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.
Cytochemical staining of equine blood and bone marrow cells.
Equine veterinary journal    October 1, 1977   Volume 9, Issue 4 205-207 doi: 10.1111/j.2042-3306.1977.tb04032.x
Tschudi P, Archer RK, Gerber H.No abstract available
Analysis of normal equine serum using the SMA 12/60 Autoanalyzer.
Veterinary medicine, small animal clinician : VM, SAC    October 1, 1977   Volume 72, Issue 10 1629-1633 
Porter T, McCashin FB.No abstract available
Nucleolar fragmentation in cells infected with alphaviruses (39886).
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)    October 1, 1977   Volume 156, Issue 1 109-112 doi: 10.3181/00379727-156-39886
Stanton GJ, Osborne LC, Albrecht TB.No abstract available
Semisynthetic cytochrome c.
Proceedings of the National Academy of Sciences of the United States of America    October 1, 1977   Volume 74, Issue 10 4248-4250 doi: 10.1073/pnas.74.10.4248
Barstow LE, Young RS, Yakali E, Sharp JJ, O'Brien JC, Berman PW, Harbury HA.Horse heart cytochrome c can be split with cyanogen bromide into a heme peptide (residues 1-65) and a nonheme peptide (residues 66-104). In a process involving (i) complex formation between the two fragments and (ii) restoration of the severed peptide linkage, a fully active cytochrome c preparation can be re-formed. Use has been made of this process to couple the heme peptide to peptide 66-104 synthesized by the Merrifield solid-phase procedure. The semisynthetic product formed in this manner is indistinguishable from reconstituted cytochrome c prepared with nonsynthetic peptide 66-104.
[Fibrinogen level in clinically healthy horses].
Veterinarni medicina    October 1, 1977   Volume 22, Issue 10 605-611 
Dusek J.Various sets of horses were examined in view of the necessity of widening the range of biochemical substances for diagnostic purposes in the field of veterinary medicine. The aim of the investigations was to obtain basic information on fibrinogen level and its variability. The average value stated was 280 mg% s = 89, sx = 12, V% = 32). The fibrinogen level in horses of the pronounced oxidation type was lower than in those with reduced metabolism, the difference being connected with the speed of sedimentation of erythrocytes. Repeated examination of a part of the set of horses (n = 10) on three...
Methods in the evaluation of antiparasitic drugs in the horse.
American journal of veterinary research    October 1, 1977   Volume 38, Issue 10 1581-1586 
Drudge JH, Lyons ET.The critical test is the primary method used for the efficacy evaluation of drugs against the major internal parasites (bots, ascarids, large strongyles, small strongyles, and pinworms) of the horse. The critical test determines: (1) spectrum of activity, (2) effectiveness of removal, (3) pattern of discharge, and (4) physical condition of each species of these parasites. General characteristics of the major parasitisms of the horse are discussed briefly. Criteria of the critical test also are considered including: (1) number of tests, (2) strain variation and drug resistance, (3) selection of...
Chromatographic separations of alphavirus strains by hydroxylapatite.
Journal of clinical microbiology    September 1, 1977   Volume 6, Issue 3 238-243 doi: 10.1128/jcm.6.3.238-243.1977
Jahrling PB, Beall JL.Hydroxylapatite column chromatography methods were developed to characterize selected alphavirus populations. Different conditions of pH and phosphate molarity were required to obtain satisfactory elution profiles and separations for Western equine encephalomyelitis virus strains, compared with Eastern equine encephalomyelitis virus and Semliki Forest virus strains. Raising the pH of the buffers effected earlier elutions of all viruses. Selection of phosphate gradients with more gentle slopes and adjustment to the proper pH effected better separations of virus subpopulations. Elution profiles ...
Effects of storage on the methaemoglobin content of equine blood.
Research in veterinary science    September 1, 1977   Volume 23, Issue 2 241-243 
Dixon PM, Brown R.Equine blood containing different levels of methaemoglobin was stored under varying conditions and the methaemoglobin content was monitored during the storage period. Only under aerobic storage at 4 degrees C did the methaemoglobin content of all samples appear to remain stable.
Practical methods of determining serum immunoglobulin M and immunoglobulin G concentrations in foals.
Journal of the American Veterinary Medical Association    September 1, 1977   Volume 171, Issue 5 455-458 
Buening GM, Perryman LE, McGuire TC.Serum concentrations of immunoglobulin M (IgM) and immunoglobulin G (IgG) can be determined in the horse with a satisfactory degree of accuracy, using commercially available reagents. Selected lots of anti-human IgM can be used in precipitation tests to detect and quantitate equine IgM. Commercially available anti-equine IgG tended to overestimate the amount of IgG in single radial immunodiffusion tests. Even with these limitations, commercial reagents can be used to differentiate immunodeficiency disorders of foals, including combined immunodeficiency and failure of passive transfer of colost...
Inhibition of the growth of some strains of Mycoplasma mycoides subsp mycoides by the blood of certain horses.
Research in veterinary science    September 1, 1977   Volume 23, Issue 2 252-254 
Dyson DA, Smith GR.When incorporated in solid medium at a concentration of 15 per cent, the defibrinated blood of certain horses strongly suppressed the growth of some, but not all, strains of Mycoplasma mycoides subsp mycoides so that many colonies failed to develop to a visible size. Blood from a single rabbit was tested and found to exert a similar effect. There was striking variation in the degree of inhibition produced by different samples of horse blood and, of five strains of the organism examined, the T1 vaccine strain was the most susceptible. The results suggested that the effect was not due to antibod...
The structure of horse methaemoglobin at 2-0 A resolution.
Journal of molecular biology    August 15, 1977   Volume 114, Issue 3 385-414 doi: 10.1016/0022-2836(77)90256-x
Ladner RC, Heidner EJ, Perutz MF.No abstract available
(Mg2+ + K+)-dependent inhibition of NaK-ATPase due to a contaminant in equine muscle ATP.
Biochemical and biophysical research communications    August 8, 1977   Volume 77, Issue 3 1024-1029 doi: 10.1016/s0006-291x(77)80080-6
Hudgins PM, Bond GH.No abstract available
The oxidation of ferrocytochrome c in nonbinding buffer.
Canadian journal of biochemistry    August 1, 1977   Volume 55, Issue 8 796-803 doi: 10.1139/o77-118
Peterman BF, Morton RA.The apparent equilibrium constant and rate of oxidation was investigated for the reaction of cytochrome c with iron hexacyanide. It was found that if horse heart ferricytochrome c was exposed to ferricyanide (to oxidize traces of reduced protein) the cytochrome subsequently, even after extensive dialysis, had an apparent equilibrium constant different from that of electrodialyzed protein. The effect of ferricyanide ion apparently cannot be removed by ordinary dialysis. The ionic strength dependence of the apparent equilibrium constant and bimolecular oxidation rate constant was measured in the...
Electron-transfer protein reactivities. Kinetic studies of the oxidation of horse heart cytochrome c, Chromatium vinosum high potential iron-sulfur protein, Pseudomonas aeruginosa azurin, bean plastocyanin, and Rhus vernicifera stellacyanin by pentaamminepyridineruthenium(III).
Journal of the American Chemical Society    July 20, 1977   Volume 99, Issue 15 5158-5167 doi: 10.1021/ja00457a042
Cummins D, Gray HB.No abstract available
Studies on the antigenicity of an inactivated, aluminum hydroxide adjuvant equine influenza vaccine. Kucera CJ, Beckenhauer WH.An inactivated, aluminum hydroxide adjuvant equine influenza vaccine was tested in horses and guinea pigs to determine the levels of antigen that would elicit maximum serological responses. Vaccine containing serial twofold increments of A/Equi-1/Prague and A/Equi-2/Miami strains of equine influenza virus was administered to random groupings of both types of test animals. The hemagglutination inhibition antibody response for each group was then measured. Results in horses and guinea pigs were compared to determine if the equine serological values could be related to a potency test in laborator...
Lactic acid concentration in peritoneal fluid of normal and diseased horses.
Research in veterinary science    July 1, 1977   Volume 23, Issue 1 117-118 
Moore JN, Traver DS, Turner MF, White FJ, Huesgen JG, Butera TS.Peritoneal fluid from each of 15 clinically healthy horses and five horses with acute abdominal disease was evaluated for lactic acid concentration. The normal range was 2-7--13-4 mg/dl. Simultaneous blood and peritoneal fluid samples from healthy horses revealed consistently lower lactic acid concentrations in the peritoneal fluid than in the blood, whereas peritoneal fluid lactic acid levels were consistently greater than blood levels in the diseased horses. The diseased horses had highly significant (P less than 0-005) increases in both blood and peritoneal fluid lactic acid concentrations ...
Direct radioimmunoassay of progesterone in mare plasma.
Steroids    July 1, 1977   Volume 30, Issue 1 33-39 doi: 10.1016/0039-128x(77)90134-9
Mathieu HP, Mathieu-Nast C, Vrignaud C.A rapid and low cost radioimmunologic procedure for progesterone assay in mare plasma is proposed. Radioimmunoassay is performed directly on 10 microliter of unextracted plasma. Free progesterone is adsorbed on dextran-charcoal, then the aqueous phase is decanted and extracted by 1 ml of scintillation fluid. Counting is performed directly on this two-phase system. Results are comparable to those obtained with radioimmunoassays using extracted plasma.
Bovine reaginic antibody III. Cross-reaction of antihuman IgE and antibovine reaginic immunoglobulin antisera with sera from several species of mammals. Nielsen KH.Using antisera specific for the heavy chain of human IgE and bovine reaginic immunoglobulin, the degree of cross-reaction amongst sera from pig, rat, rabbit, guinea pig, goat, cow, horse, dog, cat and human was tested. Antihuman IgE antiserum gave strong reactions with pig, rabbit, cow, goat and human sera (100% to 15.1%) and weak reactions with rat, guinea pig, horse, dog and cat sera (10.1% to 3.22%). Antibovine reagin antiserum produced a considerable amount of cross-reaction with sera from pig, rat, rabbit, goat, horse and human (43.6% to 20.1%) with limited reactions with guinea pig, dog ...
Analysis of serum proteins and cerebrospinal fluid in clinically normal horses, using agarose electrophoresis.
American journal of veterinary research    July 1, 1977   Volume 38, Issue 7 1089-1092 
Kristensen F, Firth EC.Using agarose as a supporting matrix, electrophoresis was conducted on 50 serum samples and 20 cerebrospinal fluid samples from clinically normal horses (n = 50) of various ages and breeds. The technique was shown to be reliable. A positive correlation between age and gamma-globulin concentration was found in young horses. Features of the electrophoretograms of serum and cerebrospinal fluid samples are discussed, and a nomenclature based on Rf values is proposed.
Electronic and steric factors affecting ligand binding: horse hemoglobins containing 2,4-dimethyldeuteroheme and 2,4-dibromodeuteroheme.
The Journal of biological chemistry    June 25, 1977   Volume 252, Issue 12 4225-4231 
Seybert DW, Moffat K, Gibson QH, Chang CK.Horse globin has been recombined with 2,4-dimethyldeuteroheme and 2,4-dibromodeuteroheme to yield the corresponding reconstituted hemoglobins, and the ligand binding reactions of these reconstituted hemoglobins have been examined in detail. Both hemoglobins exhibit relatively high n values, but 2,4-dimethyldeuterohemoglobin displays a consistently higher oxygen affinity than native hemoglobin, whereas the oxygen affinity of 2,4-dibromodeuterohemoglobin is consistently lower than that of native hemoglobin. The rate constants l’, and 1’4 for the binding of the first and fourth molecules of C...
Application of radioimmunoassay method for detecting 19-nortestosterone (nandrolone) in equine and canine plasma.
The Veterinary record    June 25, 1977   Volume 100, Issue 26 560-562 doi: 10.1136/vr.100.26.560
Jondorf WR, Macdougall DF.No abstract available
Laboratory methods of equine pregnancy diagnosis.
The Veterinary record    June 18, 1977   Volume 100, Issue 25 536 doi: 10.1136/vr.100.25.536-a
Allen WE, Cox JE, Newcombe .No abstract available
On the detectability of anabolic steroids in horse urine [proceedings].
British journal of pharmacology    June 1, 1977   Volume 60, Issue 2 297P-298P 
Jondorf WR, Moss MS.No abstract available
Influence of foetal genotype on the follicle-stimulating hormone:luteinizing hormone ratio of pregnant mare serum gonadotrophin.
The Journal of endocrinology    June 1, 1977   Volume 73, Issue 3 419-425 doi: 10.1677/joe.0.0730419
Stewart F, Allen WR, Moor RM.Rat testicular radioreceptor assays specific for FSH and LH were used to determine the FSH:LH ratio of PMSG produced by horse, donkey, mule and hinny conceptuses. Measurements of FSH and LH activities in PMSG produced both in vivo and in vitro by the four types of conceptuses showed that the genotype of the foetus markedly influences the FSH:LH ratio of PMSG. The FSH:LH ratio of PMSG produced by the horse conceptus was around unity whereas the ratio of PMSG produced by the donkey conceptus was as low as 0-2. Furthermore, the hybrid mule and hinny conceptuses both produced PMSG with an FSH:LH r...
Laboratory methods of equine pregnancy diagnosis.
The Veterinary record    May 7, 1977   Volume 100, Issue 19 396-399 doi: 10.1136/vr.100.19.396
Walker D.Rectal examination is a reliable method of diagnosing pregnancy in the mare. Also, test kits are available for the simple quick detection of pregnant mare serum gonadotrophin. Nevertheless there is a considerable demand by practitioners for an independent laboratory service in equine pregnancy diagnosis, particularly during the gestational phase when placental gonadotrophin is concentrated in the blood. An initial attempt to provide a service by means of the agar gel diffusion test was disappointing and alternatives were sought. The primary requirements for an ideal alternative technique were ...
Equine angiotensin converting enzyme: a zinc metalloenzyme.
Clinical and experimental pharmacology & physiology    May 1, 1977   Volume 4, Issue 3 267-281 doi: 10.1111/j.1440-1681.1977.tb02624.x
Fernley RT.1. Angiotensin I converting enzyme from horse plasma has been extensively purified and shown to be homogeneous by disc-gel electrophoresis. 2. The metal ion involved in the catalytic reaction of the enzyme has been identified for the first time as zinc by atomic absorption spectrometry. 3. A number of other physicochemical properties of the enzyme are described and compared with results obtained by other investigators. The molecular weight was determined by gel filtration to be 113 000 daltons. The pH maximum was found to be 7-4. The chloride activation of the enzyme appears to act by facilita...
New techniques to measure blood cholinesterase activity in domesticated animals.
American journal of veterinary research    May 1, 1977   Volume 38, Issue 5 659-662 
Silvestri R.A macromethod and a semimicromethod were developed to measure erythrocyte acetylcholinesterase activity in cattle, sheep, goats, horses, dogs, and swine, and to measure plasma cholinesterase activity in horses, dogs, and swine. Comparison of the 2 methods with erythrocytes of sheep, cattle, goats, and horses indicated both methods gave similar results. They can be done in a shorter time and are more sensitive than Michel's method. Normal deltapH values per minutes, with standard deviations for blood cholinesterase activity of animals of different ages, sexes, breeds, and species, were: 0.76 +/...
Methods for quantifying mammalian spermatogenesis: a review.
Journal of animal science    May 1, 1977   Volume 44, Issue 5 818-833 doi: 10.2527/jas1977.445818x
Berndtson WE.No abstract available
Electron-microscopic study of the development of an equine adenovirus in cultured fetal equine kidney cells.
Canadian journal of microbiology    May 1, 1977   Volume 23, Issue 5 497-509 doi: 10.1139/m77-074
Shahrabadi MS, Marusyk RG, Crawford TB.Sequential changes induced by an equine adenovirus in cultured fetal equine kidney cells were studied by electron microscopy. The first morphological change was the appearance of type I inclusions. These inclusions developed to type II inclusions which appeared as ring forms. Type III inclusions were formed within the central part of type II inclusions and finally filled up most of the nuclear space. As the infection proceeded, type IV inclusions which appeared as dense dark-staining spheres were formed at the center of the type III inclusions and also inside the cytoplasm. These dark-staining...
Immunoglobulin G subclass [IgG and IgG(T)] interaction with the P26 group specific antigen of equine infectious anemia virus: immunodiffusion and complement-fixation reactions.
American journal of veterinary research    May 1, 1977   Volume 38, Issue 5 655-658 
McGuire TC.Isolated equine immunoglobulin (Ig)G(T) antibodies to equine infectious anemia virus P26 antigen did not precipitate with antigen when the ratio of antibody to antigen was high. However, at lower ratios of antibody to antigen precipitation occurred. In addition, complement-fixation by IgG and P26 antigen was inhibited by high concentrations of IgG(T). The unusual reaction pattern noted with IgG(T) antibodies was still detectable by the immunodiffusion test for equine infectious anemia virus. In situations of nonprecipitability by IgG(T), the adjacent positive control line was inhibited, and th...