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1.
Chem Biol Interact ; 291: 245-252, 2018 Aug 01.
Article in English | MEDLINE | ID: mdl-29964003

ABSTRACT

We conducted an investigation to evaluate the effects of Brazilian Pampa biome honey and its major phenolic compounds on the development of an erected wings posture phenotype and related mitochondrial aspects induced by Hypoxia/Reoxygenation (H/R) in Drosophila melanogaster. Flies were pre-treated for 3 days with a 10% honey solution and different concentrations of caffeic acid and ρ-coumaric acid and then submitted to hypoxia for 3 h. We observed that after reoxygenation, some flies acquired an erected wings posture and that this feature may be related to mortality. In addition, H/R induced down-regulation of ewg mRNA expression, which could be associated to the observed complex phenotype. H/R also caused a dysregulation in opa1-like, ldh and diap genes expression and reduced O2 fluxes in flie's mitochondria. Honey mitigated opa1-like mRNA expression changes provoked by H/R. Differently from honey, caffeic and ρ-coumaric acids displayed no protective effects. In conclusion, we report for the first time the protective effects of honey against complex phenotypes and mitochondrial changes induced by H/R in adult flies.


Subject(s)
Aging/physiology , Drosophila melanogaster/metabolism , Honey , Hypoxia/pathology , Mitochondria/metabolism , Oxygen/pharmacology , Protective Agents/pharmacology , Wings, Animal/metabolism , Animals , Behavior, Animal/drug effects , Cell Respiration/drug effects , Drosophila melanogaster/drug effects , Gene Expression Regulation/drug effects , Locomotion/drug effects , Mitochondria/drug effects , Muscles/cytology , Muscles/drug effects , RNA, Messenger/genetics , RNA, Messenger/metabolism , Wings, Animal/drug effects
2.
Ecotoxicol Environ Saf ; 61(3): 353-60, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15922801

ABSTRACT

Antioxidant responses and oxidative stress were evaluated in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Brachyura) after oral microcystin administration. Responses were evaluated through antioxidant enzyme activities (catalase-(CAT), superoxide dismutase, glutathione-S-transferase- (GST)). Nonproteic sulfhydril (NP-SH) groups, oxygen consumption, lipid peroxides (LPO), and oxidized proteins were also measured. Microcystin administration increased the oxygen consumption. GST activity and NP-SH concentration showed transient increases and CAT activity showed a peak and then a reduction. Oxidative damage was evidenced with regard to LPO content and suggested by the inhibition of CAT activity at the end of the experiment, indicating that the antioxidant response induced by the toxin was insufficient. A lowering in the number of hepatopancreatic B cells should be related to microcystin elimination.


Subject(s)
Antioxidants/physiology , Brachyura/physiology , Enzyme Inhibitors/toxicity , Hepatopancreas/physiology , Oxidative Stress , Peptides, Cyclic/toxicity , Animals , Glutathione Transferase/metabolism , Microcystins , Oxygen Consumption
3.
Ecotoxicol Environ Saf ; 61(3): 361-5, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15922802

ABSTRACT

Microcystins are hepatotoxins suspected to generate oxidative stress. This mechanism was evaluated in gills of the estuarine crab Chasmagnathus granulatus (Decapoda, Brachyura). Adult male crabs were fed ground beef with or without vitamin E (600 mg/kg). Microcystin (1.21 microg/kg) was daily administered through forced ingestion, for 7 days. After exposure, catalase activity was reduced in posterior gills of crabs supplemented with vitamin E. A lower increment in glutathione S-transferase activity (GST) was observed in organisms pretreated with vitamin E and then exposed to microcystin with respect to those exposed to the toxin but not pretreated with the vitamin. Pretreatment with vitamin E also increased nonproteic sulfhyrdil groups and this effect was not observed after microcystin exposure. The fact that supplementation with antioxidants such as vitamin E modulates GST activity indicates the direct or indirect involvement of microcystin in oxidative stress generation.


Subject(s)
Antioxidants/pharmacology , Antioxidants/physiology , Brachyura/physiology , Peptides, Cyclic/toxicity , Vitamin E/pharmacology , Animals , Environmental Exposure , Gills/physiology , Glutathione Transferase/metabolism , Microcystins
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