Potential Effects of Essential Oil from Plinia cauliflora (Mart.) Kausel on Leishmania: In Vivo, In Vitro, and In Silico Approaches

Author:

Holanda Vanderlan N.1,Brito Thaíse G. S.1,Oliveira João R. S. de1,Cunha Rebeca X. da1,Silva Ana P. S. da1,Silva Welson V. da2,Araújo Tiago F. S.3,Tavares Josean F.4ORCID,Santos Sócrates G. dos5ORCID,Figueiredo Regina C. B. Q.2,Lima Vera L. M.1ORCID

Affiliation:

1. Laboratório de Lipídios e Aplicação de Biomoléculas em Doenças Prevalentes e Negligenciadas, Departamento de Bioquímica, Centro de Biociências, Universidade Federal de Pernambuco, Avenida Professor Moraes Rego, 1235, Recife 50670-901, PE, Brazil

2. Laboratório de Biologia Celular de Patógenos, Instituto Aggeu Magalhães, Departamento de Microbiologia, Avenida Professor Moraes Rego, 1235, Recife 50670-901, PE, Brazil

3. Colegiado de Ciências Farmacêuticas, Universidade Federal do Vale do São Francisco, José de Sá Maniçoba, S/N, Petrolina 56304-917, PE, Brazil

4. Departamento de Ciências Farmacêuticas, Universidade Federal da Paraíba, Rua Tabelião Stanislau Eloy, 41, Castelo Branco III, João Pessoa 58033-455, PB, Brazil

5. Laboratório de Tecnologia Farmacêutica, Instituto de Pesquisa em Drogas e Medicamentos, Universidade Federal da Paraíba, Cidade Universitária, Campus I, Castelo Branco III, S/N, João Pessoa 58033-455, PB, Brazil

Abstract

In the search for new chemotherapeutic alternatives for cutaneous leishmaniasis (CL), essential oils are promising due to their diverse biological potential. In this study, we aimed to investigate the chemical composition and leishmanicidal and anti-inflammatory potential of the essential oil isolated from the leaves of Plinia cauliflora (PCEO). The chemical composition of PCEO showed β-cis-Caryophyllene (24.4%), epi-γ-Eudesmol (8%), 2-Naphthalenemethanol[decahydro-alpha] (8%), and trans-Calamenene (6.6%) as its major constituents. Our results showed that the PCEO has moderate cytotoxicity (CC50) of 137.4 and 143.7 μg/mL on mice peritoneal exudate cells (mPEC) and Vero cells, respectively. The PCEO was able to significantly decrease mPEC infection by Leishmania amazonensis and Leishmania braziliensis. The value of the inhibitory concentration (IC50) on amastigote forms was about 7.3 µg/mL (L. amazonensis) and 7.2 µg/mL (L. braziliensis). We showed that PCEO induced drastic ultrastructural changes in both species of Leishmania and had a high selectivity index (SI) > 18. The in silico ADMET analysis pointed out that PCEO can be used for the development of oral and/or topical formulation in the treatment of CL. In addition, we also demonstrated the in vivo anti-inflammatory effect, with a 95% reduction in paw edema and a decrease by at least 21.4% in migration immune cells in animals treated with 50 mg/kg of PCEO. Taken together, our results demonstrate that PCEO is a promising topical therapeutic agent against CL.

Funder

Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Instituto Aggeu Magalhães and Inova-Fiocruz Program

FACEPE

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

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