552 research outputs found

    Robustness of reserve selection procedures under temporal species turnover

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    Complementarity-based algorithms for the selection of reserve networks emphasize the need to represent biodiversity features efficiently, but this may not be sufficient to maintain those features in the long term. Here, we use data from the Common Birds Census in Britain as an exemplar data set to determine guidelines for the selection of reserve networks which are more robust to temporal turnover in features. The extinction patterns found over the 1981-1991 interval suggest that two such guidelines are to represent species in the best sites where they occur (higher local abundance) and to give priority to the rarer species. We tested five reserve selection strategies, one which finds the minimum representation set and others which incorporate the first or both guidelines proposed. Strategies were tested in terms of their efficiency (inversely related to the total area selected) and effectiveness (inversely related to the percentage of species lost) using data on eight pairs of ten-year intervals. The minimum set strategy was always the most efficient, but suffered higher species loss than the others, suggesting that there is a trade-off between efficiency and effectiveness. A desirable compromise can be achieved by embedding the concerns about the long-term maintenance of the biodiversity features of interest in the complementarity-based algorithms

    Alteraciones en la tasa de respiración de Daphnia magna bajo concentraciones subletales de anatoxina-a

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    Anatoxina-a es una potente neurotoxina producida por cianobacterias dulceacuícolas que puede representar un riesgo, por sus efectos agudos, para diferentes formas de vida, incluyendo los seres humanos. Aunque se conocen los efectos agudos y crónicos de esta toxina, pocos estudios aportan datos de medidas de efectos subletales sobre la respiración del zooplancton. En este trabajo se cuantifican cambios en la respiración de Daphnia magna bajo una concentración subletal de anatoxina-a, en condiciones experimentales, por medio de un sistema automatizado de medida en continuo de consumo de Oxígeno. Los resultados indican que la presencia de anatoxina-a en dosis subletales reduce significativamente la actividad respiratoria en esta especie, con efectos, dependientes de la edad del organismo.Anatoxin-a is a potent neurotoxin produced by some freshwater cyanobacteria which, because of its acute toxic effects, may represent a hazard to aquatic organisms, and even to human beings. Both the acute and chronic effects of this toxin are rather well known, but few studies provided information about its sublethal effect on the zooplankton respiration. In this paper we have quantified respiration changes in Daphnia magna under sublethal anatoxin-a concentrations in experimental conditions, using an automatic open-flow system of continuous measurement of oxygen consumption. Our results show that the presence of anatoxin-a at sublethal doses reduces significantly the respiratory activity of the animals, being the effects greatly dependent on the individual age

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

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    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

    Historical summer distribution of the endangered North Atlantic right whale (Eubalaena glacialis): a hypothesis based on environmental preferences of a congeneric species

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    Aim: To obtain a plausible hypothesis for the historical distribution of North Atlantic right whales (NARWs) (Eubalaena glacialis) in their summer feeding grounds. Previously widespread in the North Atlantic, after centuries of hunt- ing, these whales survive as a small population off eastern North America. Because their exploitation began before formal records started, information about their historical distribution is fragmentary

    Transforming growth factor-β (TGF-β) maintains follicular ultrastructure and stimulates preantral follicle growth in caprine ovarian tissue cultured in vitro

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    O objetivo desse estudo foi investigar se o TGF-β afeta a sobrevivência, ativação e crescimento de folículos primordiais caprinos inclusos no córtex ovariano após o cultivo in vitro. Ovários de cabras foram coletados em abatedouro e fragmentos de tecido ovariano foram cultivados por um e sete dias em meio essencial mínimo alfa (α-MEM+) sozinho ou suplementado com TGF-β (1, 5, 10 ou 50ng/mL). Fragmentos ovarianos não cultivados e cultivados foram processados para análise histológica e ultraestrutural. Os resultados mostraram que, comparado ao controle fresco, houve diminuição no percentual de folículos morfologicamente normais em todos os tratamentos somente após sete dias de cultivo. O TGF-β não afetou a ativação folicular independente da concentração testada, contudo, o diâmetro folicular foi superior (P<0.05) no tratamento com 10ng/mL de TGF-β quando comparado ao controle fresco e aos demais tratamentos. Além disso, essa mesma concentração manteve a ultraestrutura normal dos folículos após sete dias de cultivo. Em conclusão, o TGF-β apresentou efeito adicional no crescimento folicular e na manutenção da integridade ultraestrutural de folículos pré-antrais caprinos inclusos no tecido ovariano quando utilizado na concentração de 10ng/mL durante sete dias de cultivo.The objectives of this study were to investigate whether TGF-β affect the survival, activation and further growth of goat primordial follicles enclosed in ovarian cortex after in vitro culture. Goat ovaries were collected from an abattoir and pieces of ovarian tissues were cultured for one or seven days in a supplemented alpha Minimum Essential Medium, alone or containing TGF-β (1, 5, 10 or 50ng/mL). Ovarian tissues from the fresh control as well as those cultured were processed for histological and ultrastructural studies. The results showed that when compared with fresh control, there was decrease in the percentages of histologically normal follicles in all treatments only after seven days culture. TGF-β did not affect the activation of preantral follicles regardless of its concentration, however, larger follicles diameter (P<0.05) was observed using 10ng/mL TGF-β than in the fresh control and other treatments. Moreover, this concentration maintained the normal ultrastructure after seven days of culture. In conclusion, TGF-β showed additional effect on the follicle growth and the maintenance of ultrastructural integrity of goat preantral follicles enclosed in ovarian tissue when used at 10ng/mL during seven days of culture

    Increase in Ca2+ current by sustained cAMP levels enhances proliferation rate in GH3 cells

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    Aims: Ca2 + and cAMP are important intracellular modulators. In order to generate intracellular signals with various amplitudes, as well as different temporal and spatial properties, a tightly and precise control of these modulators in intracellular compartments is necessary. The aim of this study was to evaluate the effects of elevated and sustained cAMP levels on voltage-dependent Ca2 + currents and proliferation in pituitary tumor GH3 cells. Main methods: Effect of long-term exposure to forskolin and dibutyryl-cyclic AMP (dbcAMP) on Ca2 + current density and cell proliferation rate were determined by using the whole-cell patch-clamp technique and real time cell monitoring system. The cAMP levels were assayed, after exposing transfected GH3 cells with the EPAC-1 cAMP sensor to forskolin and dbcAMP, by FRET analysis. Key findings: Sustained forskolin treatment (24 and 48 h) induced a significant increase in total Ca2 + current density in GH3 cells. Accordingly, dibutyryl-cAMP incubation (dbcAMP) also elicited increase in Ca2 + current density. However, the maximum effect of dbcAMP occurred only after 72 h incubation, whereas forskolin showed maximal effect at 48 h. FRET-experiments confirmed that the time-course to elevate intracellular cAMP was distinct between forskolin and dbcAMP. Mibefradil inhibited the fast inactivating current component selectively, indicating the recruitment of T-type Ca2 + channels. A significant increase on cell proliferation rate, which could be related to the elevated and sustained intracellular levels of cAMP was observed. Significance: We conclude that maintaining high levels of intracellular cAMP will cause an increase in Ca2 + current density and this phenomenon impacts proliferation rate in GH3 cells

    Higher spin quaternion waves in the Klein-Gordon theory

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    Electromagnetic interactions are discussed in the context of the Klein-Gordon fermion equation. The Mott scattering amplitude is derived in leading order perturbation theory and the result of the Dirac theory is reproduced except for an overall factor of sixteen. The discrepancy is not resolved as the study points into another direction. The vertex structures involved in the scattering calculations indicate the relevance of a modified Klein-Gordon equation, which takes into account the number of polarization states of the considered quantum field. In this equation the d'Alembertian is acting on quaternion-like plane waves, which can be generalized to representations of arbitrary spin. The method provides the same relation between mass and spin that has been found previously by Majorana, Gelfand, and Yaglom in infinite spin theories

    Strange stars in Krori-Barua space-time

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    The singularity space-time metric obtained by Krori and Barua\cite{Krori1975} satisfies the physical requirements of a realistic star. Consequently, we explore the possibility of applying the Krori and Barua model to describe ultra-compact objects like strange stars. For it to become a viable model for strange stars, bounds on the model parameters have been obtained. Consequences of a mathematical description to model strange stars have been analyzed.Comment: 9 pages (two column), 12 figures. Some changes have been made. " To appear in European Physical Journal C
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