antileishmanial effect against L. amazonensis and to promote lesion healing in animal model. Herein, we evaluated the in vitro and in vivo antileishmanial and healing effects of CLF-1 against L. braziliensis. CLF-1 treatment showed low toxicity in macrophages and significantly reduced parasite load in vitro. CLF-1 induced higher IL-12 and TNF-α production and more discrete IL-4 and IL-10 production. For in vivo evaluation, a CLF-1 cream formulation was prepared to treat hamsters infected with L. braziliensis. CLF-1 treatment was able to reduce parasite load on the infected skin and lymph node more efficiently than the conventional treatment. Histopathological analysis indicated a strong inflammatory response accompanied by an important healing response. Data from this study indicate that topical CLF-1 treatment was effective and non-toxic in L. braziliensis infected hamsters suggesting its potential for further development as a future therapeutic intervention.