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1.
Benef Microbes ; 11(8): 767-778, 2020 Dec 02.
Article in English | MEDLINE | ID: mdl-33267751

ABSTRACT

This study is based on our previous research showing that commercial probiotic fermented milk (PFM) intake mitigates respiratory allergy development to ovalbumin (OVA) in adult mice (6-weeks old) increasing specific immunoglobulin (Ig)G2a and interferon (IFN)-γ rather than IgE. The aim was to determine if PFM exerts a protective effect when an allergy model is induced 5 days after weaning and whether the mechanisms involved are similar to those previously reported. Before inducing allergy, a group of 21-day old BALB/c mice received PFM for 10 days to analyse the impact on intestinal epithelial cells (IECs) activation. Two more groups received PFM for 5 days and were sensitised with OVA; only one group continued taking PFM until the end of the experiment. Sensitisation scheme: 3 OVA injections 1% in phosphate buffered saline (PBS) plus 7 days OVA aerosol exposure and re-stimulus 15 days later. The contents of specific- IgE, IgG, total-secretory-IgA and Th1/Th2 balance in serum, bronchoalveolar lavage (BAL) and gut were measured at 7 and 15 days post-sensitisation (dPS) and 2 days post-re-stimulus (2dPR). Treg cells in lungs were also quantified. Results were compared with normal and sensitised controls. PFM induced mild activation of IECs increasing monocyte chemoattractant protein-1 (MCP-1 or CCL2) and interleukin (IL)-6 production. In sensitised mice, PFM controlled the response inducing IgG rather than IgE at 7 and 15-dPS and 2dPR (60 days old). Th1-balance (IFN-γ) was favoured by PFM in lungs at 7 dPS with low levels of IL-10 released to regulate the response. Total-S-IgA increased in lungs and gut; however, PFM intake did not affect Treg cells in lungs. PFM maintains controlled stimulation of the immune cells involved in Th1 response, favouring IgG at the respiratory mucosal site. Although the effect was not as strong as that reported previously, PFM promoted maturation and activation of gut immune cells preserving intestinal homeostasis and lung immune response.


Subject(s)
Fermented Foods , Immunoglobulin A/blood , Immunoglobulin G/blood , Intestinal Mucosa/physiology , Milk/microbiology , Probiotics/pharmacology , Animals , Cytokines/blood , Disease Models, Animal , Immunoglobulin E/blood , Mice , Mice, Inbred BALB C , Ovalbumin/immunology , Th1-Th2 Balance/drug effects
2.
Int J Immunopathol Pharmacol ; 23(4): 1235-44, 2010.
Article in English | MEDLINE | ID: mdl-21244773

ABSTRACT

Probiotics may offer protection against Salmonella enteritidis serovar Typhimurium infection via different mechanisms. The aim of this study is to investigate, using mouse models, the effect of the administration of fermented milk containing the probiotic bacteria L. casei DN-114 001 in the protection against Salmonella enteritidis serovar Typhimurium when this product is administered continuously before and after infection or only post-infection. The adjuvant effect of this probiotic fermented milk (PFM) against S. Typhimurium was also evaluated in newborn mice, whose mothers received the PFM during the suckling period or their offspring after weaning. The results obtained showed that PFM administration after salmonella infection was useful to decrease the severity of the infection. The best effect was obtained with continuous PFM administration. In the newborn mice model, PFM administration to the newborn mice after weaning showed the best effect against the pathogen. PFM administration to the mother during the suckling period was beneficial against this enterophatogen when their offspring did not receive probiotics after weaning. Continuous PFM administration to adult mice (before and after infection) was important to maintain the intestinal barrier and the immune surveillance in optimal conditions to diminish the pathway of entrance of salmonella and the spread of this pathogen to deeper tissues. In the newborn mice model, it was observed that PFM administration to the offspring after weaning or their mother during the suckling period had a protective effect against salmonella infection, however, in the mice from mothers that received PFM during nursing which were fed with PFM after weaning, we found a down regulated immune maturity that was not protective against this infection.


Subject(s)
Fermentation , Milk , Probiotics/pharmacology , Salmonella Infections/prevention & control , Salmonella typhimurium , Animals , Chemokine CCL3/analysis , Cytokines/biosynthesis , Immunoglobulin A/biosynthesis , Liver/microbiology , Macrophages/immunology , Mice , Mice, Inbred BALB C , Peyer's Patches/immunology , Spleen/microbiology , Toll-Like Receptor 4/analysis
3.
Biol Trace Elem Res ; 127(2): 143-7, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18802669

ABSTRACT

The purpose of the present work was to evaluate the iron bioavailability of a new ferric pyrophosphate salt stabilized and solubilized with glycine. The prophylactic-preventive test in rats, using ferrous sulfate as the reference standard, was applied as the evaluating methodology both using water and yogurt as vehicles. Fifty female Sprague-Dawley rats weaned were randomized into five different groups (group 1: FeSO(4); group 2: pyr; group 3: FeSO(4) + yogurt; group 4: pyr + yogurt and group 5: control). The iron bioavailability (BioFe) of each compound was calculated using the formula proposed by Dutra-de-Oliveira et al. where BioFe % = (HbFef - HbFei) x 100/ToFeIn. Finally, the iron bioavailability results of each iron source were also given as relative biological value (RBV) using ferrous sulfate as the reference standard. The results showed that both BioFe % and RBV % of the new iron source tested is similar to that of the reference standard independently of the vehicle employed for the fortification procedure (FeSO(4) 49.46 +/- 12.0% and 100%; Pyr 52.66 +/- 15.02% and 106%; FeSO(4) + yogurth 54.39 +/- 13.92% and 110%; Pyr + yogurt 61.97 +/- 13.54% and 125%; Control 25.30 +/- 6.60, p < 0.05). Therefore, the stabilized and soluble ferric pyrophosphate may be considered as an optimal iron source for food fortification.


Subject(s)
Diphosphates/chemistry , Food, Fortified , Iron, Dietary/pharmacokinetics , Iron/chemistry , Analysis of Variance , Animals , Biological Availability , Diet , Diphosphates/pharmacokinetics , Female , Ferrous Compounds/chemistry , Ferrous Compounds/pharmacokinetics , Iron/pharmacokinetics , Random Allocation , Rats , Rats, Sprague-Dawley , Reference Standards , Solubility , Water , Yogurt
4.
Immunobiology ; 213(2): 97-108, 2008.
Article in English | MEDLINE | ID: mdl-18241694

ABSTRACT

The effect of the long-term administration of commercial fermented milk containing probiotic bacteria in the mucosal immune response and peritoneal macrophages was analyzed. BALB/c mice were fed with fermented milk for 98 consecutive days. Small and large intestines were removed for histology; IgA, CD4, CD8 cells and cytokines-producing cells were counted. The influence on the immune cells associated with bronchus and mammary glands as well as on peritoneal macrophages was also analyzed. Continuous oral administration of fermented milk increased IgA+ cells in both parts of the intestine (small and large intestine). IL-10, a regulatory cytokine, increased in the intestinal cells in most samples. TNFalpha, IFNgamma and IL-2 producing cells were also enhanced. Values for CD4 and CD8(+) cell populations in lamina propria of the intestine were increased in relation to the control throughout the assay. No modifications in the histology of intestines were observed. Long-term consumption of fermented milk enhanced intestinal mucosa immunity, mediated by IgA+ cells and by cytokine production. This improvement of gut immunity was maintained and down-regulated by cytokines such as IL-10, preventing gut inflammatory immune response. The effect of this fermented milk on mucosal sites distant to the gut, such as bronchus and mammary glands, showed that in both tissues the increase in IgA+ cells was only observed at the beginning of the continuous consumption and no modifications in the number of cytokine positive cells were found. Similar observations were found when phagocytic activity of peritoneal macrophages was measured. It was demonstrated that the most evident effect of long-term consumption of fermented milk was observed in the intestine. Immunodulatory effects and the maintenance of intestinal homeostasis without secondary effects after long-term administration of fermented milk were also observed.


Subject(s)
Bacteria , Cultured Milk Products , Gastric Mucosa/immunology , Macrophages, Peritoneal/immunology , Probiotics , Administration, Oral , Animals , Bronchi/immunology , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Immunity, Mucosal/immunology , Immunoglobulin A/metabolism , Macrophages, Peritoneal/metabolism , Mammary Glands, Animal/immunology , Mice , Mice, Inbred BALB C , Models, Animal , Time
5.
Biol Trace Elem Res ; 110(1): 73-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16679549

ABSTRACT

The aim of the present study was to assess dietary zinc effects on femur weight and mineral content in growing rats. For this purpose, 70 weanling Sprague-Dawley rats were divided into four groups. Each group was subject to a diet containing 2 (BZ), 5 (DZ), 10 (MZ), and 30 (CZ) ppm zinc. The calcium and magnesium content in all diets was 5 g/kg and 507 mg/kg, respectively. The animals were kept on this regime for 28 d and then sacrificed and their femurs were removed for analysis using atomic absorption spectrophotometry. The weights of the BZ and DZ groups were significantly different from the MZ and CZ groups (38.5+/-10.5, 89.9+/-13.7, 118.6+/-13.6, and 134+/-19.9 g, p<0.01) respectively. There were no differences between the MZ and CZ groups. Femur weight also varied with dietary zinc, as it was significantly different among all groups (BZ, 265+/-49 mg; DZ, 380+/-40 mg; MZ, 452+/-54 mg; CZ, 735+/-66 mg; p<0.01). The femur zinc content varied with diets, following a different pattern than the above parameters. Femur zinc from the BZ group (51.5+/-5.4 ppm) was significantly different from the MZ and CZ groups (115.9+/-14.2 and 175.0+/-13.5 ppm, respectively), whereas the DZ group (62.5+/-11.3 ppm) did not differ from the other three groups. The femur content of calcium (BZ, 83.2+/-9.8 mg/g; DZ, 88.0+/-9.2 mg/g; MZ, 90.2+/-13.6 mg/g; CZ, 83.1+/-14.7 mg/g) and magnesium (BZ, 1.82+/-0.13 mg/g; DZ, 1.98+/-0.09 mg/g; MZ, 1.93+/-14 mg/g; CZ, 1.83+/-0.19 mg/g) were not significantly different among the groups, nor was the calcium-magnesium ratio. These results suggest that although dietary zinc deficiency retards growth and causes bone fragility, bone deposition of calcium and magnesium and its ratio are not affected.


Subject(s)
Bone Development/physiology , Bone and Bones/metabolism , Calcium/metabolism , Diet , Magnesium/metabolism , Zinc/physiology , Animals , Dose-Response Relationship, Drug , Femur/growth & development , Male , Organ Size/physiology , Rats , Weight Gain/physiology
6.
Biol Trace Elem Res ; 109(2): 195-200, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16444009

ABSTRACT

In this research, we measured the iron bioavailability of ferrous gluconate stabilized with glycine (SFG) when it is used to fortify petit suisse cheese using the prophylactic-preventive method in rats. Three groups of male, weaned rats received a basal diet (control diet; 5.2 ppm Fe), a reference standard diet (SO4Fe; 9.2 ppm Fe), and a basal diet using iron-fortified petit suisse cheese as the iron source (cheese diet; 8.8 ppm Fe) for 22 d. The iron bioavailability was calculated as the ratio between the mass of iron incorporated into hemoglobin and the total iron intake per animal during the treatment. These values (BioFe) were 68% and 72% for SFG and ferrous sulfate, respectively. The value of the Relative Biological Value (RBV) was 95% for SFG in petit suisse cheese. These results show that according to this method, the iron bioavailability from industrial fortified petit suisse cheese can be considered as a high bioavailability rate.


Subject(s)
Anemia, Iron-Deficiency/prevention & control , Cheese/analysis , Iron, Dietary/therapeutic use , Iron/pharmacokinetics , Analysis of Variance , Animals , Biological Availability , Body Weight , Ferrous Compounds/pharmacokinetics , Glycine/pharmacokinetics , Hemoglobins/chemistry , Iron/analysis , Iron/blood , Iron, Dietary/analysis , Iron, Dietary/blood , Male , Rats , Rats, Sprague-Dawley
7.
Biol Trace Elem Res ; 104(3): 261-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15930595

ABSTRACT

The aim of the study was to determine the relative bioavailability of zinc gluconate stabilized with glycine in a Petit Suisse cheese from an infant dessert. Weight gain and bone zinc content were the nutritional responses evaluated for the diets of different zinc content: 2 ppm (basal) and 5, 10, and 30 ppm from zinc gluconate stabilized with glycine and zinc sulfate. Nonlinear regression analysis of the fitted curves for weight gain determined a relative zinc bioavailability of 100% for the Ymax ratio and 96% for Ymax/t1/2 ratio for zinc gluconate stabilized with glycine (R2=0.7996 for zinc sulfate and 0.8665 for zinc gluconate stabilized with glycine). The slope ratio analysis from linear regression of femur zinc determined a relative zinc bioavailability of 93% for zinc gluconate stabilized with glycine (R2=0.8693 for zinc sulfate and 0.8307 for zinc gluconate stabilized with glycine). Zinc gluconate stabilized with glycine has similar bioavailability as zinc sulfate in a Petit Suisse cheese nutritional matrix, with the advantage that the stabilized compound does not modify the sensorial characteristics of the fortified cheese.


Subject(s)
Biomarkers , Cheese/analysis , Weight Gain/drug effects , Zinc/pharmacokinetics , Animals , Biological Availability , Femur/anatomy & histology , Femur/chemistry , Gluconates/administration & dosage , Glycine/administration & dosage , Male , Rats , Rats, Sprague-Dawley , Zinc/administration & dosage , Zinc Sulfate/administration & dosage
8.
Biol Trace Elem Res ; 104(3): 269-73, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15930596

ABSTRACT

Fortification of a Petit Suisse cheese with zinc sulfate and zinc gluconate stabilized with glycine was used as a tool to overcome zinc-deficiency effects on total-body growth and skeletal growth. Animals were divided in 4 groups of 10 rats: basal (B), control (C), depletion-repletion 1 (DR1), and depletion-repletion 2 (DR2). These four groups were fed with four diets: basal (2 ppm Zn), control (30 ppm Zn), DR1, and DR2; they received a basal diet for 14 d and a control diet for the other 14 d of the experiment, using zinc sulfate for DR1 and zinc gluconate stabilized with glycine for DR2. After 28 d of the experiment, total-body weight and weight gain of the control and DR1 and DR2 animals were not statistically different (p<0.05), Femur weight and femur zinc content of DR1 and DR2 did not achieve the values of control animals (p<0.05), but they were higher than that of basal animals. Our results show that restoration of dietary zinc levels by means of food fortification normalized weight gain, as an indicator of total-body growth, and presented a trend to normalize bone weight, as a marker of skeletal growth, in young rats and independently of the zinc source used.


Subject(s)
Cheese , Deficiency Diseases/diet therapy , Food, Fortified , Zinc Sulfate/therapeutic use , Zinc/deficiency , Animals , Femur/anatomy & histology , Femur/chemistry , Gluconates/therapeutic use , Glycine/therapeutic use , Hematocrit , Hemoglobins/analysis , Male , Rats , Rats, Sprague-Dawley , Weight Gain/drug effects , Zinc/therapeutic use
9.
Biol Trace Elem Res ; 99(1-3): 49-69, 2004.
Article in English | MEDLINE | ID: mdl-15235141

ABSTRACT

Zinc deficiency remains a serious health problem worldwide affecting developed as well as developing countries. Despite the evidence proving that zinc deprivation during the periods of rapid growth negatively affects the cognitive brain as well as sexual development, there are few complete studies carried out in children. The present article proposes a revision of the evidence gathered until now on the relationship existing between zinc deficiency and intellectual and sexual development during the stages of childhood, preadolescence, and adolescence.


Subject(s)
Human Development/physiology , Sexual Development/physiology , Zinc/deficiency , Animals , Central Nervous System/metabolism , Cognition/physiology , Humans , Malnutrition/physiopathology , Zinc/metabolism
10.
Arch. latinoam. nutr ; 53(2): 119-132, jun. 2003.
Article in Spanish | LILACS | ID: lil-356578

ABSTRACT

Iron is an essential micronutrient involved in multiple biochemical and physiological process. In this review we discuss the most relevant aspect of its metabolism in order to reach a better comprehension of the relevant roll that this micronutrient plays in human health.


Subject(s)
Humans , Iron/metabolism , Micronutrients/metabolism , Absorption , Iron/pharmacokinetics , Micronutrients/pharmacokinetics
11.
Biol Trace Elem Res ; 81(3): 215-28, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11575679

ABSTRACT

Diabetes mellitus is a group of metabolic disorders, the incidence of which varies widely throughout the world. The treatment of diabetes mellitus includes insulin, oral antidiabetic agents, and dietary regimens. Although the emphasis is on macronutrients intakes, there is strong evidence that there is an abnormal metabolism of several micronutrients in diabetic individuals. Zinc is one of the essential micronutrients of which status and metabolism is altered in this condition. This work is a short review about the close relation among zinc, glucose metabolism, and insulin physiology, as well as about the few experimental data about zinc absorption and zinc supplementation in diabetes mellitus patients.


Subject(s)
Diabetes Mellitus/blood , Diabetes Mellitus/drug therapy , Zinc/pharmacology , Diabetes Complications , Dietary Supplements , Free Radicals , Glucose/metabolism , Humans , Insulin/metabolism
12.
J Trace Elem Med Biol ; 15(4): 255-9, 2001.
Article in English | MEDLINE | ID: mdl-11846015

ABSTRACT

Microencapsulated ferrous sulfate with soy lecithin (SFE-171) has been used as an iron source for the fortification of milk and dairy products. With the purpose to extend the use of this agent to other kind of foods or even to pharmaceutical preparations for oral administration, the SFE-171 was turned into a fluid powder (SFE-171-P) by means of vacuum drying. The iron bioavailability (BioFe) of SFE-171-P was evaluated in this work by means of the prophylactic-preventive method in rats, using ferrous sulfate as reference standard. Both iron sources were separately added to a basal diet of low iron content in a concentration of 10 mg iron/kg diet. Two groups of 10 weaned rats 25 days old received the fortified diets during 28 days, while a third group of the same size received the basal diet without iron additions. The weights and haemoglobin concentrations (HbC) of every animal were determined before and after the treatment, thus allowing the calculation of the mass of iron incorporated into haemoglobin (HbFe) during this period. The BioFe of the iron sources were obtained as the percentage ratio between the HbFe and the mass of iron consumed by each animal. The results were also given as Relative Biological Value (RBV), which relates the BioFe of the studied source with that of the reference standard. The liver iron concentration (LIC) of each animal was determined at the end of the experiment in order to evaLuate the influence of the studied iron sources on the liver iron stores. SFE-171-P presented BioFe, RBV and LIC values of (47 +/- 7)%, 109% and (46.6 +/- 3.4) mg/kg respectively, while the corresponding values for the reference standard were of (43 +/- 7)%, 100% and (45.0 +/- 4.7) mg/kg. These results show that the drying process used to produce the SFE-171-P does not affect its bioavailability, which is also adequate for the potential use of this product in food fortification or with pharmaceutical purposes.


Subject(s)
Ferrous Compounds/pharmacokinetics , Iron/pharmacokinetics , Phosphatidylcholines/pharmacokinetics , Animals , Chemistry, Clinical/methods , Dietary Supplements , Dose-Response Relationship, Drug , Drug Compounding , Female , Hemoglobins/metabolism , Rats , Rats, Sprague-Dawley
13.
Biol Trace Elem Res ; 76(3): 193-205, 2000 Sep.
Article in English | MEDLINE | ID: mdl-11049218

ABSTRACT

The essentiality of zinc for humans was first documented by Prasad in the 1960s. The main clinical manifestations associated with zinc deficiency are growth retardation, hypogonadism, diarrhea, and increased susceptibility to infectious diseases. Thus, in the past 25 yr, there was an increased interest of researchers in studying the role of zinc in human immunity. Although mechanistic research has been carried out using animal models, there are several studies in humans with similar results. This work is an attempt to review the information available in this field to understand the important role that zinc plays in the normal development and function of the immune system.


Subject(s)
Immune System/physiology , Nutritional Status , Zinc/metabolism , Aged , Animals , Child , Humans , Thymus Gland/metabolism , Thymus Gland/physiology
14.
Nutrition ; 16(9): 762-6, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10978858

ABSTRACT

Food fortification with a proper zinc compound is an economic and effective strategy to prevent zinc deficiency. BioZn-AAS, a zinc gluconate stabilized with glycine, was compared with zinc sulfate (reference standard), zinc hydroxide, and zinc gluconate, all of them labeled with (65)Zn. This preclinical study was performed on Sprague-Dawley rats of both sexes, and the administered dose was 85 microg/kg of zinc. Bioavailability studies showed that absorption of BioZn-AAS was not statistically different than absorption from other sources in female rats (25.65% +/- 2.20% for BioZn-AAS, 28.24% +/- 4. 60% for ZnSO(4), 24.91% +/- 4.02% for Zn[OH](2), and 25.51% +/- 2. 70% for Zn-gluconate). In the case of the male rats, absorption of BioZn-AAS (27.97% +/- 4.20%) was higher (P<0.05) than that from the other compounds (23.15% +/- 2.90% for ZnSO(4), 22.62% +/- 3.90% for Zn[OH](2), and 22.30% +/- 3.90% for Zn-gluconate). Biodistribution studies demonstrated that the zinc from BioZn-AAS followed the same metabolic pathway as zinc from the other sources. Toxicity studies were performed with 50 female and 50 male rats. The value of oral lethal dose 50 (LD(50)) was 2000 mg/kg for female rats and 1900 mg/kg for male rats. Therefore, we conclude that BioZn-AAS has adequate properties to be considered a proper zinc compound for food fortification or dietary supplementation.


Subject(s)
Organ Specificity , Zinc Compounds/pharmacokinetics , Zinc Compounds/toxicity , Absorption , Animals , Biological Availability , Female , Gluconates/pharmacokinetics , Hydroxides/pharmacokinetics , Lethal Dose 50 , Male , Rats , Rats, Sprague-Dawley , Zinc Sulfate/pharmacokinetics
16.
J Nutr Sci Vitaminol (Tokyo) ; 46(3): 125-9, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10955278

ABSTRACT

Radio-iron tests are frequently used to measure the bioavailability of different iron sources for food fortification. As the labeling procedures must be done under laboratory conditions, complementary studies should be carried out to evaluate the bioavailability of iron sources produced on an industrial scale. The iron bioavailability of SFE-171 (ferrous sulfate microencapsulated with phospholipids) was studied in previous reports using the compounds labeled with 59Fe and 55Fe; the results showed an iron bioavailability similar to that of ferrous sulfate. In the present work, the iron bioavailability of industrial SFE-171 was studied by the prophylactic-preventive method in rats using ferrous sulfate as the reference standard. Elemental iron powder was also studied by the same method for comparative purposes. The liver iron concentration of each animal was determined at the end of the experiment in order to evaluate the influence of each iron source on the liver iron stores. Relative biological values of 98 and 34% were found for SFE-171 and elemental iron powder, respectively, while the corresponding relative liver iron concentrations were 104 and 45%. The results provided by the prophylactic-preventive method show that the iron bioavailability of industrial SFE-171 is similar to that of ferrous sulfate; these results are also in agreement to those obtained with the radioactive compounds. We can conclude that the SFE-171 obtained by industrial procedures for massive use in iron food fortification has the same bioavailability as that of the SFE-171 produced and labeled under laboratory conditions.


Subject(s)
Ferrous Compounds/pharmacokinetics , Intestinal Absorption , Iron/metabolism , Animals , Biological Availability , Drug Compounding , Ferrous Compounds/administration & dosage , Food, Fortified , Iron/administration & dosage , Liver/chemistry , Liver/metabolism , Male , Phospholipids , Rats , Rats, Sprague-Dawley , Reference Standards
17.
Article in Spanish | MEDLINE | ID: mdl-10797835

ABSTRACT

It is now well known that zinc is an essential micronutrient. Even though much information is available, there are many points that remain to be studied. zinc is absorbed by the intestine and transported in the plasma by albumin, forming a small exchangeable pool, which is rapidly exhausted even in cases of mild deficiency. zinc is essential for the activity of about 70 enzymes among other functions. Therefore, zinc deficiency produces a great number of clinical disorders, the symptoms of which may range between mild up to serious dysfunctions. These problems are corrected by a dietary supplementation with zinc. The lack of a reliable method to determine the zinc nutritional status reflects the problem to estimate the metal recommended dietary allowances, which are difficulty met specially by children, old persons and pregnant women which constitute the main risk groups. Although our knowledge concerning zinc toxicity is scarce, it is well known that the amounts of zinc that produces toxic effects are much higher than those that are contained in regular diets as well as in diets supplemented with this metal. Therefore, the need of the development of effective strategies, like food fortification with proper zinc compounds, appears as an attractive alternative in order to prevent and/or correct the deficiency of this vital element and to improve the health and the life quality of the whole population.


Subject(s)
Zinc/physiology , Age Factors , Animals , Female , Humans , Intestinal Absorption/physiology , Male , Mice , Nutritional Requirements , Nutritive Value , Pregnancy , Rats
18.
Article in Spanish | BINACIS | ID: bin-14769

ABSTRACT

Se ha postulado que el aporte de hierro a las células usuarias se halla bajo un control dependiente del tamaño de la fracción intracelular libre del metal, cuyos cambios se reflejarían en mensajes a la expresión de los receptores séricos o de membrana para ajustar la oferta a la demanda. La posibilidad de que los receptores de membrana pudieran estar afectados por la malnutrición calórico-proteica se exploró en estudios a través de los cambios de la capacidad de los reticulocitos circulantes de ratón normal para incorporar hierro in vitor, observando el diferente comportamiento ocasionado por la incubación de las células con suero humano de dadores normales y de pacientes de anemia nutricional. Los resultados muestran una significativa caída de dicha capacidad cuando se utilizó suero de pacientes afectados de anemia nutricional. Se discute el probable mecanismo responsable de dicha diferencia. (AU)


Subject(s)
Child , Animals , Humans , Rats , Mice , Adult , Zinc , Nutritional Requirements , Nutritive Value , Intestinal Absorption/physiology , Zinc/physiology , Zinc/deficiency , Zinc/metabolism , Zinc/pharmacokinetics
19.
Article in Spanish | BINACIS | ID: bin-40143

ABSTRACT

It is now well known that zinc is an essential micronutrient. Even though much information is available, there are many points that remain to be studied. zinc is absorbed by the intestine and transported in the plasma by albumin, forming a small exchangeable pool, which is rapidly exhausted even in cases of mild deficiency. zinc is essential for the activity of about 70 enzymes among other functions. Therefore, zinc deficiency produces a great number of clinical disorders, the symptoms of which may range between mild up to serious dysfunctions. These problems are corrected by a dietary supplementation with zinc. The lack of a reliable method to determine the zinc nutritional status reflects the problem to estimate the metal recommended dietary allowances, which are difficulty met specially by children, old persons and pregnant women which constitute the main risk groups. Although our knowledge concerning zinc toxicity is scarce, it is well known that the amounts of zinc that produces toxic effects are much higher than those that are contained in regular diets as well as in diets supplemented with this metal. Therefore, the need of the development of effective strategies, like food fortification with proper zinc compounds, appears as an attractive alternative in order to prevent and/or correct the deficiency of this vital element and to improve the health and the life quality of the whole population.

20.
Article in Spanish | LILACS | ID: lil-245927

ABSTRACT

Se ha postulado que el aporte de hierro a las células usuarias se halla bajo un control dependiente del tamaño de la fracción intracelular libre del metal, cuyos cambios se reflejarían en mensajes a la expresión de los receptores séricos o de membrana para ajustar la oferta a la demanda. La posibilidad de que los receptores de membrana pudieran estar afectados por la malnutrición calórico-proteica se exploró en estudios a través de los cambios de la capacidad de los reticulocitos circulantes de ratón normal para incorporar hierro in vitor, observando el diferente comportamiento ocasionado por la incubación de las células con suero humano de dadores normales y de pacientes de anemia nutricional. Los resultados muestran una significativa caída de dicha capacidad cuando se utilizó suero de pacientes afectados de anemia nutricional. Se discute el probable mecanismo responsable de dicha diferencia.


Subject(s)
Child , Animals , Humans , Rats , Mice , Adult , Zinc , Intestinal Absorption/physiology , Nutritional Requirements , Nutritive Value , Zinc/deficiency , Zinc/metabolism , Zinc/pharmacokinetics , Zinc/physiology
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