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1.
Physiol Behav ; 222: 112892, 2020 08 01.
Article in English | MEDLINE | ID: mdl-32302609

ABSTRACT

Abnormalities in the thyroid hormones, like in hypothyroidism, are closely related to dementia and Alzheimer's disease demonstrating the main symptom of these disorders: memory deficit. In this study we evaluated the effect of chrysin on deficit spatial and aversive memories and the contribution of glutamatergic, cholinergic pathways and Na+, K+-ATPase activity on hippocampus and prefrontal cortex in hypothyroid adult female mice C57BL/6. Hypothyroidism was induced by the continuous exposure to 0.1% methimazole (MTZ) in drinking water for 31 days. The exposure to MTZ was associated to low plasma levels of thyroid hormones (TH) compared to the control group on the 32nd. Subsequently, euthyroid and MTZ-induced hypothyroid mice received (intragastrically) either vehicle or chrysin (20 mg/kg) once a day for 28 consecutive days. After treatments mice performed the following behavioral assessments: open-field test (OFT), morris water maze (MWM) and passive avoidance test. Additionally, plasma TH levels were measured again, as well as glutamate levels, Na+,K+-ATPase and acetylcholinesterase (AChE) activities were analyzed in the hippocampus and prefrontal cortex of mice. Mice with hypothyroidism showed a deficit of spatial and aversive memory and chrysin treatment reversed these deficits. It also reduced the levels of glutamate and decreased Na+,K+-ATPase activity in both cerebral structures in the hypothyroid mice compared with the euthyroid ones, with the exception of glutamate in the hippocampus, which was a partial reversal. AChE activity was not altered by treatments. Together, our results demonstrate that chrysin normalized hippocampal glutamate levels and Na+,K+-ATPase activity, which could be involved in the reversal of memory deficit.


Subject(s)
Glutamic Acid , Hypothyroidism , Animals , Female , Flavonoids , Hippocampus/metabolism , Hypothyroidism/chemically induced , Hypothyroidism/drug therapy , Mice , Mice, Inbred C57BL , Sodium-Potassium-Exchanging ATPase/metabolism
2.
Behav Brain Res ; 351: 104-113, 2018 10 01.
Article in English | MEDLINE | ID: mdl-29803654

ABSTRACT

The etiopathogenesis of depression may involve repeated exposure to several unpredictable stressors. This study was conducted to investigate changes induced by chronic unpredictable mild stress (CUMS) and to assess behavioral and neurochemical changes that predict depressive-like behavior in Drosophila melanogaster. Male Drosophila melanogaster flies were exposed to CUMS with several stressors (cold, heat, starvation, and sleep deprivation) in an unpredictable and chronic manner for ten days. At the end of treatment, in vivo behavioral tests (open field, aggression, forced swimming, mating, light/dark box, male fertility evaluation, sucrose preference, weight evaluation) and ex vivo analyses (dopamine and serotonin levels) were performed. Using this CUMS model, we obtained results that contribute to the construction of a depressive model in Drosophila, where we reproduce some behavioral phenotypes corresponding to depressive symptoms, such as immobility in the forced swimming test, less exploration in the light/dark test, changes in mating behavior, changes in the aggressiveness test, reduced sucrose preference, and weight-loss, in addition to a significant reduction in the levels of serotonin and dopamine when compared to the control group. Fluoxetine was used in our study as a positive control to demonstrate that CUMS-induced depressive-like behaviors in flies can be reversed by antidepressants. In conclusion, male Drosophila melanogaster exposed to CUMS display a depressive-like phenotype, and, while this poses some limitations as an animal model for depression, it meets some of the criteria required to be a valid model, such as good face and construct validity.


Subject(s)
Biogenic Amines/metabolism , Depressive Disorder/metabolism , Disease Models, Animal , Drosophila melanogaster , Stress, Psychological/metabolism , Animals , Antidepressive Agents/pharmacology , Behavior, Animal/drug effects , Behavior, Animal/physiology , Brain/drug effects , Brain/metabolism , Depressive Disorder/drug therapy , Depressive Disorder/etiology , Fluoxetine/pharmacology , Male , Motor Activity/drug effects , Motor Activity/physiology , Stress, Psychological/drug therapy , Uncertainty
3.
Eur J Pharmacol ; 822: 78-84, 2018 Mar 05.
Article in English | MEDLINE | ID: mdl-29355556

ABSTRACT

Hypothyroidism is often associated with psychiatric disorders such as depression. In this study, we evaluated the effect of chrysin on depressive-like behavior and monoamine levels in hypothyroid female mice. Hypothyroidism was induced by continuous exposure to 0.1% methimazole (MTZ) in drinking water for 31 days. Exposure to MTZ was associated with low plasma levels of thyroid hormones T3 and T4 compared with the control group. Subsequently, euthyroid and MTZ-induced hypothyroid mice were intragastrically administered vehicle or chrysin (20mg/kg) once a day for 28 consecutive days. After treatments, the following behavioral assessments were performed: Open-Field Test (OFT), Tail suspension test (TST), and Forced Swimming Test (FST). Additionally, T3 and T4 levels were measured again, and serotonin (5HT), dopamine, and noradrenaline levels were analyzed in the prefrontal cortex and the hippocampus. Chrysin treatment could not reverse T3 and T4 levels. Hypothyroid mice showed an increased immobility time in TST and FST; chrysin treatment reversed these effects. Reduced levels of 5HT and dopamine in the prefrontal cortex and the hippocampus were observed in the hypothyroid mice than in the euthyroid mice. Chrysin treatment recovered 5HT content in both structures and dopamine content only in the hippocampus. Noradrenaline content was not altered by treatments. Together, our results have demonstrated that chrysin treatment reverses depressive-like behaviors in hypothyroid female mice and suggests the involvement of 5HT and dopamine in these effects.


Subject(s)
Behavior, Animal/drug effects , Depression/drug therapy , Dopamine/metabolism , Flavonoids/pharmacology , Hippocampus/drug effects , Hypothyroidism/complications , Serotonin/metabolism , Animals , Depression/etiology , Depression/metabolism , Female , Flavonoids/therapeutic use , Hippocampus/metabolism , Mice , Prefrontal Cortex/drug effects , Prefrontal Cortex/metabolism , Thyroid Hormones/metabolism
4.
J Cell Biochem ; 118(4): 709-717, 2017 04.
Article in English | MEDLINE | ID: mdl-27496677

ABSTRACT

This study aims to investigate the protective effect of p-chloro-phenyl-selenoesterol [PCS; 0,2 mg/kg; 10 ml/kg i.g.) in colitis induced by 2,4,6-trinitrobenzene sulfonic acid [TNBS; 2 mg/100 µl 50% ethanol; intrarectally) in mice. Several parameters including weight, length, histological analyses determination, thiobarbituric acid reactive species, reactive species levels, superoxide dismutase, catalase, and myeloperoxidase (MPO) activity of colon were evaluated. The serum levels of tumor necrosis factor alpha [TNF-α) and interleukin 6 [IL-6) were also assessed. Treatment with PCS reduced the clinical and histopathologic severity of TNBS-induced colitis, characterized by colon length reduction and increased colon weight and microscopic intestinal inflammation. The therapeutic effects of PCS in this model were associated with significant decrease in proinflammatory cytokines TNF-α and IL-6 and decrease in MPO activity. Furthermore, combined with improvements in inflammatory parameters, treatment with the PCS was able to decrease oxidative stress and to prevent the decrease in antioxidant defenses in animals with TNBS-induced colitis. This finding suggests that PCS can improve experimental colitis in mice and it could be a potential therapeutic agent for the treatment of patients with IBD. J. Cell. Biochem. 118: 709-717, 2017. © 2016 Wiley Periodicals, Inc.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Inflammatory Bowel Diseases/drug therapy , Organoselenium Compounds/pharmacology , Animals , Cytokines/biosynthesis , Disease Models, Animal , Female , Inflammation Mediators/metabolism , Inflammatory Bowel Diseases/metabolism , Inflammatory Bowel Diseases/pathology , Mice , Oxidative Stress/drug effects , Peroxidase/metabolism , Trinitrobenzenesulfonic Acid/toxicity
5.
Neurotoxicology ; 51: 96-105, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26366809

ABSTRACT

The γ-orizanol present in rice bran oil contains a mix of steryl triterpenyl esters of ferulic acid, which is believed to be linked to its antioxidant potential. In this study we investigated the neuroprotective actions of γ-orizanol (ORY) against the toxicity induced by rotenone (ROT) in Drosophila melanogaster. The flies (both genders) aged between 1 and 5 days old were divided into four groups of 50 flies each: (1) control, (2) ORY 25 µM, (3) ROT 500 µM, (4) ORY 25 µM+ROT 500 µM. Flies were concomitantly exposed to a diet containing ROT and ORY for 7 days according to their respective groups. Survival and behavior analyses were carried out in vivo, and ex vivo analyses involved acetylcholinesterase activity (AChE), determination of dopaminergic levels, cellular viability and mitochondrial viability, activities of superoxide dismutase (SOD), catalase (CAT), glutathione-S-transferase (GST), reactive species levels (RS), lipid peroxidation (TBARS) and contents of total thiols and non-proteic thiols (NPSH). Our results show for the first time that ORY not only acts as an endogenous activator of the cellular antioxidant defenses, but it also ameliorates rotenone induced mortality, oxidative stress and mitochondrial dysfunction. Our salient findings regarded the restoration of cholinergic deficits, dopamine levels and improved motor function provided by ORY. These results demonstrate the neuroprotective potential of ORY and that this effect can be potentially due to its antioxidant action. In conclusion, the present results show that ORY is effective in reducing the ROT induced toxicity in D. melanogaster, which showed a neuroprotective action, possibly due to the presence of the antioxidant constituents such as the ferulic acid.


Subject(s)
Dopamine/metabolism , Insecticides/toxicity , Oxidative Stress/drug effects , Parkinsonian Disorders/metabolism , Parkinsonian Disorders/physiopathology , Phenylpropionates/administration & dosage , Rotenone/toxicity , Acetylcholinesterase/metabolism , Animals , Antioxidants/metabolism , Cell Survival/drug effects , Drosophila melanogaster , Female , Insecticides/administration & dosage , Male , Motor Activity/drug effects , Parkinsonian Disorders/chemically induced , Rotenone/administration & dosage
6.
Rev. patol. trop ; 44(2): 163-169, 2015. tab
Article in Portuguese | LILACS | ID: lil-776167

ABSTRACT

O consumo da alface (Lactuca sativa) pode ser um importante meio de transmissão de váriasdoenças parasitárias. Assim, o controle parasitológico constitui um grande desafio quando se verificaa inclusão cada vez mais frequente de hortaliças na dieta da população mundial. O objetivo destetrabalho foi avaliar a contaminação por parasitos de interesse em saúde pública em alfaces (L. sativa)comercializadas no município de Itaqui, RS. No processo de amostragem, foram selecionadossupermercados e produtores locais da cidade de Itaqui. Foram investigadas 60 amostras de alface (Lsativa) da variedade crespa, sendo 30 de produtores locais e 30 dos mercados locais, todas adquiridasaleatoriamente. As amostras de alface foram acondicionadas em sacos de polietileno limpos eidentificados. As folhas foram separadas uma a uma e lavadas em recipientes de vidro esterilizadoscom 250 mL de água destilada. A água resultante do processo de lavagem foi analisada utilizando-setrês técnicas parasitológicas: exame direto, sedimentação espontânea (Lutz) e centrífugo-flutuaçãoem sulfato de zinco a 33 por cento (Faust). Para a caracterização morfológica dos parasitos, utilizou-semicroscópio óptico. Das 60 amostras analisadas, 29 (48,3 por cento) apresentaram algum tipo de parasito,das quais 19 (63,3 por cento) eram procedentes de produtores locais e 10 (36,7 por cento), dos mercados locais.Foram encontrados ovos de Ascaris sp (5 por cento) e cistos de Giardia lamblia (38 por cento) e Entamoeba sp(13 por cento). A verificação da presença de parasitos, sobretudo helmintos e protozoários, especialmenteem hortaliças, é de grande interesse para a saúde pública, visto que fornece subsídios para o serviçode vigilância sanitária sobre o estado higiênico desses produtos.


The consumption of lettuce (Lactuca sativa) can be an important means of transmission of severalparasitic diseases, so the increasing inclusion of vegetables in the diet of the world populationpresents an important challenge. The objective of this study was to evaluate the contamination oflettuce (L. sativa) marketed in the municipality of Itaqui (RS) by parasites of interest to public health.A sampling process was used, selecting supermarkets and local producers in the city of Itaqui. Weinvestigated 60 samples of lettuce (L. sativa) of the curly variety, from 30 local producers and 30local markets, all acquired at random. The lettuce samples were placed in clean plastic bags andidentified. The leaves were separated and washed in a glass container with 250 ml of sterile distilledwater. The wash water was analyzed using three parasitological techniques: direct examination,spontaneous sedimentation technique (Lutz) and flotation of zinc sulfate to 33 percent (Faust). Themorphological features of the parasite were examined by means of an optical microscope. Of the60 samples analyzed, 29 (48.33 percent) had some type of parasites. Of these, 19 (63.34 percent) were fromlocal producers and 10 (36.66 percent) from local markets. Eggs were found of Ascaris sp. (5 percent) andcysts of Giardia lamblia (38 percent) and Entamoeba sp. (13 percent). Checking for the presence of parasites,particularly helminths and protozoa, especially in vegetables, has great interest for public health,because it supplements health surveillance on the hygienic condition of the goods.


Subject(s)
Lactuca/parasitology , Food Contamination , Parasitic Diseases , Vegetables
7.
J Toxicol Environ Health A ; 77(1-3): 115-24, 2014.
Article in English | MEDLINE | ID: mdl-24555652

ABSTRACT

The adverse effects of the alga Prasiola crispa extract (PcE) were investigated in a fruit fly (Drosophila melanogaster) and cockroach (Nauphoeta cinerea) model. In flies, toxicity was assessed as mortality and biochemical alterations including acetylcholinesterase (AChE) activity and oxidative stress markers. The cardiotoxic action of PcE was also examined in a model of semi-isolated cockroach heart. The administration of PcE (2 mg/ml) to flies for 24 h resulted in a marked increase in mortality rate (7.6-fold rise compared to control). AChE activity, glutathione (GSH) levels, and hydroperoxide formation remained unchanged. Fly glutathione S-transferase (GST) and catalase (CAT) activity were significantly altered after PcE treatment. Fraction III (ethyl acetate) of PcE was significantly more toxic to flies compared to fractions I (methanol) and II (ethanol). A significant decrease was noted in cockroach semi-isolated heart function. The addition of 5,5'-dithiobis-(2-nitrobenzoic acid (DTNB), an oxidizing agent, concomitant with the extract significantly blocked this effect, suggesting that reduced compounds may be involved in the cardiotoxic action produced by PcE. Our results show for the first time the adverse effects of PcE in two insect models, Drosophila melanogaster and Nauphoetacinerea. The insecticidal properties of PcE may be related to changes in important antioxidant/detoxifying systems, as well as to changes in insect cardiac function.


Subject(s)
Chlorophyta/toxicity , Cockroaches/drug effects , Drosophila melanogaster/drug effects , Insecticides/toxicity , Plant Extracts/toxicity , Acetylcholinesterase/metabolism , Animals , Biomarkers/metabolism , Cockroaches/metabolism , Dose-Response Relationship, Drug , Drosophila melanogaster/metabolism , Glutathione/metabolism , Heart/drug effects , Heart/physiopathology , Hydrogen Peroxide/metabolism , Male , Oxidative Stress/drug effects
8.
EXCLI J ; 13: 1239-53, 2014.
Article in English | MEDLINE | ID: mdl-26417337

ABSTRACT

Embryonic animals are especially susceptible to metal exposure. Manganese (Mn) is an essential element, but in excess it can induce toxicity. In this study we used Drosophila melanogaster as an embryonic model to investigate biochemical and behavioral alterations due to Mn exposure. Flies were treated with standard medium supplemented with MnCl2 at 0.1 mM, 0.5 mM or 1 mM from the egg to the adult stage. At 0.5 mM and 1 mM Mn, newly ecloded flies showed significantly enhanced locomotor activity when assessed by negative geotaxis behavior. In addition, a significant increase in Mn levels (p < 0.0001) was observed, while Ca, Fe, Cu, Zn and S levels were significantly decreased. A significant drop in cell viability occurred in flies exposed to 1 mM Mn. There was also an induction of reactive oxygen species at 0.5 mM and 1 mM Mn (p < 0.05). At 1 mM, Mn increased Catalase (p < 0.005), Superoxide Dismutase (p < 0.005) and Hsp83 (p < 0.0001) mRNA expression, without altering Catalase or Superoxide Dismutase activity; the activity of Thioredoxin reductase and Glutatione-S-transferase enzymes was increased. Mn treatment did not alter ERK or JNK1/2 phosphorylation, but at 1 mM caused an inhibition of p38(MAPK) phosphorylation. Together these data suggest mechanisms of adaptation in the fly response to Mn exposure in embryonic life.

9.
Toxicol Rep ; 1: 200-208, 2014.
Article in English | MEDLINE | ID: mdl-28962239

ABSTRACT

Chrysin (5,7-dihydroxyflavone) is a flavonoid, natural component of traditional medicinal herbs, present in honey, propolis and many plant extracts. The objective of this study was to investigate the hypolipidemic properties of chrysin on Triton WR-1339-induced hyperlipidemia in female C57BL/6 mice. Triton WR-1339 was administered intraperitoneally (400 mg/kg) to overnight-fasted mice to develop acute hyperlipidemia. Chrysin was administered orally (10 mg/kg) 30 min before Triton WR-1339. At 24 h after Triton WR-1339 injection, blood samples were collected to measure plasma lipid levels. The hepatic thiobarbituric acid reactive substances (TBARS), carbonyl content, non-protein sulfhydryl (NPSH) and ascorbic acid (AA) levels, as well as catalase (CAT) and superoxide dismutase (SOD) activity were recorded. Chrysin administration significantly decreased total cholesterol levels. In addition, it partially decreased non-high density lipoprotein-cholesterol and triglycerides levels in plasma of hyperlipidaemic mice. In addition chrysin administration prevented the increase on TBARS levels and prevented the decrease in SOD activity induced by Triton WR-1339. These findings indicated that chrysin was able to decrease plasma lipids concentration and that its antioxidant properties was, at least in part, involved in the hypolipidaemic action of chrysin.

10.
Arch Toxicol ; 85(6): 645-51, 2011 Jun.
Article in English | MEDLINE | ID: mdl-20924558

ABSTRACT

Diphenyl diselenide (PhSe)(2) is a synthetic organoselenium compound displaying glutathione peroxidase-like activity. Protective and antioxidant potential of (PhSe)(2) have been extensively investigated in in vivo and in vitro studies. In spite of this, there is a lack of studies addressed to the investigation of potential cytotoxic effect and signaling pathways modulated by this compound. Herein, we aimed to analyze the effects of 24-h treatment with (PhSe)(2) on cell viability and a possible modulation of signaling pathways in human neuroblastoma cell line SH-SY5Y. For this purpose, cells were incubated with (PhSe)(2) (0.3-30 µM) for 24 h and cell viability, apoptotic cell death and modulation of MAPKs (ERK1/2 and p38(MAPK)), and PKC substrates phosphorylation was determined. (PhSe)(2) treatment significantly decreased cell viability and increased the number of apoptotic cells with induction of PARP cleavage. An increase in ERK1/2 phosphorylation was observed at (PhSe)(2) 3 µM. In contrast, higher concentrations of the chalcogenide inhibited ERK1/2, p38(MAPK) and PKC substrate phosphorylation. Pre-treatment with ERK1/2 inhibitor, U0126, increased cell susceptibility to (PhSe)(2). Together, these data indicate a cytotoxic potential of (PhSe)(2) in a neuronal cell line, which appears to be mediated by the ERK1/2 pathway.


Subject(s)
Antioxidants/toxicity , Apoptosis/drug effects , Benzene Derivatives/toxicity , Extracellular Signal-Regulated MAP Kinases/metabolism , MAP Kinase Signaling System/drug effects , Neurons/drug effects , Organoselenium Compounds/toxicity , Benzene Derivatives/agonists , Cell Line, Tumor , Cell Survival/drug effects , Extracellular Signal-Regulated MAP Kinases/chemistry , Humans , Isoenzymes/metabolism , Mitogen-Activated Protein Kinase 1/antagonists & inhibitors , Mitogen-Activated Protein Kinase 1/chemistry , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3/antagonists & inhibitors , Mitogen-Activated Protein Kinase 3/chemistry , Mitogen-Activated Protein Kinase 3/metabolism , Molecular Weight , Neurons/metabolism , Organoselenium Compounds/agonists , Peptide Fragments/chemistry , Peptide Fragments/metabolism , Phosphorylation/drug effects , Poly(ADP-ribose) Polymerases/chemistry , Poly(ADP-ribose) Polymerases/metabolism , Protein Kinase C/metabolism , Protein Kinase Inhibitors/pharmacology , Protein Processing, Post-Translational/drug effects , p38 Mitogen-Activated Protein Kinases/chemistry , p38 Mitogen-Activated Protein Kinases/metabolism
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