Details

Autor(en) / Beteiligte

• dos Santos, Marinalva Cardoso
• Scaini, João Luís Rheingantz
• Lopes, Márcio Vinicius Costa
• Rodrigues, Beatriz Gonçalves
• Silva, Nichole Osti
• Borges, Carla Roberta Lopes
• dos Santos, Sandra Cruz
• dos Santos Machado, Karina
• Werhli, Adriano Velasque
• da Silva, Pedro Eduardo Almeida
• Lourenço, Maria C.S.
• da Silva, Emerson T.
• de Souza, Marcus V.N.
• de Lima, Vânia Rodrigues
• Gonçalves, Raoni Schroeder B.

Titel

Mefloquine synergism with anti-tuberculosis drugs and correlation to membrane effects: Biologic, spectroscopic and molecular dynamics simulations studies

Ist Teil von

• Bioorganic chemistry, 2021-05, Vol.110, p.104786-104786, Article 104786

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2021

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• [Display omitted] •Mefloquine presents a synergism with different drugs against M. tuberculosis.•Mefloquine increases the membrane lateral diffusion and enhance its permeability.•Mefloquine effect in membrane can contribute to synergistic interactions. Studies displaying the combination of mefloquine (MFL) with anti-tuberculosis (TB) substances are limited in the literature. In this work, the effect of MFL-association with two first-line anti-TB drugs and six fluoroquinolones was evaluated against Mycobacterium tuberculosis drug resistant strains. MFL showed synergistic interaction with isoniazid, pyrazinamide, and several fluoroquinolones, reaching fractional inhibitory concentration indexes (FICIs) ranging from 0.03 to 0.5. In order to better understand the observed results, two approaches have been explored: (i) spectroscopic responses attributed to the effect of MFL on physicochemical properties related to a liposomal membrane model composed by soybean asolectin; (ii) molecular dynamics (MD) simulation data regarding MFL interaction with a membrane model based on PIM2, a lipid constituent of the mycobacterial cell wall. FTIR and NMR data showed that MFL affects expressively the region between the phosphate and the first methylene groups of soybean asolectin membranes, disordering these regions. MD simulations results detected high MFL density in the glycolipid interface and showed that the drug increases the membrane lateral diffusion, enhancing its permeability. The obtained results suggest that synergistic activities related to MFL are attributed to its effect of lipid disorder and membrane permeability enhancement.