Tissue iron distribution and adaptation of iron absorption in rats exposed to a high dietary level of NaFeEDTA

Although it has been shown that iron absorption from NaFeEDTA, a promising iron fortificant, is effectively down-regulated in iron-loaded rats, effects of prolonged exposure to high dietary levels of NaFeEDTA are not well understood. The objectives of this study were to determine whether rats can adapt to a high dietary level of NaFeEDTA by down-regulating iron absorption, and to determine effects on tissue iron distribution, with or without an iron absorption inhibitor. Male Sprague-Dawley rats were exposed to diets supplemented with FeSO4 or NaFeEDTA at 1200 mg of Fe/kg of diet, with or without tea, for 27 days. Iron absorption measured by whole-body counting before and after exposure showed that rats adapted to the high dietary level of FeSO4 or NaFeEDTA by down-regulating iron absorption to a similar extent. However, nonheme iron concentrations in liver and spleen were about 35-50% lower, whereas the concentration in kidney was about 300% higher in rats fed NaFeEDTA, compared to rats fed FeSO4. Tea had no major impact on iron absorption or iron status, regardless of iron source. Our results showed that although iron absorption was down-regulated similarly, body iron distribution was markedly different between rats exposed to FeSO4 and those exposed to NaFeEDTA. Further studies are warranted to determine the effects of prolonged exposure to dietary NaFeEDTA on kidney iron accumulation and kidney function.     

Tissue iron distribution and urinary mineral excretion vary depending on the form of iron (FeSO4 or NaFeEDTA) and the route of administration (oral or subcutaneous) in rats given high doses of iron

Sodium iron ethylenediaminetetraacetate (NaFeEDTA) has considerable promise as an iron fortificant in food. However, effects of administering high levels of NaFeEDTA on tissue iron distribution and mineral excretion are not well understood. The objectives of this study were to assess nonheme iron distribution in the body and urinary excretion of Ca, Mg, Cu, Fe, and Zn after daily administration of high levels of iron to rats over 21 days. Iron was either given orally with food or injected subcutaneously, as either FeSO 4 or NaFeEDTA. Selected tissues were collected for nonheme iron analysis. Estimated total body nonheme iron levels were similar in rats fed NaFeEDTA or FeSO 4, but the tissue distribution was different: it was 53% lower in the liver and 86% higher in the kidneys among rats fed NaFeEDTA than among those fed FeSO 4. In contrast, body nonheme iron was 3.2-fold higher in rats injected with FeSO 4 than in rats injected with NaFeEDTA. Administering NaFeEDTA orally elevated urinary Cu, Fe, and Zn excretion compared with FeSO 4 (1.41-, 11.9-, and 13.9-fold higher, respectively). We conclude that iron is dissociated from the EDTA complex prior to or during intestinal absorption. A portion of intact FeEDTA may be absorbed via a paracellular route at high levels of intake but is mostly excreted in the urine. Metal-free EDTA may be absorbed and cause elevated urinary excretion of Fe, Cu, and Zn.     

Iron and zinc absorption from two bean (Phaseolus vulgaris L.) genotypes in young women

Extrinsic and intrinsic iron and zinc labels were used to test iron and zinc absorption from two bean (Phaseolus vulgaris) genotypes, containing normal (common beans, CB) or higher (HFeZnB) iron and zinc concentrations, fed in single meals to young women with low iron reserves. The women were divided into two groups, with one receiving a CB test meal (n = 12) and the other, an HFeZnB test meal (n = 11). The beans were intrinsically labeled hydroponically with (55)Fe (CB and HFeZnB) and with (70)Zn (HFeZnB). Concentrations of zinc and iron were 98 and 65% higher, respectively, in HFeZnB as compared to CB, but phytic acid contents were similar. Extrinsic labels were (59)Fe (CB and HFeZnB), (67)Zn (CB), and (68)Zn (HFeZnB). Iron and zinc percent absorption levels were calculated from radio-iron activity in red blood cells and from urinary excretion of zinc isotopes. Intrinsic and extrinsic iron absorption measures were highly correlated (R (2) = 0.986) (average extrinsic/intrinsic ratio was 1.00). Iron absorption was low (geometric mean < 2%) in both bean types, and total iron absorbed was not different between types. Intrinsic zinc absorption from the HFeZn beans was higher than extrinsic absorption (15.2% vs 13.4%, p < 0.05) (average extrinsic/intrinsic was 0.90). The correlation between intrinsic and extrinsic zinc measures was not as high as that for iron (R (2) = 0.719). Percent zinc absorption levels were similar in both bean types, but total extrinsic zinc absorbed was 90% higher (p < 0.05) from the HFeZnB meal. Thus, the less expensive and time-consuming extrinsic labeling may be used to screen various varieties of beans for iron bioavailability in humans, but it underestimates zinc absorption by approximately 10%. Selective breeding for high-zinc bean genotypes may improve zinc status. However, high-iron genotypes appear to have little effect on iron status when fed alone in single meals to women with low iron reserves.     

Carotenoid absorption in humans consuming tomato sauces obtained from tangerine or high-beta-carotene varieties of tomatoes

Tomato sauces were produced from unique tomato varieties to study carotenoid absorption in humans. Tangerine tomatoes, high in cis-lycopene, especially prolycopene (7Z,9Z,7'Z,9'Z), and high-beta-carotene tomatoes as an alternative dietary source of beta-carotene were grown and processed. Sauces were served after 2 week washout periods and overnight fasting for breakfast to healthy subjects (n = 12, 6M/6F) in a randomized crossover design. The serving size was 150 g (containing 15 g of corn oil), tangerine sauce containing 13 mg of lycopene (97.0% as cis-isomers) and high-beta-carotene sauce containing 17 mg of total beta-carotene (1.6% as the 9-cis-isomer) and 4 mg of lycopene. Blood samples were collected 0, 2, 3, 4, 5, 6, 8, and 9.5 h following test meal consumption and carotenoids determined in the plasma triacylglycerol-rich lipoprotein fraction by HPLC-electrochemical detection. Baseline-corrected areas under the concentration vs time curves (AUC) were used as a measure of absorption. AUC0-9.5h values for total lycopene in the tangerine sauce group were 870 +/- 187 (nmol.h)/L (mean +/- SEM) with >99% as cis-isomers (59% as the tetra-cis-isomer). The AUC0-9.5h values for total beta-carotene and lycopene after consumption of the high-beta-carotene sauce were 304 +/- 54 (4% as 9-cis-carotene) and 118 +/- 24 (nmol.h)/L, respectively. Lycopene dose-adjusted triacylglycerol-rich lipoprotein AUC responses in the tangerine sauce group were relatively high when compared to those in the literature and the high-beta-carotene group. The results support the hypothesis that lycopene cis-isomers are highly bioavailable and suggest that special tomato varieties can be utilized to increase both the intake and bioavailability of health-beneficial carotenoids.     

Moisture stress and calcium absorption from immersions during the seed‐filling stage of soybean

Abstract

Calcium (Ca) uptake was studied by immersing the central tip of a trifoliate leaf in various concentrations of ⁴⁵CaCl₂ solutions and under moisture stress conditions during the seed‐filling period of soybean. Beta‐ray gauging and the diurnal leaf temperature variation showed similar characteristics for leaf water status. The activities of ⁴⁵Ca were significantly higher (p < 0.0001) at 5, 10, 20, and 30 mM concentrations for water stressed and non‐stressed leaves compared with the control. Calcium (⁴⁵Ca) activities at 5, 10, and 20 mM Ca concentrations between stressed and non‐stressed leaves were not significant, but the difference in their mean values at 30 mM Ca concentration was significant (p = 0.0159). The relationship between ⁴⁵Ca uptake and Ca concentration was parabolic for both stressed (R² = 0.77) and non‐stressed (R² = 0.81) leaves. Autoradiographs indicated Ca movement through the mid‐rib and veins of the tip‐immersed trifoliate leaf but showed no activity in other plant parts. An activity gradient developed between seeds when a pod‐tip was immersed in the radioactive solution.     

Enzymatic digestion-high-pressure homogenization prior to slurry introduction graphite furnace atomic absorption spectrometry for selenium determination in plant and animal tissues.

Homogenization using a new flat valve homogenizer in combination with enzymatic digestion with a crude protease was investigated as a means of releasing Se compounds from zoological and botanical matrixes prior to slurry introduction GFAAS. Timed trials with four zoological certified reference materials (CRMs), three botanical reference materials (RMs), and a food crop indicated that Se release into 5% (v/v) ethanol-0.03 M TRIS containing 20 mg of protease was quantitative after homogenization or became quantitative within 1 h of digestion at 60 degrees C. For each of the zoological RMs (whole egg powder, dogfish muscle, and dogfish liver), three passes through the homogenizer in the presence of protease provided a quantitative release of selenium, and incubation with the enzyme was not necessary. No separation of the Se between the liquid phase and the particulate phase was evident even after several days of subsequent storage at 4 degrees C. The botanical matrixes (three milled wheat RMs and a rapeseed sample) were more resistant to selenium release and required up to 1 h of digestion with protease at 60 degrees C. Alternatively, 10 passes through the homogenizing valve (in the presence of the enzyme) resulted in the quantitative release of analyte.     

Difructose anhydride III promotes absorption of the soluble flavonoid alphaG-rutin in rats

A highly soluble quercetin glycoside, alphaG-rutin, is a glucose adduct of insoluble rutin. We examined the effects of difructose anhydride III (DFAIII; di-D-fructofuranosyl 1,2':2,3'-dianhydride) on intestinal absorption of alphaG-rutin by rat experiments. alphaG-rutin, rutin, quercetin, and the quercetin conjugate appeared in the portal blood after an intubation of alphaG-rutin (100 micromol), DFAIII effected higher portal concentrations of alphaG-rutin in portal cannulated rats. In ligated jejunal and ileal loops of rats, alphaG-rutin, rutin, quercetin, and the quercetin conjugate appeared in the intestinal mesenteric blood at both 30 and 60 min in both loops; the concentration of alphaG-rutin was 1.5-3 times higher when absorbed in the presence DFAIII. In the isolated mucosae of the jejunum and ileum, mucosal-to-serosal passage of alphaG-rutin increased with the addition of 100 micromol of DFAIII. These results indicate that alphaG-rutin is absorbed as the intact form and that DFAIII stimulates its absorption in the small intestine.     

Influence of foam structure on the release kinetics of volatiles from espresso coffee prior to consumption

The relationship between the physical structure of espresso coffee foam, called crema, and the above-the-cup aroma release was studied. Espresso coffee samples were produced using the Nespresso extraction system. The samples were extracted with water with different levels of mineral content, which resulted in liquid phases with similar volatile profiles but foams with different structure properties. The structure parameters foam volume, foam drainage, and lamella film thickness at the foam surface were quantified using computer-assisted microscopic image analysis and a digital caliper. The above-the-cup volatile concentration was measured online by using PTR-MS and headspace sampling. A correlation study was done between crema structure parameters and above-the-cup volatile concentration. In the first 2.5 min after the start of the coffee extraction, the presence of foam induced an increase of concentration of selected volatile markers, independently if the crema was of high or low stability. At times longer than 2.5 min, the aroma marker concentration depends on both the stability of the crema and the volatility of the specific aroma compounds. Mechanisms of above-the-cup volatile release involved gas bubble stability, evaporation, and diffusion. It was concluded that after the initial aroma burst (during the first 2-3 min after the beginning of extraction), for the present sample space a crema of high stability provides a stronger aroma barrier over several minutes.     

Iron oxides in two Oxisols from the Brazilian coastal plain

Two Oxisols from the B2 horizon at similar locations 2 km apart on the Brazilian coastal plain with a udic, isohyperthermic regime were practically identical in chemical composition but differed markedly in colour; one was a dark reddish brown, the other a pale ochre. Mossbauer spectra at 295 K, 80 K and 4.2 K indicated a clear difference in iron oxide mineralogy. Iron was present as aluminous hematite and goethite, with Al substitutions of approximately 20% in the two phases. However, the relative proportion of iron present in hematite and goethite was 45:55 in the first sample and 12:88 in the second. Possible reasons for these differences are discussed.     

Combination of lipids and emulsifiers enhances the absorption of orally administered quercetin in rats

The effects of lipids, emulsifiers, and ethanol on the absorption of orally administered quercetin in rats were investigated for its efficient intestinal absorption. Rats were administered 150 micromol/kg quercetin in water supplemented with lipids and/or emulsifiers, or ethanol, and blood was collected from the tail for 6 h after administration. Co-administration of lipids such as lecithin and soybean oil or emulsifiers including sucrose fatty acid ester, polyglycerol fatty acid ester, and sodium taurocholate had no statistically significant effects on quercetin absorption, although these constituents rather increased the accumulation of conjugated forms of quercetin and those of isorhamnetin in rat plasma. However, the combination of lipids and emulsifiers enhanced the absorption of quercetin significantly. Thirty and fifty percent (v/v) of the ethanol in the vehicle raised the efficiency of quercetin absorption in a concentration-dependent manner. Quercetin absorption-enhancing effects of these constituents seemed to be affected by quercetin's solubility in respective vehicles used for the administration. Ethanol is not helpful for the effective absorption of quercetin, as a high concentration is required. In conclusion, a combination of lipids and emulsifiers is necessary for enhancing quercetin absorption.     

Effect of the carbamate pesticide Sevin on the intestinal absorption of some nutrients in the teleost fish,Channa Punctatus

The effect of four concentrations (0.1, 1, 10, and 100 ppm) of Sevin on the rate of uptake of two sugars (glucose and fructose) and an aminoacid (tryptophan) by the intestine of the fresh water snake-head fish,Channa punctatus has been investigated. All four concentrations of the pesticide decreased the rate of transport of the three nutrients. No direct relationship could be established between the concentration of Sevin in the medium and decrease in the rate of transport of nutrients, although, increase in the concentration of Sevin reduced the absorption of nutrients by the intestine to a greater extent. Experiments conductedin vivo andin vitro showed that in both cases the pesticide decreased the brush border enzyme activity.     

Cadmium induced alterations in the intestinal absorption of glucose and fructose in a freshwater cat fish,Heteropneustes fossilis

The effect of four concentrations (1.0, 0.1, 0.01, and 0.001 mM) of Cd on the rate of absorption of two sugars, glucose and fructose by the intestine of the fresh water cat fish, Heteropneustes fossilis has been studied after 1 h at 23 °C. Intestinal glucose and fructose transport was also assessed in fish exposed to a sublettral concentration (0.0023 mM) of Cd in the ambient water for 15 and 30 days. Control fish showed no marked difference in the rates of absorption of glucose and fructose. All four concentrations of Cd decreased the rate of transport of glucose and fructose significantly. Among the two sugars, decrease in the rate of transport of fructose was more marked than glucose. In fish exposed to Cd in the ambient water, reduction of glucose and fructose absorption was greater after 30 days of exposure than after 15 days.     

Interactions of lipid metabolism and intestinal physiology with Tremella fuciformis Berk edible mushroom in rats fed a high-cholesterol diet with or without Nebacitin

Male adult Wistar rats were randomly divided into six groups in a 2 x 3 factorial design and fed diets containing different levels of Tremella fuciformis Berk (TFB) dietary fiber (0, 5, or 10%) and 1 g of cholesterol/100 g of diet with or without 0.7% Nebacitin for 4 weeks. TFB contained 6.2% soluble dietary fiber and 57.3% insoluble dietary fiber. The results showed that the serum LDL-cholesterol, hepatic total cholesterol, and triglyceride levels were significantly decreased (P < 0.05) in the rats fed diets with TFB content with or without Nebacitin. However, the serum total cholesterol, VLDL-cholesterol, and triglyceride levels were significantly decreased (P < 0.05) by Nebacitin. In feces, the presence of TFB (T5, T10, AT5, and AT10) in the diet significantly increased the total neutral steroids and bile acid excretions and undigested fiber concentrations as compared to T0 or AT0. In the small intestine, the Nebacitin diets increased the weights of both cecum and colon-rectum contents and lowered short-chain fatty acid (SCFA) concentrations of serum and cecal contents more than no Nebacitin diets did. It was suggested that the hypocholesterolemic effect of TFB dietary fiber may be mediated by the increase in fecal neutral steroids and total bile acids excretion and the increase in SCFA productions. The TFB edible mushroom dietary supplement altered the intestinal physiology of the rats.     

Acid-induced phase separation of anionic surfactants for the extraction of 1,4-dichlorobenzene from honey prior to liquid chromatography

The acid-induced liquid-liquid phase separation of anionic surfactants in aqueous solutions and its applicability to cloud point extraction methodology were applied as a tool for the extraction of 1,4-dichlorobenzene (p-DCB) from aqueous samples. p-DCB is extracted into the micelles of sodium dodecane sulfonate (SDSA) in a 4.2 M HCl solution. The micellar phase is separated from the bulk aqueous solution after centrifugation and collected from the surface of the suspension. The micellar extracts are injected into a high-performance liquid chromatographic apparatus and quantified at 225 nm with a reference wavelength of 280 nm. Following the proposed methodology, a preconcentration factor of ca. 160 is achieved (starting from 50 mL solutions) allowing for detection limits at the low microg/L level. Application to honey samples produced detection limits of 2.5 microg/kg with quantification limits of 7.5 microg/kg, while the recoveries of the method ranged from 85% at high concentrations to 95% at lower concentrations of p-DCB. The combined uncertainty of the entire analytical procedure was 4.5% at the concentration level of 30 microg/kg allowing for reliable and reproducible results for the determination of p-DCB at the concentration levels considered as thresholds for EU and U.S. legislation (10 microg/kg).     

稻田改为茶园后土壤铁形态与磁学性质演变特征

以四川省雅安市名山区稻田及由稻田改造的茶园土壤为研究对象,采用铁形态连续分级提取与环境磁学技术相结合的方法,分析铁氧化物与磁学特征随土壤利用方式及植茶时间变化而变化的特征。结果表明:稻田及不同植茶年限(3、6、10 a)茶园土壤110 cm土体各形态铁含量均表现为可还原铁(Red-Fe)>可氧化态铁(Oxi-Fe)>酸溶态铁(Acid-Fe);稻田改为茶园以及随着植茶年限延长,表层(0～10 cm)及亚表层(10～20 cm)土壤Acid-Fe、Oxi-Fe含量明显增加,而整个土体Red-Fe含量降低。稻田改为茶园3 a后,0～30 cm土壤表现出质量磁化率(MS)、饱和等温剩磁(SIRM)、软剩磁(IRMs)升高,而硬剩磁(IRMh)降低;随着植茶年限的延长,土体总体表现出各磁性参数均降低的趋势,亚铁磁性矿物主导土壤磁性特征变化。稻田改为茶园后土壤逐渐酸化且有机质积累,使亚铁磁性矿物不稳定,进一步导致Red-Fe溶解并向Acid-Fe、Oxi-Fe转化,且随植茶年限的延长,部分铁氧化物结晶度会增加。     

Iron absorption,localization, and biomineralization of Cynodon dactylon,a perennial grass from the Río Tinto basin (SW Iberian Peninsula)

Cynodon dactylon (L.) Pers. is a perennial rhizomatous grass (Poaceae), grown for cattle nutrition on the riverbanks of Río Tinto (Southwest Iberian Peninsula, Spain), a highly acidic area with high concentrations of iron (Fe) and other metals. This study focuses on the absorption, distribution, and accumulation of Fe in the root, rhizome, and leaves of C. dactylon under controlled conditions. Plants collected from Río Tinto were grown in a Hoagland solution containing 500 mg kg^–1 of ferrous Fe. Samples were collected up to 2 months after exposure and analyzed for total Fe concentration using inductively coupled plasma–mass spectrometry (ICP‐MS) and for Fe distribution and bioformations by scanning electron microscopy (SEM) with an energy‐dispersive x‐ray analyzer (EDX). The results show high concentrations of Fe in all plant organs, with fast Fe translocation from roots to leaves. Iron bioformations composed mainly of Fe, S, and K were detected in all plant organs and were especially apparent in roots and leaves. These results differ from those reported for another species of Poaceae, Imperata cylindrica, which grows under the same environmental conditions, suggesting the existence of different resistance strategies between species of the same family.     

Interaction of Different Iron Chelates with an Alkaline and Calcareous Soil: A Complementary Methodology to Evaluate the Performance of Iron Compounds in the Correction of Iron Chlorosis

Abstract

A great number of studies have shown that the stability of iron chelates as a function of pH is not the unique parameter that must be considered in order to evaluate the potential effectiveness of Fe‐chelates to correct iron chlorosis in plants cultivated in alkaline and calcareous soils. In fact, other factors, such as soil sorption on soil components or the competition among Fe and other metallic cations for the chelating agent in soil solution, have a considerable influence on the capacity of iron chelates to maintain iron in soil solution available to plants. In this context, the aim of this work is to study the variation in concentration of the main iron chelates employed by farmers under field conditions—Fe‐EDDHA (HA), Fe‐EDDHMA (MA), Fe‐EDDHSA (SA), Fe‐EDDCHA (CA), Fe‐EDTA (EDTA), and Fe‐DTPA (DTPA)—in the soil solution of a calcareous soil over time. To this end, soil incubations were carried out using a soil:Fe solution ratio corresponding to soil field capacity, at a temperature of 23°C. The soil used in the experiments was a calcareous soil with a very low organic matter content. The variation in concentration of Fe and Fe‐chelates in soil solution over time were obtained by measuring the evolution in soil solution of both the concentration of total Fe (measured by AAS), and the concentration of the ortho‐ortho isomers for Fe‐EDDHA and analogs or chelated Fe for Fe‐EDTA and Fe‐DTPA (measured by HPLC). The following chelate samples were used: a HA standard prepared in the laboratory and samples of HA, MA, SA, CA, Fe‐EDTA, and Fe‐DTPA obtained from commercial formulations present in the market. The percentage of iron chelated as ortho‐ortho isomers for HAs was: HA standard (100%); HA (51.78%); MA (60.06%); SA (22.50%); and CA (27.28%). In the case of Fe‐EDTA and Fe‐DTPA the percentages of chelated iron were 96.09 and 99.12, respectively. Results show that it is possible to classify the potential effectiveness of the different types of iron chelates used in our experiments as a function of two practical approaches: (i) considering the variation of total iron in soil solution over time, MA is the best performing product, followed by HA, CA, SA, DTPA, EDTA, and ferrous sulfate in the order listed and (ii) considering the capacity of the different iron chelates to maintain the fraction of chelated iron (ortho‐ortho isomers for HA, MA, SA, and CA and total chelated iron for EDTA and DTPA) in soil solution, the order is: SA > CA > HA > MA > EDTA ≈ DTPA. This result, that is related to the nature of the chelate and does not depend on the degree of chelated Fe in the products, indicates that SA and CA might be very efficient products to correct iron chlorosis. Finally, our results also indicate the suitability of this soil incubation methodology to evaluate the potential efficiency of iron compounds to correct iron chlorosis.     

The response of pearl millet to changes in nitrogen concentration or form during grain fill

Pearl millet [Pennisetum glaucum (L.) R. Br.] is a potentially productive, high‐yielding grain crop in the southeastern USA. A lack of response in pearl millet grain yield to fertilizer N in field studies indicates pearl millet may be able to remobilize N from vegetative to reproductive tissue. The N remobilization capabilities of a plant can be affected by the form of N supplemented. The objectives of this study were to evaluate the effects of N‐form ratio (NH₄ ⁺ : NO₃ ^‐) on the N remobilization capabilities of pearl millet when N is removed from the nutrient solution at the boot stage and to evaluate the effects of changing N‐form ratios at the boot stage on the seed yield and N content of pearl millet. Pearl millet was grown in solution culture under greenhouse conditions. There were 10 treatments: an initial NH₄ ⁺ : NO₃ ^‐ ratio of 3:1 followed by a change at the boot stage to either all NO₃ ^‐, no N, or a continuation of the initial ratio; an initial NH₄ ⁺ : NO₃ ^‐ ratio of 1:1 followed by a change at the boot stage to either all NO₃ ^‐, all NH₄ ⁺ no N, or a continuation of the initial ratio; and an initial NH₄ ⁺ : NO₃ ^‐ ratio of 1:3 followed by a change at the boot stage to either all NH₄ ⁺ no N, or a continuation of the initial ratio. Pearl millet dry matter accumulation was insensitive to changes in N‐form ratio or N removal at the boot stage. The lack of seed yield response to removal of N was a result of pearl millet utilizing N present in culms and leaves for seed production. Applications of N after the boot stage did not increase seed yield, but led to luxury consumption of N.