Croton campestris A. St.-Hill Methanolic Fraction in a Chlorpyrifos-Induced Toxicity Model in Drosophila melanogaster: Protective Role of Gallic Acid

Author:

Gomes Karen Kich1,Macedo Giulianna Echeverria1,Rodrigues Nathane Rosa12,Ziech Cynthia Camila1,Martins Illana Kemmerich1,Rodrigues Jéssica Ferreira1,de Brum Vieira Patrícia1,Boligon Aline Augusti3,de Brito Junior Francisco Elizaudo4,de Menezes Irwin R. A.4,Franco Jeferson Luis12ORCID,Posser Thaís1ORCID

Affiliation:

1. Oxidative Stress and Cell Signaling Research Group, Interdisciplinary Research Center on Biotechnology-CIPBIOTEC, Universidade Federal do Pampa, Campus São Gabriel, RS, Brazil

2. Department of Chemistry, Post Graduate Program in Toxicological Biochemistry, Universidade Federal de Santa Maria, RS, Brazil

3. Postgraduate Program in Pharmaceutical Sciences, Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil

4. Department of Biological Chemistry, Universidade Regional do Cariri, Crato, CE, Brazil

Abstract

Croton campestris A. St-Hill popularly known as “velame do campo” is a native species of the savannah from northeastern Brazil, being used in folk medicine due to its beneficial effects in the treatment of many diseases, inflammation, detoxification, gastritis, and syphilis; however, its potential use as an antidote against organophosphorus compound poisoning has not yet been shown. Here, the protective effect of the methanolic fraction of C. campestris A. St.-Hill (MFCC) in Drosophila melanogaster exposed to chlorpyrifos (CP) was investigated. Flies were exposed to CP and MFCC during 48 h through the diet. Following the treatments, parameters such as mortality, locomotor behavior, and oxidative stress markers were evaluated. Exposure of flies to CP induced significant impairments in survival and locomotor performance. In parallel, increased reactive oxygen species and lipoperoxidation occurred. In addition, the activity of acetylcholinesterase was inhibited by CP, and superoxide dismutase and glutathione S-transferase activity was induced. Treatment with MFCC resulted in a blockage of all CP-induced effects, with the exception of glutathione S-transferase. Among the major compounds found in MFCC, only gallic acid (GA) showed a protective role against CP while quercetin and caffeic acid alone were ineffective. When in combination, these compounds avoided the toxicity of CP at the same level as GA. As far as we know, this is the first study reporting the protective effect of MFCC against organophosphate toxicity in vivo and highlights the biotechnological potential of this fraction attributing a major role in mediating the observed effects to GA. Therefore, MFCC may be considered a promising source for the development of new therapeutic agents for the treatment of organophosphate intoxications.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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