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

• Published in: Oxidative medicine and cellular longevity 2020, Vol.2020 (2020), p.1-10
• Main Authors: de Menezes, Irwin R. A., Franco, Jeferson Luis, Posser, Thaís, Bolignon, Aline, Vieira, Patrícia de Brum, Rodrigues, Jéssica Ferreira, Kemmerich Martins, Illana, Ziech, Cynthia Camila, Rodrigues, Nathane Rosa, Echeverria Macedo, Giulianna, Gomes, Karen Kich, Júnior, Francisco E. B.
• Format: Article
• Language: English
• Subjects: Acids; Agriculture; Antioxidants; Care and treatment; Chromatography; Drosophila; Enzyme inhibitors; Enzymes; Ethanol; Flavonoids; Flour; Glutathione transferase; Health aspects; Insects; Leaves; Lipid peroxidation; Oxidative stress; Phenols; Poisoning; Proteins; Reactive oxygen species; Signal transduction; Sucrose; Superoxide
• ISSN: 1942-0900; 1942-0994
• DOI: 10.1155/2020/3960170

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.