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Bibliografia Linea Ferro

BIODIFer – 20 capsule

- Sevda ER, et al. Anticandidal activities of lactic acid bacteria isolated from the vagina. Turk J Med Sci. 2019; 49:375-383

- Goossens D, et al. Survival of the probiotic, L. plantarum 299v® and its effects on the faecal bacterial flora, with and without gastric acid inhibition. Dig Liver Dis. 2005; 37:44-50

- Jacobsen CN, et al. Screening of probiotic activities of forty-seven strains of Lactobacillus spp. by in vitro techniques and evaluation of the colonization ability of five selected strains in humans. Appl Environ Microbiol. 1999; 65:4949-4956

- Hoppe M, et al. Probiotic strain Lactobacillus plantarum 299vincreases iron absorption from an iron-supplemented fruit drink: a double-isotope cross-over single-blind study in women of reproductive age. Br J Nutr. 2015; 114:1195-202.

- Bering S, et al. A lactic acid-fermented oat gruel increases non-haem iron absorption from a phytate-rich meal in healthy women of childbearing age. Br J Nutr. 2006; 96:80-5

- Hoppe M, et al. Freeze-dried Lactobacillus plantarum 299vincreases iron absorption in young females-Double isotope sequential single-blind studies in menstruating women. PLoS One. 2017; 12: e0189141

- Axling U, et al. The Effect of Lactobacillus plantarum 299von Iron Status and Physical Performance in Female Iron-Deficient Athletes: A Randomized Controlled Trial. Nutrients. 2020; 12:1279

- Axling U, et al. The effect of Lactiplantibacillus plantarum 299v® together with a low dose of iron on iron status in healthy pregnant women: A randomized clinical trial. Acta Obstet Gynecol Scand. 2021; [Online ahead of print]

- Pretzer G, et al. Biodiversity-based identification and functional characterization of the mannose-specific adhesin of Lactobacillus plantarum. J Bacteriol 2005; 187: 6128-36

- Adlerberth I, et al. A mannose-specific adherence mechanism in Lactobacillus plantarum conferring binding to the human colonic cell line HT-29. Appl Environ Microbiol. 1996; 62:2244-51

- Tallon R, et al. Strain- and matrix-dependent adhesion of Lactobacillus plantarum is mediated by proteinaceous bacterial compounds. J Appl Microbiol. 2007; 102: 442-51

- Mack DR, et al. Extracellular MUC3 mucin secretion follows adherence of Lactobacillus strains to intestinal epithelial cells in vitro. Gut 2003; 52: 827-33

- Simovich M, et al. Localization of the iron transport proteins Mobilferrin and DMT-1 in the duodenum: the surprising role of mucin. Am J Hematol. 2003; 74:32-45

- Sandberg AS, et al. Iron Supplements Containing Lactobacillus plantarum 299vIncrease Ferric Iron and Up-regulate the Ferric Reductase DCYTB in Human Caco-2/HT29 MTX Co-Cultures. Nutrients. 2018; 10:1949

- Goossens D, et al. The effect of Lactobacillus plantarum 299von the bacterial composition and metabolic activity in faeces of healthy volunteers: a placebo-controlled study on the onset and duration of effects. Aliment Pharmacol Ther. 2003; 18:495-505

- Johansson ML, et al. Survival of Lactobacillus plantarum DSM 9843 (299v®), and effect on the short-chain fatty acid content of faeces after ingestion of a rose-hip drink with fermented oats. Int J Food Microbiol. 1998; 42:29-38

- Kaźmierczak-Siedlecka K, et al. Effects of 4 weeks of Lactobacillus plantarum 299vsupplementation on nutritional status, enteral nutrition tolerance, and quality of life in cancer patients receiving home enteral nutrition - a double-blind, randomized, and placebo-controlled trial. Eur Rev Med Pharmacol Sci. 2020; 24:9684-9694

- Ducrotté P, et al. Clinical trial: Lactobacillus plantarum 299v(DSM 9843) improves symptoms of irritable bowel syndrome. World J Gastroenterol. 2012; 18:4012-8

- Andersson H, et al. Oral Administration of Lactobacillus plantarum 299vReduces Cortisol Levels in Human Saliva during Examination Induced Stress: A Randomized, Double-Blind Controlled Trial. Int J Microbiol. 2016; 2016:8469018

- Rudzki L, et al. Probiotic Lactobacillus plantarum 299vdecreases kynurenine concentration and improves cognitive functions in patients with major depression: A double-blind, randomized, placebo controlled study. Psychoneuroendocrinology. 2019; 100:213-222

- Harrington M, et al. A comparison of the bioavailability of ferrous fumarate and ferrous sulfate in non-anemic Mexican women and children consuming a sweetened maize and milk drink. Eur J Clin Nutr. 2011; 65:20-5

- Balay KS, et al. Orange but not apple juice enhances ferrous fumarate absorption in small children. J Pediatr Gastroenterol Nutr. 2010; 50:545-50

- Jeroense F, et al. Consumption of Galacto-Oligosaccharides Increases Iron Absorption from Ferrous Fumarate: A Stable Iron Isotope Study in Iron-Depleted Young Women. J Nutr. 2019; 149:738-746

- Jeroense F, et al. Acute Consumption of Prebiotic Galacto-Oligosaccharides Increases Iron Absorption from Ferrous Fumarate, but not from Ferrous Sulfate and Ferric Pyrophosphate: Stable Iron Isotope Studies in Iron-Depleted Young Women. J Nutr. 2020; 150:2391-2397

- Devaki SJ & Raveendran RL. Vitamin C: Sources, Functions, Sensing and Analysis. DOI: 10.5772/intechopen.70162

- Atanassova BD & Tzatchev KN. Ascorbic Acid – important for iron metabolism. Folia Med (Plovdiv) 2008; 50:11-6

- McKie AT, et al. An iron-regulated ferric reductase associated with the absorption of dietary iron. Science 2001; 291:1755-1759

- Lane DJR & Richardson DR. The active role of vitamin C in mammalian iron metabolism: Much more than just enhanced iron absorption! Free Radic Biol Med. 2014; 75:69-83

- Toth I & Bridges KR. Ascorbic Acid Enhances Ferritin mRNA Translation by an IRP/Aconitase Switch. J Biol Chem 1995; 270: 19540-19544

- Bridges KR. Ascorbic acid inhibits lysosomal autophagy of ferritin. J Biol Chem 1987; 262:14773-14778

- Bridges KR & Hoffmann KE. The effects of ascorbic acid on the intracellular metabolism of iron and ferritin. J Biol Chem 1986; 261:14273-14277

- Lykkesfeldt J & Tveden-Nyborg P. The Pharmacokinetics of Vitamin C. Nutrients. 2019; 11:2412

- Hasselholt S, et al. Distribution of vitamin C is tissue specific with early saturation of the brain and adrenal glands following differential oral dose regimens in guinea pigs. Br J Nutr 2015; 113:1539-1549

- Levine M, et al. A new recommended dietary allowance of vitamin C for healthy young women. Medical Sciences. PNAS 2001; 98: 9842–9846

- Rosenberg IH. A history of the isolation and identification of folic acid (folate). Ann Nutr Metab. 2012; 61:231-5

- Iyer R & S K Tomar. Folate: a functional food constituent. J Food Sci. 2009; 74: R114-22

- McNulty H, & Pentieva K. Folate bioavailability. Proc Nutr Soc. 2004; 63:529-36

- Allen L & Casterline-Sabel J. Prevalence and causes of nutritional anemias. In: Ramakrishnan U, ed. Nutritional Anemias. Boca Raton, FL: CRC Press, 2001; 7-21

- Bailey LB & Gregory JF III. Folate metabolism and requirements. J Nutr. 1999; 129:779-82

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