Analyze Diet

Topic:Metabolomics

Metabolomics in horses involves the comprehensive study and analysis of metabolites within the equine biological systems. This field focuses on identifying and quantifying small molecules, known as metabolites, which are the end products of cellular processes. Metabolomics provides insights into the metabolic pathways and physiological states of horses, contributing to a better understanding of their health, nutrition, and disease conditions. By analyzing biofluids such as blood, urine, or tissue samples, researchers can detect changes in metabolic profiles that may indicate disease or responses to environmental factors. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and implications of metabolomics in equine research.
Beyond blood sugar: the potential of NMR-based metabonomics for type 2 human diabetes, and the horse as a possible model.
Analytical and bioanalytical chemistry    November 28, 2006   Volume 387, Issue 2 533-537 doi: 10.1007/s00216-006-0979-z
Hodavance MS, Ralston SL, Pelczer I.Metabonomic analysis is a powerful tool for identifying and characterizing metabolic disorders, for example type 2 diabetes and the metabolic syndrome. Nuclear magnetic resonance (NMR) spectroscopy is an essential tool for such analysis, with special benefits. The review assesses the current status and potential of NMR-based metabonomics of type 2 diabetes. The horse is proposed as a possible model for studying this condition and disease. Some examples are shown of horse blood analyses by NMR.
Resolution, quantification and confirmation of betamethasone and dexamethasone in equine plasma by liquid chromatography/tandem mass spectrometry.
Rapid communications in mass spectrometry : RCM    February 17, 2005   Volume 19, Issue 6 825-832 doi: 10.1002/rcm.1851
Luo Y, Uboh CE, Soma LR, Guan F, Rudy JA, Tsang DS.This method describes the simultaneous separation, identification, quantification and confirmation of betamethasone (BTM) and dexamethasone (DXM) in equine plasma by liquid chromatography (LC) integrated with multidimensional tandem mass spectrometry. Analytes were directly extracted from equine plasma by methyl tert-butyl ether (MTBE). The residues were reconstituted with sample solvent. LC separation of the analytes was performed on a Hypercarb column using acetonitrile/water/formic acid (95:5:0.5, v/v/v) as the mobile phase. Sample screening, quantification and confirmation were performed i...
Analysis of the variations of follicular fluid composition during follicular growth and maturation in the mare using proton nuclear magnetic resonance (1H NMR).
Reproduction (Cambridge, England)    July 27, 2002   Volume 124, Issue 2 241-248 doi: 10.1530/rep.0.1240241
Gérard N, Loiseau S, Duchamp G, Seguin F.Follicular development and ovulatory processes in mammals involve local biochemical changes as a result of substantial modifications in cellular metabolism, the most well known of which is steroid variation. In the present study, the intrafollicular variation of several other components was studied using proton nuclear magnetic resonance ((1)H NMR). This approach made it possible to demonstrate that the intrafollicular biochemical content changes during follicular growth and maturation. Follicular fluid was aspirated by ovarian puncture of the dominant follicle at various physiological stages ...
Analysis of protein ions in the range 3000-12000 Th under partial (no discharge) atmospheric pressure chemical ionization conditions using ion trap mass spectrometry.
Rapid communications in mass spectrometry : RCM    July 12, 2002   Volume 16, Issue 12 1153-1159 doi: 10.1002/rcm.693
Cristoni S, Bernardi LR, Biunno I, Guidugli F.A new approach, based on the use of atmospheric pressure chemical ionization ion trap mass spectrometry (APCI-ITMS), but without a corona discharge, was investigated for application to creating and monitoring protein ions. It must be emphasized that APCI is not usually used in protein analysis. In order to verify the applicability of the proposed method to the analysis of proteins, two standard proteins (horse cytochrome c and horse myoglobin) were analyzed. A mixture of the two proteins was also analyzed showing that this novel approach, based on the use of APCI, can be used in the analysis o...
Metabolism of methandrostenolone in the horse: a gas chromatographic-mass spectrometric investigation of phase I and phase II metabolism.
Journal of chromatography. B, Biomedical sciences and applications    January 31, 2002   Volume 765, Issue 1 71-79 doi: 10.1016/s0378-4347(01)00409-1
McKinney AR, Ridley DD, Suann CJ.The phase I and phase II metabolism of the anabolic steroid methandrostenolone was investigated following oral administration to a standardbred gelding. In the phase I study, metabolites were isolated from the urine by solid-phase extraction, deconjugated by acid catalysed methanolysis and converted to their O-methyloxime trimethylsilyl derivatives. GC-MS analysis indicated the major metabolic processes to be sequential reduction of the A-ring and hydroxylation at C6 and C16. In the phase II study, unconjugated, beta-glucuronidated and sulfated metabolites were fractionated and deconjugated us...
GC-MS characterization of urinary metabolites and changes of ethisterone and testosterone profile after oral administration of danazol in equine.
Journal of veterinary pharmacology and therapeutics    July 10, 2001   Volume 24, Issue 2 147-153 doi: 10.1046/j.1365-2885.2001.00317.x
Kim JY, Choi MH, Kim SJ, Kyong JB, Chung BC.No abstract available
Variations in cartilage catabolism in different equine joints in response to interleukin-1 in vitro.
The Veterinary record    March 27, 2001   Volume 148, Issue 7 204-206 doi: 10.1136/vr.148.7.204
Fuller CJ, Barr AR, Dieppe PA.An explant system was used to investigate the hypothesis that cartilage from different equine joints might respond differently to challenge with interleukin-1alpha (IL-1alpha). Pairs of normal cartilage samples were taken from the metacarpophalangeal, proximal interphalangeal and distal interphalangeal joints of six horses. One of each pair was stimulated with 10 ng/ml human recombinant IL-1alpha for three days, and the supernatants and remaining cartilage explants were analysed for their total content of glycosaminoglycans. A significantly higher percentage of glycosaminoglycans was released ...
A new method for quantitation of spin concentration by EPR spectroscopy: application to methemoglobin and metmyoglobin.
Journal of magnetic resonance (San Diego, Calif. : 1997)    January 29, 2000   Volume 142, Issue 2 266-275 doi: 10.1006/jmre.1999.1935
Svistunenko DA, Sharpe MA, Nicholls P, Wilson MT, Cooper CE.A new method of EPR spectral analysis is developed to quantitate overlapping signals. The method requires double integration of a number of spectra containing the signals in different proportions and the subsequent solution of a system of linear equations. The result gives the double integral values of the individual lines, which can then be further used to find the concentrations of all the paramagnetic species present. There is no requirement to deconvolute the whole spectrum into its individual components. The method is employed to quantify different heme species in methemoglobin and metmyo...
Pathogenicity of Vibrio alginolyticus for cultured gilt-head sea bream (Sparus aurata L.).
Applied and environmental microbiology    October 31, 1998   Volume 64, Issue 11 4269-4275 doi: 10.1128/AEM.64.11.4269-4275.1998
Balebona MC, Andreu MJ, Bordas MA, Zorrilla I, Moriñigo MA, Borrego JJ.The in vivo and in vitro pathogenic activities of whole cells and extracellular products of Vibrio alginolyticus for cultured gilt-head sea bream were evaluated. The 50% lethal doses ranged from 5.4 x 10(4) to 1.0 x 10(6) CFU/g of body weight. The strains examined had the ability to adhere to skin, gill, and intestinal mucus of sea bream and to cultured cells of a chinook salmon embryo cell line. In addition, the in vitro ability of V. alginolyticus to adhere to mucus and skin cells of sea bream was demonstrated by scanning electron microscopy. The biological activities of extracellular produc...
Evidence that commercial calf and horse sera can contain substantial amounts of trans-10,cis-12 conjugated linoleic acid.
Lipids    September 4, 1998   Volume 33, Issue 8 817-819 doi: 10.1007/s11745-998-0275-x
Park Y, Pariza MW.We analyzed fetal calf, newborn calf, horse, and adult cow sera for conjugated linoleic acid (CLA). All sera samples contained CLA, but the amounts varied. The predominant isomer was cis-9,trans-11 CLA but some samples appeared to contain substantial amounts of an isomer with the retention time of trans-10,cis-12 CLA.
Identification of metabolites of azaperone in horse urine.
Journal of pharmaceutical sciences    January 1, 1996   Volume 85, Issue 1 79-84 doi: 10.1021/js950205j
Sams RA, Gerken DF, Detra RL, Stanley SD, Wood WE, Tobin T, Yang JM, Tai HH, Jegananthan A, Watt DS.Two metabolites of the tranquilizer azaperone were extracted from alkalinized horse urine after treatment with beta-glucuronidase/sulfatase from limpets (Patella vulgata). The metabolites were identified by a combination of independent chemical synthesis and GC/MS and 1H NMR analysis. The metabolites were identified as 1-(fluorophenyl)-4-[4-(5-hydroxy-2-pyridinyl)-1-piperazinyl]-1-butanol, designated as 5'-hydroxy-azaperol, and 1-(fluorophenyl)-4-[4-(5-hydroxy-2-pyridinyl)-1-piperazinyl]-1-butanone, designated as 5'-hydroxyazaperone. A TLC screening test was developed for detecting both metabo...
[The metabolism of foreign substances in the horse with reference to other animal species].
Zentralblatt fur Veterinarmedizin. Reihe A    September 1, 1994   Volume 41, Issue 7 493-508 
Schmid A, Schmid H.In this paper, the metabolism of xenobiotics in the horse, including differences to other species, is discussed. The most important metabolic reactions of phase I (oxidation, reduction and hydrolysis of substrates), as well as of phase II (conjugation of substrates with glucuronic acid, sulphuric acid, acetic acid, alkyl groups, amino acids, amino acid derivatives, glutathione etc.), are discussed and enzymes involved in the metabolic reactions are considered.
[Ganglioside GM3 from horse erythrocytes: structure and effect on cell proliferation].
Bioorganicheskaia khimiia    August 1, 1993   Volume 19, Issue 8 817-824 
Menzeleev RF, Smirnova GP, Chekareva NV, Zvonkova EN, Krasnopol'skiĭ IuM, Shvets VI.An increase of the mouse fibroblast proliferation by ganglioside GM3 from equine erythrocytes is described. The structure of GM3 has been established on the basis of chemical methods, enzymatic degradation, GC-MS, as well as plasma desorption mass spectrometry and HPLC of 9-anthrylmethyl esters of gangliosides to characterize the long-chain base composition. The oligosaccharide moiety includes an N-glycolylneuraminic acid residue, whereas the main components of the lipid moiety are 20:1 sphingosine and 24:0 fatty acids.
A comparative study of the metabolic effort expended by horse riders during a jumping competition.
British journal of sports medicine    March 1, 1992   Volume 26, Issue 1 33-35 doi: 10.1136/bjsm.26.1.33
Gutiérrez Rincón JA, Vives Turcó J, Muro Martínez I, Casas Vaqué I.The three main Olympic horse riding disciplines are dressage, jumping, and three-day eventing (including dressage, cross country and jumping). In the jumping discipline (obstacle race), the 'team' (horse rider) is judged under the different conditions that might take place in a varied run. The horse is expected to show power and ability; the rider must show riding skill and good physical condition. However, the different conditions encountered by the rider during competition (duration of event, continuous isometric working level, especially in the inferior trunk, lead us to consider the need f...
The identification of hepatotoxic pyrrolizidine alkaloid exposure in horses by the demonstration of sulphur-bound pyrrolic metabolites on their hemoglobin.
Veterinary and human toxicology    June 1, 1991   Volume 33, Issue 3 286-287 
Seawright AA, Hrdlicka J, Wright JD, Kerr DR, Mattocks AR, Jukes R.No abstract available
The effect of cryopreservation on the metabolic activity of day-6.5 horse embryos.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 411-417 
Rieger D, Bruyas JF, Lagneaux D, Bézard J, Palmer E.The decrease in embryo viability caused by cryopreservation may be due, in part, to metabolic disturbances. To determine the effect of cryopreservation on metabolism, Day -6.5 horse embryos were either frozen and thawed using glycerol as the cryoprotectant, given only the glycerol treatment or washed an equal number of times in phosphate buffered saline (PBS). Before and after treatment, individual embryos were incubated with L-[14C(U)]-glutamine, to measure Krebs cycle activity, and D-[5-3H]-glucose, to measure Embden-Meyerhof pathway activity. Before treatment, glucose metabolism ranged from...
Changes in the metabolic profile of equine muscle from birth through 1 yr of age.
Journal of applied physiology (Bethesda, Md. : 1985)    April 1, 1990   Volume 68, Issue 4 1399-1404 doi: 10.1152/jappl.1990.68.4.1399
Kline KH, Bechtel PJ.The purpose of this study was to investigate metabolic changes in equine muscle from birth to 1 yr of age. Duplicate biopsies from the middle portion of the gluteus medius were obtained from a depth of 2 cm beneath the superficial fascia at 1 day, 7 days, 1 mo, 3 mo, 6 mo, and 1 yr of age in 11 quarter horses and at 1 day, 3 mo, 6 mo, and 1 yr of age in 5 Standardbreds. Muscle enzyme activities determined were citrate synthase, 3-hydroxyacyl-CoA dehydrogenase, phosphorylase, and lactate dehydrogenase. Percent fast-twitch, fast-twitch high oxidative, and slow-twitch oxidative fiber types were d...
The identification of a dihydrodiol metabolite of propranolol excreted in horse urine.
Biomedical & environmental mass spectrometry    November 1, 1989   Volume 18, Issue 11 1030-1033 doi: 10.1002/bms.1200181113
Dumasia MC, Houghton E.No abstract available
Analysis of fatty acids in equine cerebrospinal fluid using gas chromatography with electron-capture detection.
Journal of chromatography    September 29, 1989   Volume 494 278-282 doi: 10.1016/s0378-4347(00)82676-6
Sweeney RW, Beech J, Whitlock RH, Castelli PL.No abstract available
Metabolism of naturally occurring [13C]glucose given orally to horses.
American journal of veterinary research    August 1, 1988   Volume 49, Issue 8 1259-1262 
Klein HJ, Schulze E, Deegen E, Giese W.In 5 horses, 13CO2/12CO2 ratios in expired air were determined using isotope mass spectroscopy to investigate metabolism of naturally occurring [13C]glucose. Oral glucose tolerance tests (OGTT) were performed using maize or beet glucose. Maize has a higher 13C concentration than that of most plants. The 13CO2/12CO2 ratios after OGTT was performed using maize glucose were compared with 13CO2/12CO2 ratios in expired air after OGTT was performed using beet glucose. The ratio also was determined during the period horses were not fed. Using OGTT, all horses were glucose tolerant. The OGTT performed...
[Testing of a reflection photometer for the determination of enzymes and metabolites in the blood plasma of racehorses].
DTW. Deutsche tierarztliche Wochenschrift    March 1, 1988   Volume 95, Issue 3 104-105 
Hambitzer R, Sommer H.No abstract available
Changes in the metabolic profile of the equine gluteus medius as a function of sampling depth.
Comparative biochemistry and physiology. A, Comparative physiology    January 1, 1988   Volume 91, Issue 4 815-819 doi: 10.1016/0300-9629(88)90969-3
Kline KH, Bechtel PJ.1. Cross sections from the middle of the gluteus medius were removed from 10 adult horses and used to evaluate changes in histochemically determined muscle fiber type and biochemically determined metabolic enzyme activities as a function of sample depth. 2. Muscle fiber types determined using histochemical methods for myosin ATPase (pH 9.4) and succinic dehydrogenase (SDH) activity indicated percent fast-twitch glycolytic (FG) muscle fibers decreased and slow-twitch oxidative (SO) fibers increased as a function of increasing sampling depth. 3. Percent histochemically determined fast-twitch oxi...
Identification of a flunixin metabolite in the horse by gas chromatography-mass spectrometry.
Journal of chromatography    December 25, 1987   Volume 423 123-130 doi: 10.1016/0378-4347(87)80334-1
Jaussaud P, Courtot D, Guyot JL, Paris J.The main metabolite of flunixin, a hydroxylated product, has been identified by gas chromatography-mass spectrometry and 1H NMR spectroscopy in equine urine and plasma. The method also permits the qualitative monitoring of the urinary elimination of the drug and its metabolite. The two products are detected up to 175 and 54 h, respectively, after a single intravenous administration at the dose of 1 mg/kg. Simultaneous detection of the two compounds increases the reliability of anti-doping control analysis.
High-speed liquid chromatography/tandem mass spectrometry for the determination of drugs in biological samples.
Analytical chemistry    October 1, 1986   Volume 58, Issue 12 2453-2460 doi: 10.1021/ac00125a022
Covey TR, Lee ED, Henion JD.No abstract available
The organism as bioreactor. Interpretation of the reduction law of metabolism in terms of heterogeneous catalysis and fractal structure.
Journal of theoretical biology    November 21, 1985   Volume 117, Issue 2 209-230 doi: 10.1016/s0022-5193(85)80218-6
Sernetz M, Gelléri B, Hofmann J.Organisms and bioreactors are open, dissipative systems in steady state. They are functionally equivalent with respect to turnover and kinetics, and structurally analogous with respect to fractal organization and self-similar scaling. As heterogeneous catalytic systems both are governed by interaction of mass transport and reaction. The structural equivalent to turbulence in the reactor, yielding high efficiency, is the fractal folding and branching of the transport systems of the organism. Dimensionally and in terms of fractals, organisms and reactors are therefore area-volume hybrids. The ph...
Identification of metabolites of methylprednisolone in equine urine.
Steroids    August 1, 1985   Volume 46, Issue 2-3 755-765 doi: 10.1016/0039-128x(85)90055-8
Gallicano KD, Ng RM, Young LM.Methylprednisolone and three metabolites, 17,21-dihydroxy-6 alpha-methyl-1,4-pregnadiene-3,11,20-trione, 6 alpha-methyl-17,20 beta,21-trihydroxy-1,4-pregnadiene-3,11-dione, and 6 alpha-methyl-11 beta,17,20 beta,21-tetrahydroxy-1,4-pregnadien-3-one were detected in equine urine after intraarticular administration of methylprednisolone acetate. All four compounds were excreted both in the unconjugated form and as glucuronic acid conjugates. They were identified by comparing data obtained from analyses by high performance liquid chromatography, thin-layer chromatography, ultraviolet spectroscopy ...
Blood metabolite profiles of broodmares and foals.
Equine veterinary journal    May 1, 1984   Volume 16, Issue 3 192-196 doi: 10.1111/j.2042-3306.1984.tb01902.x
Rogers PA, Fahey GC, Albert WW.Serum amino acid profiles and other serum characteristics of broodmares and their foals wee studied. Compared with mares, foals had significantly higher concentrations of serum leucine, threonine, aspartic acid, asparagine, glutamic acid, glutamine, proline and tyrosine, glucose, cholesterol, creatinine and phosphorus. Foals had significantly less serum histidine, glycine, cystine, taurine, protein and urea nitrogen. Lysine and/or methionine supplementation of pregnant and lactating broodmare diets were conducted. Changes in serum amino acid profiles caused by dietary amino acid supplemented w...
On-line direct liquid introduction interface for micro-liquid chromatography/mass spectrometry: application to drug analysis.
Clinical chemistry    September 1, 1982   Volume 28, Issue 9 1882-1886 
Eckers C, Skrabalak DS, Henion J.We describe an integrated micro-liquid chromatograph/mass spectrometer (micro-LC/MS) system capable of performing routine determinations for 1--10 ng of drugs and their metabolites extracted from biological fluids. The micro-LC is constructed from conventional "high-performance" liquid-chromatographic instrumentation by using commercially available components. The mass spectrometer is operated in the chemical ionization mode. The direct liquid introduction micro-LC/MS interface can be constructed from commercially available materials. Chromatographic and mass spectral results demonstrate the a...
An attempt to establish metabolic indices useful in evaluating the training of thoroughbred racehorses.
Zentralblatt fur Veterinarmedizin. Reihe A    January 1, 1981   Volume 28, Issue 9-10 750-759 doi: 10.1111/j.1439-0442.1981.tb01247.x
Szarska E.No abstract available
Biochemical changes in horses during endurance rides.
The Veterinary record    May 27, 1978   Volume 102, Issue 21 469 doi: 10.1136/vr.102.21.469
Orton RG.No abstract available