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Topic:In Vitro Research

In vitro research involving horses refers to the study of equine cells, tissues, or biological molecules outside their normal biological context, typically in controlled laboratory environments. This research approach allows scientists to investigate cellular processes, molecular interactions, and the effects of various treatments without the ethical and logistical complexities of in vivo studies. In vitro studies contribute to understanding equine physiology, pathology, and pharmacology by providing insights into cellular responses to pathogens, drugs, and other stimuli. This page compiles peer-reviewed research studies and scholarly articles that explore various in vitro methodologies and their applications in equine science, including cell culture techniques, molecular assays, and drug efficacy testing.
Detection of proviral DNA in horse cells infected with equine infectious anemia virus.
Journal of virology    June 1, 1978   Volume 26, Issue 3 577-583 doi: 10.1128/JVI.26.3.577-583.1978
Rice NR, Simek S, Ryder OA, Coggins L.Equine infectious anemia virus (EIAV) recently has been shown to possess a high-molecular-weight RNA genome and a virion reverse transcriptase. We completed the demonstration that EIAV is a retrovirus by showing the presence of proviral DNA in equine cells infected in vitro, but not in normal horse DNA. These studies were performed by using a highly representative cDNA probe synthesized by the virion polymerase. It was found that this cDNA reassociated extensively, and with high thermal stability, with either viral RNA or DNA extracted from infected cells, but showed no detectable reassociatio...
A non-phosphate-buffered physiological saline for in vitro electrophysiological studies on the mammalian neuromuscular junction [proceedings].
The Journal of physiology    May 1, 1978   Volume 278 8P-9P 
Rees D.No abstract available
Measurement of neutralizing antibody to equid herpesvirus 1 by single radial hemolysis.
Journal of clinical microbiology    May 1, 1978   Volume 7, Issue 5 495-496 doi: 10.1128/jcm.7.5.495-496.1978
Klingeborn B, Dinter Z.Antibody to equid herpesvirus 1, which mediates single radial hemolysis, is that responsible for neutralization. Hemagglutination inhibition antibody is not necessarily involved in neutralization or hemolysis.
[Effectiveness of coumaphos against chorioptes bovis in a horse with foot-mange (author’s transl)].
Tijdschrift voor diergeneeskunde    April 1, 1978   Volume 103, Issue 7 377-380 
Boersema JH.A horse with foot-mange failed to recover following a number of courses of treatment with coumaphos. Mites isolated from this horse were tested in vitro for their sensitivity to coumaphos and lindane. The mites were resistant to coumaphos and sensitive to lindane. Following treatment with lindane, the horse recovered within four weeks.
A laboratory system for production of flexion rates and forces in the forelimb of the horse.
American journal of veterinary research    March 1, 1978   Volume 39, Issue 3 365-369 
Kingsbury HB, Quddus MA, Rooney JR, Geary JE.The distal portion of the forelimb of the horse is provided with a stay apparatus composed of tendons, ligaments, and fascia. This stay apparatus provides the major resistance to joint flexion during the support phase of the stride. The laboratory test system described was shown to be able to reproduce in vitro limb motions and hoof forces measured with a running horse. These results indicated the stay apparatus operates in a largely passive mode, active muscle contraction apparently serving to provide rigidity only early in the support phase of the stride. The testing system described was des...
In vitro and in vivo effects of corticosteroids on peripheral blood lymphocytes from ponies.
American journal of veterinary research    March 1, 1978   Volume 39, Issue 3 393-398 
Magnuson NS, McGuire TC, Banks KL, Perryman LE.The in vitro and in vivo effects of corticosteroids on peripheral blood lymphocytes (PBL) from ponies were studied. Prednisolone inhibited lymphocyte stimulation by phytohemagglutin (PHA) in a dose-dependent manner, without inducing lysis even at large doses. The PBL from horses heterozygous for the combined immunodeficiency trait responded to corticosteroid treatment the same as did PBL from normal ponies. Removal of the corticosteroid after incubation with PBL from normal ponies partially restored responsiveness of these cells to PHA. Chronic in vivo treatment of ponies with corticosteroids ...
Microculture method for mixed lymphocyte cultures in the horse.
American journal of veterinary research    February 1, 1978   Volume 39, Issue 2 337-339 
McClure JJ, Muscoplat CC, Johnson DW, Senogles DR.A miniaturized method for the mixed lymphocyte culture test in the horse is described. The test is performed in either round- or flat-bottom microtitration tissue culture plates. Concentrations of responsing and stimulating cells are varied, depening on the experiment. Significant discrimination between isogeneic and allogenic mixtures is possible after 120 hours' culture when cells are labeled ([3H]thymidine) for the last 16 to 18 hours of the test.
Production of Venezuelan equine encephalitis virus in cells grown on artificial capillaries.
Applied and environmental microbiology    February 1, 1978   Volume 35, Issue 2 431-434 doi: 10.1128/aem.35.2.431-434.1978
Johnson AD, Eddy GA, Gangemi JD, Ramsburg HH, Metzger JF.Primary cell cultures, a continuous cell line, and a diploid cell line were grown on an artificial capillary system. The cells were subsequently infected with Venezuelan equine encephalitis virus, and viral replication was studied. Extracellular fluids harvested from this system contained high titers of virus and were relatively free of cell debris.
Circular dichroic properties and conformation of thionicotinamide dinucleotides bound to horse-liver alcohol dehydrogenase.
European journal of biochemistry    February 1, 1978   Volume 83, Issue 2 593-599 doi: 10.1111/j.1432-1033.1978.tb12128.x
Joppich-Kuhn R, Luisi PL.The interaction between horse liver alcohol dehydrogenase and the oxidized and reduced forms of the 3-thionicotinamide--adenine dinucleotide coenzyme analogues (sNAD and sNADH) has been investigated by ultraviolet absorption, fluorescence and circular dichroism. The fluorescence of sNADH is enhanced when bound to the enzyme, and the protein fluorescence is quenched by both sNADH (60--65%) and sNAD (65%). The possible origin of the larger quenching produced by sNAD with respect to that of NAD is discussed. Coenzyme dissociation constants have been determined by monitoring the quenching of the p...
Stability of horse muscle acylphosphatase to heat and to urea.
Physiological chemistry and physics    January 1, 1978   Volume 10, Issue 2 153-162 
Berti A, Stefani M, Camici G, Manao G, Ramponi G.The thermal stability of horse muscle acylphosphatase was investigated by measuring the inactivation constants at various pH and temperature values, and by differential spectra technique. This enzyme has high thermal stability in an acidic environment but is inactivated in an alkaline medium. It was found that the enzyme can be protected against such inactivation at pH 8.0 by increasing its concentration and the ionic strength of the solution. The effect of high urea concentrations on stability was also measured. It was found that spectral changes at 230 nm are related to urea inactivation of ...
Synthetic antigens. Horse “natural” antibodies against interpolymer of styrene and maleic acid (PSM).
Archivum immunologiae et therapiae experimentalis    January 1, 1978   Volume 26, Issue 1-6 67-71 
Ugorski M, Mikulska J, Skibiński G, Wieczorek Z, Lisowski J.Properties of horse natural anti-PSM antibodies are described. The antibodies were of IgG class. Electrostatic forces were mainly involved in reaction of PSM with horse antibodies. The reaction was inhibited by low molecular compounds resembling structural unit of PSM. Studies of difference spectra and ORD and CD spectra showed no major conformational changes in horse antibodies after reaction with PSM.
Stability and kinetic behavior of carboxymethylated horse muscle acylphosphatase.
Physiological chemistry and physics    January 1, 1978   Volume 10, Issue 4 367-373 
Stefani M, Berti A, Camici G, Manao G, Cappugi G, Ramponi G.Horse muscle acylphosphatase consists of a main chain S-S bound to glutathione. It was found that removal of the glutathione by reduction and successive carboxymethylation of the only cysteine of the main chain affects the stability of the enzyme, mainly with respect to thermal inactivation. On the other hand, the kinetic properties of the enzyme are affected very little.
Enzymes in organic synthesis. Influence of substrate structure on rates of horse liver alcohol dehydrogenase-catalysed oxidoreductions.
Journal of the Chemical Society. Perkin transactions 1    January 1, 1978   Volume 12 1636-1642 doi: 10.1039/p19780001636
Irwin AJ, Lok KP, Huang KW, Jones JB.No abstract available
Horse pancreatic colipase: isolation by a detergent method and amino terminal sequence of the polypeptide chain.
Biochimie    January 1, 1978   Volume 60, Issue 1 103-107 doi: 10.1016/s0300-9084(78)80207-7
Julien R, Rathelot J, Canioni P, Sarda L, Gregoire J, Rochat H.No abstract available
Sensitivity of contagious equine metritis bacteria to antibiotics: evaluation by in vitro disk method. Rommel F, Dardiri AH, Sahu SP.No abstract available
Isoelectric focusing of horse serum esterase isozymes and detection of new phenotypes.
Animal blood groups and biochemical genetics    January 1, 1978   Volume 9, Issue 4 207-213 doi: 10.1111/j.1365-2052.1978.tb01438.x
Fisher RA, Scott AM.A new method for separating the isozymes of horse serum esterase is described. The improved resolution has enabled us to detect several previously undescribed phenotypes. This method has also been used to detect two different apparently 'silent' alleles.
The mini-pig as a model for penetration of penicillins.
Scandinavian journal of infectious diseases. Supplementum    January 1, 1978   Issue 14 135-142 
Bergan T, Versland I.To be active, antimicrobials must reach the bacteria in the infectious foci in adequate concentrations. Direct measurements of levels in the various foci are difficult to perform, but a number of animal models with artificial extravascular foci have been developed. In many ways, the physiology of pigs resemble that of humans. Consequently, it was thought that pigs might also parallel humans in the handling of penicillins. General pharmacokinetics of ampicillin and flucloxacillin and the penetration of the substances to subcutaneously implanted teflon tistisue chambers were investigated. Ampici...
The ‘normal range’ and precision of phytohaemagglutinin-induced equine lymphocyte transformation in vitro.
Research in veterinary science    January 1, 1978   Volume 24, Issue 1 87-91 
Dixon JB, Allan D, West CR.Data are presented on lymphocyte transformation by phytohaemagglutinin in 20 normal horses. The logarithms of transformation ratios were found to have an approximately normal distribution, giving (for the transformation ratios themselves) a geometric mean of 23.6, a range of 1.92 to 97.3, and an estimated 95 per cent tolerance interval of 1.1 to 488. Analysis of variance on the logarithms of the transformation ratios gave a coefficient of variation of 140 per cent of the transformation ratios themselves for the variation between horses; whereas the coefficient of variation between duplicate sa...
Antigenic relatedness of equine herpes virus types 1 and 3.
Archives of virology    January 1, 1978   Volume 56, Issue 1-2 33-45 doi: 10.1007/BF01317281
Gutekunst DE, Malmquist WA, Becvar CS.Antiserums prepared in specific pathogen free (SPF) ponies were used in direct and indirect immunofluorescence, immunodiffusion, complement fixation and serum neutralization procedures to study the interrelationships of the three types of equine herpes viruses (EHV-1, EHV-2, and EHV-3). Equine cell cultures infected with each type virus fluoresced when stained with homologous conjugated antiserum. In reciprocal tests EHV-1 and EHV-3 cross-fluoresced, but EHV-2 did not cross-fluoresce. Non-infected cell cultures did not fluoresce when stained with the 3 conjugates. EHV-1 and EHV-3 cross-fluores...
The null allele in the horse esterase (Es) system detected by enzyme assay and rocket immunoelectrophoresis in heterozygous animals.
Animal blood groups and biochemical genetics    January 1, 1978   Volume 9, Issue 4 197-205 doi: 10.1111/j.1365-2052.1978.tb01437.x
Kaminski M.The detection of the recessive null allele of horse serum esterase (Es) is possible in heterozygotes Es+/EsO which by starch gel electrophoresis appear like homozygotes Es+/Es+. Two methods are proposed, the titration of enzymatic activity of esterase and the immunochemical titration of esterase as antigen. These methods can be applied to solve the cases of suspect parentage or in population studies.
Special topics in clinical pathology.
The Cornell veterinarian    January 1, 1978   Volume 68 Suppl 7 306-317 
Bentinck-Smith J, Tasker JB.The following topics are discussed in this presentation: A. Recent advances in the use and interpretation and methodology of antibiotic susceptibility testing. B. Improvements in sample submittal to obtain accurate results from your laboratory. C. Staining blood, bone marrow, and cytology specimens in the office laboratory. D. Pathogenesis and differential diagnosis of lipemia. E. Differential diagnosis of abdominal effusions.
Regulation of the synthesis of M protein by sugars, Todd Hewitt broth, and horse serum, in growing cells of Streptococcus pyogenes.
Microbios    January 1, 1978   Volume 21, Issue 85-86 185-212 
Pine L, Reeves MW.Various sugars were tested for their effect on the differential rate of synthesis of M protein during the growth of Streptococcus pyogenes strain 0055 M12T12. In a semisynthetic medium alone, a high rate of M protein synthesis occurred with glucose as a substrate; decreasing rates of synthesis occurred with sucrose and trehalose, in that order, although the rates of growth were approximately equal with all sugars. A period of derepressed synthesis of M protein occurred in the lag phase of growth and in the stationary period as the substrates were being depleted. Although glucose inhibited the ...
Replication of equine herpesvirus type 1 and type 3: resistance to hydroxyurea and thymidine.
Intervirology    January 1, 1978   Volume 9, Issue 5 276-285 doi: 10.1159/000148945
Allen GP, Cohen JC, Randall CC, O'Callaghan DJ.The replication of equine herpesvirus type 1 (EHV-1) and type 3 (EHV-3) was unimpeded in three different cell types-equine epithelial cells, equine fibroblasts, and mouse fibroblasts-which had been blocked in their capacity to synthesize host DNA by 2.5 mM hydroxyurea (HU) or 2 mM thymidine (TdR). The rate of DNA synthesis in uninfected or equine herpesvirus-infected cells in the presence of HU or TdR was measured by pulse-labeling cell samples with a labeled DNA precursor at different times after infection. DNA synthesis in uninfected cultures was completely inhibited by both compounds. Howev...
[Uterine motility in vitro induced by PGF2alpha in cattle and horses in various stages of pregnancy].
Bollettino della Societa italiana di biologia sperimentale    November 15, 1977   Volume 53, Issue 21 1964-1970 
Minoia P, Mitolo-Chieppa D, Renna G, Lograno M.No abstract available
Lactoperoxidase-catalyzed iodination of horse cytochrome c:monoiodotyrosyl 74 cytochrome c.
The Journal of biological chemistry    November 10, 1977   Volume 252, Issue 21 7743-7751 
Osheroff N, Feinberg BA, Margoliash E, Morrison M.Iodination of horse cytochrome c with the lactoperoxidase-hydrogen peroxide-iodide system results initially in the formation of the monoiodotyrosyl 74 derivative. This singly modified protein was obtained in pure form by ion exchange chromatography and preparative column electrophoresis. It shows an intact 695 nm absorption band, the midpoint potential of the native protein, a nuclear magnetic resonance spectrum which indicates an undisturbed heme crevice structure, a normal reaction with antibodies directed against native horse cytochrome c, and circular dichroic spectra in which the only cha...
A subunit-sized butyrylcholinesterase present in high concentrations in pooled rabbit serum.
The Biochemical journal    November 1, 1977   Volume 167, Issue 2 367-376 doi: 10.1042/bj1670367
Main AR, McKnelly SC, Burgess-Miller SK.A butyrylcholinesterase of mol.wt. approx. 83000 was observed in pooled rabbit serum. The enzyme was named monomeric butyrylcholinesterase to distinguish it from the larger oligomeric butyrylcholinesterase of horse and human serum whose subunits are the same size as the monomeric enzyme. The active-site concentration of monomeric butyrylcholinesterase in the pooled serum was 0.18mum, which is five times the concentration of butyrylcholinesterase in pooled horse serum. This was surprising, since the horse serum is regarded as a rich source of butyrylcholinesterase, whereas rabbit serum is not g...
Circular dichroism of porcine, bovine, and equine pancreatic phospholipases A2 and their zymogens. Unusual conformations simulating helix content.
Biochimica et biophysica acta    October 26, 1977   Volume 494, Issue 2 285-292 doi: 10.1016/0005-2795(77)90157-x
Jirgensons B, de Haas GH.Conformation of porcine, bovine, and equine pancreatic phospholipases A2 (EC 3.1.1.4) and their zymogens was studied by the circular dichroism (CD) probe in the far and near ultraviolet spectral zones. All these phospholipases and their zymogens displayed CD curves suggesting the presence of moderate amounts of α-helical conformation. However, on the basis of known primary structure and recent X-ray structural analysis of prophospholipase A2 crystals (Drenth, J., Enzing, C.M., Kalk, K.H. and Vessies, J.C.A. (1976) Nature 264, 373–377), it has to be concluded that the positive CD band cen...
[Phantoms for the collection of genital secretions in stallions].
DTW. Deutsche tierarztliche Wochenschrift    October 5, 1977   Volume 84, Issue 10 382-385 
Klug E, Brinkhoff D, Flüge A, Scherbarth R, Essich G, Kienzler M.Practical experiences of the phantom method for collection of genital secretions from stallions are reported. Taking a phantom used in the Richard-Götze-Haus Tierärztliche Hochschule Hannover as a prototype two further models slightly modified have been constructed, baring a flat hollow in the right side of the caudal phantom body for manual inserting of the Artificial Vagina. These three models fulfill four important conditions for routine use: (1) sufficient sexual attractivity for the stallions; 80-85% successful collections of presecretions out of a total of 1050 using the dummy and 70% ...
[Dilution of stallion sperm].
Veterinariia    October 1, 1977   Issue 10 86-88 
Naumenkov AI, Roman'kova NK.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.