Nematostatic activity of isoprenylated guanidine alkaloids from Pterogyne nitens and their interaction with acetylcholinesterase.


Journal

Experimental parasitology
ISSN: 1090-2449
Titre abrégé: Exp Parasitol
Pays: United States
ID NLM: 0370713

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 09 02 2023
revised: 03 04 2023
accepted: 03 05 2023
medline: 6 6 2023
pubmed: 14 5 2023
entrez: 13 5 2023
Statut: ppublish

Résumé

Although new nematicides have appeared, the demand for new products less toxic and more efficient for the control of plant-parasitic nematodes are still high. Consequently, studies on natural secondary metabolites from plants, to develop new nematicides, have increased. In this work, nineteen extracts from eleven Brazilian plant species were screened for activity against Meloidogyne incognita. Among them, the extracts of Piterogyne nitens showed a potent nematostatic activity. The alkaloid fraction obtained from the ethanol extract of leaves of P. nitens was more active than the coming extract. Due to the promising activity from the alkaloid fraction, three isoprenylated guanidine alkaloids isolated from this fraction, galegine (1), pterogynidine (2), and pterogynine (3) were tested, showing similar activity to the alkaloid fraction, which was comparable to that of the positive control Temik at 250 μg/mL. At lower concentrations (125-50 μg/mL), compound 2 showed to be the most active one. As several nematicides act through inhibition of acetylcholinesterase (AChE), the guanidine alkaloids were also employed in two in vitro AChE assays. In both cases, compound 2 was more active than compounds 1 and 3. Its activity was considered moderated compared to the control (physostigmine). Compound 2 was selected for an in silico study with the electric eel (Electrophorus electricus) AChE, showing to bind mostly to the same site of physostigmine in the AChEs, pointing out that this could be the mechanism of action for this compound. These results suggested that the guanidine alkaloids 1,2 and 3 from P. nitens are promising for the development of new products to control M. incognita, especially guanidine 2, and encourage new investigations to confirm the mechanism of action, as well as to determine the structure-activity relationship of the guanidine alkaloids.

Identifiants

pubmed: 37178971
pii: S0014-4894(23)00083-8
doi: 10.1016/j.exppara.2023.108542
pii:
doi:

Substances chimiques

Acetylcholinesterase EC 3.1.1.7
Guanidine JU58VJ6Y3B
Physostigmine 9U1VM840SP
Alkaloids 0
Plant Extracts 0
Guanidines 0
Antinematodal Agents 0
Cholinesterase Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108542

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Aline Coqueiro (A)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil; Department of Chemistry, Federal University of Technology - Paraná (UTFPR), Ponta Grossa, PR, 84017-220, Brazil. Electronic address: alinedqi@utfpr.edu.br.

Daniara Cristina Fernandes (DC)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil; Federal Institute of Education, Science and Technology of São Paulo (IFSP), Matão, SP, 15991-502, Brazil.

Amanda Danuello (A)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil; Institute of Chemistry, Federal University of Uberlândia (UFU), Uberlândia, MG, 38408-100, Brazil.

Luis Octávio Regasini (LO)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil; Departme nt of Chemistry and Environmental Sciences, Institute of Biosciences, Humanities and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, SP, 15054-000, Brazil.

Elaine Monteiro Cardoso-Lopes (EM)

Institute of Environmental Research, São Paulo, SP, 01061-970, Brazil.

Maria Cláudia Marx Young (MCM)

Institute of Environmental Research, São Paulo, SP, 01061-970, Brazil.

Luce Maria Brandão Torres (LM)

Institute of Environmental Research, São Paulo, SP, 01061-970, Brazil.

Vicente Paulo Campos (VP)

Department of Phytopathology, Federal University of Lavras (UFLA), Lavras, MG, 37200-000, Brazil.

Dulce Helena Siqueira Silva (DHS)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil.

Vanderlan da Silva Bolzani (V)

Nuclei of Bioassays, Biosynthesis and Ecophysiology of Natural Products (NuBBE), Department of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, SP, 14801-970, Brazil.

Denilson Ferreira de Oliveira (DF)

Department of Chemistry, Federal University of Lavras (UFLA), Lavras, MG, 37200-900, Brazil. Electronic address: denilson@ufla.br.

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Classifications MeSH