16 research outputs found

    Efectos de dietas ricas en ácidos grasos monoinsaturados en la gestión y prevención de la resistencia a la insulina: Una revisión sistemática

    Get PDF
    Insulin resistance (IR), which is linked to obesity, is a mechanism associated with metabolic diseases, mainly type 2 diabetes mellitus. Studies have shown that monounsaturated fatty acids (MUFAs) have anti-inflammatory and anti-oxidative properties which positively affect IR. This systematic review examined the effects of MUFAs from different sources on IR in obese or overweight patients with or without metabolic syndrome. A search was carried out in the PubMed/Medline and Bireme/VHL databases, and data from 16 studies were analysed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. The intervention time ranged from 1 day to 5.2 years. All participants were overweight or obese; some had central obesity, a moderate risk of cardiovascular disease, low high-density lipoprotein levels, altered fasting glucose levels, prediabetes or type 2 diabetes mellitus. This systematic review provides evidence that MUFA-rich diets can improve IR.La resistencia a la insulina (RI), que está ligada a la obesidad, es un mecanismo asociado a enfermedades metabólicas, principalmente a la diabetes mellitus tipo 2. Los estudios han demostrado que los ácidos grasos monoinsaturados (AGMI) tienen propiedades antiinflamatorias y antioxidantes, que afectan positivamente a la RI. Esta revisión sistemática examinó los efectos de los AGMI de diferentes fuentes sobre la RI en pacientes obesos o con sobrepeso con o sin síndrome metabólico. Se realizó una búsqueda en las bases de datos PubMed/Medline y Bireme/VHL, y se analizaron los datos de 16 estudios de acuerdo con las pautas Preferred Reporting Items for Systematic Reviews and Meta-Analyses. El tiempo de intervención osciló entre 1 día y 5,2 años. Todos los participantes tenían sobrepeso u obesidad; algunos tenían obesidad central, riesgo moderado de enfermedad cardiovascular, niveles bajos de lipoproteínas de alta densidad, niveles alterados de glucosa en ayunas, prediabetes o diabetes mellitus tipo 2. Esta revisión sistemática proporciona evidencia de que las dietas ricas en MUFA pueden mejorar la RI

    Fish oil ingestion reduces the number of aberrant crypt foci and adenoma in 1,2-dimethylhydrazine-induced colon cancer in rats

    Get PDF
    We determined the effect of fish oil (FO) ingestion on colonic carcinogenesis in rats. Male Wistar rats received 4 subcutaneous injections (40 mg/kg body weight each) of 1,2-dimethylhydrazine (DMH) at 3-day intervals and were fed a diet containing 18% by weight FO (N = 10) or soybean oil (SO, N = 10) for 36 weeks. At sacrifice, the colon was removed, aberrant crypt foci were counted and the fatty acid profile was determined. Intestinal tumors were removed and classified as adenoma or carcinoma. Liver and feces were collected and analyzed for fatty acid profile. FO reduced the mean (± SEM) number of aberrant crypt foci compared to SO (113.55 ± 6.97 vs 214.60 ± 18.61; P 0.05). In conclusion, our findings indicate that chronic FO ingestion protected against the DMH-induced preneoplastic colon lesions and adenoma development, but not against carcinoma in rats

    Consistency analysis of a nonbirefringent Lorentz-violating planar model

    Full text link
    In this work analyze the physical consistency of a nonbirefringent Lorentz-violating planar model via the analysis of the pole structure of its Feynman propagators. The nonbirefringent planar model, obtained from the dimensional reduction of the CPT-even gauge sector of the standard model extension, is composed of a gauge and a scalar fields, being affected by Lorentz-violating (LIV) coefficients encoded in the symmetric tensor κμν\kappa_{\mu\nu}. The propagator of the gauge field is explicitly evaluated and expressed in terms of linear independent symmetric tensors, presenting only one physical mode. The same holds for the scalar propagator. A consistency analysis is performed based on the poles of the propagators. The isotropic parity-even sector is stable, causal and unitary mode for 0κ00<10\leq\kappa_{00}<1. On the other hand, the anisotropic sector is stable and unitary but in general noncausal. Finally, it is shown that this planar model interacting with a λφ4\lambda|\varphi|^{4}-Higgs field supports compactlike vortex configurations.Comment: 11 pages, revtex style, final revised versio

    Pervasive gaps in Amazonian ecological research

    Get PDF
    Biodiversity loss is one of the main challenges of our time, and attempts to address it require a clear understanding of how ecological communities respond to environmental change across time and space. While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes, vast areas of the tropics remain understudied. In the American tropics, Amazonia stands out as the world's most diverse rainforest and the primary source of Neotropical biodiversity, but it remains among the least known forests in America and is often underrepresented in biodiversity databases. To worsen this situation, human-induced modifications may eliminate pieces of the Amazon's biodiversity puzzle before we can use them to understand how ecological communities are responding. To increase generalization and applicability of biodiversity knowledge, it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple organism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region's vulnerability to environmental change. 15%–18% of the most neglected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lost

    Long-term aerobic swimming training by rats reduces the number of aberrant crypt foci in 1,2-dimethylhydrazine-induced colon cancer

    No full text
    We determined the effect of long-term aerobic swimming training regimens of different intensities on colonic carcinogenesis in rats. Male Wistar rats (11 weeks old) were given 4 subcutaneous injections (40 mg/kg body weight each) of 1,2-dimethyl-hydrazine (DMH, dissolved in 0.9% NaCl containing 1.5% EDTA, pH 6.5), at 3-day intervals and divided into three exercise groups that swam with 0% body weight (EG1, N = 11), 2% body weight (EG2, N = 11), and 4% body weight of load (EG3, N = 10), 20 min/day, 5 days/week for 35 weeks, and one sedentary control group (CG, N = 10). At sacrifice, the colon was removed and counted for tumors and aberrant crypt foci. Tumor size was measured and intra-abdominal fat was weighed. The mean number of aberrant crypt foci was reduced only for EG2 compared to CG (26.21 ± 2.99 vs 36.40 ± 1.53 crypts; P < 0.05). Tumor incidence was not significantly different among groups (CG: 90%; EG1: 72.7%; EG2: 90%; EG3: 80%). Swimming training did not affect either tumor multiplicity (CG: 2.30 ± 0.58; EG1: 2.09 ± 0.44; EG2: 1.27 ± 0.19; EG3: 1.50 ± 0.48 tumors) or size (CG: 1.78 ± 0.24; EG1: 1.81 ± 0.14; EG2: 1.55 ± 0.21; EG3: 2.17 ± 0.22 cm3). Intra-abdominal fat was not significantly different among groups (CG: 10.54 ± 2.73; EG1: 6.12 ± 1.15; EG2: 7.85 ± 1.24; EG3: 5.11 ± 0.74 g). Aerobic swimming training with 2% body weight of load protected against the DMH-induced preneoplastic colon lesions, but not against tumor development in the rat

    Long-term aerobic swimming training by rats reduces the number of aberrant crypt foci in 1,2-dimethylhydrazine-induced colon cancer

    Get PDF
    We determined the effect of long-term aerobic swimming training regimens of different intensities on colonic carcinogenesis in rats. Male Wistar rats (11 weeks old) were given 4 subcutaneous injections (40 mg/kg body weight each) of 1,2-dimethyl-hydrazine (DMH, dissolved in 0.9% NaCl containing 1.5% EDTA, pH 6.5), at 3-day intervals and divided into three exercise groups that swam with 0% body weight (EG1, N = 11), 2% body weight (EG2, N = 11), and 4% body weight of load (EG3, N = 10), 20 min/day, 5 days/week for 35 weeks, and one sedentary control group (CG, N = 10). At sacrifice, the colon was removed and counted for tumors and aberrant crypt foci. Tumor size was measured and intra-abdominal fat was weighed. The mean number of aberrant crypt foci was reduced only for EG2 compared to CG (26.21 ± 2.99 vs 36.40 ± 1.53 crypts; P < 0.05). Tumor incidence was not significantly different among groups (CG: 90%; EG1: 72.7%; EG2: 90%; EG3: 80%). Swimming training did not affect either tumor multiplicity (CG: 2.30 ± 0.58; EG1: 2.09 ± 0.44; EG2: 1.27 ± 0.19; EG3: 1.50 ± 0.48 tumors) or size (CG: 1.78 ± 0.24; EG1: 1.81 ± 0.14; EG2: 1.55 ± 0.21; EG3: 2.17 ± 0.22 cm³). Intra-abdominal fat was not significantly different among groups (CG: 10.54 ± 2.73; EG1: 6.12 ± 1.15; EG2: 7.85 ± 1.24; EG3: 5.11 ± 0.74 g). Aerobic swimming training with 2% body weight of load protected against the DMH-induced preneoplastic colon lesions, but not against tumor development in the rat

    Fish oil ingestion reduces the number of aberrant crypt foci and adenoma in 1,2-dimethylhydrazine-induced colon cancer in rats

    Get PDF
    We determined the effect of fish oil (FO) ingestion on colonic carcinogenesis in rats. Male Wistar rats received 4 subcutaneous injections (40 mg/kg body weight each) of 1,2-dimethylhydrazine (DMH) at 3-day intervals and were fed a diet containing 18% by weight FO (N = 10) or soybean oil (SO, N = 10) for 36 weeks. At sacrifice, the colon was removed, aberrant crypt foci were counted and the fatty acid profile was determined. Intestinal tumors were removed and classified as adenoma or carcinoma. Liver and feces were collected and analyzed for fatty acid profile. FO reduced the mean (± SEM) number of aberrant crypt foci compared to SO (113.55 ± 6.97 vs 214.60 ± 18.61; P 0.05). In conclusion, our findings indicate that chronic FO ingestion protected against the DMH-induced preneoplastic colon lesions and adenoma development, but not against carcinoma in rat

    Vibrio Variabilis Sp. Nov. And Vibrio Maritimus Sp. Nov., Isolated From Palythoa Caribaeorum

    No full text
    Two novel vibrio isolates (R-40492 T and R-40493 T) originating from the zoanthid Palythoa caribaeorum in Brazil in 2005 were taxonomically characterized by means of a polyphasic approach comprising multilocus sequence analysis (MLSA), DNA-DNA hybridization (DDH), ΔTm analysis and phenotypic characterization. Phylogenetic analysis based on 16S rRNA gene sequences showed that R-40492 T and R-40493 T fell within the genus Vibrio and were most closely related to each other with 99% similarity; similarities of these two novel isolates towards Vibrio neptunius LMG 20536 T, Vibrio coralliilyticus LMG 20984 T, Vibrio nigripulchritudo LMG 3896 T, Vibrio sinaloensis LMG 25238 T and Vibrio brasiliensis LMG 20546 T varied between 97.1 and 98.5%. DDH experiments showed that the two isolates had less than 15% relatedness to the phylogenetically most closely related Vibrio species. R-40492 T and R-40493 T had 55-57% relatedness to each other. The ΔTm between R-40492 T and R-40493 T was 6.12 °6C. In addition, MLSA of concatenated sequences (16S rRNA, ftsZ, gyrB, recA, rpoA, topA, pyrH and mreB; 6035 bp in length) showed that the two novel isolates formed a separate branch with less than 92% concatenated gene sequence similarity towards known species of vibrios. Two novel species are proposed to accommodate these novel isolates, namely Vibrio variabilis sp. nov. (type strain, R-40492 T=LMG 25438 T=CAIM 1454 T) and Vibrio maritimus sp. nov. (type strain, R-40493 T=LMG 25439 T=CAIM 1455 T)., © 2011 IUMS.611230093015Baumann, P., Schubert, R.H.W., Genus I.Vibrio.In Bergey's Manual of Systematic Bacteriology (1984), 1, pp. 518-538. , Edited by N. R. Krieg J. G. Holt. Baltimore: Williams WilkinsBen-Haim, Y., Thompson, F.L., Thompson, C.C., Cnockaert, M.C., Hoste, B., Swings, J., Rosenberg, E., Vibrio coralliilyticus sp.nov.,a temperature-dependent pathogen of the coral Pocillopora damicornis (2003) Int J Syst Evol Microbiol, 53, pp. 309-315Bourne, D.G., Garren, M., Work, T.M., Rosenberg, E., Smith, G.W., Harvell, C.D., Microbial disease and the coral holobiont (2009) Trends Microbiol, 17, pp. 554-562Chimetto, L.A., Brocchi, M., Thompson, C.C., Martins, R.C.R., Ramos, H.R., Thompson, F.L., Vibrios dominate as culturable nitrogen-fixing bacteria of the Brazilian coral Mussismilia hispida (2008) Syst Appl Microbiol, 31, pp. 312-319Chimetto, L.A., Brocchi, M., Gondo, M., Thompson, C.C., Gomez-Gil, B., Thompson, F.L., Genomic diversity of vibrios associated with the Brazilian coral Mussismilia hispida and its sympatric zoanthids (Palythoa caribaeorum, Palythoa variabilis and Zoanthus solanderi) (2009) J Appl Microbiol, 106, pp. 1818-1826Chimetto, L.A., Cleenwerck, I., Alves Jr., N., Silva, B.S., Brocchi, M., Willems, A., de Vos, P., Thompson, F.L., Vibrio communis sp.nov.,isolated from the marine animals Mussismilia hispida, Phyllogorgia dilatata, Palythoa caribaeorum, Palythoa variabilis and Litopenaeus vannamei (2011) Int J Syst Evol Microbiol, 61, pp. 362-368Eck, R.V., Dayhoff, M.O., (1966) Atlas of Protein Sequence and Structure, , Silver Springs, MD: National Biomedical Research FoundationEzaki, T., Hashimoto, Y., Yabuuchi, E., Fluorometric deoxyribonucleic acid-deoxyribonucleic acid hybridization in microdilution wells as an alternative to membrane filter hybridization in which radioisotopes are used to determine genetic relatedness among bacterial strains (1989) Int J Syst Bacteriol, 39, pp. 224-229Felsenstein, J., Confidence limits on phylogenies: An approach using the bootstrap (1985) Evolution, 39, pp. 783-791Gomez-Gil, B., Fajer-Avila, E., Garcia-Vargas, F., Vibrios of the spotted rose snapper Lutjanus guttatus Steindachner, 1869 from northwestern Mexico (2007) J Appl Microbiol, 102, pp. 1518-1526Gomez-Gil, B., Fajer-Avila, E., Pascual, J., Macian, M.C., Pujalte, M.J., Garay, E., Roque, A., Vibrio sinaloensis sp.nov.,isolated from the spotted rose snapper,Lutjanus guttatus Steindachner, 1869 (2008) Int J Syst Evol Microbiol, 58, pp. 1621-1624Goris, J., Suzuki, K., de Vos, P., Nakase, T., Kersters, K., Evaluation of a microplate DNA-DNA hybridization method compared with the initial renaturation method (1998) Can J Microbiol, 44, pp. 1148-1153Huys, G., Vancanneyt, M., Coopman, R., Janssen, P., Falsen, E., Altwegg, M., Kersters, K., Cellular fatty-acid composition as a chemotaxonomic marker for the differentiation of phenospecies and hybridization groups in the genus Aeromonas (1994) Int J Syst Bacteriol, 44, pp. 651-658Kovacs, N., Identification of Pseudomonas pyocyanea by the oxidase reaction (1956) Nature, 178, p. 703Macian, M.C., Ludwig, W., Aznar, R., Grimont, P.A.D., Schleifer, K.H., Garay, E., Pujalte, M.J., Vibrio lentus sp.nov.,isolated from Mediterranean oysters (2001) Int J Syst Evol Microbiol, 51, pp. 1449-1456Mesbah, M., Premachandran, U., Whitman, W.B., Precise measurement of the G+C content of deoxyribonucleic acid by high performance liquid chromatography (1989) Int J Syst Bacteriol, 39, pp. 159-167Moreira, A.P.B., Pereira Jr., N., Thompson, F.L., Usefulness of a real-time PCR platform for G+C content and DNA-DNA hybridization estimations in vibrios (2011) Int J Syst Evol Microbiol, 61, pp. 2379-2383Oigman-Pszczol, S.S., Figueiredo, M.A.O., Creed, J.C., Distribution of benthic communities on the tropical rocky subtidal of Armac ̧a ̃o dos Bu ́zios, southeastern Brazil (2004) Mar Ecol (Berl), 25, pp. 173-190Rossello-Mora, R., Amann, R., The species concept for prokaryotes (2001) FEMS Microbiol Rev, 25, pp. 39-67Saitou, N., Nei, M., The neighbor-joining method: A new method for reconstructing phylogenetic trees (1987) Mol Biol Evol, 4, pp. 406-425Sawabe, T., Kita-Tsukamoto, K., Thompson, F.L., Inferring the evolutionary history of vibrios by means of multilocus sequence analysis (2007) J Bacteriol, 189, pp. 7932-7936Sheu, S.Y., Jiang, S.R., Chen, C.A., Wang, J.T., Chen, W.M., Vibrio stylophorae sp.nov.,isolated from the reef-building coral Stylophora pistillata (2011) Int J Syst Evol Microbiol, 61, pp. 2180-2185Sussman, M., Willis, B.L., Victor, S., Bourne, D.G., Coral pathogens identified for White Syndrome (WS) epizootics in the Indo-Pacific (2008) PLoS ONE, 2393, p. 3Tamura, K., Dudley, J., Nei, M., Kumar, S., MEGA4:Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0 (2007) Mol Biol Evol, 24, pp. 1596-1599Thompson, F.L., Hoste, B., Vandemeulebroecke, K., Swings, J., Genomic diversity amongst Vibrio isolates from different sources determined by fluorescent amplified fragment length polymorphism (2001) Syst Appl Microbiol, 24, pp. 520-538Thompson, F.L., Hoste, B., Thompson, C.C., Huys, G., Swings, J., The coral bleaching Vibrio shiloi Kushmaro 2001 is a later synonym of Vibrio mediterranei Pujalte and Garay 1986 (2001) Syst Appl Microbiol, 24, pp. 516-519Thompson, F.L., Hoste, B., Vandemeulebroecke, K., Engelbeen, K., Denys, R., Swings, J., Vibrio trachuri Iwamoto 1995 is a junior synonym of Vibrio harveyi (Johnson and Shunk 1936) Baumann 1981 (2002) Int J Syst Evol Microbiol, 52, pp. 973-976Thompson, F.L., Li, Y., Gomez-Gil, B., Thompson, C.C., Hoste, B., Vandemeulebroecke, K., Rupp, G.S., de Bem, M.M., Vibrio neptunius sp.nov.,Vibrio brasiliensis sp.nov.and Vibrio xuii sp.nov.,isolated from the marine aquaculture environment (bivalves, fish, rotifers and shrimps) (2003) Int J Syst Evol Microbiol, 53, pp. 245-252Thompson, F.L., Iida, T., Swings, J., Biodiversity of vibrios (2004) Microbiol Mol Biol Rev, 68, pp. 403-431Thompson, F.L., Gevers, D., Thompson, C.C., Dawyndt, P., Naser, S., Hoste, B., Munn, C.B., Swings, J., Phylogeny and molecular identification of vibrios on the basis of multilocus sequence analysis (2005) Appl Environ Microbiol, 71, pp. 5107-5115Thompson, F.L., Gomez-Gil, B., Vasconcelos, A.T.R., Sawabe, T., Multilocus sequence analysis reveals that Vibrio harveyi and V.campbellii are distinct species (2007) Appl Environ Microbiol, 73, pp. 4279-4285Thompson, C.C., Vicente, A.C.P., Souza, R.C., Vasconcelos, A.T.R., Vesth, T., Alves Jr., N., Ussery, D.W., Thompson, F.L., Genomic taxonomy of vibrios (2009) BMC Evol Biol, 9, pp. 1-16Wang, H., Liu, J., Wang, Y., Zhang, X.H., Vibrio marisflavi sp.nov.,isolated from seawater (2011) Int J Syst Evol Microbiol, 61, pp. 568-573Waterhouse, A.M., Procter, J.B., Martin, D.M.A., Clamp, M., Barton, G.J., Jalview Version 2-a multiple sequence alignment editor and analysis workbench (2009) Bioinformatics, 25, pp. 1189-1191Wayne, L.G., Brenner, D.J., Colwell, R.R., Grimont, P.A.D., Kandler, O., Krichevsky, M.I., Moore, L.H., Murray, R.G.E., International Committee on Systematic Bacteriology.Report of the ad hoc committee on reconciliation of approaches to bacterial systematics (1987) Int J Syst Bacteriol, 37, pp. 463-464Willems, A., Doignon-Bourcier, F., Goris, J., Coopman, R., de Lajudie, P., de Vos, P., Gillis, M., DNA-DNA hybridization study of Bradyrhizobium strains (2001) Int J Syst Evol Microbiol, 51, pp. 1315-132
    corecore