FB2026_02 , released June 18, 2026
Reference Report
Open Close
Reference
Citation
Macedo, G.E., Gomes, K.K., Rodrigues, N.R., Martins, I.K., Wallau, G.D.L., Carvalho, N.R., Cruz, L.C.D., Costa Silva, D.G.D., Boligon, A.A., Franco, J.L., Posser, T. (2017). Senecio brasiliensis impairs eclosion rate and induces apoptotic cell death in larvae of Drosophila melanogaster.  Comp. Biochem. Physiol. C. Toxicol. Pharmacol. 198(): 45--57.
FlyBase ID
FBrf0235675
Publication Type
Research paper
Abstract
Senecio brasilienis (Spreng) Less., is a species native from Brazil, popularly known as "Maria mole", and known to induce hepatotoxicity due to its high content of Pyrrolizidine alkaloids. Despite its toxicity, this plant is widely used in Brazilian folk medicine. Considering the antagonizing effects described for S. brasiliensis, we describe here molecular markers involved in the toxicity of hydroalcoholic extract from leaves of S. brasiliensis (HESB) in Drosophila melanogaster. Phytochemical analysis of HESB revealed the presence of phenolic acids and flavonoids. A significant antioxidant potential against ABTS(+) and DPPH radical was found in parallel. Ingestion of extract did not alter the survival and locomotor activity of adult flies. However when ingested along the larval developmental phase, the eclosion rate of flies was interrupted at higher concentration of extract. To comprehend this phenomenon several analysis were conducted in larvae. HESB stimulated activity of antioxidant enzymes SOD and GST, and increased GSH/GSSG ratio and ROS production. Additionally, HESB caused a significant decrease of cell viability. The mRNA expression of Nrf2, TrxR, CAT, Drice and Dilp6 were also significantly up-regulated. HESB caused significant decrease on the phosphorylation of MAPKs and AKT. In parallel, PARP cleavage and caspases 3/7 activity were stimulated. In addition, glucose, glycogen and triglycerides levels were decreased. Taken together our study depicts a disruption in the eclosion of D. melanogaster possibly attributed to the inhibition of kinases implied in developmental process, energetic demand and induction of apoptotic cell death process.
PubMed ID
PubMed Central ID
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Comp. Biochem. Physiol. C. Toxicol. Pharmacol.
    Title
    Comparative biochemistry and physiology. Toxicology & pharmacology : CBP
    Publication Year
    2000--
    ISBN/ISSN
    1532-0456
    Data From Reference
    Chemicals (1)
    Genes (10)