scholarly journals 109 Phytate supplementation has minimal impact on mineral digestibility in horses

2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 89-90
Author(s):  
Katy Brinkley-Bissinger ◽  
Laura M Cersosimo ◽  
Kathleen E Sullivan ◽  
Shannon E Livingston ◽  
Jill M Bobel ◽  
...  

Abstract Phosphorus in equine rations is supplied by inorganic mineral fortification or naturally-occurring P in forages and grains. Up to 70% of P in plant material is bound to phytate. In monogastrics like poultry and swine, phytate can reduce absorption of P and divalent cations, but the extent that this occurs in horses is unknown. This study tested the hypothesis that phytate decreases mineral digestibility in horses. Six mature Quarter Horse geldings (mean ± SE, 586 ± 19 kg, 10 ± 1.5 y) were randomly assigned to two treatments applied in a cross-over design: IP6 (Ca-Mg-phytate isolated from rice bran fed at 15 mg phytic acid/kg BW) or CON (equivalent Ca, Mg and P from inorganic minerals to match intake from IP6). The level of phytate added represented an amount present in grain-rich rations typically fed to broodmares, growing horses and performance athletes. Supplements were added to a basal diet (1.75% BW, DM basis) consisting of 75% timothy hay and 25% roughage-based concentrate. Each 14-d period had an 11-d treatment adaptation followed by a 3-d total fecal collection. After acid digestion, P was determined colorimetrically and other minerals were determined by inductively coupled plasma spectrometry. Data were analyzed using mixed model ANOVA. Intakes of Ca, P, Mg, Zn, Cu and Fe were similar between treatments (140, 72, 40, 1.05, 0.24, and 1.78 mg/kg BW respectively). Apparent P digestibility (18.8 and 17%, SEM 1.9; P = 0.41) and estimates of true P digestibility (32.8 and 30.8%, SEM 1.9; P = 0.39) were similar between CON and IP6. Apparent digestibilities of other minerals were also not affected by IP6 supplementation. Findings suggest horses have sufficient microbial phytase activity in the gastrointestinal tract to mitigate impacts of dietary phytate. Higher levels or different forms of phytate and marginal mineral intake may yield different results.

2010 ◽  
Vol 8 (2) ◽  
pp. 341-346 ◽  
Author(s):  
Joanna Kurczewska ◽  
Grzegorz Schroeder ◽  
Urszula Narkiewicz

AbstractThe synthesis of metal (Fe, Co, Ni)-encapsulated carbon nanomaterials coated with cyclam-bonded silica has been described. The organic layer was identified by Fourier transform infrared spectroscopy and elemental analysis. The functionalized magnetic nanomaterials were employed to extract the divalent cations: copper, calcium, cobalt, manganese and nickel from aqueous solutions. Their adsorption capacities were studied by the batch procedure. The concentration of cations extracted was determined by inductively coupled plasma mass spectrometry. Influence of different parameters viz. pH, amount of the compound studied, contact time, on the cation extraction was investigated. Under optimum conditions copper extraction was significantly more efficient when compared with other coexisting ions.


2021 ◽  
Vol 64 (2) ◽  
pp. 251-259
Author(s):  
Rajesh Rangasamy ◽  
Praveen Kumar Malekadi ◽  
D. Peer Mohamed ◽  
Dheeraj Kumar Tyagi ◽  
Rahul Raveendran ◽  
...  

The present study arose from the need of to determine inorganic arsenic (iAs) at low levels in rice. Ultra-high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry (UHPLC-ICPMS) using Kinetic Energy Discrimination (KED) mode to eliminate spectral interferences was used for analysis of iAs. Sample preparation involves extraction of inorganic arsenic (sum of As3+ and As5+) with water by heating at 90 °C for 5 min in water bath. Separation is accomplished with a reversed-phase ion pack column using a gradient chromatographic method followed by ICPMS analysis within 5 min. The method was validated in accordance with Commission Regulation (EU) No 836/2011 and performance characteristics were verified. Acceptable values were obtained for specificity, repeatability (HorRatr < 0.6), within-lab reproducibility (HorRatR < 0.3) with recovery 80-90%, limit of quantification (0.02 mg/kg), fitness-for-purpose and trueness (using CRM); thus, the method can be considered for official control purposes.


2020 ◽  
Vol 44 (5) ◽  
pp. 490-498
Author(s):  
Abdul Khader Karakka Kal ◽  
Zubair Perwad ◽  
Tajudheen K Karatt ◽  
Jahfar Nalakath ◽  
Michael Subhahar

Abstract Recently, an increased tendency to use various metals has been observed in the sports competition fields. Many of these metals and their organic complexes reportedly have good pharmacologic, therapeutic and performance-enhancement uses; they are banned or recommended as controlled medications in competitive sports. The objective of this research was to determine the concentration of pharmacologically relevant metals in urine samples collected from racehorses at various sport events, develop a method and assess the concentrations of above metals using inductively coupled plasma mass spectrometry (ICP-MS). Seven alkali–alkaline earth metals (lithium, sodium, potassium, magnesium, calcium, strontium and barium) and six heavy metals (chromium, cobalt, copper, zinc, arsenic and selenium) were studied in detail. To compare and confirm the concentrations of these metals, the screening was carried out on the basis of region and sex of the animal. ICP-MS provides extremely high sensitivity that enables the determination of the metals at very low concentration from complex biological matrices. From the research, it is clear that irrespective of sex and region the concentration of metal is very high in some samples, might be accidental or intentional doping to improve sporting performances. This research work is of significant importance in setting threshold values for screening metals in race day samples in order to avoid potential harmful effects on athletes and the depth of malpractices, it can bring to sports.


2016 ◽  
Vol 80 (6) ◽  
pp. 977-983 ◽  
Author(s):  
C. H. Yoder ◽  
N. T. Landes ◽  
L. K. Tran ◽  
A. K. Smith ◽  
J. D. Pasteris

AbstractCarbonated calcium apatites doped with a monovalent cation (Li+, Na+, or K+) or a divalent cation (Mg2+ or Zn2+) were prepared in aqueous solution and analysed by powder X-ray diffraction, inductively coupled plasma atomic emission spectroscopy and infrared spectroscopy. The hypothesis that the location of carbonate in the apatite structure, either in place of hydroxide ions in the c-axis channels (A-type substitution) or in place of phosphate (B-type substitution), is affected by the solution energetics of the cation (specifically its enthalpy of hydration) was strengthened by the observation of larger amounts of Atype carbonate in apatites containing the monovalent cations in aqueous solution. It is shown that cations with low negative enthalpies of hydration favour A-type substitution, whereas cations with higher negative hydration enthalpies, such as divalent cations (Mg2+, Zn2+), favour B-type substitution.


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