Zinc(II)-Sterol Hydrazone Complex as a Potent Anti-Leishmania Agent: Synthesis, Characterization, and Insight into Its Mechanism of Antiparasitic Action

Author:

Visbal Gonzalo1,Justo Rodrigo M. S.2ORCID,dos Santos da Silva e Miranda Gabrielle3,Teixeira de Macedo Silva Sara4,de Souza Wanderley56,Rodrigues Juliany Cola Fernandes3,Navarro Maribel2ORCID

Affiliation:

1. Laboratório de Ácidos Nucleicos (Laban), Coordenação Geral de Biologia (Cobio), Diretoria de Metrologia Científica e Industrial, DIMCI, Instituto Nacional de Metrologia, Qualidade e Tecnologia, INMETRO, Rio de Janeiro 25250-020, Brazil

2. Laboratório de Químicas Bioinorgânica e Catalise (LaQBIC), Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Juiz de Fora Juiz De Fora, Juiz de Fora 36036-900, Brazil

3. Núcleo Multidisciplinar de Pesquisa em Biologia (NUMPEX-Bio), Campus UFRJ-Duque de Caxias Prof. Geraldo Cidade, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, Brazil

4. Centro Nacional de Biologia Estrutural e Bioimagem, CENABIO, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, Brazil

5. Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, Brazil

6. Centro Multiusuário para Análise de Fenômenos Biológicos, Escola Superior de Saúde, Universidade do Estado do Amazonas, Manaus 69850-000, Brazil

Abstract

Searching for new alternatives for treating leishmaniasis, we present the synthesis, characterization, and biological evaluation against Leishmania amazonensis of the new ZnCl2(H3)2 complex. H3 is 22-hydrazone-imidazoline-2-yl-chol-5-ene-3β-ol, a well-known bioactive molecule functioning as a sterol Δ24-sterol methyl transferase (24-SMT) inhibitor. The ZnCl2(H3)2 complex was characterized by infrared, UV-vis, molar conductance measurements, elemental analysis, mass spectrometry, and NMR experiments. The biological results showed that the free ligand H3 and ZnCl2(H3)2 significantly inhibited the growth of promastigotes and intracellular amastigotes. The IC50 values found for H3 and ZnCl2(H3)2 were 5.2 µM and 2.5 µM for promastigotes, and 543 nM and 32 nM for intracellular amastigotes, respectively. Thus, the ZnCl2(H3)2 complex proved to be seventeen times more potent than the free ligand H3 against the intracellular amastigote, the clinically relevant stage. Furthermore, cytotoxicity assays and determination of selectivity index (SI) revealed that ZnCl2(H3)2 (CC50 = 5 μΜ, SI = 156) is more selective than H3 (CC50 = 10 μΜ, SI = 20). Furthermore, as H3 is a specific inhibitor of the 24-SMT, free sterol analysis was performed. The results showed that H3 was not only able to induce depletion of endogenous parasite sterols (episterol and 5-dehydroepisterol) and their replacement by 24-desalkyl sterols (cholesta-5,7,24-trien-3β-ol and cholesta-7,24-dien-3β-ol) but also its zinc derivative resulting in a loss of cell viability. Using electron microscopy, studies on the fine ultrastructure of the parasites showed significant differences between the control cells and parasites treated with H3 and ZnCl2(H3)2. The inhibitors induced membrane wrinkle, mitochondrial injury, and abnormal chromatin condensation changes that are more intense in the cells treated with ZnCl2(H3)2.

Funder

CAPES doctoral scholarship

FAPEMIG

Fundep

CNPq

FAPERJ

FAPEAM

Publisher

MDPI AG

Subject

Pharmaceutical Science

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