91 research outputs found

    Valor nutritivo de silagens de bagaço de sorgo sacarino produzido na Beira Interior Sul

    Get PDF
    Pelas utilizações diversificadas que lhe estão associadas, o sorgo sacarino (Sorghum bicolor (L.) Moench) é uma cultura que tem vindo a receber assinalável atenção nos meios académicos. Apesar de em regra ser encarada como uma matéria-prima para a produção de biocombustíveis, nomeadamente bioetanol, a verdade é que a cultura e os seus subprodutos, designadamente a fração fibrosa da planta, apresentam a capacidade de ser utilizados com outros fins, nomeadamente na alimentação de ruminantes. O objetivo deste estudo foi comparar o valor nutritivo da silagem de bagaço de três cultivares de sorgo sacarino (Sugargraze, Sugar-T e 23402), com o valor nutritivo da silagem das mesmas cultivares processadas sem e com pré-fenação. Os resultados obtidos (% na MS) para as silagens de sorgo sacarino sem pré-fenação vs silagens de sorgo sacarino com pré-fenação vs silagens de bagaço de sorgo sacarino foram, respetivamente, os seguintes: MS 23,23% (±2,045) vs 26,52% (±1,233) vs 28,56% (±4,115) (P<0,05); PB 6,47% (±0,589) vs 5,96% (±0,164) vs 4,81% (±0,392) (P<0,05); GB 1,11% (±0,084) vs 1,01% (±0,096) vs 0,86% (±0,041) (P<0,05); NDF 55,05% (±2,613) vs 54,39% (±0,638) vs 74,53% (±1,283) (P<0,05); ADF 31,16% (±1,530) vs 31,76% (±0,725) vs 45,46% (±1,073) (P<0,05); ADL 3,22% (±0,497) vs 3,39% (±0,708) vs 4,87% (±0,474) (P<0,05); Cinzas 4,41% (±0,437) vs 4,33% (±0,489) vs 3,17% (±0,263) (P<0,05); Digestibilidade da MO 59,25% (±1,584) vs 59,40% (±1,708) vs 48,32% (±0,988) (P<0,05). Estes resultados levam-nos a concluir que as silagens de bagaço de sorgo sacarino apresentam valores de PB, GB e Digestibilidade da MO mais baixos (P<0,05) e valores de NDF, ADF e ADL mais elevados (P<0,05). No entanto, parecem apresentar valor nutritivo adequado para serem utilizadas na alimentação de ruminantes. Serão necessários estudos futuros para avaliar o efeito da utilização deste subproduto na produção de leite e carne

    Chronic Ethanol Intake Promotes Double Gluthatione S-transferase/transforming Growth Factor-α-positive Hepatocellular Lesions In Male Wistar Rats

    Get PDF
    The chronic ethanol intake influence on the gluthatione S-transferase (GST-P) and transforming growth factor α (TGF-α) expression in remodeling/persistent preneoplastic lesions (PNLs) was evaluated in the resistant hepatocyte model. Male Wistar rats were allocated into five groups: G1, non-treated, fed water and chow ad libitum; G2, non-treated and pair-fed chow (restricted to match that of G3 group) and a maltodextrin (MD) solution in tap water (matched ethanol-derived calories); G3, fed 5% ethanol in drinking water and chow ad libitum; G4, diethylnitrosamine (DEN, 200 mg/kg, body weight) plus 200 parts per million of 2-acetylaminofluorene (2-AAF) for 3 weeks and pair-fed chow (restricted to match that of G5 group) and an MD solution in tap water (matched ethanol-derived calories); G5, DEN/2-AAF treatment, fed ethanol 5% and chow ad libitum. All animals were subjected to 70% partial hepatectomy at week 3 and sacrificed at weeks 12 or 22, respectively. Liver samples were collected for histological analysis or immunohistochemical expression of GST-P, TGF-α and proliferating cell nuclear antigen or zymography for matrix metalloproteinases-2 and-9. At the end of ethanol treatment, there was a significant increase in the percentage of liver area occupied by persistent GST-P-positive PNLs, the number of TGF-α-positive PNLs and the development of liver tumors in ethanol-fed and DEN/2-AAF-treated groups (G5 versus G4, P < 0.001). In addition, ethanol feeding led to a significant increase in cell proliferation mainly in remodeling and persistent PNLs with immunoreactivity for TGF-α at week 22 (P < 0.001). Gelatinase activities were not altered by ethanol treatment. The results demonstrated that ethanol enhances the selective growth of PNL with double expression of TGF-α and GST-P markers. © 2008 Japanese Cancer Association.992221228Pöschl, G., Seitz, H.K., Alcohol and cancer (2004) Alcohol Alcohol, 39, pp. 155-165Bofetta, P., Hashibe, M., Alcohol and cancer (2006) Lancet Oncol, 7, pp. 149-156Brown, L.M., Epidemiology of alcohol-associated cancers (2005) Alcohol, 35, pp. 161-168Voight, M.D., Alcohol in hepatocellular cancer (2005) Clin Liver Dis, 9, pp. 151-169Vidal, F., Toda, R., Gutiérrez, C., Influence of chronic alcohol abuse and liver disease on hepatic aldehyde dehydrogenase activity (1998) Alcohol, 15, pp. 3-8Lieber, C.S., Abittan, C.S., Pharmacology and metabolism of alcohol, including its metabolics effects and interactions with other drugs (1999) Clin Dermatol, 17, pp. 365-379Bunout, D., Nutritional and metabolic effects of alcoholism: Their relationship with alcoholic liver disease (1999) Nutrition, 15, pp. 583-589Niemellä, O., Distribution of ethanol-induced protein adducts in vivo: Relationship to tissue injury (2001) Free Rad Biol Med, 31, pp. 1533-1538Brooks, T.J., Theruvathu, J.A., DNA adducts from acetaldehyde: Implications for alcohol-related carcinogenesis (2005) Alcohol, 35, pp. 187-193Verna, L., Whysner, J., Williams, G.M., N-Nitrosodiethylamine mechanistic data and risk assessment: Bioactivation, DNA-Adduct formation, mutagenicity and tumor initiation (1996) Pharmacol Ther, 71, pp. 57-81Friedman, S.L., Mechanisms of disease: Mechanisms of hepatic fibrosis and therapeutic implication (2004) Nat Clin Pract Gastroenterol Hepatol, 1, pp. 98-105Purohit, V., Brenner, D.A., Mechanisms of alcohol-induced hepatic fibrosis: A summary of the Ron Thurman symposium (2006) Hepatology, 43, pp. 872-878Arthur, M.J.P., Fibrogenesis: Metalloproteinases and their inhibitors in liver fibrosis (2000) Am J Physiol Gastrointest Liver Phisiol, 279, pp. 245-249Tatsuta, M., Iishi, H., Baba, M., Enhancement by ethyl alcohol experimental hepatocarcinogenesis induced by N-nitrosomorpholine (1997) Int J Cancer, 71, pp. 1045-1048Karim, M.R., Wanibuchi, H., Wei, M., Morimura, K., Salim, E., Fukushima, S., Enhancing risk of ethanol on MeIQx-induced rat hepatocarcinogenesis is accompanied with increased levels of cellular proliferation and oxidative stress (2003) Cancer Lett, 192, pp. 37-47Kushida, M., Wanibuchi, H., Morimura, K., Dose-dependence of promotion of 2-amino-dimethylimidazo[4,5-f]quinoxaline-induced rat hepatocarcinogenesis by ethanol: Evidence for a threshold (2005) Cancer Sci, 96, pp. 747-757Stickel, F., Schuppan, D., Hahn, E.G., Seitz, H.K., Cocarcinogenic effects of alcohol in hepatocarcinogenesis (2002) Gut, 51, pp. 132-139Croager, E.J., Smith, P.G.J., Yeoh, G.C.T., Ethanol interactions with a choline-deficient, ethionine-supplemented feeding regime potentiate pre-neoplastic cellular alterations in rat liver (2002) Carcinogenesis, 23, pp. 1685-1693Wanibuchi, H., Wei, M., Karim, R., Existence of no hepatocarcinogenic effect levels of 2-amino-dimethylimidazo[4,5-f]quinoxaline with or without coadministration with ethanol (2006) Toxicol Pathol, 34, pp. 232-236Yanagi, S., Yamashita, M., Hiasa, Y., Kamiya, T., Effect of ethanol on hepatocarcinogenesis initiated in rats with 3′-methyl-4-dimethylaminoazobenzene in the absence of liver injuries (1989) Int J Cancer, 44, pp. 681-684Cho, K.J., Jang, J.J., Effects of carbon tetrachloride, ethanol, and acetaldehyde on diethylnitrosamine-induced hepatocarcinogenesis in rats (1993) Cancer Lett, 70, pp. 33-39Holmberg, B., Ekstrom, T., The effects of long-term oral administration of ethanol on Sprague-Dawley rats - A condensed report (1995) Toxicology, 96, pp. 133-145Solt, D., Farber, E., New principles for the analysis of chemical carcinogenesis (1976) Nature, 263, pp. 701-703Semple-Roberts, E., Hayes, M.A., Armstrong, D., Becker, R.A., Racz, W.J., Farber, E., Alternative methods of selecting hepatocellular nodules resistant to 2-acetylaminefluorene (1987) Int J Cancer, 40, pp. 643-645Tatematsu, M., Nagamine, Y., Farber, E., Redifferentiation as a basis for remodeling of carcinogen-induced hepatocyte nodules to normal appearing liver (1983) Cancer Res, 43, pp. 5049-5058Wood, G.A., Sarma, D.S.R., Archer, M.C., Resistance to the promotion of glutathione S-transferase 7-7-positive liver lesions in Copenhagen rats (1999) Carcinogenesis, 20, pp. 1169-1175Bannasch, P., Zerban, H., Predictive value of hepatic preneoplastic lesions as indicators of carcinogenic response (1992) Mechanism of Carcinogenesis in Risk Identification, pp. 389-427. , In: Vainio H, Magee PN, McGregor DB, McMichal AJ, eds. Lyon: IARC. Sci Publications, no. 116Pinheiro, F., Faria, R.R., de Camargo, J.L., Spinardi-Barbisan, A.L., da Eira, E.F., Barbisan, L.F., Chemoprevention of preneoplastic liver foci development by dietary mushroom Agaricus blazei Murrill in the rat (2003) Food Chem Toxicol, 41, pp. 1543-1550Schulte-Hermann, R., Kraupp-Grasl, B., Bursch, W., Gerbracht, U., Timmermann-Trosiener, I., Effects of non-genotoxic hepatocarcinogens phenobarbital and nafenopin on phenotype and growth of different populations of altered foci in rat liver (1989) Toxicol Pathol, 17, pp. 642-649Levin, S., Bucci, T.J., Cohen, S.M., The nomenclature of cell death: Recommendations of an ad hoc Committee of the Society of Toxicologic Pathologists (1999) Toxicol Pathol, 27, pp. 484-490Bradford, M.M., A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding (1976) Anal Biochem, 72, pp. 248-254Bitsch, A., Hadjiolov, N., Klöhn, P.-C., Bergmann, O., Zwwirner-Baier, I., Neumann, H.-G., Dose-response of early effects related to tumor promotion of 2-acetylaminofluorene (2000) Toxicol Sci, 55, pp. 44-51Imai, T., Masui, T., Ichinose, M., Reduction of glutathione S-transferase P-form mRNA expression in remodeling nodules in rat liver revealed by in situ hybridization (1997) Carcinogenesis, 18, pp. 545-551De Miglio, M.R., Simile, M.M., Muroni, M.R., Phenotypic reversion of rat neoplastic liver nodules is under genetic control (2003) Int J Cancer, 105, pp. 70-75Kaufmann, W.K., Zhang, Y., Kaufmann, D.G., Association between expression of transforming growth factor-alpha and progression of hepatocellular foci to neoplasms (1992) Carcinogenesis, 13, pp. 1481-1483Tamano, S., Merlino, G.T., Ward, J.M., Rapid development of hepatic tumors in transforming growth factor alpha transgenic mice associated with increased cell proliferation in precancerous hepatocellular lesions initiated by N-nitrosodiethylamine and promoted by phenobarbital (1994) Carcinogenesis, 15, pp. 1791-1798Burr, A.W., Toole, K., Mathew, J., Hines, J.E., Chapman, C., Burt, A.D., Transforming growth factor-α expression is altered during experimental hepatocarcinogenesis (1996) J Pathol, 179, pp. 276-282Kitano, M., Wada, J., Ariki, Y., Possible tumour development from double positive foci for TGF-alpha and GST-P observed in early stages on rat hepatocarcinogenesis (2006) Cancer Sci, 97, pp. 478-483Sandgren, E.P., Luetteke, N.C., Qiu, T.H., Palmiter, R.D., Brinster, R.L., Lee, D.C., Transforming growth factor alpha dramatically enhances oncogene-induced carcinogenesis in transgenic mouse pancreas and liver (1993) Mol Cell Biol, 13, pp. 320-330Thorgeirsson, S.S., Santoni-Rugiu, E., Transgenic mouse models in carcinogenesis: Interaction of c-myc with transforming growth factor alpha and hepatocyte growth factor in hepatocarcinogenesis (1996) Br J Clin Pharmacol, 42, pp. 43-52Kato, J., Sato, Y., Inui, N., Ethanol induces transforming-growth factor-α expression in hepatocytes, leading to a stimulation of collagen synthesis by hepatic stellate cells (2003) Alcohol Clin Exp Res, 27, pp. 58S-63SZerban, H., Radig, S., Kopp-Schneider, A., Bannasch, P., Cell proliferation and cell death (apoptosis) in hepatic preneoplasia and neoplasia are closely related to phenotypic cellular diversity and instability (1994) Carcinogenesis, 15, pp. 2467-2473Grasl-Kraupp, B., Ruttkay-Nedecky, B., Müllauer, H., Taper, H., Huber, W., Bursch, W., Schulte-Hermann R Inherent increase of apoptosis in liver tumors: Implications for carcinogenesis and tumor regression (1997) Hepatology, 25, pp. 906-912Tanaka, T., Hirota, Y., Kuriyama, M., Nishiguchi, S., Otani, S., Time course of change in glutathione s-transferase positive foci and ornithine decarboxylase activity after cessation of long-term alcohol administration in rats (2001) Asian Pac J Cancer Prev, 2, pp. 131-134Mazzantini, R.P., de Conti, A., Moreno, F.S., Persistent and remodeling hepatic preneoplastic lesions present differences in cell proliferation and apoptosis, as well as in p53, Bcl-2 and NF-kappaB pathways (2007) J Cell BiochemFoda, H.D., Zucker, S., Matrix metalloproteinases in cancer invasion, metastasis and angiogenesis (2001) Drug Discov Today, 6, pp. 478-482Aye, M.M., Cuiling, M.A., Lin, H., Bower, K.A., Wiggins, R.C., Luo, J., Ethanol-induced in vitro invasion of breast cancer cells. the contribution of MMP-2 by fibroblasts (2004) Int J Cancer, 112, pp. 738-746Ke, Z., Lin, H., Fan, Z., MMP-2 mediates ethanol-induced invasion of mammary epithelial cells over-expressing ErbB2 (2006) Int J Cancer, 119, pp. 8-1

    Membrane-associated proteins of ejaculated sperm from Morada Nova rams

    Get PDF
    AbstractThe objective was to describe the profile of membrane proteins from sperm of tropically adapted Morada Nova rams (N = 5). Samples from protein-enriched fractions of ejaculated sperm (containing 400 μg of protein) were separated by two-dimensional electrophoresis and respective maps analyzed using PDQuest software (version 7.3.0; Bio-Rad). Proteins were identified using tandem mass spectrometry. Also, membrane proteins were incubated with antibodies against binder of sperm protein (BSP) 1 and bodhesin 2 (Bdh-2), components of vesicular gland secretion. For membrane proteins of ejaculated sperm, an average of 133 ± 4.6 spots were detected per gel, of which, 107 spots were consistently present on all gels. Sixty-eight spots and 37 proteins were identified using mass spectrometry, corresponding to 71.6% of the intensity of all spots detected. Three major spots identified as ram seminal vesicle protein (RSVP) 14 represented approximately 30% of the intensity of all spots. Two of the most intense spots in the gel reacted against anti-BSP1, at 14 kDa. In addition, four low molecular weight spots reacted with anti-Bdh-2 antibodies. Proteins RSVP and Bdh-2 belong to the BSP and spermadhesin families, respectively, and were previously reported as major components of ram seminal proteins. Additional proteins identified in the sperm membrane two-dimensional maps included alpha-2-heparan sulfate-glycoprotein, plasma glutamate carboxypeptidase, arylsulfatase A, cathelicidin, heat shock protein 70 kDa, angiotensin-converting enzyme, leucine aminopeptidase, and clusterin. Some proteins were present as multiple isoforms, such as tubulin (12), alpha-2-heparan sulfate-glycoprotein (5), ATP synthase (5), Bdh-2 (4) and RSVP14 (3). Based on gene ontology analysis, the most common biological processes associated with the membrane proteins were cellular processes (34%), response to stimulus (14%), and metabolic processes (11%). Binding (37%) and catalytic activity (32%) corresponded to the most frequent molecular functions for those proteins. In conclusion, we identified a diverse cohort of components of membrane proteins in ram sperm. Major proteins previously reported in seminal plasma, such as RSVP14 and Bdh-2, were also extracted from sperm membranes. Knowledge of sperm proteins is crucial for elucidating mechanisms underlying their association with sperm function

    Three-dimensional analysis of jaw kinematic alterations in patients with chronic TMD - disc displacement with reduction

    Get PDF
    The study investigated whether chronic TMD patients with disc displacement with reduction (DDR), performing non-assisted maximum jaw movements, presented any changes in their mandibular kinematics with respect to an age-matched control group. Moreover, it was examined whether jaw kinematics and a valid clinic measure of oro-facial functional status have significant associations. Maximum mouth opening, mandible protrusion and bilateral laterotrusions were performed by 20 patients (18 women, 2 men; age, 18-34 years) and 20 healthy controls (17 women, 3 men; age, 20-31 years). The three-dimensional coordinates of their mandibular interincisor and condylar reference points were recorded by means of an optoelectronic motion analyser and were used to quantitatively assess their range of motion, velocity, symmetry and synchrony. Three functional indices (opening-closing, mandibular rototranslation, laterotrusion - right and left - and protrusion) were devised to summarise subject's overall performance, and their correlation with the outcome of a clinical protocol, the oro-facial myofunctional evaluation with scores (OMES), was investigated. TMD patients were able to reach maximum excursions of jaw movements comparable to healthy subjects' performances. However, their opening and closing mandibular movements were characterised by remarkable asynchrony of condylar translation. They had also reduced jaw closing velocity and asymmetric laterotrusions. The functional indices proved to well summarise the global condition of jaw kinematics, highlighting the presence of alterations in TMD-DDR patients, and were linearly correlated with the oro-facial functional status. The jaw kinematic alterations seem to reflect both oro-facial motor behaviour adaptation and a DDR-related articular impairment

    Prediction of apparent digestibility of hays from natural pastures of the Northeast region of Portugal

    Get PDF
    In the Northeast region of Portugal hays from natural pastures are traditionally used as the main feed during the period of drought and the evaluation of its nutritive value is essential. The aim of this study was to predict the apparent organic matter digestibility (OMD) of 21 hays from natural pastures based on chemical composition, pepsin-cellulase solubility of organic matter (OMS) and in vitro organic matter digestibility. Chemical composition of hays showed a wide range of values and acid detergent lignin (ADL) was the component that presented the highest variation (CV = 18.4%). The OMD varied between 516 and 658 g/kg OM. The best single OMD predictor was OMS (RSD = 2.8%, R2 = 0.52, P<0.001). Using multiple regression to predict OMD, the variables included in the model were OMS and ADL (OMD = 21.51 + 0.94 OMS – 0.83 ADL; RSD = 2.75%; R2 = 0.54; P<0.0001). According to principal component analysis (PCA) hays were divided in 3 groups and the multiple regression established for the larger group of hays (n=10) was: OMD = 4.13 + 0.85 OMS – 1.03 ADL; RSD = 2.13%, R2 = 0.77, P<0.0001. The OMS method was superior to chemical composition and to the in vitro rumen fluid method in predicting OMD of hays from natural pastures. Results from PCA suggested that it may be useful to group these hays according to its chemical composition to accurately predict OMD
    • …
    corecore