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    Modulation Of Insulin Secretion By Physical Training During Recovery From Protein Malnutrition In Rats

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    Objective: The purpose of the present study was to examine insulin secretion in rats submitted to protein restriction and nutritional recovery associated or not to physical training. Methods: The experiment was designed in two sets of five weeks each. In the first set the rats were fed a nonnal-protein diet(17%-control group) or a low-protein diet (6%-malnourished group) for five weeks. After this, all animals were fed the 17% protein diet and separated into four groups: sedentary control(SC); trained eontrol(TC); sedentary recovered(SR) and trained recovered(TR). TC and TR rats performed swimming exercise. Results: The results indicated efficiency of the 6% protein diet in producing signs of malnutrition, as reduction in body weight gain and serum albumin levels, as well as liver fat. Serum insulin in the fed state and insulin secretion by isolated pancreatic islets in response to glucose were Keduced,but peripheral sensitivity to insulin was increased and glucose tolerance was not changed in the protein deficient rats, indicating adaptation to malnutrition. Diet protocol for nutritional recovery was efficient in repairing body weight gain, serum albumin and liver fat levels of the previously malnourished rats. Glucose induced insulin release by pancreatic islets remained low after nutritional recovery. Insulin secretion by the islets isolated from rats submitted to exercise training during nutritional recovery was improved when compared with the sedentary animals. Conclusion: This indicates that exercise training may be useful in the treatment of protein calorie malnutrition, concerning to glucose induced insulip secretion.45258268Uvin, O., The state of world hunger (1994) Nutr Re, 52 (5), pp. 151-161(2008) World Health Organization Statistical Information Indicators of child undernutrition in World, , http://www.who.int/whosis/database/core/core_select_process.afm?countries=all&indicators=child_undernutritionTorun B, Chew F. Proteín-energy malnutrition. In: Shils ME, Olson JA, Shike EM. Modem Nutrition in health and disease, Philadelphia, PH: Lea & Febiger,1994:950-997Santhiago, V., Silva, A.S.R., Gobatto, C.A., Mello, M.A.R., Treinamento físico durante a recupera?? o nutricional n? o afeta o metabolismo muscular da glicose de ratos. (2006) Rev Bras Med Esporte, 12, p. 2Rao, H.R., Adaptations in glucose homeostasis during chronic nutritional deprivation in rats: He patic resistance to both insulin and glucagon (1995) Metabolism, 44, pp. 817-824Rao, H.R., Fasting glucose homeostasis in the adaptation to chronic nutritional deprivation in rats (1995) Am J Physiol, 268, pp. E873-E879Swenne, I., Crace, C.J., Milner, R.D.G., Persistent impairment of insulin secretory response to glucose in adult rats after limited period of protein-calorie malnutrition early in life (1987) Diabetes, 36, pp. 454-458Koranji, L.I., Bourey, R.E., Slentz, C.A., Holloszy, J.O., PErmutt, A.A., Coordinate reduction of rat pancreatic islet glucokinase and proinsulin mRNA by exercise training (1991) Diabetes, 40, pp. 401-404Engdahl, J.H., Veldhuis, J.D., Farrell, P., Altered pulsatile insulin secretion associated with endurance training (1995) J Appl Physiol, 79, pp. 1977-1987Fluckey, J.D., Kraemer, W.J., Farrell, P.A., Pancreatic islet insulin secretion is inereased after resistance exercise in rats (1995) J App Physiol, 79, pp. 1100-1105Oliveira, C.A.M., Luciano, E., Mello, M.A.R., The rate of exercise on longterm effect of alloxan administrated in neonatal rats (2004) Exp Physiol, 90, pp. 79-96Torun, B., Viterife. Influence of exercise on linear growth (1994) Europ J Clin Nut, 48, pp. S186-S190Reeves, P.G., Components of the AIN-93 diets as improvements in the AIN-76 diet (1993) J Nutr, 127, pp. 838S-841SNogueira, D.M., Strufaldi, B., Hirata, M.H., Abdalla, D.S.P., Hirata, R.D.C., (1990) Métodos de bioquímica clínica: Técnico-interpretação, , São Paulo, SP: PancasatHerbert, V., Lau, K.S., Gotlieb, C.W., Bleicher, S.T., Coated charcoal immunoassay of insulin (1965) J Clin Endocrinol, 25, pp. 1375-1384Dubois, B., Gilles, K.A., Hamilton, J.K., Rebers, P.A., Colorimetric method for determination of sugar and related substances (1956) Anal Chem, 28, pp. 350-356Mathews, J.N.S., Altman, D.G., Campbel, M.S., Royston, P., Analysis of serial in medical research (1990) Br Med J, 27, pp. 230-235Lundbaeck, K., Intravenous glucose tolerance test as a tool in definition and diagnosis of diabetes mellitus (1962) Br Med J, 2, pp. 1507-1513Lacy, P.E., Kostianovsky, M., Method of the isolation of intact islets of Langerhans from the rat pancreas (1967) Diabetes, 16, pp. 35-39McArdle, W.D., Katch, F.I., Katch, V.L., (2003) Fisiologia do Exercício: Energia, Nutrição e Desempenho Hamann, , Rio de Janeiro, RJ: Guanabara KooganIzawa, T., Komabayashi, T., Ca2+ and lipolysis in adipocytes from exercise-trained rats (1994) J Appl Physiol, 977, pp. 2618-2624Borer, K.T., Hormonal and nutritional determinants of catch-up growth in hamsters (1987) Growth, 51, pp. 103-117Whitehead, R.G., Harland, P.S.E.G., Blood glucose, lactate and pyruvate in kwashiorkor (1966) Br J Nutr, 20, pp. 825-831Latorraca, M.Q., Reis, M.A.B., Carneiro, E.M., Mello, M.A.R., Velloso, L.A., Saad, M.I.A., Protein deficiency and nutrition mal recovery modulated insulin secretation and early steps of insulin secretation in rats (1998) J Nutr, 128, pp. 1643-1349Almeida, P.B.L., Mello, M.A.R., Efeitos da desnutrição protéica fetal/neonatal sobre a ação da insulina e a homeostase glicêmica na vida adulta. (2005) Rev Bras Ativ Fis e Saúde, 10, pp. 17-28Nóbrega FJ de. DesnutriçǎIntra-Uterina e Pós-Natal. São Paulo. SP: Panamed Editoiial, 1986Silva, M.P., Stevanato, E., Moreira, V.M., Porto, M., Mello, M.A.R., Efeitos da desnutrição intra-uterina e da recuperação nutricional sobre respostas metabólicas an exercício crônico em ratos jovens. (1999) Motriz, 5, pp. 152-159Saltin, B., Wade, C.E., Metabolic fundamentals in exercise (1973) Med Science in Sports, 5, pp. 137-146Okitolonda, W., Brichard, S.M., Henquin, J.C., Repercutions of chronic protein-calorie malnutrition on glucose homeostasis in the rat (1987) Diabetologia, 30, pp. 946-951Latorraca, M.Q., Reis, M.A.B., Carneiro, E.M., Mello, M.A.R., Velloso, L.A., Saad, M.J., Boschero, A.C., Protein deficiency and nutritional recovery modulate insulin secretion and the early steps of insulin action in rats (1998) J Nutr Philadelphia, 128, pp. 1643-1649Santos, R.V.T., Caperuto, E.C., Rosa, L.F.B.P.C., Efeitos do aumento, na sobrecarga de treinamento sobre parâmetros bioquímicos e hormonais em ratos. (2006) Rev Bras Med Esporte, 12, p. 3Kumar, V., Den, M.G., Ramalingaswami, V., Mechanism of fatty liver in protein deficiency (1972) Gastroenterology, 62, pp. 445-451Carneiro, E.M., Mello, M.A.R., Gobatto, C.A., Boschero, A.C., Low protein diet impairs glucose-induced insulin secretion from and 45Ca uptake by pancreatic rat islets (1995) J Nutr Biochem, 6, pp. 314-318Slentz, C.A., Gulve, E.A., Rodnick, K.J., Henriksen, E.J., Youn, J.H., Holloszy, J.O., Glucose transporters and maximal transport are increased in endurance-trained rat soleus (1992) J Appl Physiol, 73, pp. 486-492Ropelle, E.R., Pauh, J.R., Carvalheira, J.B.C., Efeitos moleculares do exercício físico sobre as vias de sinalização insulíinica. 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    Protein Deficiency Attenuates The Effects Of Alloxan On Insulin Secretion And Glucose Homeostasis In Rats

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    We have investigated the effect of alloxan on insulin secretion and glucose homeostasis in rats maintained on a 17% protein (normal protein, NP) or 6% protein (low protein, LP) diet from weaning (21 days old) to adulthood (90 days old). The incidence of alloxan diabetes was higher in the NP (3.5 times) than in the LP group. During an oral glucose tolerance test, the area under serum glucose curve was lower in LP (57%) than in NP rats while there were no differences between the two groups in the area under serum insulin curve. The serum glucose disappearance rate (Kitt) after exogenous insulin administration was higher in LP (50%) than in NP rats. In pancreatic islets isolated from rats not injected with alloxan, acute exposure to alloxan (0.05 mmol/L) reduced the glucose- or arginine-stimulated insulin secretion of NP islets by 78% and 56%, respectively, whereas for islets from LP rats, the reduction was 47% and 17% in the presence of glucose and arginine, respectively. Alloxan treatment reduced the glucose oxidation in islets from LP rats to a lesser extent than in NP islets (23% vs. 56%). In conclusion, alloxan was less effective in producing hyperglycemia in rats fed a low protein diet than in normal diet rats. This effect is attributable to an increased peripheral sensivity to insulin in addition to a better preservation of glucose oxidation and insulin secretion in islets from rats fed a low protein diet.3317382Blachier, F., Murtada, A., Sener, A., Malaisse, W.J., Stimulus-secretion coupling of arginine-induced insulin release. Uptake of metabolized and nonmetabolized cationic amino acids by pancreatic islets (1989) Endocrinology, 124, pp. 134-141Borg, A.H., Cagliero, E., Sandler, S., Eizirik, D.L., Welsh, N., Welsh, M., Interleukin-1 B increases the activity of superoxide dismutase in rat pancreatic islet (1992) Endocrinology, 130, pp. 2851-2857Brooks, S.E.H., Patch, F.R., Golden, M.H.N., Payne-Robinson, H.M., Ultrastructure of the islets of Langerhans in protein energy malnutrition (1993) W.I. Med. J., 42, pp. 101-106Carneiro, E.M., Mello, M.A.R., Gobatto, C.A., Boschero, A.C., Low protein diet impairs glucose induced insulin release and 45Ca uptake by pancreatic rat islets (1995) Nutr. Biochem., 6, pp. 314-318Grace, C.J., Swenne, I., Khon, P.G., Strain, A.J., Milner, R.D.G., Protein energy malnutrition induces changes in insulin sensitivity (1990) Diabetes Metabol., 16, pp. 484-491De Vos, A., Heimberg, H., Quartier, E., Huypens, P., Bouwens, L., Pipeleers, D., Schuit, F., Human and rat beta cells differ in glucose transporter but not in glucokinase gene expression (1995) J. Clin. Invest., 96, pp. 2489-2495Desai, M., Crowter, N.J., Lucas, A., Hales, C.N., Organ selective growth in the offspring of protein restricted mothers (1996) Br. J. Nutr., 76, pp. 591-603Dixit, P.K., Kaung, K.L.C., Pancreatic B cell in malnutrition: A study involving morphometric analysis and alloxan effects (1985) J. Nutr., 115, pp. 375-381Eizirik, D.L., Bjorklund, A., Cagliero, E., Genotoxic agents increase the expression of growth arrest and DNA damage-induced genes gadd 153 and gadd 45 in rat pancreatic islets (1993) Diabetes, 42, pp. 438-445Eizirik, D.L., Welsh, M., Strandell, E., Welsh, N., Sandler, S., Interleukin-1 B depletes insulin messenger RNA and increases heat shock protein Hsp 70 in mouse pancreatic islets without impairing glucose metabolism (1990) Endocrinology, 127, pp. 2290-2297Escriva, F., Kergoat, M., Bailbé, D., Pascual-Leone, A.M., Portha, B., Increased insulin action in the rat after protein malnutrition early in life (1991) Diabetologia, 34, pp. 559-564Gasa, R., Senner, A., Malaisse, W.J., Gomis, R., Apparent starvation induced repression of pancreatic islet glucokiriase (1995) Biochem. Mol. Med., 56, pp. 99-103James, W.P.T., Coore, H.G., Persistent impairment of insulin secretion and glucose tolerance after malnutrition (1970) Am. J. Clin. Nutr., 23, pp. 386-389Latorraca, M.Q., Carneiro, E.M., Mello, M.A.R., Boschero, A.C., Protein deficiency during pregnancy and lactation impairs glucose induced insulin secretion but increases the sensitivity to insulin in weaned rats (1998) Br. J. Nutr., 80, pp. 291-297Lenzen, S., Panten, U., Alloxan: History and mechanism of action (1988) Diahetologia, 31, pp. 337-342Lundebaek, K., Intravenous glucose tolerance as a tool in definition and diagnosis of diabetes mellitus (1962) Br. Med. J., 3, pp. 1057-1513Malaisse, W.J., Alloxan toxicity to B cell: A new hypothesis (1982) Biochem. Pharmacol., 31, pp. 3527-3534Malaisse, W.J., Malaisse-Lagae, F., Wright, P., Effect of fasting upon insulin secretion in the rat (1967) Am. J. Physiol., 213, pp. 843-848Mathews, J.N.S., Altman, D.G., Campbel, M.S., Royston, P., Analysis of serial measurements in medical research (1990) Br. Med. J., 27, pp. 230-235Matschinsky, F., Glucokinase as a sensor and metabolic signal generator in pancreatic β-cell and hepatocytes (1990) Diabetes, 39, pp. 647-652Mello, M.A.R., Cury, L., Valle, L.B.S., Oliveira-Filho, R.M., Pregnancy in young rats: Effects of malnutrition (1987) Nutr. Rep. Int., 36, pp. 527-535Mello, M.A.R., Luciano, E., Effects of protein malnutrition on glucose tolerance in rats with alloxan induced diabetes (1995) Braz. J. Med. Biol. Res., 28, pp. 467-470Munday, R., Ludwig, K., Lenzen, S., The relationship between the physicochemical properties and the biological effects of alloxan and several N-alkyl substituted alloxan derivatives (1993) J. 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    pinheirorbp/nestedness: A novel perspective on nestedness and a theory-oriented procedure for the use of null models: codes.

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    <p>Scripts to reproduce the full set of analysis performed in our study.</p> <p>Authors: Pinheiro R. B. P., Dormann C.F., Felix G.M.F., and Mello M.A.R.</p&gt

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Variations on the Author

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    “Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship

    Appropriate Similarity Measures for Author Cocitation Analysis

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    We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis

    Evaluation Of A Protein Deficient Diet In Rats Through Blood Oxidative Stress Biomarkers

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    Protein malnutrition leads to functional impairment in several organs, which is not fully restored with nutritional recovery. Little is known about the role of oxidative stress in the genesis of these alterations. This study was designed to assess the sensitivity of blood oxidative stress biomarkers to a dietary protein restriction. Male Wistar rats were divided into two groups, according to the diet fed from weaning (21 days) to 60 day old: normal protein (17% protein) and low protein (6% protein). Serum protein, albumin, free fatty acid and liver glycogen and lipids were evaluated to assess the nutritional status. Blood glutathione reductase (GR) and catalase (CAT) activities, plasma total sulfhydryl groups concentration (TSG) as well as plasma thiobarbituric acid reactive substances (TBARs) and reactive carbonyl derivatives (RCD) were measured as biomarkers of the antioxidant system and oxidative damage, respectively. The glucose metabolism in soleus muscle was also evaluated as an index of stress severity imposed to muscular mass by protein malnutrition. No difference was observed in muscle glucose metabolism or plasma RCD concentration between both groups. However, our results showed that the low protein group had higher plasma TBARs (62%) concentration and lower TSG (44%) concentration than control group, indicating increased reactive oxygen species production in low protein group. The enhancement of erythrocyte GR (29%) and CAT (28%) activities in this group also suggest an adaptation to the stress generated by the protein deficiency. Taken together, the results presented here show that the biomarkers used were able to reflect the oxidative stress level induced by this specific protein deficient diet.113-114213228Aebi, H., Catalase in vitro (1984) Meth. Enzymol., 105, pp. 121-126Report of the American Institute of Nutrition ad hoc committee on standards for nutritional studies (1977) J. 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Chem., 28, pp. 350-356Eston, Finney, R.G., Finney, S., Baker, S., Baltzopoulos, V., Muscle tenderness and peak torque changes after downhill running following a prior bout of isokinetic eccentric exercise (1996) J. Sports Sci., 14, pp. 291-299Faure, P., Lafond, J.-L., Measurement of plasma sulfhydryl and carbonyl groups as a possible indicator of protein oxidation (1995) Analysis of Free Radicals in Biological Systems, pp. 237-248. , A. E. Favier, J. Cadet, B. Kalyanaraman, M. Fontecave, J.-L Pierre (Eds.) Basel, Switzerland: Birkhäuser VerlagFechner, A., Böhme, C.C., Gromer, S., Funk, M., Schimer, R.H., Becker, Leichsenring, K., Antioxidant status and nitric oxide in malnutrition syndrome kwashiorkor (2001) Pediat. Res., 49, pp. 237-243Holbrook, F., (2000) Nature, 408, pp. 239-247Galdino, R., Almeida, C.C.S., Luciano, E., Mello, M.A.R., Protein malnutrition does not impair glucose metabolism adaptations to exercise-training (2000) Nutr. 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    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

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