Effects of insecticide acephate on membrane mimetic systems: The role played by electrostatic interactions with lipid polar headgroups

Pesticides are important agrochemicals to yield high crop productivity but their indiscriminate use may harm the environment and human health. In order to seek a compromise between effectiveness as insecticide and safety for humans, it is essential to correlate their physiological action with molecu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of molecular liquids 2021-06, Vol.332, p.115868, Article 115868
Hauptverfasser: Morato, Luis F.C., Ruiz, Gilia C.M., Pazin, Wallance M., Gomes, Orisson P., Oliveira, Osvaldo N., Batagin-Neto, Augusto, Constantino, Carlos J.L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Pesticides are important agrochemicals to yield high crop productivity but their indiscriminate use may harm the environment and human health. In order to seek a compromise between effectiveness as insecticide and safety for humans, it is essential to correlate their physiological action with molecular-level interaction with cell membranes. In this study, we found that acephate interacts preferentially with positively charged Langmuir monolayers that represent simplified cell membranes. This was proven by comparing surface pressure-molecular area (π-A) isotherms and polarization-modulated infrared reflection absorption spectroscopy (PM-IRRAS) data on monolayers of the zwitterionic 1,2-dipalmitoyl-sn-glycerol-3-phosphocholine (DPPC) and 1-palmitoyl-2-oleoyl-glycero-3-phosphocholine (POPC), the cationic dimethyldioctadecyl ammonium bromide (DODAB) and 1,2-dipalmitoyl-3-trimethylammonium-propane (DPTAP), and the anionic dihexadecyl phosphate (DHP) and 1,2-dipalmitoyl-sn-glycero-3-phosphate (DPPA). While acephate induced a closer packing of DODAB and DPTAP monolayers upon binding to their quaternary ammonium and choline groups, respectively, almost no effects were observed in the π-A isotherms of the other lipids. Such preferred interaction between acephate and the positively-charged groups was confirmed with density-functional theory (DFT) calculations. Acephate also changed the size and zeta potential of large unilamellar vesicles (LUVs) formed with cationic lipids. Taken together these results point to a physiological action related to acephate binding to positively charged groups owing to its negative character, which may help establish conditions for the safe use of this insecticide. •Langmuir monolayers of DODAB and DPTAP are more affected by acephate.•Acephate causes the molecular area reduction of cationic monolayers.•PM-IRRAS reveals electrostatic interactions between acephate and lipids headgroups.•Acephate interacts on the surface of the cationic large vesicles.
ISSN:0167-7322
1873-3166
DOI:10.1016/j.molliq.2021.115868