185 research outputs found

    Controle quĂ­mico de parreira-brava (Cissampelos glaberrimay)

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    The aim of this study was to find a chemical alternative for the control of C. g/aberrima, a weed that has became a serious problem in sugar cane plantations. The post emergent herbicides tested included: glyphosate, by itself and mixed with carfentrazone or sulfentrazone, metribuzin, 2,4-D + diuron, acetochlor, ametryne and oxyfluorfen mixed with diuron and acetochlor. In preemergence, oxytluorfen mixed with diuron, 2,4-D/picloram, clomazone, imazapyr, carfentrazone and sulfentrazone, tebuthiuron, 2,4-D/picloram, clomazone mixed with imazapyr, and diuron/hexazinone mixed with MSMA were tested at recommended rates. A third trial was setup under semi controlled conditions aiming at a pre emergence controI of this plant. A PVC cylindrical container containing 42 I of soil was used. The rhizomes were placed at two differents depths: 30 and 55 em, In relation to postemergence herbicide treatments only oxyfluorfen mixed with acetochlor showed good control during the first 30 days after application, after which this treatment started to lose effect. The pre emergent treatments with 2,4-D/picloram and tebuthiuron showed the best control over 90 days and the treatments with imazapyr mixed with oxyfluorfen and clomazone resulted in an excellent control during 60 days in preemergence. The treatment with 2,4-D/picloram did not cause toxicity to the crop. None ofthe preemergence treatments killed the rhizomes at 55 em depth, but 2,4-D/picloram caused death ofthe new shoots, this being the most promising herbicide to control this weed.O trabalho teve por objetivo encontrar uma alternativa para o controle quĂ­mico da parreira-brava, uma planta daninha que vem se constituindo em sĂ©rio problema para a cultura da cana-de-açĂșcar. Os herbicidas utilizados em pĂłs-emergĂȘncia foram glyphosate, isolado e em mistura em tanque com carfentrazone e com sulfentrazone, metribuzin, 2,4-D+diuron, acetochlor, ametryne e oxytluorfen em mistura com diuron e com acetochlor. Em prĂ©-ernergĂȘncia foram testadas as misturas oxytluorfen+diuron, oxyfluorfen+2,4-D/picloram, oxyfluorfen+clomazone, oxyfluorfen+imazapyr, oxyfluorfen+carfentrazone oxytluorfen+sulfentrazone, 2,4-D/picloram, clomazone+imazapyr, diuron/hexazinone+MSMA, e o tebuthiuron isolado, todos em suas doses recomendadas. Um terceiro ensaio foi realizado sob condiçÔes semicontroladas, visando o controle em prĂ©-emergĂȘncia, no qual os rizomas foram colocados em duas profundidades diferentes, 30 e 55 em, em tubos de PVC com capacidade de 42 Ide solo e submetido aos seguintes tratamentos: 2,4-D/picloram (12001320, 1440/384 e 1680/448 g/ha), 2,4-D/picloram+imazapyr (1200/320+500,1200/320+750 e 1200/320+ I000 g/ha), 2,4-D/picloram+metribuzin (1200/ 320+1920, 1200/320+2400 e 1200/320+2880 g/ha), imazapyr (750 g/ha) e metribuzin (2400 g/ha). Como resultado do controle quĂ­mico em pĂłs-emergĂȘncia, apenas o tratamento contendo a mistura oxyfluorfen+acetochlor proporcionou um bom controle durante os primeiros 30 dias apĂłs a aplicação, quando começou a perder eficiĂȘncia. Os tratamentos em prĂ©-emergĂȘncia com 2,4-D/picloram e tebuthiuron proporcionaram excelente controle da planta daninha durante 90 dias, e os tratamentos com imazapyr em 'mistura com oxytluorfen e com clomazone resultaram em excelente controle durante os primeiros 60 dias, apĂłs os quais a eficiĂȘncia diminuiu. O tratamento com 2,4-D/picloram nĂŁo causou intoxicação Ă  cultura. Nenhum dos tratamentos em prĂ©-emergĂȘncia matou os rizomas que se encontravam atĂ© 55 em de profundidade, mas o 2,4-D/picloram causou mortalidade das brotaçÔes, mostrando ser o herbicida mais promissor no controle dessa planta daninha

    The Interplay of Mitochondrial Oxidative Stress and Endoplasmic Reticulum Stress in Cardiovascular Fibrosis in Obese Rats

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    We have evaluated the role of mitochondrial oxidative stress and its association with endoplasmic reticulum (ER) stress activation in the progression of obesity-related cardiovascular fibrosis. MitoQ (200 ”M) was orally administered for 7 weeks to male Wistar rats that were fed a high-fat diet (HFD, 35% fat) or a control diet (CT, 3.5% fat). Obese animals presented cardiovascular fibrosis accompanied by increased levels of extracellular matrix proteins and profibrotic mediators. These alterations were associated with ER stress activation characterized by enhanced levels (in heart and aorta vs. CT group, respectively) of immunoglobulin binding protein (BiP; 2.1-and 2.6-fold, respectively), protein disulfide-isomerase A6 (PDIA6; 1.9-fold) and CCAAT-enhancer-binding homologous protein (CHOP; 1.5- and 1.8-fold, respectively). MitoQ treatment was able to prevent (p < 0.05) these modifications at cardiac and aortic levels. MitoQ (5 nM) and the ER stress inhibitor, 4-phenyl butyric acid (4 ”M), were able to block the prooxidant and profibrotic effects of angiotensin II (Ang II, 10−6 M) in cardiac and vascular cells. Therefore, the data show a crosstalk between mitochondrial oxidative stress and ER stress activation, which mediates the development of cardiovascular fibrosis in the context of obesity and in which Ang II can play a relevant role

    The consequences of growth hormone-releasing hormone receptor haploinsufficiency for bone quality and insulin resistance

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    Objective Growth hormone (GH)/insulin-like growth factor (IGF) axis and insulin are key determinants of bone remodelling. Homozygous mutations in the GH-releasing hormone receptor (GHRHR) gene (GHRHR) are a frequent cause of genetic isolated GH deficiency (IGHD). Heterozygosity for GHRHR mutation causes changes in body composition and possibly an increase in insulin sensitivity, but its effects on bone quality are still unknown. The objective of this study was to assess the bone quality and metabolism and its correlation with insulin sensitivity in subjects heterozygous for a null mutation in the GHRHR. Patients and methods A cross-sectional study was performed on 76 normal subjects (68.4% females) (N/N) and 64 individuals (64.1% females) heterozygous for a mutation in the GHRHR (MUT/N). Anthropometric features, quantitative ultrasound (QUS) of the heel, bone markers [osteocalcin (OC) and CrossLaps], IGF-I, glucose and insulin were measured, and homeostasis model assessment of insulin resistance (HOMAIR) was calculated. Results There were no differences in age or height between the two groups, but weight (P = 0.007) and BMI (P = 0.001) were lower in MUT/N. There were no differences in serum levels of IGF-I, glucose, T-score or absolute values of stiffness and OC, but insulin (P = 0.01), HOMAIR (P = 0.01) and CrossLaps (P = 0.01) were lower in MUT/N. There was no correlation between OC and glucose, OC and HOMAIR in the 140 individuals as a whole or in the separate MUT/N or N/N groups. Conclusions This study suggests that one allele mutation in the GHRHR gene has a greater impact on energy metabolism than on bone quality.NIH, National Institutes of Health USA [1 R01 DK065718]FAPITEC/SE, BrazilCAPESFAEP

    Mitochondrial Oxidative Stress Promotes Cardiac Remodeling in Myocardial Infarction through the Activation of Endoplasmic Reticulum Stress

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    We have evaluated cardiac function and fibrosis in infarcted male Wistar rats treated with MitoQ (50 mg/kg/day) or vehicle for 4 weeks. A cohort of patients admitted with a first episode of acute MI were also analyzed with cardiac magnetic resonance and T1 mapping during admission and at a 12-month follow-up. Infarcted animals presented cardiac hypertrophy and a reduction in the left ventricular ejection fraction (LVEF) and E- and A-waves (E/A) ratio when compared to controls. Myocardial infarction (MI) rats also showed cardiac fibrosis and endoplasmic reticulum (ER) stress activation. Binding immunoglobulin protein (BiP) levels, a marker of ER stress, were correlated with collagen I levels. MitoQ reduced oxidative stress and prevented all these changes without affecting the infarct size. The LVEF and E/A ratio in patients with MI were 57.6 ± 7.9% and 0.96 ± 0.34, respectively. No major changes in cardiac function, extracellular volume fraction (ECV), or LV mass were observed at follow-up. Interestingly, the myeloperoxidase (MPO) levels were associated with the ECV in basal conditions. BiP staining and collagen content were also higher in cardiac samples from autopsies of patients who had suffered an MI than in those who had died from other causes. These results show the interactions between mitochondrial oxidative stress and ER stress, which can result in the development of diffuse fibrosis in the context of MI

    Evaluation of in vitro Antifungal Activity of Xylosma prockia (Turcz.) Turcz. (Salicaceae) Leaves Against Cryptococcus spp.

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    Cryptococcus species are responsible for important systemic mycosis and are estimated to cause millions of new cases annually. The available therapy is limited due to the high toxicity and the increasing rates of yeast resistance to antifungal drugs. Popularly known as “sucarĂĄ,” Xylosma prockia (Turcz.) Turcz. (Salicaceae) is a native plant from Brazil with little information on its pharmacological potential. In this work, we evaluated in vitro anticryptococcal effects of the leaf ethanolic extract of X. prockia and its fractions against Cryptococcus gattii and Cryptococcus neoformans. We also evaluated phenotypic alterations caused by ethyl acetate fraction (EAF) (chosen according to its biological results). The liquid chromatography–mass spectrometry (LC-MS) analysis of EAF demonstrated the presence of phenolic metabolites that belong to three structurally related groups as majority compounds: caffeoylquinic acid, coumaroyl-glucoside, and caffeoyl-glucoside/deoxyhexosyl-caffeoyl glucoside derivatives. The minimum inhibitory concentration (MIC) values against C. gattii and C. neoformans ranged from 8 to 64 mg/L and from 0.5 to 8 mg/L, for ethanolic extract and EAF, respectively. The EAF triggered an oxidative burst and promoted lipid peroxidation. EAF also induced a reduction of ergosterol content in the pathogen cell membrane. These effects were not associated with alterations in the cell surface charge or in the thermodynamic fingerprint of the molecular interaction between EAF and the yeasts evaluated. Cytotoxic experiments with peripheral blood mononuclear cells (PBMCs) demonstrated that EAF was more selective for yeasts than was PBMCs. The results may provide evidence that X. prockia leaf extract might indeed be a potential source of antifungal agents.Fil: Folly, Mariany L. C.. Universidade Federal de Juiz de Fora; BrasilFil: Ferreira, Gabriella F.. Universidade Federal de Juiz de Fora; BrasilFil: Salvador, Maiara R.. Universidade Federal de Juiz de Fora; BrasilFil: Sathler, Ana A.. Universidade Federal de Juiz de Fora; BrasilFil: da Silva, Guilherme F.. Universidade Federal de Juiz de Fora; BrasilFil: Santos, Joice Castelo Branco. Ceuma University; BrasilFil: Santos, Julliana R. A. dos. Ceuma University; BrasilFil: Nunes Neto, Wallace Ribeiro. Ceuma University; BrasilFil: Rodrigues, JoĂŁo Francisco Silva. Ceuma University; BrasilFil: Fernandes, Elizabeth Soares. Ceuma University; BrasilFil: da Silva, LuĂ­s ClĂĄudio Nascimento. Ceuma University; BrasilFil: de Freitas, Gustavo JosĂ© Cota. Universidade Federal de Minas Gerais; BrasilFil: Denadai, Ângelo M.. Universidade Federal de Minas Gerais. Instituto de CiĂȘncias BiolĂłgicas; BrasilFil: Rodrigues, Ivanildes V.. Universidade Federal de Juiz de Fora; BrasilFil: Mendonça, Leonardo M.. Universidade Federal de Juiz de Fora; BrasilFil: Monteiro, Andrea Souza. Ceuma University; BrasilFil: Santos, Daniel Assis. Universidade Federal de Minas Gerais; BrasilFil: Cabrera, Gabriela Myriam. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Ciudad Universitaria. Unidad de MicroanĂĄlisis y MĂ©todos FĂ­sicos en QuĂ­mica OrgĂĄnica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de MicroanĂĄlisis y MĂ©todos FĂ­sicos en QuĂ­mica OrgĂĄnica; ArgentinaFil: Siless, GastĂłn Ezequiel. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Ciudad Universitaria. Unidad de MicroanĂĄlisis y MĂ©todos FĂ­sicos en QuĂ­mica OrgĂĄnica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de MicroanĂĄlisis y MĂ©todos FĂ­sicos en QuĂ­mica OrgĂĄnica; ArgentinaFil: Lang, Karen L.. Universidade Federal de Juiz de Fora; Brasi

    Septic shock in older people: a prospective cohort study

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    Abstract\ud \ud Background\ud Septic shock is the first cause of death in Intensive Care Units. Despite experimental data showing increased inflammatory response of aged animals following infection, the current accepted hypothesis claims that aged patients are immunocompromised, when compared to young individuals.\ud \ud \ud Results\ud Here, we describe a prospective cohort study designed to analyze the immune profile of this population.\ud \ud \ud Conclusion\ud Older people are as immunocompetent as the young individual, regarding the cytokines, chemokines and growth factors response to devastating infection

    Cardiac-Oxidized Antigens Are Targets of Immune Recognition by Antibodies and Potential Molecular Determinants in Chagas Disease Pathogenesis

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    Trypanosoma cruzi elicits reactive oxygen species (ROS) of inflammatory and mitochondrial origin in infected hosts. In this study, we examined ROS-induced oxidative modifications in the heart and determined whether the resultant oxidized cardiac proteins are targets of immune response and of pathological significance in Chagas disease. Heart biopsies from chagasic mice, rats and human patients exhibited, when compared to those from normal controls, a substantial increase in protein 4-hydroxynonenal (4-HNE), malondialdehyde (MDA), carbonyl, and 3-nitrotyrosine (3-NT) adducts. To evaluate whether oxidized proteins gain antigenic properties, heart homogenates or isolated cardiomyocytes were oxidized in vitro and one- or two-dimensional gel electrophoresis (2D-GE)/Western blotting (WB) was performed to investigate the proteomic oxidative changes and recognition of oxidized proteins by sera antibodies in chagasic rodents (mice, rats) and human patients. Human cardiomyocytes exhibited LD50 sensitivity to 30 ”M 4-HNE and 100 ”M H2O2 at 6 h and 12 h, respectively. In vitro oxidation with 4-HNE or H2O2 resulted in a substantial increase in 4-HNE- and carbonyl-modified proteins that correlated with increased recognition of cardiac (cardiomyocytes) proteins by sera antibodies of chagasic rodents and human patients. 2D-GE/Western blotting followed by MALDI-TOF-MS/MS analysis to identify cardiac proteins that were oxidized and recognized by human chagasic sera yielded 82 unique proteins. We validated the 2D-GE results by enzyme-linked immunosorbent assay (ELISA) and WB and demonstrated that oxidation of recombinant titin enhanced its immunogenicity and recognition by sera antibodies from chagasic hosts (rats and humans). Treatment of infected rats with phenyl-α-tert-butyl nitrone (PBN, antioxidant) resulted in normalized immune detection of cardiac proteins associated with control of cardiac pathology and preservation of heart contractile function in chagasic rats. We conclude that ROS-induced, cardiac-oxidized antigens are targets of immune recognition by antibodies and molecular determinants for pathogenesis during Chagas disease

    Blood Meal-Derived Heme Decreases ROS Levels in the Midgut of Aedes aegypti and Allows Proliferation of Intestinal Microbiota

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    The presence of bacteria in the midgut of mosquitoes antagonizes infectious agents, such as Dengue and Plasmodium, acting as a negative factor in the vectorial competence of the mosquito. Therefore, knowledge of the molecular mechanisms involved in the control of midgut microbiota could help in the development of new tools to reduce transmission. We hypothesized that toxic reactive oxygen species (ROS) generated by epithelial cells control bacterial growth in the midgut of Aedes aegypti, the vector of Yellow fever and Dengue viruses. We show that ROS are continuously present in the midgut of sugar-fed (SF) mosquitoes and a blood-meal immediately decreased ROS through a mechanism involving heme-mediated activation of PKC. This event occurred in parallel with an expansion of gut bacteria. Treatment of sugar-fed mosquitoes with increased concentrations of heme led to a dose dependent decrease in ROS levels and a consequent increase in midgut endogenous bacteria. In addition, gene silencing of dual oxidase (Duox) reduced ROS levels and also increased gut flora. Using a model of bacterial oral infection in the gut, we show that the absence of ROS resulted in decreased mosquito resistance to infection, increased midgut epithelial damage, transcriptional modulation of immune-related genes and mortality. As heme is a pro-oxidant molecule released in large amounts upon hemoglobin degradation, oxidative killing of bacteria in the gut would represent a burden to the insect, thereby creating an extra oxidative challenge to the mosquito. We propose that a controlled decrease in ROS levels in the midgut of Aedes aegypti is an adaptation to compensate for the ingestion of heme
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