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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Anthelmintic effect of Pterogyne nitens (Fabaceae) on eggs and larvae of Haemonchus contortus: Analyses of structure-activity relationships based on phenolic compounds

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Author(s):
Lima, Caroline Sprengel [1] ; Pereira, Matheus Henrique [1] ; Gainza, Yousmel Aleman [2] ; Hoste, Herve [3] ; Regasini, Luis Octavio [1] ; de Souza Chagas, Ana Carolina [2]
Total Authors: 6
Affiliation:
[1] Sao Paulo State Univ UNESP, Inst Biosci Humanities & Exact Sci, Sao Jose Do Rio Preto, SP - Brazil
[2] Embrapa Pecuaria Sudeste, BR-13560970 Sao Carlos, SP - Brazil
[3] INRA, UMR 1225, Interact Hote Agents Pathogens, F-31076 Toulouse - France
Total Affiliations: 3
Document type: Journal article
Source: INDUSTRIAL CROPS AND PRODUCTS; v. 164, JUN 2021.
Web of Science Citations: 1
Abstract

Due to high prevalence and large pathogenicity, Haemonchus contortus is the main gastrointestinal nematode in tropical and subtropical regions. This species is responsible for severe economic losses to sheep and goat breeders in Brazil. The control of this parasite is currently compromised, mainly, due to anthelmintic resistance. In the search for natural anthelmintic alternatives, Pterogyne nitens, a native Brazilian tree with potential ethnopharmacological activity, has been identified. The aim of this study was to evaluate the anthelmintic activity of ethanolic extracts and phenolic compounds from P. nitens, as well as two commercial flavonoids (chrysin and morin), to derive the chemical structure and anthelmintic activity. The ovicidal and larvicidal activity of ethanolic extracts from leaves (EEL) and fruits (EEFR), as well as natural compounds from P. nitens on H. contortus were evaluated through egg hatch assay (EHA) and larval development assay (LDA). The results showed that all extracts, especially the phenolic compounds were active in the EHA and LDA. The egg hatch inhibitory effects of EEL (EC50 = 316 mu g/mL) were more potent than EEFR (EC50 = 512 mu g/mL). However, larval development inhibitory effects of EEL (EC50 = 47 mu g/mL) and EEFR (EC50 = 35 mu g/mL) were similar. Among the compounds, the flavones (sorbifolin, pedalitin, and chrysin) did not have inhibitory effects on egg hatching but presented some activity against larval development of H. contortus. In contrast, the flavonols (quercetin, rutin, and morin) showed high activity in the EHA but were inactive in the LDA. The addition of at hydroxyl group and rutinose group to the flavonoid structure increased the ovicidal and larvicidal activity, respectively. The phenolic acids showed potent anthelmintic activity: caffeic acid, ferulic acid, and gallic acid had the highest anthelmintic effects, presenting EC50 values of 1.48, 0.56, and 4.93 mu g/mL in the EHA; and 31, 22, and 33 mu g/mL in the LDA, respectively. These results suggest that P. nitens might be a source of effective alternative compounds to control H. contortus. (AU)

FAPESP's process: 18/15083-2 - Synthesis and biological evaluation of isobavachalcone (IBC) and analogs as potential agents against tuberculosis
Grantee:Luis Octávio Regasini
Support Opportunities: Regular Research Grants
FAPESP's process: 14/18330-0 - Synthesis and biological evaluation of curcumin-cinnamaldehyde hybrids as bacterial cell division inhibitors
Grantee:Luis Octávio Regasini
Support Opportunities: Regular Research Grants