Susceptibility of Leishmania to novel pentavalent organometallics: Investigating impact on DNA and membrane integrity in antimony(III)‐sensitive and ‐resistant strains

Author:

Islam Arshad123ORCID,do Prado Bruno Rodrigues2,Dittz Dalton4,Rodrigues Bernardo Lages2,Silva Sydnei Magno da5,do Monte‐Neto Rubens L.6,Shabeer Muhammad2ORCID,Frézard Frédéric1,Demicheli Cynthia2

Affiliation:

1. Department of Physiology and Biophysics, Postgraduate Program in Physiology and Pharmacology, Institute of Biological Sciences Universidade Federal de Minas Gerais (UFMG) Belo Horizonte Brazil

2. Department of Chemistry, Institute of Exact Sciences Universidade Federal de Minas Gerais (UFMG) Belo Horizonte Brazil

3. Department of Pathology Government Lady Reading Hospital Medical Teaching Institution Peshawar Pakistan

4. Department of Biochemistry and Pharmacology, Health Sciences Center Federal University of Piauí (UFPI), Av. Universitária Teresina Brazil

5. Institute of Biomedical Sciences Universidade Federal de Uberlândia, Av Amazonas, s/n Umuarama Brazil

6. Instituto René Rachou – IRR/Fiocruz Minas, Av. Augusto de Lima Belo Horizonte Brazil

Abstract

AbstractThe aim the present study was to investigate the impact of novel pentavalent organobismuth and organoantimony complexes on membrane integrity and their interaction with DNA, activity against Sb(III)‐sensitive and ‐resistant Leishmania strains and toxicity in mammalian peritoneal macrophages. Ph3M(L)2 type complexes were synthesized, where M = Sb(V) or Bi(V) and L = deprotonated 3‐(dimethylamino)benzoic acid or 2‐acetylbenzoic acid. Both organobismuth(V) and organoantimony(V) complexes exhibited efficacy at micromolar concentrations against Leishmania amazonensis and L. infantum but only the later ones demonstrated biocompatibility. Ph3Sb(L1)2 and Ph3Bi(L1)2 demonstrated distinct susceptibility profiles compared to inorganic Sb(III)‐resistant strains of MRPA‐overexpressing L. amazonensis and AQP1‐mutated L. guyanensis. These complexes were able to permeate the cell membrane and interact with the Leishmania DNA, suggesting that this effect may contribute to the parasite growth inhibition via apoptosis. Taken altogether, our data substantiate the notion of a distinct mechanism of uptake pathway and action in Leishmania for these organometallic complexes, distinguishing them from the conventional inorganic antimonial drugs.

Funder

Third World Academy of Sciences

Publisher

Wiley

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