Analyze Diet

Topic:Laboratory Methods

Laboratory methods in equine research encompass a variety of techniques and procedures used to analyze biological samples from horses to study health, disease, genetics, and physiology. These methods include hematological analyses, biochemical assays, molecular biology techniques, and microbiological cultures. Commonly utilized laboratory techniques involve blood tests for complete blood count (CBC) and serum chemistry, polymerase chain reaction (PCR) for genetic and infectious disease studies, and enzyme-linked immunosorbent assays (ELISA) for detecting specific proteins or antibodies. These methods provide valuable data that contribute to understanding equine health and disease mechanisms. This page compiles peer-reviewed research studies and scholarly articles that explore the application, development, and outcomes of laboratory methods in the context of equine research.
High-performance liquid chromatography/tandem mass spectrometry: its use for the identification of stanozolol and its major metabolites in human and equine urine.
Biomedical & environmental mass spectrometry    January 1, 1990   Volume 19, Issue 1 37-51 doi: 10.1002/bms.1200190106
Mück WM, Henion JD.A screening procedure for the anabolic steroid stanozolol in human and equine urine was developed based on enzymatic hydrolysis, liquid-liquid extraction and reversed-phase liquid chromatography combined on-line with tandem mass spectrometry. The column effluent was introduced into the atmospheric pressure ionization source of a triple-quadrupole mass spectrometer via a heated pneumatic nebulizer liquid chromatograph/mass spectrometer interface. Abundant protonated molecular ions were generated by corona discharge ionization. Confirmation of stanozolol and several of its hydroxylated and dihyd...
Rapid determination of methandrostenolone in equine urine by isotope dilution liquid chromatography-tandem mass spectrometry.
Journal of chromatography    December 29, 1989   Volume 497 49-57 doi: 10.1016/0378-4347(89)80004-0
Edlund O, Bowers L, Henion J, Covey TR.Urine samples were spiked with [17-methyl-2H3]methandrostenolone as internal standard and extracted with a mixture of dichloromethane and cyclohexane. The organic phase was concentrated and injected onto a short octyl-silica column (30 mm x 4.6 mm I.D.) for separation of methandrostenolone and 17-epimethandrostenolone. The effluent from the column was connected to a Sciex TAGA 6000E triple quadrupole mass spectrometer equipped with an atmospheric pressure ion source for sampling of ions generated by a heated pneumatic nebulizer with corona discharge ionization. This ion source produced abundan...
Primary structure of horse serotransferrin glycans. Demonstration that heterogeneity is related to the number of glycans and to the presence of N-acetylneuraminic acid and N-acetyl-4-O-acetylneuraminic acid.
European journal of biochemistry    December 22, 1989   Volume 186, Issue 3 583-590 doi: 10.1111/j.1432-1033.1989.tb15248.x
Coddeville B, Stratil A, Wieruszeski JM, Strecker G, Montreuil J, Spik G.Three serotransferrin variants Tf 2a, Tf 4b and Tf 5b were isolated in an homogeneous form from a preparation of homozygous horse serotransferrin Tf 0. On the basis of the results concerning molecular mass determination and the carbohydrate analysis, it is concluded that the serotransferrin variant Tf 2a contains only one glycan while variants Tf 4b and Tf 5b contain two glycans. The structure of all of the glycans has been established by combining methylation analysis, mass spectrometry and 400-MHz 1H-NMR spectroscopy. From the obtained results, it appears that the two glycans of Tf 5b varian...
Transbilayer movement of phosphatidylserine in nonhuman erythrocytes: evidence that the aminophospholipid transporter is a ubiquitous membrane protein.
Biochemistry    December 12, 1989   Volume 28, Issue 25 9680-9685 doi: 10.1021/bi00451a021
Connor J, Schroit AJ.A 31-32-kDa integral membrane protein has been previously identified in erythrocytes as the protein most likely to be responsible for the transbilayer movement of phosphatidylserine (PS) [Connor & Schroit (1988) Biochemistry 27, 848-851]. Using similar techniques, we have identified analogous proteins of identical molecular weights in bovine, equine, ovine, porcine, canine, caprine, and rhesus red blood cells. Similar to human red blood cells, all of the mammalian cells were able to specifically transport an exogenously supplied fluorescent PS analogue from their outer-to-inner membrane le...
Structure determination of three neutral oligosaccharides obtained from horse colostrum.
Carbohydrate research    December 1, 1989   Volume 194 280-287 doi: 10.1016/0008-6215(89)85026-8
Urashima T, Sakamoto T, Ariga H, Saito T.No abstract available
[Preliminary experience with a buffy coat analyser in horses].
Tijdschrift voor diergeneeskunde    December 1, 1989   Volume 114, Issue 23 1193-1194 
van de Velde LF.The present author's practice was offered the opportunity of testing a so-called buffy-coat analyser of the firm of Becton & Dickinson for its use in the field. He does not deny readers the report of his preliminary experience. In addition, the interpretation of the results and the limitations of the apparatus are briefly discussed.
Serum uric acid concentrations in horses heterozygous for combined immunodeficiency.
American journal of veterinary research    December 1, 1989   Volume 50, Issue 12 2155-2157 
Kettler MK, Weil MR, Perryman LE.Serum uric acid concentrations were determined in horses known to be carriers of combined immunodeficiency gene(s) and in presumed noncarrier horses. Uric acid concentrations were significantly higher (P less than 0.005) in carrier horses than in presumed noncarrier horses. However, there was some overlap in serum uric acid concentrations between carrier and presumed noncarrier horses.
Biotransformation of 5(10)-estrene-3 alpha,17 beta-diol by equine testicular preparations in vitro.
Biochemical Society transactions    December 1, 1989   Volume 17, Issue 6 1019-1020 doi: 10.1042/bst0171019
Dumasia MC, Houghton E.The research investigates the biosynthesis of a particular isomer called 5(10)-estrene-3 alpha, 17 beta-diol in stallion testes and how it affects the formation of 19-nor steroids and oestrogens. Summary of […]
[Detection of streptococci from various serological groups in animals].
Veterinarni medicina    December 1, 1989   Volume 34, Issue 12 743-749 
Havelka B, Skarková A.During the period from 1985 to 1988 we determined 228 strains of streptococci isolated from samples of various sorts of biomaterials, mainly animals. From this set of streptococci we classified 207 strains into serological groups according to the Lancefield classification and about 30% strains into species by means of serological and biochemical methods. Most of the strains were allocated to group C (37.28%) and group Q (17.39%). 89 streptococci strains originated from pigs, 40 strains from horses, 13 from cattle, 12 from dogs, 9 from poultry and 8 from coypu. The other streptococci strains or...
In vitro transport of L-alanine by equine cecal mucosa.
American journal of veterinary research    December 1, 1989   Volume 50, Issue 12 2138-2144 
Freeman DE, Kleinzeller A, Donawick WJ, Topkis VA.When sheets of mucosa from the cecum of clinically normal horses were incubated in vitro with radiolabeled L-alanine, they could accumulate this amino acid against an apparent concentration gradient after 60 to 150 minutes of incubation. The active transport system for L-alanine was on the serosal surface of the mucosal sheet only. L-Alanine accumulation at 60 minutes was partly inhibited by 20 mM glycine (P less than 0.01), 0.5 mM ouabain (P less than 0.05), and Na deprivation (P less than 0.02). Anoxia for 60 minutes increased L-alanine accumulation, but had adverse effects on cell structure...
Effect of dietary linolenic acid on endotoxin-induced thromboxane and prostacyclin production by equine peritoneal macrophages.
Circulatory shock    December 1, 1989   Volume 29, Issue 4 311-318 
Morris DD, Henry MM, Moore JN, Fischer K.In laboratory animals, the incorporation of alpha linolenic acid or other n-3 series fatty acids into the diet results in marked changes in cell membrane composition as well as arachidonic acid metabolism. The purpose of the present study was to determine whether endotoxin-induced thromboxane A2 (TxA2) and/or prostacyclin (PGI2) production by equine peritoneal macrophages was altered by feeding horses a diet containing 8% linseed oil as a source of alpha linolenic acid for 8 weeks. Peritoneal macrophages were cultured in vitro in the presence of endotoxin (LPS) (0.5-500 ng/ml) or calcium ionop...
Influence of technical parameters on the in vitro motility of equine neutrophils in the presence of streptococcal culture supernatant.
Veterinary immunology and immunopathology    November 30, 1989   Volume 23, Issue 1-2 85-101 doi: 10.1016/0165-2427(89)90112-8
Blancquaert AB, Colgan SP, Bruyninckx WJ.To identify the influence of technical factors on the in vitro motility of equine neutrophils towards streptococcus culture supernatant in an under-agarose assay, we studied the changes in eight cell migration parameters. The distances the phagocytes travelled by directed, random and spontaneous migration increased with incubation time, cell concentration and the gelatin and serum contents of the migration plates. The contribution of chemotaxis to the phagocyte migrations, however, decreased simultaneously. The directed and random, though not the spontaneous, migrations of the phagocytes incre...
A hemolytic assay for the measurement of equine complement.
Veterinary immunology and immunopathology    November 30, 1989   Volume 23, Issue 1-2 129-137 doi: 10.1016/0165-2427(89)90115-3
Reis KJ.A hemolytic assay was developed for the measurement of functional equine complement activity. The assay utilizes antibody sensitized chicken erythrocytes as the target cell and was specific for classical pathway (antibody dependent) complement activity. The assay was found to be reproducible and more sensitive than previous reports using other species of target cells. Total serum complement (CH50) values were determined for five mares and their foals and followed over a period of 3 months.
Thin-layer chromatographic screening procedure for some drugs in horse plasma.
Journal of chromatography    November 24, 1989   Volume 496, Issue 2 407-415 doi: 10.1016/s0378-4347(00)82588-8
Tanaka T, Aramaki S, Momose A.A thin-layer chromatographic screening procedure for some basic, neutral and acidic drugs was developed using 3 ml of horse plasma. Chloroform-2-propanol (95:5, v/v) was used as the extraction solvent. The drugs were identified by a high-performance thin-layer chromatographic plate and spraying successively with some detection reagents. In this study, the extraction recovery rates and the detection limits were determined at the same time.
Simultaneous analysis of furosemide and bumetanide in horse plasma using high performance liquid chromatography.
Biomedical chromatography : BMC    November 1, 1989   Volume 3, Issue 6 262-265 doi: 10.1002/bmc.1130030607
Singh AK, McArdle C, Gordon B, Ashraf M, Granley K.A high performance liquid chromatographic method is described for the simultaneous determination of furosemide and bumetanide in horse plasma. The C8 (3 microns) reversed phase column (4.8 x 150 mm) provided clear separation of furosemide and bumetanide with other components present in the horse plasma. The detection limit for both the drugs was 10 ng/mL. Both drugs were stable in plasma (at natural or acidic pH) for up to 24 h. The method is sufficiently sensitive to detect furosemide levels in plasma obtained from horses receiving a therapeutic dose of furosemide.
An improved TLC method for the detection of flunixin in equine serum.
Research in veterinary science    November 1, 1989   Volume 47, Issue 3 406-407 
Pemberton AD, Slater JS, Milne EM.A method for flunixin detection in equine serum extracts involving thin layer chromatography, spraying the chromatogram with alkaline sodium hypochlorite solution and heating with a detection limit of 50 ng ml-1 is described.
Histochemical and molecular determination of fiber types in chemically skinned single equine skeletal muscle fibers.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society    November 1, 1989   Volume 37, Issue 11 1731-1738 doi: 10.1177/37.11.2530270
Sosnicki AA, Lutz GJ, Rome LC, Goble DO.Until now, there has been no reliable method for histochemical determination of fiber types of single skinned muscle fibers. The major problem arises from the fact that most histochemical techniques use cross-sections of a large group of fibers and compare a given fiber with those surrounding it. This is not possible with a single skinned fiber which has been separated from a bundle to be used for mechanical analysis. A further problem is that the skinning procedure itself may alter the staining pattern. We have developed a procedure by which multiple cross-sections of single skinned fibers ca...
Androgen and 19-norandrogen aromatization by equine and human placental microsomes.
Journal of steroid biochemistry    November 1, 1989   Volume 33, Issue 5 949-954 doi: 10.1016/0022-4731(89)90245-8
Dintinger T, Gaillard JL, Moslemi S, Zwain I, Silberzahn P.The ability of equine and human placental microsomes to aromatize testosterone and 19-nortestosterone was studied. When 3 microM [1 beta,2 beta-3H]testosterone was used as substrate, the specific activity of equine placental microsomal aromatase was 2.5 times higher than that of the human microsomal enzyme. Although 19-nortestosterone was aromatized 67 times more rapidly by equine than by human aromatase, we found that equine aromatase exhibited a markedly weaker affinity for this substrate than did the human enzyme. Competitive inhibition of testosterone aromatization by 19-nortestosterone oc...
A new method for hydrolyzing sulfate and glucuronyl conjugates of steroids.
Analytical biochemistry    November 1, 1989   Volume 182, Issue 2 289-294 doi: 10.1016/0003-2697(89)90596-4
Tang PW, Crone DL.A new method for hydrolyzing steroid conjugates (both sulfates and glucuronides conjugates) that is efficient, effective, and inexpensive is described. This method comprises incubation of the conjugates--after salting-out into ethyl acetate or elution from a C18 cartridge--with anhydrous methanolic hydrogen chloride (methanolysis) for 10 min. It has been successfully applied to our routine radioimmunoassay screening and GC/MS confirmation studies of steroids in prerace and postrace equine urine samples. Comparative GC/MS studies on entire (male horse) urine samples showed that methanolysis gav...
Comparison of the binding of Ca2+ and Mn2+ to bovine alpha-lactalbumin and equine lysozyme.
Journal of inorganic biochemistry    November 1, 1989   Volume 37, Issue 3 185-191 doi: 10.1016/0162-0134(89)80041-8
Desmet J, Van Dael H, Van Cauwelaert F, Nitta K, Sugai S.The enthalpy change of the binding of Ca2+ and Mn2+ to equine lysozyme was measured at 25 degrees C and pH 7.5 by batch microcalorimetry: delta H degrees Ca2+ = -76 +/- 5 kJ mol-1, delta H degrees Mn2+ = -21 +/- 10 kJ mol-1. Binding constants, log KCa2+ = 6.5 +/- 0.2 and log KMn2+ = 4.1 +/- 0.5, were calculated from the calorimetric data. Therefore, delta S degrees Ca2+ = -131 +/- 20 JK-1 mol-1 and delta S degrees Mn2+ = 8 +/- 44 JK-1 mol-1. Removal of Ca2+ induces small but significant changes in the circular dichroism spectrum, indicating the existence of a partially unfolded apo-conformatio...
Determination of leucine enkephalin and methionine enkephalin in equine cerebrospinal fluid by microbore high-performance liquid chromatography and capillary zone electrophoresis coupled to tandem mass spectrometry.
Journal of chromatography    October 27, 1989   Volume 495 41-59 doi: 10.1016/s0378-4347(00)82608-0
Mück WM, Henion JD.The performance of microbore high-performance liquid chromatography and capillary zone electrophoresis, both equipped with on-line tandem mass spectrometric detection capability, was evaluated critically for the determination of endogenous amounts of leucine enkephalin and methionine enkephalin in equine cerebrospinal fluid. Using an identical sample clean-up and enrichment procedure, capillary zone electrophoresis-mass spectrometry is limited in its concentration detection capacity owing to its much smaller injection volume. Leucine enkephalin was identified in post-mortem equine cerebrospina...
Screening of steroids in horse urine and plasma by using electron impact and chemical ionization gas chromatography-mass spectrometry.
Journal of chromatography    October 6, 1989   Volume 479, Issue 2 233-242 doi: 10.1016/s0021-9673(01)83339-2
Singh AK, Gordon B, Hewetson D, Granley K, Ashraf M, Mishra U, Dombrovskis D.Gas chromatography with chemical ionization mass spectrometry and selected-ion monitoring provided a sensitive method for the screening and confirmation of steroids in horse urine and plasma. Chemical ionization mass spectrometry was more sensitive than the electron impact ionization mass spectrometry for most of the steroids except for testosterone, prednisone-metabolite-2 and prednisolone-metabolite-2. The chromatographic conditions used in this study provided clean separation of different natural and synthetic steroids. Approximately 75-85% of the steroids added to plasma and approximately ...
A dot-immunobinding assay for the detection of antibody to Getah virus in horses.
Australian veterinary journal    October 1, 1989   Volume 66, Issue 10 340-341 doi: 10.1111/j.1751-0813.1989.tb09724.x
Sugiura Y, Ohta C, Goto H.No abstract available
Difference in content ratio of components among horse serum transferrin variants.
Nihon juigaku zasshi. The Japanese journal of veterinary science    October 1, 1989   Volume 51, Issue 5 969-974 doi: 10.1292/jvms1939.51.969
Watanabe K, Sohara T, Takeda M, Ueno K, Suzumura N, Rokurouda Y, Rokurouda I, Yamamoto S.Each of five genetic variants of horse serum transferrin (Tf), D, F, H, O, and R, was separated into two bands by polyacrylamide gel isoelectric focusing (PAGIEF). The more acidic band, termed component a, was more abundant than the other one, termed component b, in all variants. Components a and b of TFO variant were immunologically indistinguishable from each other by double immunodiffusion test. Determination of the content ratio of component a to component b in each variant revealed that the variants were classified into two groups: one group (D, F, and H) had a relatively high ratio withi...
Urinary eCG patterns in the mare during pregnancy.
Theriogenology    October 1, 1989   Volume 32, Issue 4 607-622 doi: 10.1016/0093-691x(89)90282-3
Roser JF, Lofstedt RM.Blood and urine samples collected from 12 mares at frequent intervals from 25 to 210 d of pregnancy were analyzed for equine chorionic gonadotropin (eCG). Blood and urine samples were collected daily through two consecutive ovulatory periods from five cyclic mares for comparative purposes. Separate radioimmunoassays (RIA) were developed to detect eCG in the urine and plasma. A simple and quick commercial dipstick enzyme-linked immunospecific assay (ELISA), developed for eCG in the blood, was also utilized in this study to detect eCG in the urine. In the 12 pregnant mares, eCG concentrations in...
Isolation and characterization of equine microvascular endothelial cells in vitro.
American journal of veterinary research    October 1, 1989   Volume 50, Issue 10 1800-1805 
Bochsler PN, Slauson DO, Chandler SK, Suyemoto MM.The use of cultured tissue has not yet become widespread in research involving equine disease, and this may be attributable in part to the scarcity of published reports concerning tissue culture methods for this species. We report here the isolation of equine microvascular endothelium (EMVE) from fresh omental tissue of horses and ponies. Fresh donor tissue was minced, subjected to collagenase digestion, and filtered. Cells were layered on 5% bovine serum albumin for gravity sedimentation, the bottom layer was collected, and the cells were plated onto fibronectin-coated flasks. Medium consiste...
Histochemistry of complex carbohydrates in the horse duodenal gland.
Nihon juigaku zasshi. The Japanese journal of veterinary science    October 1, 1989   Volume 51, Issue 5 909-915 doi: 10.1292/jvms1939.51.909
Takehana K, Abe M, Iwasa K, Hiraga T.Complex carbohydrates were examined in glandular cells of the horse duodenal gland by using lectin histochemical techniques. In the horse, the duodenal gland was distributed in the area from the uppermost part of the small intestine to a point about 6m caudal to the pylorus. It consisted of two types of cells, mucous and serous cells. The former was found in glands distributed almost all over this part, but the latter was present in glands distributed restrictedly to the uppermost part of the small intestine at a point about 10 cm caudal to the pylorus. The cytoplasm of the mucous cell contain...
A retrospective study of nineteen ataxic horses.
The Canadian veterinary journal = La revue veterinaire canadienne    October 1, 1989   Volume 30, Issue 10 802-806 
Nappert G, Vrins A, Breton L, Beauregard M.A retrospective study of 19 ataxic horses admitted to the College of Veterinary Medicine of the University of Montreal during the period of January 1985 to December 1988 is presented. There were 11 cases of cervical vertebral malformation, four of equine degenerative myeloencephalopathy, two of equine protozoal myeloencephalitis, one each of vertebral osteomyelitis and intervertebral disc protrusion. The clinical diagnosis of ataxia in horses requires neurological, radiographic, myelographic, and laboratory examinations.
Epithelium- and mucosa-dependent relaxation and contraction of normal equine trachealis muscle in vitro.
American journal of veterinary research    October 1, 1989   Volume 50, Issue 10 1720-1724 
Olson LE, Perkowski SZ, Mason DE, Muir WW.Strips of trachealis muscle were dissected from the mid-cervical portion of the trachea from horses that were free of respiratory tract disease. The epithelium and mucosa were removed from one group of tissues and were left intact in a second group of tissues. Each tissue was suspended in a bath filled with Krebs-bicarbonate solution that was aerated with 5% CO2 in oxygen and maintained at 37 degrees C. Isometric tension was continuously recorded. The contractile response to square-wave electrical stimulations increased as frequency (3, 5, 10, 15, 20, 25, and 30 Hz), voltage (10, 15, 18, and 2...
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