965 resultados para N-methoxy-N-methyl-2-[(4 ` substituted)phenylsulfinyl]propanamides
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Insulin resistance is a transitory phenomenon of the metabolic response to trauma. In uncomplicated operations it lasts for 2-4 weeks postoperatively, and is directly related to the magnitude of the injury. The fasting status caused by conventional fasting protocols aggravates this resistance and may induce hyperglycemia. Conventional preoperative fasting time may aggravate this resistance and increment the elevation of glycemia especially because it is frequently longer than the expected 6-8h and may reach 10-16 hs. Additionally, overnight fasting may cause variable degrees of dehydration depending on the extension of the fasting period. Recently, various societies of anesthesia and nutrition have changed their guidelines to propose a reduction of preoperative fasting to 2h with clear fluids containing carbohydrates. These new protocols (ACERTO, ERAS) are based on the safety of this routine as consistently demonstrated by various randomized trials and a meta-analysis.
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The human body eliminates foreign compounds primarily by metabolizing them to hydrophilic forms to facilitate effective excretion through the kidneys. Cytochrome P450 (CYP) enzymes in the liver and intestine contribute to the metabolism of many drugs. Pharmacokinetic drugdrug interactions occur if the activity of CYPs are inhibited or induced by another drug. Prescribing multiple drugs to the improve effectiveness of therapy or to treat coexisting diseases is a common practice in clinical medicine. Polypharmacy predisposes patients to adverse effects because of the profound unpredictability in CYP enzymatic-mediated drug metabolism. S-ketamine is a phencyclidine derivative which functions as an antagonist of the N-methyl-Daspartate (NMDA) receptor in the central nervous system. It is a unique anaesthetic producing “dissociative anaesthesia” in high doses and analgesia in low doses. Studies with human liver microsomes suggest that ketamine is metabolized primarily via CYP3A4 and CYP2B6 enzymes. In this thesis, in healthy volunteers, randomized and controlled cross-over studies were conducted to investigate the effects of different CYP inducers and inhibitors on the pharmacokinetics and pharmacodynamics of oral and intravenous S-ketamine. The plasma concentrations of ketamine and its metabolite, norketamine, were determined at different timepoints over a 24 hour period. Other pharmacodynamic variables were examined for 12 hours. Results of these studies showed that the inhibition of the CYP3A4 pathway by clarithromycin or grapefruit juice increased the exposure to oral S-ketamine by 2.6- and 3.0-fold. Unexpectedly, CYP3A4 inhibition by itraconazole caused no significant alterations in the plasma concentrations of oral S-ketamine. CYP3A4 induction by St. John´s wort or rifampicin decreased profoundly the concentrations of oral S-ketamine. However, after rifampicin, there were no significant differences in the plasma concentrations of S-ketamine when it was administered intravenously. This demonstrated that rifampicin inhibited the metabolism of Sketamine at the intestinal level. When CYP2B6 was inhibited by ticlopidine, there was a 2.4- fold increase in the exposure of S-ketamine. These studies demonstrated that low dose oral Sketamine is metabolized both via CYP3A4 and CYP2B6 pathways. The concomitant use of drugs that affect CYP3A4 or CYP2B6, during oral S-ketamine treatment, may cause clinically significant drug-drug interactions.
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Background: Type 2 diabetes patients have a 2-4 fold risk of cardiovascular disease (CVD) compared to the general population. In type 2 diabetes, several CVD risk factors have been identified, including obesity, hypertension, hyperglycemia, proteinuria, sedentary lifestyle and dyslipidemia. Although much of the excess CVD risk can be attributed to these risk factors, a significant proportion is still unknown. Aims: To assess in middle-aged type 2 diabetic subjects the joint relations of several conventional and non-conventional CVD risk factors with respect to cardiovascular and total mortality. Subjects and methods: This thesis is part of a large prospective, population based East-West type 2 diabetes study that was launched in 1982-1984. It includes 1,059 middle-aged (45-64 years old) participants. At baseline, a thorough clinical examination and laboratory measurements were performed and an ECG was recorded. The latest follow-up study was performed 18 years later in January 2001 (when the subjects were 63-81 years old). The study endpoints were total mortality and mortality due to CVD, coronary heart disease (CHD) and stroke. Results: Physically more active patients had significantly reduced total, CVD and CHD mortality independent of high-sensitivity C-reactive protein (hs-CRP) levels unless proteinuria was present. Among physically active patients with a hs-CRP level >3 mg/L, the prognosis of CVD mortality was similar to patients with hs-CRP levels ≤3 mg/L. The worst prognosis was among physically inactive patients with hs-CRP levels >3 mg/L. Physically active patients with proteinuria had significantly increased total and CVD mortality by multivariate analyses. After adjustment for confounding factors, patients with proteinuria and a systolic BP <130 mmHg had a significant increase in total and CVD mortality compared to those with a systolic BP between 130 and 160 mmHg. The prognosis was similar in patients with a systolic BP <130 mmHg and ≥160 mmHg. Among patients without proteinuria, a systolic BP <130 mmHg was associated with a non-significant reduction in mortality. A P wave duration ≥114 ms was associated with a 2.5-fold increase in stroke mortality among patients with prevalent CHD or claudication. This finding persisted in multivariable analyses. Among patients with no comorbidities, there was no relationship between P wave duration and stroke mortality. Conclusions: Physical activity reduces total and CVD mortality in patients with type 2 diabetes without proteinuria or with elevated levels of hs-CRP, suggesting that the anti-inflammatory effect of physical activity can counteract increased CVD morbidity and mortality associated with a high CRP level. In patients with proteinuria the protective effect was not, however, present. Among patients with proteinuria, systolic BP <130 mmHg may increase mortality due to CVD. These results demonstrate the importance of early intervention to prevent CVD and to control all-cause mortality among patients with type 2 diabetes. The presence of proteinuria should be taken into account when defining the target systolic BP level for prevention of CVD deaths. A prolongation of the duration of the P wave was associated with increased stroke mortality among high-risk patients with type 2 diabetes. P wave duration is easy to measure and merits further examination to evaluate its importance for estimation of the risk of stroke among patients with type 2 diabetes.
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Este trabalho teve como objetivo avaliar a eficiência de misturas de herbicidas no controle de duas espécies de trapoeraba, Commelina diffusa e Commelina benghalensis. Para isso, segmentos de caule dessas espécies foram transplantados em vasos contendo 12 L de substrato. Após 120 dias, foram aplicados os seguintes tratamentos: carfentrazone-ethyl (30 g ha¹) em mistura com glyphosate (720 g ha-1) e/ou glyphosate potássico (720 g ha-1); glyphosate (720 g ha-1) em mistura com flumioxazin (60 g ha-1) e/ou 2,4-D (670 g ha-1) e/ou metsulfuron methyl (4 g ha-1); oxyfluorfen em mistura com sulfentrazone (480 + 375 g ha¹); aplicações seqüenciais, com intervalo de 21 dias, de [(paraquat + diuron) / (carfentrazone-ethyl + glyphosate)] [(200+400)/(30+720)] e de [(paraquat + diuron) / (paraquat + diuron)] [(200+400)/(200+400)]; e testemunha sem aplicação de herbicida. Cada espécie constituiu um experimento, sendo ambos conduzidos no delineamento em blocos casualizados, com quatro repetições. Foram feitas avaliações de controle das trapoerabas e da biomassa fresca da parte aérea. Os tratamentos mais eficientes no controle das trapoerabas foram as aplicações seqüenciais, com intervalo de 21 dias, de (paraquat + diuron) / (carfentrazone-ethyl + glyphosate) e de (paraquat + diuron) / (paraquat + diuron), seguidas das misturas em tanque de 2,4-D + glyphosate e de carfentrazone-ethyl + glyphosate e/ou glyphosate potássico.
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Foi realizado um levantamento referente à comercialização de herbicidas no Estado do Paraná, visando quantificar o volume de sua utilização durante o ano de 2000. Em seguida, com base nas propriedades químicas desses herbicidas, estudaram-se critérios teóricos para classificá-los de acordo com o potencial de lixiviação. A análise dos dados do levantamento indicou que o maior volume comercializado ocorreu no quarto trimestre, relacionando-se provavelmente ao aumento da demanda provocada pela safra de verão. Os grupos de mecanismos de ação cujo consumo é mais significativo são, pela ordem, os inibidores da síntese de aminoácidos (36,9% do total comercializado), os inibidores da fotossíntese (31,3%), os mimetizadores da auxina (11%) e os inibidores da divisão celular (8,8%). Os herbicidas glyphosate (4.562,28 t), atrazine (3.075,91 t), 2,4-D (1.659,33 t) e sulfosate (631,60 t) representam, em conjunto, cerca de 65% do volume total comercializado no Estado. A classificação quanto ao potencial de lixiviação demonstrou que acifluorfen-sódio, alachlor, atrazine, chlorimuron-ethyl, fomesafen, hexazinone, imazamox, imazapyr, imazaquin, imazethapyr, metolachlor, metribuzin, metsulfuron-methyl, nicosulfuron, picloram, sulfentrazone e tebuthiuron são potencialmente lixiviadores, de acordo com os três critérios teóricos adotados (GUS, CDFA e Cohen).
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As condições climáticas, no momento da aplicação, determinam em grande parte a eficácia de herbicidas pós-emergentes. Com o objetivo de avaliar a influência das condições climáticas sobre a eficácia de diferentes herbicidas, aplicados na pós-emergência da cultura de trigo, para o controle de Raphanus raphanistrum (nabiça), foi conduzido um experimento em condições de campo, na Estação Experimental da Fundação ABC, município de Tibagi-PR, na safra de 2002. A cultura de trigo foi instalada em sistema de plantio direto, utilizando o cultivar OR1. O delineamento experimental adotado foi o de blocos ao acaso em esquema fatorial 5 x 4 (cinco herbicidas e quatro horários de aplicação), em quatro repetições. Os herbicidas utilizados foram, em g de i.a. ha-1: metsulfuron-methyl (3,6), iodosulfuron-methyl (5,0), metribuzin (144,0), 2,4-D amina (1005,0) e 2,4-D éster (400,0); os horários de aplicação durante o dia foram 7h, 10h30, 13h30 e 17h45. A aplicação dos tratamentos herbicidas foi feita com a cultura do trigo em pleno perfilhamento, e com uma infestação de 288 pl m-2 de nabiça, que possuíam em média cinco a sete folhas. As características avaliadas foram eficácia de controle da nabiça e porcentagem de fitotoxicidade na cultura aos 8, 16, 22 e 30 dias após aplicação dos tratamentos (DAA). Os dados obtidos foram submetidos à análise de variância pelo teste F no programa SAS, sendo as médias comparadas pelo teste de LSD de Fishes a 5% de probabilidade. Houve interação entre os herbicidas e os horários de aplicação em relação ao controle de nabiça. Metribuzin e iodosulfuron-methyl foram os herbicidas menos influenciados pelas condições climáticas nos diferentes horários para o controle de nabiça. O metribuzin foi mais eficiente no seu controle, mas evidenciou sintomas de fitotoxicidade que desapareceram aos 30 DAA. As condições climáticas que ocorreram para os diferentes horários de aplicação influenciaram o desempenho dos herbicidas. O metsulfuron-methyl, o 2,4-D amina e o 2,4-D éster apresentaram grandes diferenças de controle conforme o horário de aplicação, sendo os horários das 7h00 e 17h45 os que proporcionaram menor controle quando comparados aos horários das 10h30 e 13h30. Esses resultados evidenciam a importância das condições climáticas no momento das aplicações de defensivos agrícolas no inverno, na cultura de trigo.
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A aplicação de um mesmo herbicida, ou de herbicidas com o mesmo mecanismo de ação, durante anos consecutivos, numa mesma área, pode resultar na seleção de biótipos de plantas daninhas resistentes a herbicidas. O objetivo deste trabalho foi confirmar a resistência de um biótipo da planta daninha losna-branca (Parthenium hysterophorus) aos herbicidas inibidores da enzima acetolactato sintase (ALS), proveniente de uma propriedade rural no município de Mandaguari, norte do Estado do Paraná. Plantas com suspeita de resistência foram tratadas com diversos herbicidas e doses e comparadas com plantas de uma população suscetível. Os tratamentos foram as doses recomendadas dos herbicidas, duas e quatro vezes superiores à dose recomendada. Os produtos e as doses aplicadas foram cloransulam-methyl a 0,0; 33,6; 67,2; e 134,4 g i.a. ha-1 mais o adjuvante Agral a 0,2% v/v, chlorimuron-ethyl a 0,0; 20,0; 40,0; e 80,0 g i.a. ha-1, imazethapyr a 0,0; 100,0; 200,0; e 400,0 g i.a. ha-1 e iodosulfuron-methyl-sodium mais foramsulfuron a 0,0; 3,0 + 45,0 g i.a. ha-1 (150,0 g p.c. ha¹); 6,0 + 90,0 g i.a. ha-1 (300,0 g p.c. ha-1); e 12,0 + 180,0 g i.a. ha-1 (600,0 g p.c. ha-1). Foi acres centado um tratamento com o herbicida 2,4-D na dose de 536,0 g e.a. ha-1. As curvas de doseresposta do biótipo resistente foram inferiores às do biótipo suscetível em todas as doses e herbicidas estudados. O biótipo de losna-branca foi confirmado como resistente aos herbicidas inibidores da ALS. A ocorrência de resistência cruzada foi observada em relação aos herbicidas pertencentes aos grupos químicos das imidazolinonas (imazethapyr), triazolopirimidinas (cloransulam-methyl) e sulfoniluréias (chlorimuron-ethyl e iodosulfuron-methyl-sodium mais foramsulfuron). O herbicida 2,4-D, apresentou alto índice de controle de ambos os biótipos de losna-branca avaliados, confirmando que esse mecanismo de ação do herbicida é uma importante alternativa para manejar áreas com problemas de resistência.
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O glyphosate é um herbicida não-seletivo utilizado para controlar plantas daninhas há mais de 20 anos no Rio Grande do Sul. A buva (Conyza bonariensis) é uma espécie daninha comum nos Estados da região Sul do Brasil e tradicionalmente controlada com uso de glyphosate. Entretanto, nos últimos anos plantas de buva têm apresentado poucos sintomas de toxicidade em resposta ao tratamento com glyphosate, sugerindo que estas plantas são resistentes ao herbicida. Assim, com o objetivo de avaliar a resposta de uma população de plantas de buva a glyphosate, foram realizados três experimentos: um em campo e dois em casa de vegetação. No experimento em campo, os tratamentos avaliados constaram de doses crescentes de glyphosate (0, 360, 720, 1.440, 2.880 e 5.760 g ha-1), e os herbicidas paraquat (400 g ha-1) e 2,4-D (1.005 g ha-1) foram empregados como produtos testemunhas, com diferentes mecanismos de ação nas plantas. No experimento em casa de vegetação os tratamentos constaram de doses crescentes de glyphosate (0, 360, 720, 1.440, 2.880 e 5.760 g ha-1), mais os herbicidas testemunhas, aplicados sobre plantas de um biótipo considerado resistente e de outro considerado sensível. No segundo experimento realizado em casa de vegetação, foram avaliados os tratamentos contendo glyphosate (720, 1.440 e 2.880 g ha-1), mais os herbicidas chlorimuron-ethyl (40 g ha-1), metsulfuron-methyl (4 g ha-1), 2,4-D (1.005 g ha-1), paraquat (400 g ha-1) e diuron + paraquat (200 + 400 g ha-1), bem como a testemunha sem tratamento herbicida. A toxicidade dos tratamentos herbicidas foi avaliada aos 7, 15 e 30 DAT (dias após tratamento). Os resultados obtidos nos experimentos em condições de campo e em casa de vegetação, de forma geral, evidenciam que o biótipo sensível é controlado pelo glyphosate e pelos demais herbicidas avaliados. Demonstram ainda que o biótipo resistente apresenta-se, igualmente ao biótipo sensível, altamente suscetível aos herbicidas com mecanismo de ação distinto daquele do glyphosate. Entretanto, o biótipo resistente mostra baixa resposta ao herbicida glyphosate, mesmo se este for empregado em doses elevadas, evidenciando ter adquirido resistência a esse produto.
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Os efeitos dos herbicidas bentazon, metolachlor, trifluralin, imazethapyr, imazethapyr+lactofen, haloxyfop-methyl, glyphosate e chlorimuron-ethyl, testados em duas concentrações (duas e dez vezes a dose média recomendada por hectare), sobre a atividade microbiana foram estudados em amostras de solo que nunca haviam recebido tratamento com pesticidas. Como bioindicadores, utilizou-se a respiração microbiana, quantificando a emissão de CO2 aos 2, 4, 8, 12, 16, 20 e 24 dias após incubação, a atividade da enzima desidrogenase e a hidrólise de diacetato de fluoresceína (FDA), aos 8 e 28 dias. Bentazon e a mistura de imazethapyr+lactofen na maior concentração e o haloxyfop-methyl nas duas concentrações apresentaram efeitos inibitórios na respiração edáfica, embora diferentes em época e duração do efeito. Nenhum dos tratamentos herbicidas afetou a hidrólise da FDA. A atividade da desidrogenase foi inibida, o que foi verificado em análise realizada aos oito dias,nas amostras de solo com alta concentração de bentazon e imazethapyr; no entanto, foi estimulada nos tratamentos com baixa concentração de metolachlor e imazethapyr e na maior concentração de glyphosate. A respiração basal e a atividade da desidrogenase mostraram maior sensibilidade na detecção de efeitos dos herbicidas sobre a microbiota do solo que as determinações da hidrólise de FDA. Apenas foi encontrada correlação significativa entre a atividade da desidrogenase e a respiração basal aos oito dias de incubação. Os resultados destacam a importância da consideração de múltiplos indicadores na avaliação dos efeitos de herbicidas na microbiota do solo.
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Species of the orchidaceae family are grown for marketing flowers and among them the genus Cattleya stands out. However, due to its slow growth, the substrate is subjected to weed infestation. Therefore, this study aims to evaluate the selectivity and efficiency of herbicides in controlling Pilea microphylla in Cattleya orchid seedlings (Cattleya tenebrosa x Cattleya leopoldy). We used a completely randomized design with four replications. The evaluated herbicides were oxyfluorfen (0, 120, 240 and 480 g ha-1), flumioxazin (0, 12.5, 25 and 40 g ha-1), nicosulfuron (0, 20, 40 and 80 g ha-1) mesotrione (0, 96, 144 and 192 g ha-1), clethodim (0, 60, 84 and 108 g ha-1) and metsulfuron-methyl (0, 1.2, 1.8 and 2.4 g ha-1). At post-emergence applying time, the Cattleya plants had three bulb sand were 10 cm tall, while P. microphylla, where 5 cm tall. Nicosulfuron, mesotrione and clethodim herbicides did not control P. microphylla, while oxyfluorfen and flumioxazin showed over 90% efficiency level sin controlling P. microphyllafrom 14 days after application (DAA). As to metsulfuron-methyl, it showed efficiency superior to 90% from the control dose of 1.8 g ha-1 at 28 DAA. All herbicides were selective plants of Cattleya, however, only oxyfluorfen, flumioxazin and metsulfuron-methyl were effective in controlling P. microphylla.
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ABSTRACT The aim of this work was to evaluate the weed management with herbicides applied in pre and postemergence on castor crop. The treatments were constituted by management systems using herbicides in pre (PRE) and postemergence (POS): 1) S-metolachlor at 576 g ha-1 (PRE 1) and chlorimuron-methyl at 15 g ha-1 (POS 1); 2) PRE 1 + clomazone at 650 g ha-1(PRE 2) and POS 1; 3) PRE 1, POS 1 and halosulfuron-methyl at 112.5 g ha-1(POS 2); 4) PRE 1, POS 1 and ethoxysulfuron at 60 g ha-1 (POS 3); 5) PRE 1, POS 1 and ethoxysulfuron at 120 g ha-1 (POS 4); 6) PRE 1 + PRE 2, POS 1 and POS 2; 7) PRE 1 + PRE 2, POS 1 and POS 3; 8) PRE 1 + PRE 2, POS 1 and POS 4; 9) hand-hoeing control and 10) non-weeded control. The experimental design was randomized blocks with four replications. The association of the herbicides in PRE combined to sequence applications of chlorimuron-ethyl and halosulfuron-methyl or ethoxysulfuron in POS resulted in the highest control levels of Richardia scabraand Cyperus ferax. Mild phytointoxication symptoms to the crop were more persistent with ethoxysulfuron at 120 g ha-1. The acceptable control of the weed species and similar yield to the hand-hoeing control permitted to conclude that S-metolachlor + clomazone PRE, followed by chlorimuron-ethyl and halosulfuron-methyl POS proved to be more adequate as a weed management strategy on castor crop.
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Two intramolecularly quenched fluorogenic peptides containing o-aminobenzoyl (Abz) and ethylenediamine 2,4-dinitrophenyl (EDDnp) groups at amino- and carboxyl-terminal amino acid residues, Abz-DArg-Arg-Leu-EDDnp (Abz-DRRL-EDDnp) and Abz-DArg-Arg-Phe-EDDnp (Abz-DRRF-EDDnp), were selectively hydrolyzed by neutral endopeptidase (NEP, enkephalinase, neprilysin, EC 3.4.24.11) at the Arg-Leu and Arg-Phe bonds, respectively. The kinetic parameters for the NEP-catalyzed hydrolysis of Abz-DRRL-EDDnp and Abz-DRRF-EDDnp were Km = 2.8 µM, kcat = 5.3 min-1, kcat/Km = 2 min-1 µM-1 and Km = 5.0 µM, kcat = 7.0 min-1, kcat/Km = 1.4 min-1 µM-1, respectively. The high specificity of these substrates was demonstrated by their resistance to hydrolysis by metalloproteases [thermolysin (EC 3.4.24.2), angiotensin-converting enzyme (ACE; EC 3.4.24.15)], serineproteases [trypsin (EC 3.4.21.4), a-chymotrypsin (EC 3.4.21.1)] and proteases present in tissue homogenates from kidney, lung, brain and testis. The blocked amino- and carboxyl-terminal amino acids protected these substrates against the action of aminopeptidases, carboxypeptidases and ACE. Furthermore, DR amino acids ensured total protection of Abz-DRRL-EDDnp and Abz-DRRF-EDDnp against the action of thermolysin and trypsin. Leu-EDDnp and Phe-EDDnp were resistant to hydrolysis by a-chymotrypsin. The high specifity of these substrates suggests their use for specific NEP assays in crude enzyme preparations
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We describe a new simple, selective and sensitive micromethod based on HPLC and fluorescence detection to measure debrisoquine (D) and 4-hydroxydebrisoquine (4-OHD) in urine for the investigation of xenobiotic metabolism by debrisoquine hydroxylase (CYP2D6). Four hundred µl of urine was required for the analysis of D and 4-OHD. Peaks were eluted at 8.3 min (4-OHD), 14.0 min (D) and 16.6 min for the internal standard, metoprolol (20 µg/ml). The 5-µm CN-reverse-phase column (Shimpack, 250 x 4.6 mm) was eluted with a mobile phase consisting of 0.25 M acetate buffer, pH 5.0, and acetonitrile (9:1, v/v) at 0.7 ml/min with detection at lexcitation = 210 nm and lemission = 290 nm. The method, validated on the basis of measurements of spiked urine, presented 3 ng/ml (D) and 6 ng/ml (4-OHD) sensitivity, 390-6240 ng/ml (D) and 750-12000 ng/ml (4-OHD) linearity, and 5.7/8.2% (D) and 5.3/8.2% (4-OHD) intra/interassay precision. The method was validated using urine of a healthy Caucasian volunteer who received one 10-mg tablet of Declinax®, po, in the morning after an overnight fast. Urine samples (diuresis of 4 or 6 h) were collected from zero to 24 h. The urinary excretion of D and 4-OHD, Fel (0-24 h), i.e., fraction of dose administered and excreted into urine, was 6.4% and 31.9%, respectively. The hydroxylation capacity index reported as metabolic ratio was 0.18 (D/4-OHD) for the person investigated and can be compared to reference limits of >12.5 for poor metabolizers (PM) and <12.5 for extensive metabolizers (EM). In parallel, the recovery ratio (RR), another hydroxylation capacity index, was 0.85 (4-OHD: SD + 4-OHD) versus reference limits of RR <0.12 for PM and RR >0.12 for EM. The healthy volunteer was considered to be an extensive metabolizer on the basis of the debrisoquine test.