31 research outputs found

    Fungal Planet description sheets: 1042–1111

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    Novel species of fungi described in this study include those from various countries as follows: Antarctica, Cladosporium arenosum from marine sediment sand. Argentina, Kosmimatamyces alatophylus (incl. Kosmimatamyces gen. nov.) from soil. Australia, Aspergillus banksianus, Aspergillus kumbius, Aspergillus luteorubrus, Aspergillus malvicolor and Aspergillus nanangensis from soil, Erysiphe medicaginis from leaves of Medicago polymorpha, Hymenotorrendiella communis on leaf litter of Eucalyptus bicostata, Lactifluus albopicri and Lactifluus austropiperatus on soil, Macalpinomyces collinsiae on Eriachne benthamii, Marasmius vagus on soil, Microdochium dawsoniorum from leaves of Sporobolus natalensis, Neopestalotiopsis nebuloides from leaves of Sporobolus elongatus, Pestalotiopsis etonensis from leaves of Sporobolus jacquemontii, Phytophthora personensis from soil associated with dying Grevillea mccutcheonii. Brazil, Aspergillus oxumiae from soil, Calvatia baixaverdensis on soil, Geastrum calycicoriaceum on leaf litter, Greeneria kielmeyerae on leaf spots of Kielmeyera coriacea. Chile, Phytophthora aysenensis on collar rot and stem of Aristotelia chilensis. Croatia, Mollisia gibbospora on fallen branch of Fagus sylvatica. Czech Republic, Neosetophoma hnaniceana from Buxus sempervirens. Ecuador, Exophiala frigidotolerans from soil. Estonia, Elaphomyces bucholtzii in soil. France, Venturia paralias from leaves of Euphorbia paralias. India, Cortinarius balteatoindicus and Cortinarius ulkhagarhiensis on leaf litter. Indonesia, Hymenotorrendiella indonesiana on Eucalyptus urophylla leaf litter. Italy, Penicillium taurinense from indoor chestnut mill. Malaysia, Hemileucoglossum kelabitense on soil, Satchmopsis pini on dead needles of Pinus tecunumanii. Poland, Lecanicillium praecognitum on insects' frass. Portugal, Neodevriesia aestuarina from saline water. Republic of Korea, Gongronella namwonensis from freshwater. Russia, Candida pellucida from Exomias pellucidus, Heterocephalacria septentrionalis as endophyte from Cladonia rangiferina, Vishniacozyma phoenicis from dates fruit, Volvariella paludosa from swamp. Slovenia, Mallocybe crassivelata on soil. South Africa, Beltraniella podocarpi, Hamatocanthoscypha podocarpi, Coleophoma podocarpi and Nothoseiridium podocarpi (incl. Nothoseiridium gen. nov.)from leaves of Podocarpus latifolius, Gyrothrix encephalarti from leaves of Encephalartos sp., Paraphyton cutaneum from skin of human patient, Phacidiella alsophilae from leaves of Alsophila capensis, and Satchmopsis metrosideri on leaf litter of Metrosideros excelsa. Spain, Cladophialophora cabanerensis from soil, Cortinarius paezii on soil, Cylindrium magnoliae from leaves of Magnolia grandiflora, Trichophoma cylindrospora (incl. Trichophoma gen. nov.) from plant debris, Tuber alcaracense in calcareus soil, Tuber buendiae in calcareus soil. Thailand, Annulohypoxylon spougei on corticated wood, Poaceascoma filiforme from leaves of unknown Poaceae. UK, Dendrostoma luteum on branch lesions of Castanea sativa, Ypsilina buttingtonensis from heartwood of Quercus sp. Ukraine, Myrmecridium phragmiticola from leaves of Phragmites australis. USA, Absidia pararepens from air, Juncomyces californiensis (incl. Juncomyces gen. nov.) from leaves of Juncus effusus, Montagnula cylindrospora from a human skin sample, Muriphila oklahomaensis (incl. Muriphila gen. nov.)on outside wall of alcohol distillery, Neofabraea eucalyptorum from leaves of Eucalyptus macrandra, Diabolocovidia claustri (incl. Diabolocovidia gen. nov.)from leaves of Serenoa repens, Paecilomyces penicilliformis from air, Pseudopezicula betulae from leaves of leaf spots of Populus tremuloides. Vietnam, Diaporthe durionigena on branches of Durio zibethinus and Roridomyces pseudoirritans on rotten wood. Morphological and culture characteristics are supported by DNA barcodes

    Dietary Whey Protein Lessens Several Risk Factors For Metabolic Diseases: A Review

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    Obesity and type 2 diabetes mellitus (DM) have grown in prevalence around the world, and recently, related diseases have been considered epidemic. Given the high cost of treatment of obesity/DM-associated diseases, strategies such as dietary manipulation have been widely studied; among them, the whey protein diet has reached popularity because it has been suggested as a strategy for the prevention and treatment of obesity and DM in both humans and animals. Among its main actions, the following activities stand out: reduction of serum glucose in healthy individuals, impaired glucose tolerance in DM and obese patients; reduction in body weight; maintenance of muscle mass; increases in the release of anorectic hormones such as cholecystokinin, leptin, and glucagon like-peptide 1 (GLP-1); and a decrease in the orexigenic hormone ghrelin. Furthermore, studies have shown that whey protein can also lead to reductions in blood pressure, inflammation, and oxidative stress. © 2012 Souza et al.; licensee BioMed Central Ltd.11Giskes, K., Van Lenthe, F., Avendano-Pabon, M., Brug, J., A systematic review of environmental factors and obesogenic dietary intakes among adults: Are we getting closer to understanding obesogenic environments? (2011) Obes Rev, 12, pp. 595-e106. , 10.1111/j.1467-789X.2010.00769.x 20604870Pimentel, G.D., Arimura, S.T., De Moura, B.M., Silva, M.E., De Sousa, M.V., Short-term nutritional counseling reduces body mass index, waist circumference, triceps skinfold and triglycerides in women with metabolic syndrome (2010) Diabetol Metab Syndr, 2, p. 13. , 10.1186/1758-5996-2-13 20181143(2012) Global Strategy on Diet, Physical Activity and Health: Obesity and Overweight, , http://www.who.int/dietphysicalactivity/publications/facts/obesity/en, WHO, World Health Organization, GenevaMisra, A., Khurana, L., Obesity-related non-communicable diseases: South Asians vs White Caucasians (2011) Int J Obes (Lond), 35, pp. 167-187. , 10.1038/ijo.2010.135Gigante, D.P., Moura, E.C., Sardinha, L.M., Prevalence of overweight and obesity and associated factors, Brazil, 2006 (2009) Rev Saude Publica, 43 (SUPPL. 2), pp. 83-89. , 19936502Rodrigues, T.C., Canani, L.H., Gross, J.L., Metabolic syndrome, insulin resistance and cardiovascular disease in type-1 diabetes mellitus (2010) Arq Bras Cardiol, 94, pp. 134-139. , 10.1590/S0066-782X2010000100020 20414537Mortensen, L.S., Hartvigsen, M.L., Brader, L.J., Astrup, A., Schrezenmeir, J., Holst, J.J., Thomsen, C., Hermansen, K., Differential effects of protein quality on postprandial lipemia in response to a fat-rich meal in type 2 diabetes: Comparison of whey, casein, gluten, and cod protein (2009) Am J Clin Nutr, 90, pp. 41-48. , 10.3945/ajcn.2008.27281 19458012De Oliveira, E.P., Manda, R.M., Torezan, G.A., Corrente, J.E., Burini, R.C., Dietary, anthropometric, and biochemical determinants of plasma high-density lipoprotein-cholesterol in free-living adults (2011) Cholesterol, 2011, p. 851750. , 21490775Takahashi, M.M., De Oliveira, E.P., Moreto, F., Portero-Mclellan, K.C., Burini, R.C., Association of dyslipidemia with intakes of fruit and vegetables and the body fat content of adults clinically selected for a lifestyle modification program (2010) Arch Latinoam Nutr, 60, pp. 148-154. , 21425719Frestedt, J.L., Zenk, J.L., Kuskowski, M.A., Ward, L.S., Bastian, E.D., A whey-protein supplement increases fat loss and spares lean muscle in obese subjects: A randomized human clinical study (2008) Nutrition and Metabolism, 5 (1), p. 8. , DOI 10.1186/1743-7075-5-8Solah, V.A., Kerr, D.A., Adikara, C.D., Meng, X., Binns, C.W., Zhu, K., Devine, A., Prince, R.L., Differences in satiety effects of alginate- and whey protein-based foods (2010) Appetite, 54, pp. 485-491. , 10.1016/j.appet.2010.01.019 20144671Pimentel, G.D., Portero-Mclellan, K.C., De Oliveira, E.P., Spada, A.P., Oshiiwa, M., Zemdegs, J.C., Barbalho, S.M., Long-term nutrition education reduces several risk factors for type 2 diabetes mellitus in Brazilians with impaired glucose tolerance (2010) Nutr Res, 30, pp. 186-190. , 10.1016/j.nutres.2010.03.003 20417879Pilvi, T.K., Harala, S., Korpela, R., Mervaala, E.M., Effects of high-calcium diets with different whey proteins on weight loss and weight regain in high-fat-fed C57BL/6J mice (2009) Br J Nutr, 102, pp. 337-341. , 10.1017/S0007114508199445 19622178Bowen, J., Noakes, M., Clifton, P.M., Appetite regulatory hormone responses to various dietary proteins differ by body mass index status despite similar reductions in ad Libitum energy intake (2006) Journal of Clinical Endocrinology and Metabolism, 91 (8), pp. 2913-2919. , http://jcem.endojournals.org/cgi/reprint/91/8/2913, DOI 10.1210/jc.2006-0609Petersen, B.L., Ward, L.S., Bastian, E.D., Jenkins, A.L., Campbell, J., Vuksan, V., A whey protein supplement decreases post-prandial glycemia (2009) Nutr J, 8, p. 47. , 10.1186/1475-2891-8-47 19835582Gunnarsson, P.T., Winzell, M.S., Deacon, C.F., Larsen, M.O., Jelic, K., Carr, R.D., Ahren, B., Glucose-induced incretin hormone release and inactivation are differently modulated by oral fat and protein in mice (2006) Endocrinology, 147 (7), pp. 3173-3180. , http://endo.endojournals.org/cgi/reprint/147/7/3173, DOI 10.1210/en.2005-1442Takasaki, K., Nakajima, T., Ueno, K., Nomoto, Y., Higo, K., Effects of combination treatment with dipeptidyl peptidase IV inhibitor and sulfonylurea on glucose levels in rats (2004) Journal of Pharmacological Sciences, 95 (2), pp. 291-293. , DOI 10.1254/jphs.SC0040043Monograph (2008) Altern Med Rev, 13, pp. 341-347. , 19152482 Whey proteinHaraguchi, F.K., Pedrosa, M.L., De Paula, H., Dos Santos, R.C., Silva, M.E., Influência das proteínas do soro sobre enzimas hapáticas, perfil lipídico e formação ássea de ratos hipercolesterolêmicos (2009) Rev Nutr, 22, pp. 517-525Luhovyy, B.L., Akhavan, T., Anderson, G.H., Whey proteins in the regulation of food intake and satiety (2007) J Am Coll Nutr, 26, pp. 704S-712S. , 18187437Haraguchi, F.K., De Abreu, W.C., De Paula, H., Proteínas do soro do leite: Composição, propriedades nutricionais, aplicaçes no esporte e benefícios para a saúde humana (2006) Rev Nutr, 19, pp. 479-488Hulmi, J.J., Lockwood, C.M., Stout, J.R., Effect of protein/essential amino acids and resistance training on skeletal muscle hypertrophy: A case for whey protein (2010) Nutr Metab (Lond), 7, p. 51. , 10.1186/1743-7075-7-51Pal, S., Ellis, V., Ho, S., Acute effects of whey protein isolate on cardiovascular risk factors in overweight, post-menopausal women (2010) Atherosclerosis, 212, pp. 339-344. , 10.1016/j.atherosclerosis.2010.05.032 20561625Barnett, M.P., Phillips, A.R., Harris, P.M., Cooper, G.J., Impaired insulin secretion in perfused pancreases isolated from offspring of female rats fed a low protein whey-based diet (2008) Jop, 9, pp. 477-488. , 18648139Pacheco, M.T.B., Dias, N.F.G., Baldini, V.L.S., Tanikawa, C., Sgarbieri, V.C.S., Propriedades funcionais de hidrolisados obtidos a partir de concentrados protéicos de soro de leite (2005) Ciênc Tecnol Aliment, 25, pp. 333-338. , 22764363Pal, S., Ellis, V., The acute effects of four protein meals on insulin, glucose, appetite and energy intake in lean men (2010) Br J Nutr, 104, pp. 1241-1248. , 10.1017/S0007114510001911 20456814Hackney, K.J., Bruenger, A.J., Lemmer, J.T., Timing protein intake increases energy expenditure 24h after resistance training (2010) Med Sci Sports Exerc, 42, pp. 998-1003. , 10.1249/MSS.0b013e3181c12976 19997003Lan-Pidhainy, X., Wolever, T.M., The hypoglycemic effect of fat and protein is not attenuated by insulin resistance (2010) Am J Clin Nutr, 91, pp. 98-105. , 10.3945/ajcn.2009.28125 19923374Pilvi, T.K., Korpela, R., Huttunen, M., Vapaatalo, H., Mervaala, E.M., High-calcium diet with whey protein attenuates body-weight gain in high-fat-fed C57Bl/6J mice (2007) British Journal of Nutrition, 98 (5), pp. 900-907. , DOI 10.1017/S0007114507764760, PII S0007114507764760Muro Urista, C., Alvarez Fernandez, R., Riera Rodriguez, F., Arana Cuenca, A., Tellez Jurado, A., Review: Production and functionality of active peptides from milk (2011) Food Sci Technol Int, 17, pp. 293-317. , 10.1177/1082013211398801 21917640Graf, S., Egert, S., Heer, M., Effects of whey protein supplements on metabolism: Evidence from human intervention studies (2011) Curr Opin Clin Nutr Metab Care, 14, pp. 569-580. , 10.1097/MCO.0b013e32834b89da 21912246Gilbert, J.A., Bendsen, N.T., Tremblay, A., Astrup, A., Effect of proteins from different sources on body composition (2011) Nutr Metab Cardiovasc Dis, 21 (SUPPL. 2), pp. 216-231. , 21565478Dougkas, A., Reynolds, C.K., Givens, I.D., Elwood, P.C., Minihane, A.M., Associations between dairy consumption and body weight: A review of the evidence and underlying mechanisms (2011) Nutr Res Rev, pp. 1-24Madureira, A.R., Tavares, T., Gomes, A.M., Pintado, M.E., Malcata, F.X., Invited review: Physiological properties of bioactive peptides obtained from whey proteins (2010) J Dairy Sci, 93, pp. 437-455. , 10.3168/jds.2009-2566 20105516Baer, D.J., Stote, K.S., Paul, D.R., Harris, G.K., Rumpler, W.V., Clevidence, B.A., Whey protein but not soy protein supplementation alters body weight and composition in free-living overweight and obese adults (2011) J Nutr, 141, pp. 1489-1494. , 10.3945/jn.111.139840 21677076Burton-Freeman, B.M., Glycomacropeptide (GMP) is not critical to whey-induced satiety, but may have a unique role in energy intake regulation through cholecystokinin (CCK) (2008) Physiol Behav, 93, pp. 379-387. , 10.1016/j.physbeh.2007.09.010 17964616Pichon, L., Potier, M., Tome, D., Mikogami, T., Laplaize, B., Martin-Rouas, C., Fromentin, G., High-protein diets containing different milk protein fractions differently influence energy intake and adiposity in the rat (2008) British Journal of Nutrition, 99 (4), pp. 739-748. , DOI 10.1017/S0007114507831709, PII S0007114507831709Pilvi, T.K., Storvik, M., Louhelainen, M., Merasto, S., Korpela, R., Mervaala, E.M., Effect of dietary calcium and dairy proteins on the adipose tissue gene expression profile in diet-induced obesity (2008) J Nutrigenet Nutrigenomics, 1, pp. 240-251. , 10.1159/000151238 19776631Pal, S., Ellis, V., Dhaliwal, S., Effects of whey protein isolate on body composition, lipids, insulin and glucose in overweight and obese individuals (2010) Br J Nutr, 104, pp. 716-723. , 10.1017/S0007114510000991 20377924Kasim-Karakas, S.E., Cunningham, W.M., Tsodikov, A., Relation of nutrients and hormones in polycystic ovary syndrome (2007) American Journal of Clinical Nutrition, 85 (3), pp. 688-694. , http://www.ajcn.org/cgi/reprint/85/3/688Pal, S., Ellis, V., The chronic effects of whey proteins on blood pressure, vascular function, and inflammatory markers in overweight individuals (2010) Obesity (Silver Spring), 18, pp. 1354-1359. , 10.1038/oby.2009.397Pimentel, G.D., Mota, J.F., Oyama, L.M., Oxyntomodulin and obesity (2009) Rev Nutr, 22, pp. 727-737. , 10.1590/S1415-52732009000500013Pimentel, G.D., Dornellas, A.P., Rosa, J.C., Lira, F.S., Cunha, C.A., Boldarine, V.T., De Souza, G.I., Oyama, L.M., High-fat diets rich in soy or fish oil distinctly alter hypothalamic insulin signaling in rats (2012) J Nutr 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short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase (2010) J Biol Chem, 285, pp. 31806-31818. , 10.1074/jbc.M110.123638 20670938Mortensen, L.S., Holmer-Jensen, J., Hartvigsen, M.L., Jensen, V.K., Astrup, A., De Vrese, M., Holst, J.J., Hermansen, K., Effects of different fractions of whey protein on postprandial lipid and hormone responses in type 2 diabetes (2012) Eur J Clin Nutr, , In pressSantoro, S., Velhote, M.C.P., Manzoni, C.E., Mechenas, A.S.G., Strassmann, V., Scheinberg, V., Adaptação digestiva: Uma nova proposta cirúrgica para tratar a obesidade com base em fisiologia e evolução (2003) Einstein, 1, pp. 95-98Mannucci, E., Pala, L., Ciani, S., Bardini, G., Pezzatini, A., Sposato, I., Cremasco, F., Rotella, C.M., Hyperglycaemia increases dipeptidyl peptidase IV activity in diabetes mellitus (2005) Diabetologia, 48 (6), pp. 1168-1172. , DOI 10.1007/s00125-005-1749-8Veldhorst, M.A., Nieuwenhuizen, A.G., Hochstenbach-Waelen, A., Van Vught, A.J., Westerterp, K.R., Engelen, M.P., Brummer, R.J., Westerterp-Plantenga, M.S., Dose-dependent satiating effect of whey relative to casein or soy (2009) Physiol Behav, 96, pp. 675-682. , 10.1016/j.physbeh.2009.01.004 19385022Pinto, L.C., Ricardo, E.D., Leitao, C.B., Kramer, C.K., Zanatta, C.M., Gross, J.L., Canani, L.H., Inadequate blood pressure control in patients with type 2 diabetes mellitus (2010) Arq Bras Cardiol, 94, pp. 651-655. , 10.1590/S0066-782X2010005000034 20428720Takahashi, M.M., De Oliveira, E.P., De Carvalho, A.L., De Souza Dantas, L.A., Burini, F.H., Portero-Mclellan, K.C., Burini, R.C., Metabolic syndrome and dietary components are associated with coronary artery disease risk score in free-living adults: A cross-sectional study (2011) Diabetol Metab Syndr, 3, p. 7. , 10.1186/1758-5996-3-7 21554698Lee, Y.-M., Skurk, T., Hennig, M., Hauner, H., Effect of a milk drink supplemented with whey peptides on blood pressure in patients with mild hypertension (2007) 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H., Salem, A., Sayed, A., Metwalli, A., Whey protein enhances normal inflammatory responses during cutaneous wound healing in diabetic rats (2011) Lipids Health Dis, 10, p. 235. , 10.1186/1476-511X-10-235 22168406Hamad, E.M., Taha, S.H., Abou Dawood, A.G., Sitohy, M.Z., Abdel-Hamid, M., Protective effect of whey proteins against nonalcoholic fatty liver in rats (2011) Lipids Health Dis, 10, p. 57. , 10.1186/1476-511X-10-57 21489294Zavorsky, G.S., Kubow, S., Grey, V., Riverin, V., Lands, L.C., An open-label dose - Response study of lymphocyte glutathione levels in healthy men and women receiving pressurized whey protein isolate supplements (2007) International Journal of Food Sciences and Nutrition, 58 (6), pp. 429-436. , DOI 10.1080/09637480701253581, PII 779415967Chitapanarux, T., Tienboon, P., Pojchamarnwiputh, S., Leelarungrayub, D., Open-labeled pilot study of cysteine-rich whey protein isolate supplementation for nonalcoholic steatohepatitis patients (2009) J Gastroenterol 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    Inflammatory cytokines and metabolic responses to high-intensity intermittent training: Effect of the exercise intensity

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    International audienceTo examine the effects of two high-intensity intermittent training (HIIT) programs of varying intensities (100% vs. 110% of maximal aerobic velocity [MAV]) on metabolic, hormonal and inflammatory markers in young men. Thirty-seven active male volunteers were randomly assigned into: HIIT experimental groups (100% MAV [EG100, n = 9] and 110% MAV [EG110, n = 9]) and a control groups (CG100, n = 9 and CG110, n = 9). Particpants performed high intesity intermittent exercise test (HIIE) at 100% or 110% MAV. Venous blood samples were obtained before, at the end of HIIE and at 15 min of recovery, and before and after 8 weeks of HIIT programs. After training, Glucose was lower (p andlt; 0.01) in EG100 (d = 0.72) and EG110 (d = 1.20) at the end of HIIE, and at 15 min recovery only in EG110 (d = 0.95). After training, Insulin and Cortisol were lower than before training in EG100 and EG110 at the end of HIIE (p andlt; 0.001). After HIIT, IL-6 deceased (p andlt; 0.001) in EG100 (d = 1.43) and EG110 (d = 1.56) at rest, at the end of HIIE (d = 1.03; d = 1.75, respectively) and at 15 min of recovery (d = 0.88;d = 1.7, respectively). This decrease was more robust (p andlt; 0.05) in EG110 compared to EG100. After HIIT, TNF-α deceased (p andlt; 0.001) in EG100 (d = 1.43) and EG110 (d = 0.60) at rest, at the end of HIIE (0.71 andlt; d andlt; 0.98) and at 15 min of recovery (0.70 andlt; d andlt; 2.78). HIIT with 110% MAV is more effective in young males on the improvements of some metabolic (Glucose), hormonal (Cortisol) and inflammatory (IL-6) markers at rest, at the end of HIIE and 15 min of recovery than training at 100% MAV. © 2022 Institute of Sport. All rights reserved
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