Hexane extract from SpoSndias mombin L. (Anacardiaceae) prevents behavioral and oxidative status changes on model of Parkinson's disease in zebrafish.


Journal

Comparative biochemistry and physiology. Toxicology & pharmacology : CBP
ISSN: 1532-0456
Titre abrégé: Comp Biochem Physiol C Toxicol Pharmacol
Pays: United States
ID NLM: 100959500

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 22 07 2020
revised: 04 12 2020
accepted: 06 12 2020
pubmed: 15 12 2020
medline: 6 7 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

The search for new therapies, derived from natural compounds in order to prevent and treat Parkinson's disease (PD) has aroused the interest of many researchers. Spondias mombin (L) has active constituents with known antioxidant and anti-inflammatory activities. The aim of this study was to evaluate the neuroprotective potential of the hexane extract of S. mombin (EHSm) in an experimental model of DP induced by rotenone in zebrafish. The analysis of GC/MS demonstrated cyclogallipharaol (13.88%) and dl-α-tocopherol (8.08%) mostly, while HPLC-DAD indicated the presence of quercetin (<5), quercetrin (6.54 mg/g) and rutin (8.83 mg/g). The zebrafish exposed for 4 weeks to rotenone (ROT, 3 μg/L) and EHSm (5, 15, 25 mg/L). EHSm (25 mg/L) was able to reverse the behavioral damage induced by ROT in the entries and time spent in the top area of the tank. The parameters biochemicals indicated of EHSm prevented oxidative stress (TBARS e total thiols), inflammation and dopamine uptake triggered by ROT, evidenced of increased on the CAT, SOD and GSH and decreased of GST, O

Identifiants

pubmed: 33310063
pii: S1532-0456(20)30253-2
doi: 10.1016/j.cbpc.2020.108953
pii:
doi:

Substances chimiques

Plant Extracts 0
Rotenone 03L9OT429T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108953

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Glaucia Dal Santo (GD)

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.

Bruno Oliveira de Veras (BO)

Departamento de Medicina Tropical, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.

Eduardo Rico (E)

Laboratório de Neurologia Experimental, Programa de Pós-Graduação em Ciências da Saúde, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brazil.

Jacir Dal Magro (JD)

Área de Ciências Ambientais, Universidade Comunitária da Região de Chapecó (Unochapecó), Chapecó, SC, Brazil.

Jotele Fontana Agostini (JF)

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.

Leucio Duarte Vieira (LD)

Departamento de Fisiologia e Farmacologia, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.

Jean Felipe Fossá Calisto (JFF)

Área de Ciências Ambientais, Universidade Comunitária da Região de Chapecó (Unochapecó), Chapecó, SC, Brazil.

Ricieri Mocelin (R)

Programa de Pós-Graduação em Farmacologia e Terapêutica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

Vitória de Sá Fonseca (V)

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil; Programa de Pós-Graduação em Farmacologia e Terapêutica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

Almir Gonçalves Wanderley (AG)

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil; Departamento de Fisiologia e Farmacologia, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil. Electronic address: almir.wanderley@ufpe.br.

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Classifications MeSH