111 resultados para Demetrius.


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Because the potential of yerba mate (Ilex paraguariensis) has been suggested in the management of obesity, the aim of the present study was to evaluate the effects of yerba mate extract on weight loss, obesity-related biochemical parameters, and the regulation of adipose tissue gene expression in high-fat diet-induced obesity in mice. Thirty animals were randomly assigned to three groups. The mice were introduced to standard or high-fat diets. After 12 weeks on a high-fat diet, mice were randomly assigned according to the treatment (water or yerba mate extract 1.0 g/-kg). After treatment intervention, plasma concentrations of total cholesterol, high-density lipoprotein cholesterol, triglyceride, low-density lipoprotein (LDL) cholesterol, and glucose were evaluated. Adipose tissue was examined to determine the mRNA levels of several genes such as tumor necrosis factor-alpha (TNF-alpha), leptin, interleukin-6 (IL-6), C-C motif chemokine ligand-2 (CCL2), CCL receptor-2 (CCR2), angiotensinogen, plasminogen activator inhibitor-1 (PAI-1), adiponectin, resistin, peroxisome proliferator-activated receptor-gamma(2) (PPAR-gamma(2)), uncoupling protein-1 (UCP1), and PPAR-gamma coactivator-1 alpha (PGC-1 alpha). The F4/80 levels were determined by immunoblotting. We found that obese mice treated with yerba mate exhibited marked attenuation of weight gain, adiposity, a decrease in epididymal fat-pad weight, and restoration of the serum levels of cholesterol, triglycerides, LDL cholesterol, and glucose. The gene and protein expression levels were directly regulated by the high-fat diet. After treatment with yerba mate extract, we observed a recovery of the expression levels. In conclusion, our data show that yerba mate extract has potent antiobesity activity in vivo. Additionally, we observed that the treatment had a modulatory effect on the expression of several genes related to obesity.

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Mate (Ilex paraguariensis) is rich in polyphenolic compounds, which are thought to contribute to the health benefits of tea. Mate tea was administered orally to mice at a dose of 0.5, 1.0 or 2.0 g/kg for 60 d, and changes both in serum lipid concentration and fatty acid composition of liver and kidney were examined. The effects of mate tea on serum and tissue lipid peroxidation were assessed by the evaluation of thiobarbituric acid-reactive substances (TBARS). In tea-consuming mice, both MUFA (18: 1n-9) and PUFA (18: 2n-6 and 20: 4n-6) were increased (P<0.05) in the liver lipid (approximately 90 and 60%, respectively), whereas only MUFA (approximately 20%) were increased in the kidney lipid. The most altered PUFA class was n-6 PUFA, which increased by approximately 60-75 % (P<0.05). This difference in the fatty acid profile in the liver is reflected in the increased PUFA:SFA ratio. Consistent with these results, mice fed with mate tea had much lower TBARS in the liver. No differences (P>0.05) were found in the levels of serum cholesterol, HDL-cholesterol and TAG under the conditions of the present study. These results suggest that treatment with mate tea was able to protect unsaturated fatty acids from oxidation and may have selective protective effects within the body, especially on the liver.

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Yerba mate (Ilex paraguariensis) is rich in polyphenols, especially chlorogenic acids. Evidence suggests that dietary polyphenols could play a role in glucose absorption and metabolism. The aim of this study was to evaluate the antidiabetic properties of yerba mate extract in alloxan-induced diabetic Wistar rats. Animals (n = 41) were divided in four groups: nondiabetic control (NDC, n = 10), nondiabetic yerba mate (NDY, n = 10), diabetic control (DC, n = 11), and diabetic yerba mate (NDY, n = 10). The intervention consisted in the administration of yerba mate extract in a 1 g extract/kg body weight dose for 28 days; controls received saline solution only. There were no significant differences in serum glucose, insulin, and hepatic glucose-6-phosphatase activity between the groups that ingested yerba mate extract (NDY and DY) and the controls (NDC and DC). However, the intestinal SGLT1 gene expression was significantly lower in animals that received yerba mate both in upper (p = 0.007) and middle (p < 0.001) small intestine. These results indicate that bioactive compounds present in yerba mate might be capable of interfering in glucose absorption, by decreasing SGLT1 expression.

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O objetivo desta dissertação é avaliar se há correlação significativa entre a receita orçamentária municipal, em termos per capita, e seu grau de desenvolvimento humano medido pelo indicador IDH. Para tanto foi proposto um modelo econométrico com o emprego de dados em painel aplicado a uma amostra de 2264 cidades brasileiras nos anos de 1991 e 2000. Para testar a robustez dos resultados preliminares, os municípios foram segregados ainda conforme a região geográfica em que estão localizados e segundo o tamanho da população residente em seus territórios. Independentemente do agrupamento efetuado os resultados se mantiveram bastante estáveis, sendo possível concluir que a relação entre a receita orçamentária per capita municipal e o IDH é muito fraca, embora estatisticamente significante. Outra importante conclusão deste estudo é que quanto pior os indicadores sociais do município observado, maior é o aumento marginal esperado no IDH em função de acréscimos na sua arrecadação per capita.

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The generation of active chlorine on Ti/Sn(1-x)Ir (x) O-2 anodes, with different compositions of Ir (x = 0.01, 0.05, 0.10 and 0.30 ), was investigated by controlled current density electrolysis. Using a low concentration of chloride ions (0.05 mol L-1) and a low current density (5 mA cm(-2)) it was possible to produce up to 60 mg L-1 of active chlorine on a Ti/Sn0.99Ir0.01O2 anode. The feasibility of the discoloration of a textile acid azo dye, acid red 29 dye (C.I. 16570), was also investigated with in situ electrogenerated active chlorine on Ti/Sn(1-x)Ir (x) O-2 anodes. The best conditions for 100% discoloration and maximum degradation (70% TOC reduction) were found to be: NaCl pH 4, 25 mA cm(-2) and 6 h of electrolysis. It is suggested that active chlorine generation and/or powerful oxidants such as chlorine radicals and hydroxyl radicals are responsible for promoting faster dye degradation. Rate constants calculated from color decay versus time reveal a zero order reaction at dye concentrations up to 1.0 x 10(-4) mol L-1. Effects of other electrolytes, dye concentration and applied density currents also have been investigated and are discussed.

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Anopheles darlingi is the principal neotropical malaria vector, responsible for more than a million cases of malaria per year on the American continent. Anopheles darlingi diverged from the African and Asian malaria vectors ∼100 million years ago (mya) and successfully adapted to the New World environment. Here we present an annotated reference A. darlingi genome, sequenced from a wild population of males and females collected in the Brazilian Amazon. A total of 10 481 predicted protein-coding genes were annotated, 72% of which have their closest counterpart in Anopheles gambiae and 21% have highest similarity with other mosquito species. In spite of a long period of divergent evolution, conserved gene synteny was observed between A. darlingi and A. gambiae. More than 10 million single nucleotide polymorphisms and short indels with potential use as genetic markers were identified. Transposable elements correspond to 2.3% of the A. darlingi genome. Genes associated with hematophagy, immunity and insecticide resistance, directly involved in vectorhuman and vectorparasite interactions, were identified and discussed. This study represents the first effort to sequence the genome of a neotropical malaria vector, and opens a new window through which we can contemplate the evolutionary history of anopheline mosquitoes. It also provides valuable information that may lead to novel strategies to reduce malaria transmission on the South American continent. The A. darlingi genome is accessible at www.labinfo.lncc.br/index.php/anopheles- darlingi. © 2013 The Author(s).

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Esta dissertação pretende analisar a obra de cinco tomos intitulada Motins Políticos ou história dos principais acontecimentos políticos na Província do Pará desde o ano de 1821 até 1835. Elaborado em finais do século XIX pelo historiador e político Domingos Antônio Raiol (Barão de Guajará), esse estudo caracteriza-se pela descrição de uma série de conflitos políticos e sociais ocorridos no Grão-Pará, entre as décadas de 1820 e 1830, transformando-se ao longo do século XX, em fonte central para a história da Cabanagem. Ademais, o livro de Raiol foi muito além de elencar fontes sobre a superficialidade dos eventos políticos e suas lideranças amazônicas. Motins Políticos apresenta através de olhares sensíveis ou racionais, inúmeras referências direcionadas à natureza e sociedade amazônica. Analisando estas concepções românticas e cientificistas, essa dissertação investiga o percurso metodológico de seu autor, seu processo de produção, bem como as inúmeras críticas impetradas a ele e a sua obra ao longo do tempo.

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Neste artigo discute-se como alguns letrados e políticos da Amazônia compreenderam a cultura iletrada na Cabanagem, movimento ocorrido nessa região entre 1835 e 1840. Analisam-se relatórios de presidentes da província do Grão-Pará, estudos da época e centralmente a obra Motins políticos, do historiador e político imperial Domingos Antônio Raiol, o Barão de Guajará. Escrita entre as décadas de 1860 e 1890, a obra descreve as motivações para a guerra cabana pela ótica da ordem imperial, sobretudo após a ascensão do imperador D. Pedro II. Admite-se como hipótese que as mudanças educacionais e sociais, nascidas após os anos de 1870, embora tenham fomentado a criação de novas instituições escolares e ampliado o grau e a abrangência da instrução formal, elas também trouxeram temores na sua condução por se tratar de um local tão revolucionário quanto o Pará. Conclui-se que discutir os saberes cabanos - ainda que pela leitura arrevesada de Raiol - é criticar um tipo de educação formal, compreendendo o quanto ela pode desqualificar conhecimentos e saberes informais de mundo.

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Abstract Background The city of Sao Paulo has the highest AIDS case rate, with nearly 60% in Brazil. Despite, several studies involving molecular epidemiology, lack of data regarding a large cohort study has not been published from this city. Objectives This study aimed to describe the HIV-1 subtypes, recombinant forms and drug resistance mutations, according to subtype, with emphasis on subtype C and BC recombinants in the city of São Paulo, Brazil. Study design RNA was extracted from the plasma samples of 302 HIV-1-seropositive subjects, of which 211 were drug-naive and 82 were exposed to ART. HIV-1 partial pol region sequences were used in phylogenetic analyses for subtyping and identification of drug resistance mutations. The envelope gene of subtype C and BC samples was also sequenced. Results From partial pol gene analyses, 239 samples (79.1%) were assigned as subtype B, 23 (7.6%) were F1, 16 (5.3%) were subtype C and 24 (8%) were mosaics (3 CRF28/CRF29-like). The subtype C and BC recombinants were mainly identified in drug-naïve patients (72.7%) and the heterosexual risk exposure category (86.3%), whereas for subtype B, these values were 69.9% and 57.3%, respectively (p = 0.97 and p = 0.015, respectively). An increasing trend of subtype C and BC recombinants was observed (p < 0.01). Conclusion The HIV-1 subtype C and CRFs seem to have emerged over the last few years in the city of São Paulo, principally among the heterosexual population. These findings may have an impact on preventive measures and vaccine development in Brazil.

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RATIONALE Early reperfusion in patients experiencing acute ischemic stroke is critical, especially for patients with large vessel occlusion who have poor prognosis without revascularization. Solitaire™ stent retriever devices have been shown to immediately restore vascular perfusion safely, rapidly, and effectively in acute ischemic stroke patients with large vessel occlusions. AIM The aim of the study was to demonstrate that, among patients with large vessel, anterior circulation occlusion who have received intravenous tissue plasminogen activator, treatment with Solitaire revascularization devices reduces degree of disability 3 months post stroke. DESIGN The study is a global multicenter, two-arm, prospective, randomized, open, blinded end-point trial comparing functional outcomes in acute ischemic stroke patients who are treated with either intravenous tissue plasminogen activator alone or intravenous tissue plasminogen activator in combination with the Solitaire device. Up to 833 patients will be enrolled. PROCEDURES Patients who have received intravenous tissue plasminogen activator are randomized to either continue with intravenous tissue plasminogen activator alone or additionally proceed to neurothrombectomy using the Solitaire device within six-hours of symptom onset. STUDY OUTCOMES The primary end-point is 90-day global disability, assessed with the modified Rankin Scale (mRS). Secondary outcomes include mortality at 90 days, functional independence (mRS ≤ 2) at 90 days, change in National Institutes of Health Stroke Scale at 27 h, reperfusion at 27 h, and thrombolysis in cerebral infarction 2b/3 flow at the end of the procedure. ANALYSIS Statistical analysis will be conducted using simultaneous success criteria on the overall distribution of modified Rankin Scale (Rankin shift) and proportions of subjects achieving functional independence (mRS 0-2).

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Background Among patients with acute ischemic stroke due to occlusions in the proximal anterior intracranial circulation, less than 40% regain functional independence when treated with intravenous tissue plasminogen activator (t-PA) alone. Thrombectomy with the use of a stent retriever, in addition to intravenous t-PA, increases reperfusion rates and may improve long-term functional outcome. Methods We randomly assigned eligible patients with stroke who were receiving or had received intravenous t-PA to continue with t-PA alone (control group) or to undergo endovascular thrombectomy with the use of a stent retriever within 6 hours after symptom onset (intervention group). Patients had confirmed occlusions in the proximal anterior intracranial circulation and an absence of large ischemic-core lesions. The primary outcome was the severity of global disability at 90 days, as assessed by means of the modified Rankin scale (with scores ranging from 0 [no symptoms] to 6 [death]). Results The study was stopped early because of efficacy. At 39 centers, 196 patients underwent randomization (98 patients in each group). In the intervention group, the median time from qualifying imaging to groin puncture was 57 minutes, and the rate of substantial reperfusion at the end of the procedure was 88%. Thrombectomy with the stent retriever plus intravenous t-PA reduced disability at 90 days over the entire range of scores on the modified Rankin scale (P<0.001). The rate of functional independence (modified Rankin scale score, 0 to 2) was higher in the intervention group than in the control group (60% vs. 35%, P<0.001). There were no significant between-group differences in 90-day mortality (9% vs. 12%, P=0.50) or symptomatic intracranial hemorrhage (0% vs. 3%, P=0.12). Conclusions In patients receiving intravenous t-PA for acute ischemic stroke due to occlusions in the proximal anterior intracranial circulation, thrombectomy with a stent retriever within 6 hours after onset improved functional outcomes at 90 days.

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Directionality in populations of replicating organisms can be parametrized in terms of a statistical concept: evolutionary entropy. This parameter, a measure of the variability in the age of reproducing individuals in a population, is isometric with the macroscopic variable body size. Evolutionary trends in entropy due to mutation and natural selection fall into patterns modulated by ecological and demographic constraints, which are delineated as follows: (i) density-dependent conditions (a unidirectional increase in evolutionary entropy), and (ii) density-independent conditions, (a) slow exponential growth (an increase in entropy); (b) rapid exponential growth, low degree of iteroparity (a decrease in entropy); and (c) rapid exponential growth, high degree of iteroparity (random, nondirectional change in entropy). Directionality in aggregates of inanimate matter can be parametrized in terms of the statistical concept, thermodynamic entropy, a measure of disorder. Directional trends in entropy in aggregates of matter fall into patterns determined by the nature of the adiabatic constraints, which are characterized as follows: (i) irreversible processes (an increase in thermodynamic entropy) and (ii) reversible processes (a constant value for entropy). This article analyzes the relation between the concepts that underlie the directionality principles in evolutionary biology and physical systems. For models of cellular populations, an analytic relation is derived between generation time, the average length of the cell cycle, and temperature. This correspondence between generation time, an evolutionary parameter, and temperature, a thermodynamic variable, is exploited to show that the increase in evolutionary entropy that characterizes population processes under density-dependent conditions represents a nonequilibrium analogue of the second law of thermodynamics.

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Back Row: James Brown, Jon Falk, Dave Garlow, Bill Sheridan, Tom Hassel, Reggie Mitchell, Sr. Mgr. Michael Drews, Bob Tait, Pete Wentworth, Russ Miller, Larry Barrows, John Ferens, Chuck Ritter

11th Row: Paul Alexander, Alex Agase, Bob Thornbladh, Tirrel Burton, Jerry Hanlon, Elliot Uzelac, Gary Moeller, Milan Vooletich, Jerry Meter, Lloyd Carr, Cam Cameron, Michael Trgovac

10th Row: Fritz Seyferth, Andy Johnson, John Althouse, Joel Boyden, Mike Gillette, Mike Edwards, Sean LaFountaine, Olatide Ogunfitidimi, Vincent Washington, Steve Woroniecki, Gulam Kahn, Mike Gittleson

9th Row: John Kolesar, David Weil, Scott Crawford, Chris Simmons, Brian Reid, John Plantz, Mike DePalma, Keith Mitchell, Keith Cooper, Joe Holland, Frank Petroff, Anthony Mitchell, Bob Hurst

8th Row: Mike Taylor, Demetrius Brown, Dave Arnold, Mike Jones, Brent White, Pat Olszewski, John Herrman, Jeff Brown, Bobby Abrams, Derrick Walker, J.J. Grant, Rick Hassel, Cliff Dochterman

7th Row: Ernie Bock, Kyle Anderson, Mike DeBoer, John Duerr, Scott Mandel, Dave Mandel, John Whitledge, Brad Burrows, Don Lessner, Pat Fitzgerald, Geoff Bissell, Rick Sutkiewicz, Phil Logas

6th Row: Ernie Holloway, Jamie Morris, John Zingales, Chuck Adams, Chris D'Esposito, Mark Erhardt, John Vitale, Dave Dever, John Willingham, Bob Cernak, Rick Stites, Bob Stites

5th Row: Gene Lawson, Ken Mouton, Erik Campbell, Dave Chester, Michael Dames, Mike Husar, Dave Herrick, Mark Hill, Dan Holloway, Mike Kovac, Mark Messner, Keith Evens

4th Row: Ed Hood, Tim Schulte, Ken Higgins, Steve Thibert, Phil Webb, Carlitos Bostic, David Folkertsma, Andy Borowski, Monte Robbins, Todd Schulte, Jack Walker, Russell Rein

3rd Row: Pat Moons, Marty Shimko, Andre McIntyre, Garland Rivers, Dan Rice, John Mihic, John Elliott, Gerald White, Chris Zurbrugg, Billy Harris, Keith Cowan, Doug Mallory

2nd Row: Ben Logue, Greg Randall, Mark Hammerstein, Dieter Heren, Gilvanni Johnson, Paul Jokisch, Mike Reinhold, Jerry Quaerna, Mike Krauss, Andy Moeller, Paul Schmerge, Thomas Wilcher, Coach Bo Schembechler

Front Row: Tony Gant, Bob Perryman, Bob Tabachino, Jeff Akers, Brad Cochran, Mike Mallory, Mike Hammerstein, Eric Kattus, Clay Miller, Jim Scarcelli, Jim Harbaugh, Ivan Hicks

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Front Row: Anthony Mitchell, Pat Fitzgerald, David Ritter, Allen Bishop, Chris Zurbrugg, Phil Webb, Jamie Morris, Erik Campbell, Doug Mallory, Bob Cernak, Ernie Bock, Don Lessner, Rick Stites, Bob Stites.

2nd Row: Andy Borowski, Dave Chester, Dave Folkertsma, Michael Dames, John Vitale, Andre McIntyre, John Elliott, Mark Messner, Steve Thibert, Monte Robbins, Billy Harris, John Willingham, Mike Husar, Carlitos Bostic, Bo Schembechler.

3rd Row: Rick Hassel, Bobby Abrams, Derrick Walker, Jeff Brown, David Arnold, Dave Dever, Brent White, John Duerr, Dave Mandel, Scott Mandel, Michael Taylor, Demetrius Brown, John Kolesar, Mike Gillette.

4th Row: Ernie Holloway, Rick Sutkiewicz, Keith Cooper, J.J. Grant, Keith Mitchell, Dean Dingman, Pat Olszewski, David Weil, Joe Holland, John Herrmann, Frank Petroff, Olatide Ogunfitidim, Sean LaFontaine, Mike DeBoer.

5th Row: Vince Washington, Scott Herrala, David Key, Mike Teeter, John Milligan, Greg McMurtry, John Plantz, Joel Boyden, Warde Manuel, Jarrod Bunch, Allen Jefferson, Chris Calloway, Doug Matton, Gulam Khan.

6th Row: Mark Gutzwiller, Jeff Tubo, Marc Spencer, Marc Ramirez, T.J. Osman, Scott Smykowski, Tom Dohring, Doug Daugherty, Mike Kerr, Curtis Feaster, Vada Murray, Tim Williams, Tracy Williams, Trey Walker.

7th Row: Sean Eastman, Byron Lawson, Dave Knight, Todd Plate, Greg Ziegler, Steve Zacharias, Huemartin Robinson, Tony Boles, Chris Horn, Mike Edwards, Stu Duncan, Dave Herrick, Brian Reid, Ken Mouton, Chris D'Esposito.

8th Row: Eric Bush, Wilbur Odom, Erick Anderson, Brian Townsend, Ron Zielinski, Dave Diebolt, Greg Skrepenak, Dave Dingman, Alex Marshall, Chris Bohn, Rusty Fishtner, Ken Sollom, Otis Williams, Ra-Mon Watkins.

9th Row: Shawn Watson, Carlos Smith, Yale VanDyne, Mike Evans, Dave Ritter, Matt Elliott, Dan Jokisch, Mark Soehnlen, Lance Dottin, Neil Simpson, Kevin Owen, Jim Sinclair, Bill Madden, J.D. Carlson, John Rodney.

10th Row: Aaron Studwell, Jon Falk, Mike Gittleson, Mike Walters, Damon Taylor, Leon Morton, Dave Caputo, Brad Moyer, Colin Rudolph, Eric Traupe, David Papp, Fritz Seyferth, Russ Miller, Paul Schmidt, Kevin Kolcheff, Brad Andres.

Back Row: Dennis Morgan, Jeff Long, Jim Herrmann, Bill Harris, Bobby Morrison, Tom Reed, Lloyd Carr, Gary Moeller, Jerry Hanlon, Tirrel Burton, Les Miles, Cam Cameron, Alex Agase, Kevin Kalinich, Randy Fichtner, Dave Garlow, Dennis Blanchard, Charlie Baird.