Revista Brasileira de Parasitologia Veterinária (Jun 2020)

Anti-tick effect and cholinesterase inhibition caused by Prosopis juliflora alkaloids: in vitro and in silico studies

  • Hélimar Gonçalves de Lima,
  • Francianne Oliveira Santos,
  • Acidália Carine Vieira Santos,
  • Gisele Dias da Silva,
  • Rafaela Jesus dos Santos,
  • Kelli de Oliveira Carneiro,
  • Isabella Mary Alves Reis,
  • Isabela de Oliveira Estrela,
  • Humberto Fonseca de Freitas,
  • Thiago Campanharo Bahiense,
  • Samuel Silva da Rocha Pita,
  • Rosângela Soares Uzeda,
  • Alexsandro Branco,
  • Silvia Lima Costa,
  • Maria José Moreira Batatinha,
  • Mariana Borges Botura

DOI
https://doi.org/10.1590/s1984-29612020036
Journal volume & issue
Vol. 29, no. 2

Abstract

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Abstract We investigated the in vitro acaricide activity of the methanolic extract (ME) and alkaloid-rich fraction (AF) of Prosopis juliflora on Rhipicephalus microplus and correlated this effect with acetylcholinesterase (AChE) inhibition. The acaricide activity was evaluated using adult and larval immersion tests. Also, we studied the possible interaction mechanism of the major alkaloids present in this fraction via molecular docking at the active site of R. microplus AChE1 (RmAChE1). Higher reproductive inhibitory activity of the AF was recorded, with effective concentration (EC50) four times lower than that of the ME (31.6 versus 121 mg/mL). The AF caused mortality of tick larvae, with lethal concentration 50% (LC50) of 13.8 mg/mL. Both ME and AF were seen to have anticholinesterase activity on AChE of R. microplus larvae, while AF was more active with half-maximal inhibitory concentration (IC50) of 0.041 mg/mL. The LC-MS/MS analyses on the AF led to identification of three alkaloids: prosopine (1), juliprosinine (2) and juliprosopine (3). The molecular docking studies revealed that these alkaloids had interactions at the active site of the RmAChE1, mainly relating to hydrogen bonds and cation-pi interactions. We concluded that the alkaloids of P. juliflora showed acaricide activity on R. microplus and acted through an anticholinesterase mechanism.

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