Analyze Diet

Topic:Metabolites

Metabolites are small molecules involved in the metabolic processes within a horse's body. They are the intermediates and products of metabolism, encompassing a wide range of compounds, such as amino acids, lipids, carbohydrates, and nucleotides. These molecules play roles in energy production, growth, and cellular repair. The study of equine metabolites, often conducted through metabolomics, provides insights into the physiological and pathological states of horses. Changes in metabolite levels can indicate alterations in metabolic pathways, potentially reflecting health conditions or responses to environmental factors. This page compiles peer-reviewed research studies and scholarly articles that explore the identification, function, and diagnostic potential of metabolites in equine health.
Alterations in blood, sweat, urine and muscle composition during prolonged exercise in the horse.
The Veterinary record    April 17, 1982   Volume 110, Issue 16 377-384 doi: 10.1136/vr.110.16.377
Snow DH, Kerr MG, Nimmo MA, Abbott EM.No abstract available
Deuteromethylation of dimethylxanthines: a gas chromatographic mass spectrometric method for confirmatory analysis in horse urine extracts.
Biomedical mass spectrometry    March 1, 1982   Volume 9, Issue 3 103-107 doi: 10.1002/bms.1200090305
Houghton E.The methylated xanthines caffeine and/or theobromine are commonly encountered in drug-positive samples from racehorses and their metabolism and excretion in the horse and their analysis in urinary extracts has been of particular interest in this laboratory. Due to their polar nature the dimethylxanthines theobromine, theophylline and paraxanthine give unsatisfactory gas chromatographic performance and require derivatization prior to analysis by gas chromatography mass spectrometry. The present paper describes a simple deuteromethylation procedure to render the compounds amenable to analysis by...
[Volatile fatty acid and ammonia levels in the cecal contents of the horse depending on the type of feed, sequence and time of feeding].
Fortschritte in der Tierphysiologie und Tierernahrung    January 1, 1982   Volume 13 24-31 
Schwabenbauer K, Meyer H, Lindemann G.No abstract available
The use of combined high performance liquid chromatography negative ion chemical ionization mass spectrometry to confirm the administration of synthetic corticosteroids to horses.
Biomedical mass spectrometry    November 1, 1981   Volume 8, Issue 11 558-564 doi: 10.1002/bms.1200081107
Houghton E, Dumasia MC, Wellby JK.Negative ion chemical ionization mass spectra of some corticosteroids have been obtained by direct syringe introduction on to the Finnigan moving belt high-performance liquid chromatography-mass spectrometer interface. Proprietary preparations based upon dexamethasone, betamethasone and prednisolone were administered to horses at therapeutic dose level. Urine samples were extracted, the extracts purified by Sephadex LH-20 chromatography and the presence of the parent steroids in the eluates was confirmed by combined high-performance liquid chromatography negative ion chemical ionization mass s...
Kanamycin sulfate in the horse: serum, synovial fluid, peritoneal fluid, and urine concentrations after single-dose intramuscular administration.
American journal of veterinary research    October 1, 1981   Volume 42, Issue 10 1823-1825 
Brown MP, Stover SM, Kelly RH, Farver TB.Six healthy adult mares were given a single dose of kanamycin sulfate (200 mg/ml) IM at a dosage rate of 5 mg/kg of body weight. Kanamycin concentrations in serum, synovial fluid, peritoneal fluid, and urine were measured serially over a 48-hour period. The mean peak serum kanamycin concentration was 12.55 microgram/ml at 1 hour. Mean peak kanamycin concentrations in synovial fluid and peritoneal fluid were 7.25 microgram/ml and 9.27 microgram/ml at 2 hours and 3 hours, respectively. These concentrations decreased steadily in parallel with serum concentrations and were still measurable at 48 h...
Sodium oxacillin in the horse: serum, synovial fluid, peritoneal fluid, and urine concentrations after single-dose intramuscular administration.
American journal of veterinary research    October 1, 1981   Volume 42, Issue 10 1826-1828 
Stover SM, Brown MP, Kelly RH, Farver TB.Six healthy adult mares were given a single dose (25 mg/kg of body weight) of sodium oxacillin IM. Oxacillin concentrations in serum, synovial fluid, peritoneal fluid, and urine were measured serially over a 48-hour period. The mean peak serum oxacillin concentration was 9.75 microgram/ml at 0.5 hour after injection. Mean peak oxacillin concentrations in synovial and peritoneal fluids were 1.45 microgram/ml and 2.60 microgram/ml at 1 hour and 2 hours, respectively. These concentrations decreased in parallel with serum values and were not measurable at 48 hours. Urine concentrations of oxacilli...
Metabolic conjugation of some carboxylic acids in the horse.
Xenobiotica; the fate of foreign compounds in biological systems    October 1, 1981   Volume 11, Issue 10 655-663 doi: 10.3109/00498258109049085
Marsh MV, Caldwell J, Smith RL, Horner MW, Houghton E, Moss MS.1. 14C-Labelled benzoic acid, salicylic acid and 2-naphthylacetic acid were administered orally to horses, and urinary metabolites investigated by chromatographic and mass spectral techniques. 2. [14C]Benzoic acid (5 mg/kg) was eliminated rapidly in the urine, and quantitatively recovered in 24 h. The major urinary metabolite was hippuric acid (95% of dose) with much smaller amounts of benzoic acid, benzoyl glucuronide and 3-hydroxy-3-phenylpropionic acid. Administration of [ring-D5]benzoic acid together with [14C]benzoic acid to a pony permitted the mass spectral determination of metabolites ...
Analysis of phenylbutazone and its metabolites by high performance liquid chromatography.
Equine veterinary journal    July 1, 1981   Volume 13, Issue 3 201-203 doi: 10.1111/j.2042-3306.1981.tb03489.x
Taylor JB, Lees P, Gerring EL.No abstract available
Post-excretion production of ethanol in horse urine.
Journal - Forensic Science Society    July 1, 1981   Volume 21, Issue 3 201-206 doi: 10.1016/s0015-7368(81)71387-2
Chapman DI, Lloyd P, Buhagiar RW.No abstract available
Pharmacokinetics of phenylbutazone and its metabolites in the horse.
Equine veterinary journal    July 1, 1981   Volume 13, Issue 3 152-157 doi: 10.1111/j.2042-3306.1981.tb03472.x
Gerring EL, Lees P, Taylor JB.Phenylbutazone was given orally to 2 groups of horses and the plasma levels of the drug and its 2 principal metabolites oxyphenbutazone and gamma-hydroxyphenylbutazone measured by high performance liquid chromatography. Animals in Group 1 received single oral doses in a range from 1.1 to 13.2 mg/kg and were sampled over the succeeding 24 h. Considerable individual variation was observed both in timing and magnitude of the plasma drug responses between horses, but 24 h after dosing a clear dose response relation was recorded. Group 2 horses were given the recommended therapeutic dosage regimen ...
Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of testosterone and a study of the phase II metabolism.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1981   Volume 11, Issue 5 323-331 doi: 10.3109/00498258109045311
Dumasia MC, Houghton E.1. Isomers of 3,17-dihydroxyandrostan-16-one, 3,16-dihydroxyandrostan-17-one and androstane-3,16,17-triol have been identified as urinary metabolites of testosterone in the horse. 2. Following XAD-2 extraction of urine samples, Sephadex LH-20 chromatography was used to separate the extract into conjugate groups. Metabolites obtained after hydrolysis of the conjugates have been investigated by g.l.c.-mass spectrometry. 3. Testosterone, 3,17-dihydroxyandrostan-16-one and 3,16-dihydroxyandrostan-17-one were found only in the sulphate fraction. 5 alpha-Androstane-3 beta,17 beta-diol, and two isome...
In vivo metabolism of [3H]equilin in the pregnant mare.
Endocrinology    January 1, 1981   Volume 108, Issue 1 232-238 doi: 10.1210/endo-108-1-232
Bhavnani BR, Woolever CA.[3H]Equilin [3H-labeled 3-hydroxy-1,3,5(10), 7-estratetraen-17-one] was administered iv to a pregnant mare in the 10th month of gestation. Maternal urine was collected for 3 days, and blood samples were taken 35 min and 3, 6, 12, and 24 h after the injection. The half-life of the disappearance of radioactivity from the blood was approximately 2.5 h. Over 90% of the administered dose was excreted in the first 24 h. The urine was extracted, hydrolyzed, and fractionated. The bulk of the radioactive material (75%) was present in the phenolic sulfate fraction from which radiochemically pure equilin...
The metabolism of promazine and acetylpromazine in the horse.
Drug metabolism and disposition: the biological fate of chemicals    January 1, 1981   Volume 9, Issue 1 30-36 
Dewey EA, Maylin GA, Ebel JG, Henion JD.Promazine hydrochloride and acetylpromazine maleate were administered intravenously at clinical dose levels to horses. In urine from horses given promazine hydrochloride, the parent drug and four metabolites were detected. The two major metabolites, present as conjugates were identified after hydrolysis by beta-glucuronidase/arylsulfatase as 3-hydroxypromazine and 3-hydroxydesmonomethyl-promazine. Conjugated 3-hydroxypromazine has been previously identified as a major metabolite in the horse. Two minor metabolites isolated in this study were primaizine N-oxide and promazine N-oxide sulfoxide. ...
The major metabolite of fentanyl in the horse.
Drug metabolism and disposition: the biological fate of chemicals    November 1, 1980   Volume 8, Issue 6 425-427 
Frincke JM, Henderson GL.Fentanyl, a potent, synthetic narcotic analgesic, has reportedly been used to "dope" racehorses. Urine was collected from a horse dosed with 70 mg of [3H]fentanyl, and the primary metabolite, a water-soluble, amphoteric compound, was isolated by high-pressure liquid chromatography and identified by spectroscopic analysis. This metabolite was found to be N-[1-(2-phenethyl-4-piperidinyl)] malonanilinic acid.
Selected ion monitoring assay for bromhexine in biological fluids.
Biomedical mass spectrometry    November 1, 1980   Volume 7, Issue 11-12 582-587 doi: 10.1002/bms.1200071127
Jonckheere JA, Thienpont LM, De Leenheer AP, De Backer P, Debackere M, Belpaire FM.A method has been developed for quantification of bromhexine in plasma using gas chromatography mass spectrometry with selected ion monitoring. A deuterium labelled analogue was synthesized and used as the internal standard. To evaluate the gas chromatographic electron capture detection method described earlier, 23 plasma samples have been analysed by both techniques. Although a good correlation was shown, selected ion monitoring was superior to the electron capture detection method for levels below 3 ng ml-1. The mass spectrometric method has also been used to set up a pharmacokinetic study o...
Alterations in plasma corticosteroids, insulin and selected metabolites in horses used in endurance rides.
Equine veterinary journal    July 1, 1980   Volume 12, Issue 3 137-140 doi: 10.1111/j.2042-3306.1980.tb03403.x
Dybdal NO, Gribble D, Madigan JE, Stabenfelt GH.The effects of prolonged exercise on plasma concentrations of corticosteroids, insulin, glucose, lactate and beta-hydroxybutrate were studied in a group of horses competing in a 160 km endurance ride. Of the 53 horses included in the study at the outset, 23 completed the course. Plasma corticosteroids increased while glucose and insulin decreased during exercise. Little change occurred in plasma lactate or beta-hydroxybutyrate. The parameters studied did not result in the finding of any consistent significant differences beteeen individuals that completed and those that did not complete the co...
Qualitative and quantitative analysis of hydrochlorothiazide in equine plasma and urine by high-performance liquid chromatography.
Journal of analytical toxicology    July 1, 1980   Volume 4, Issue 4 185-191 doi: 10.1093/jat/4.4.185
Henion JD, Maylin GA.A sensitive, quantitative method has been developed for the determination of hydrochlorothiazide in equine plasma and urine. Thin-layer chromatography is used to screen for the presence of the drug in unknown samples. The TLC screening methods described provide minimum detection limits of 50 ng/mL in plasma and 25 ng/mL in urine. A silica micro chromatography column is used to clean up ethyl acetate extracts for HPLC analysis and mass spectral confirmation. An internal standard, trichloromethiazide, is used to derive quantitative data at concentrations as low as 25 ng/mL for plasma disappearan...
Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of 19-nortestosterone.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1980   Volume 10, Issue 5 381-390 doi: 10.3109/00498258009033771
Houghton E, Dumasia MC.1. The metabolism of 19-nor[4-14C]testosterone in a thoroughbred horse has been studied and neutral urinary metabolites obtained after enzyme hydrolysis have been investigated by g.l.c.-mass spectrometry. 2. 3-Hydroxyestran-17-one, 17 alpha- and 17 beta-nortestosterone, estrane-3,17-diol (two isomers), 3,16-dihydroxyestran-17-one (two isomers), 3,17-dihydroxyestran-16-one (two isomers) and estrane-3,16,17-triol were identified in the neutral urinary extracts.
Changes in blood gas, acid-base and metabolic parameters in horses during three-day event competition.
Research in veterinary science    May 1, 1980   Volume 28, Issue 3 393-395 
Rose RJ, Ilkiw JE, Sampson D, Backhouse JW.Sixteen horses competing in a three-day event had venous blood samples collected during the speed and endurance test (day 2) to examine changes in blood gas ands acid-base balance, and the concentrations of lactate, pyruvate, beta-hydroxybutyrate, acetoacetate, alpha-ketoglutarate and cortisol. Following the roads and tracks and steeplechase phases there was a significant metabolic and respiratory alkalosis despite a rise in lactate. After completion of the cross country section, although there was a significant decrease in total base, there was no significant change in pH from pre-event value...
Mouldy grain and the aetiology of pellagra: the role of toxic metabolites of Fusarium.
Biochemical Society transactions    February 1, 1980   Volume 8, Issue 1 147-150 doi: 10.1042/bst0080147
Schoental R.No abstract available
A technique for the conduct of nutritional balance experiments in horses.
Equine veterinary journal    October 1, 1979   Volume 11, Issue 4 232-234 doi: 10.1111/j.2042-3306.1979.tb01352.x
McKenzie RA, Blaney BJ, Gartner RJ, Dillon RD, Standfast NF.Standardbred geldings were used in a number of nutritional balance experiments. These consisted of 28-day cycles each of an 18-day equilibration period in yards and a 10-day settling and collection period in metabolism crates. The crates were made of galvanised metal tubing over wooden flooring covered by rubber matting and rubber sheets. Total faeces were collected in trays at the rear of crates and total urine by canvas funnels slung beneath the sheath of each horse.
A gas chromatographic screening procedure for the detection of non-steroidal anti-inflammatory drugs in horse urine.
Equine veterinary journal    October 1, 1979   Volume 11, Issue 4 259-263 doi: 10.1111/j.2042-3306.1979.tb01360.x
Hunt JP, Haywood PE, Moss MS.A gas chromatographic screening procedure for the non-steroidal anti-inflammatory group of drugs is described. The method invovles on-column methylation of the carboxylic acid group using trimethylanilinium hydroxide as the methylating reagent. Fifteen such drugs were studied. Eight of these were detected in urine collected from horses that had received these compounds orally and for these drugs, rates of urinary excretion are recorded. Seven other members of this group of drugs were shown to be detectable by this procedure but in these cases the drug was added to urine and not administered to...
Studies related to the metabolism of anabolic steroids in the horse: testosterone.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1979   Volume 9, Issue 5 269-279 doi: 10.3109/00498257909038730
Houghton E, Dumasia MC.1. After intramuscular administration of [4-14C]testosterone to two cross-bred gelded horses, 45% of the radioactivity was excreted in urine in 96 h. Small amounts of urinary activity could still be detected at 200 h. 2. Neutral metabolites obtained after both enzyme and acid hydrolysis of urine samples have been investigated by g.l.c.-mass spectrometry. 3. 5 alpha-Androstane-3 beta, 17 alpha-diol was found only in the enzyme-hydrolysable extract and testosterone only in the acid-hydrolysable extract. 5 alpha-Androstane-3 beta, 17 beta-diol and 3 beta-hydroxy-5 alpha-androstan-17-one were foun...
Changes of blood metabolites in horses after racing, with particular reference to uric acid.
Australian veterinary journal    February 1, 1979   Volume 55, Issue 2 54-57 doi: 10.1111/j.1751-0813.1979.tb15159.x
Keenan DM.Changes in concentration of a number of blood metabolites in 30 thoroughbred horses were recorded after an 1110 metre race. No significant changes occurred in blood urea or aspartate aminotransferase during the three hours after racing. Plasma sodium, potassium and calcium levels were increased immediately after racing but had returned to normal one hour after racing. Plasma phosphate showed a significant fall in concentration one hour after racing. Creatinine and lactic acid concentrations were elevated ten minutes after racing and although they subsequently decreased, the level of lactic aci...
Radioimmunoassay technique for detecting urinary excretion products after administration of synthetic anabolic steroids to the horse.
Xenobiotica; the fate of foreign compounds in biological systems    April 1, 1978   Volume 8, Issue 4 197-206 doi: 10.3109/00498257809056141
Jondorf WR, Moss MS.1. Cross-bred and thoroughbred geldings were injected with veterinary doses of various synthetic anabolic steroids. Urines collected sequentially from treated animals were analysed, following solvent extraction, by radioimmunoassay using 19-[3H]nortestosterone and an antibody raised against a 19-nortestosterone immunogen. 2. Urinary excretion of 19-nortestosterone and/or its cross-reacting metabolites was detectable for various times after administration of different nortestosterone esters, as follows: phenylpropionate (400 mg), greater than 14 days; cyclohexylpropionate (100 mg), greather tha...
Studies related to the metabolism of anabolic steroids in the horse: a gas chromatographic mass spectrometric method to confirm the administration of 19-nortestosterone or its esters to horses.
Biomedical mass spectrometry    February 1, 1978   Volume 5, Issue 2 170-173 doi: 10.1002/bms.1200050213
Houghton E, Oxley GA, Moss MS, Evans S.A method is described to confirm the presence of 19-nortestosterone metabolites in urine after the administration of veterinary preparations of this anabolic steroid to horses. The method is based upon the detection, by gas chromatography mass spectrometry or selected ion monitoring, of an isomer of estrane-3,17-diol in the urine.
Studies related to the metabolism of anabolic steroids in the horse: 19-nortestosterone.
Xenobiotica; the fate of foreign compounds in biological systems    November 1, 1977   Volume 7, Issue 11 683-693 doi: 10.3109/00498257709038698
Houghton E.1. The metabolism of 19-nortestosterone in a cross-bred horse has been studied using 14C-labelled material. 2. Two neutral metabolites isolated from urinary extracts by column chromatography were identified as isomers of 3-hydroxyestran-17-one and estrane-3,17-diol by g.l.c.-mass spectrometry. 3. The stereochemistry of the two metabolites has been investigated by comparison of the retention times of their trimethylsilyl derivatives with those of standard steroids of known configuration.
Drug interactions in the horse. III. Effects of furosemide on urinary concentrations of glucuronide metabolites of pentazocine.
Research communications in chemical pathology and pharmacology    July 1, 1977   Volume 17, Issue 3 447-456 
Miller JR, Roberts BL, Blake JW, Valentine RW, Tobin T.No abstract available
The urinary excretion of synthetic corticosteroids by the horse.
The Veterinary record    May 21, 1977   Volume 100, Issue 21 447-450 doi: 10.1136/vr.100.21.447
Chapman DI, Whiteside J.A radioimmunoassay method has been developed that enables the administration of therapeutic doses of synthetic corticosteroids to be detected in horse urine. Fourteen proprietary preparations of these steroids have been given by intramuscular injection to ponies and thoroughbreds. The administration of some preperations could still be detected six days after a single intramuscular injection of a therapeutic dose. The route of injection of dexamethasone-21-sodium phosphate, whether intramuscular, intravenous or intra-articular, did not appear to alter the length of time over which the steroid o...
Excretion and metabolism of nikethamide in the horse.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 116-123 doi: 10.1136/bjsm.10.3.116
Delbeke FT, Debackere M.It is well known that nikethamide (N,N-diethylnicotinamide, CoramineR) is metabolized very rapidly to nicotinamide. Hence, there is difficulty in proving that nikethamide has been used as a doping substance because nicotinamide is a normal physiological metabolite in the organism as well as a vitamin preparation. However, an intermediate metabolite (N-ethylnicotinamide) was found by us in the urine of horses treated with CoramineR. This was characterized by gas chromatography/mass spectrometry, and synthesized and identified as being N-ethylnicotinamide. The excretion and metabolism of niketha...