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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.
Observation on the morphology of contagious equine metritis bacterial colonies isolated from infected pony mares.
American journal of veterinary research    May 1, 1982   Volume 43, Issue 5 796-800 
Sahu SP, Wool S, Breese SS.In uterine or cervical specimens obtained from pony mares infected with streptomycin-resistant contagious equine metritis bacteria, several colonies of the bacteria which differed in morphologic characteristics were recognized during their primary isolation on Eugon chocolate agar and tryptose chocolate agar plates. The differences were usually not observed until plates were incubated 10 to 15 days. On Eugon chocolate agar plates, smooth colony, sandy colony with rings, and colony with blebs were recognized. On tryptose chocolate agar plates, only a round smooth convex colony was observed. By ...
Isolation of a retrovirus from cultured equine sarcoid tumor cells.
American journal of veterinary research    May 1, 1982   Volume 43, Issue 5 804-806 
Cheevers WP, Roberson SM, Brassfield AL, Davis WC, Crawford TB.A virus with the morphologic and biochemical properties of the family Retroviridae has been isolated from cultured cells explanted from a malignant tumor induced by intradermal inoculation of equine sarcoid cells into a combined immunodeficient Arabian foal. By electron microscopy, intracytoplasmic, extracellular, and budding particles measuring 89 to 120 nm with electron-lucent cores were seen. Virus purified from the medium of cultured cells had a buoyant density of 1.15 g/cm3 in isopycnic sucrose-gradient centrifugation, incorporated radiolabeled uridine but not thymidine, and had constitut...
Epidemiological significance of Venezuelan equine encephalomyelitis virus in vitro markers.
The American journal of tropical medicine and hygiene    May 1, 1982   Volume 31, Issue 3 Pt 1 561-568 doi: 10.4269/ajtmh.1982.31.561
Martin DH, Dietz WH, Alvaerez O, Johnson KM.One hundred and fifty-eight strains of Venezuelan equine encephalomyelitis virus were typed antigenically and classified epidemiologically as either epizootic or enzootic. Plaque sizes for 148 of these strains were determined, and the pH requirements for hemagglutination (HA) of goose erythrocytes of 131 were studied. Only antigenic variant group IABC strains could be classified epidemiologically as epizootic. In vitro these strains were characterized by the formation of small plaques in Vero cells and a relatively narrow pH range for optimum HA reactivity. Experimental studies in horses confi...
Monoclonal antibodies against transferrin. Precipitating mixtures and lack of inter-species cross-reactivity.
Immunology letters    May 1, 1982   Volume 4, Issue 5 231-235 doi: 10.1016/0165-2478(82)90043-8
Bártek J, Viklický V, Franĕk F, Angelisová P, Dráber P, Jarosíková T, Nĕmec M, Verlová H.Five stable hybridoma lines were prepared using the myeloma cell line P3-X63-Ag.653 and spleen cells of mice hyperimmunized by pig transferrin. All hybridomas grew well in mouse peritoneal cavity and produced antibodies of the IgG1 subclass. Antibody preparations obtained from ascitic fluids tested for their capacity of antigen precipitation. No precipitation was obtained with single antibodies and with pairs of antibodies. Three out of 10 possible triads gave clear and sharp precipitation zones and rings in immunodiffusion tests performed in agar gel. All 5 antibodies were shown by quantitati...
Energy metabolism of the contagious equine metritis bacterium.
Infection and immunity    May 1, 1982   Volume 36, Issue 2 531-534 doi: 10.1128/iai.36.2.531-534.1982
Lindmark DG, Jarroll EL, Timoney PJ, Shin SJ.The energy metabolism of the English E-CMO strain of contagious equine metritis bacterium was studied in whole cells and cell extracts. This bacterium appears to have an active Krebs cycle and probably obtains energy by oxidative phosphorylation since glycolysis and the hexose monophosphate pathways appear to be absent. These conclusions are based on the findings that [U-14C]glucose incorporation by this bacterium is below the level of detection, and that respiration is stimulated by Krebs cycle intermediates (i.e., malate, citrate, and succinate), but not by glucose, fructose, maltose, or suc...
Resonance-enhanced Raman identification of a ternary chemical intermediate during the equine liver alcohol dehydrogenase reduction of p-(dimethylamino)benzaldehyde.
Biochemistry    April 27, 1982   Volume 21, Issue 9 2193-2202 doi: 10.1021/bi00538a031
Jagodzinski PW, Funk GF, Peticolas WL.The nature of the binding of aromatic aldehyde and aromatic alcohol substrates to the catalytic zinc of equine liver alcohol dehydrogenase has been studied by using resonance-enhanced Raman spectroscopy. When an excess of both enzyme and coenzyme to substrate is used, a stable ternary chemical intermediate is formed between liver alcohol dehydrogenase and the reduced coenzyme, nicotinamide adenine dinucleotide, and the aldehyde, p-(dimethylamino)benzaldehyde, in the pH range 8.5-0.6. Resonance-enhanced Raman spectra clearly show that this same intermediate is formed between the excess enzyme, ...
The conformational transition of horse heart porphyrin c.
The Journal of biological chemistry    April 10, 1982   Volume 257, Issue 7 3864-3868 
Brems DN, Liu YC, Stellwagen E.The heme iron of horse heart cytochrome c was selectively removed using anhydrous HF. The product, porphyrin c, exhibits the viscosity, far ultraviolet circular dichroic, and fluorescence properties characteristic for native cytochrome c. However, porphyrin c is more susceptible to denaturation by guanidine hydrochloride and by heat than is the parent cytochrome. All of the conformational parameters of porphyrin c exhibit a common reversible transition centered at 0.95 m guanidine hydrochloride at 23 degrees C and pH 7.0. Guanidine denatured porphyrin c refolds in two kinetic phases having tim...
Effects of extracts of Onchocerca cervicalis from horses on the lytic activity of human, rat, and equine complement.
Clinical immunology and immunopathology    April 1, 1982   Volume 23, Issue 1 113-123 doi: 10.1016/0090-1229(82)90076-9
Coley SC, Leid RW.No abstract available
Pancreatic colipase: crystallographic and biochemical aspects.
European journal of biochemistry    April 1, 1982   Volume 123, Issue 2 347-354 doi: 10.1111/j.1432-1033.1982.tb19774.x
Pierrot M, Astier JP, Astier M, Charles M, Drenth J.A detailed study of the crystallization of hog and horse colipases has been undertaken. Several crystallographic varieties have been obtained and a 0.3-nm resolution structure determination is actually in progress. The sequence of the A form of horse colipase (one methionine) is given. From spectrophotometric experiments and sequence comparisons, the involvement of the aromatic residue in position 52 in the micelle binding site has been demonstrated.
Synthesis and properties of equine beta-melanotropin and its naturally occurring des-Asp analog.
International journal of peptide and protein research    April 1, 1982   Volume 19, Issue 4 327-333 doi: 10.1111/j.1399-3011.1982.tb02611.x
Izdebski J, Yamashiro D, Ng TB, Li CH.No abstract available
Antigenic stimulation of T lymphocytes in chronic nononcogenic retrovirus infection: equine infectious anemia.
Infection and immunity    April 1, 1982   Volume 36, Issue 1 38-46 doi: 10.1128/iai.36.1.38-46.1982
Shively MA, Banks KL, Greenlee A, Klevjer-Anderson P.Equine infectious anemia is a chronic disease of horses caused by a nononcogenic retrovirus. Studies were undertaken to determine the types of cells involved in the in vitro lymphoproliferative response to viral antigens and the dynamics of this reaction. It was observed that reactive lymphocytes were present at unpredictable times in the peripheral blood of infected horses. This reaction was shown to be specific for the interaction of equine infectious anemia virus and T lymphocytes. Enriched B-lymphocyte populations did not divide when exposed to equine infectious anemia virus. Macrophages w...
Phytohaemagglutinin skin testing of Arabian foals in Egypt. A test for detecting immune cell reactivity.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    March 1, 1982   Volume 29, Issue 2 160-163 doi: 10.1111/j.1439-0450.1982.tb01211.x
Khalil AA, Botros BA, Kerkor M, Lotfy O.No abstract available
Retropulsion-propulsion in equine large colon.
American journal of veterinary research    March 1, 1982   Volume 43, Issue 3 390-396 
Sellers AF, Lowe JE, Drost CJ, Rendano VT, Georgi JR, Roberts MC.The circular and longitudinal muscle coats of equine "midcolon" were found to be directly electrically coupled. They appear to act in concert, in healthy animals, as a pacemaker in the area of the large colon pelvic flexure, for retropulsive-propulsive myoelectrical events. The retropulsive events keep the cecum and right ventral and left ventral divisions of the colon filled, imposing a delay time for fermentation of cellulose and for bacterial protein synthesis. Point-to-point involvement of adjacent colon sections was slowed by cooling the intestinal contents with no adverse clinical signs....
Chemotaxis of radiolabeled equine neutrophils.
American journal of veterinary research    March 1, 1982   Volume 43, Issue 3 397-401 
Camp CJ, Leid RW.A method for the isolation of equine neutrophils was developed using metrizamide cushions. A purity of greater than 95% was routinely obtained with greater than 90% viability. These cells were radiolabeled and tested for their chemotactic response in Boyden chambers to zymosan-activated equine serum, the partially purified equine complement component C5a, and formyl-L-methionyl-L-leucyl-L-phenylalanine. The time and ionic requirements for chemotaxis of radiolabeled equine neutrophils were investigated and maximal movement was observed at 2 hours' incubation and 1.0 mM Ca and 0.5 mM Mg. Dinitro...
Purification of horse eosinophil peroxidase.
Biochimica et biophysica acta    February 18, 1982   Volume 701, Issue 2 185-191 doi: 10.1016/0167-4838(82)90112-1
Jörg A, Pasquier JM, Klebanoff SJ.Eosinophil peroxidase (donor: hydrogen-peroxidase oxidoreductase, EC 1.11.1.7) was isolated in a highly purified form (415/280 nm ratio, 1.05) from horse peripheral blood eosinophil. Eosinophil peroxidase was extracted from intact eosinophils (98-100% purity) or isolated eosinophil granules with 0.05 M acetate buffer (pH 4.7)/0.18 M NaCl and purified by chromatography on Sephadex G-200 and carboxymethylcellulose. Final elution was with 0.05 M acetate buffer (pH 4.7)/ 1 M NaCl. Horse eosinophil peroxidase is a strongly basic protein with bacterial properties when combined with H2O2 and iodide, ...
Leukotriene generation by eosinophils.
The Journal of experimental medicine    February 1, 1982   Volume 155, Issue 2 390-402 doi: 10.1084/jem.155.2.390
Jörg A, Henderson WR, Murphy RC, Klebanoff SJ.Horse eosinophils purified to greater than 98% generated slow reacting substance (SRS) when incubated with the calcium ionophore A23187. On a per cell basis, eosinophils generated four to five times the SRS produced by similarly treated horse neutrophils. Eosinophil SRS production was inhibited by 5,8,11,14-eicosatetraynoic acid and augmented by indomethacin and arachidonic acid, suggesting that it was a product(s) of the lipoxygenase pathway of arachidonic acid metabolism. Compounds with SRS activity were purified by high-pressure liquid chromatography (HPLC) and identified by ultraviolet spe...
Critical concentration of cadmium estimated by studies on horse kidney metallothionein.
Developments in toxicology and environmental science    January 1, 1982   Volume 9 37-46 
Elinder CG, Nordberg M.No abstract available
[Culture of human chorionic villi].
Revista da Faculdade de Farmacia e Odontologia de Ribeirao Preto    January 1, 1982   Volume 19, Issue 1 43-46 
Sala MA, Benedetti WL, Alvarez H.No abstract available
Experiments in the freezing and storage of equine embryos.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 399-403 
Yamamoto Y, Oguri N, Tsutsumi Y, Hachinohe Y.No abstract available
Antibodies to the zona pellucida in mares.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 309-313 
Liu IK, Shivers CA.Cross-reactivity tests indicated that the equine zona pellucida shares common antigen(s) with porcine zona. Porcine oocytes were therefore used to test for the presence of zona antibodies in the sera of horses. Serum samples were collected from 65 mares infertile for unexplained causes: 7 mares were strongly positive for antibodies reactive to porcine zona pellucida as determined by an indirect immunofluorescence method. Of these 7 mares, aged 8-23 years, 2 were nulliparous and 5 were multiparous. Zona-covered horse oocytes were treated with sera from 4 mares previously identified as zona posi...
The cryo-jaw, a clamp designed for in vitro rheology studies of horse digital flexor tendons.
Journal of biomechanics    January 1, 1982   Volume 15, Issue 8 619-620 doi: 10.1016/0021-9290(82)90073-2
Riemersa DJ, Schamhardt HC.A clamp designed for holding tendons in force/elongation studies is described. No slippage occurred when tensile forces up to 13,800 N were applied to horses digital flexor tendons fixed in this clamp.
Simultaneous isolation and partial characterization of antithrombin III and alpha 1-proteinase inhibitor from horse plasma.
Acta biochimica Polonica    January 1, 1982   Volume 29, Issue 1-2 95-103 
Kurdowska A, Koj A, Jaśkowska M.No abstract available
Purification of horse muscle acylphosphatase antibodies by affinity chromatography.
Physiological chemistry and physics    January 1, 1982   Volume 14, Issue 3 307-311 
Berti A, Liguri G, Stefani M, Nassi P, Ramponi G.Horse muscle acylphosphatase antibodies were obtained by immunizing rabbits with the highly purified antigen cross-linked with glutaraldehyde. Specific antibodies were purified from the immunoglobulin fraction by affinity chromatography using a matrix coupled with the pure antigen as immunoadsorbent. The purified antibodies were partially characterized by immunodiffusion and immunoprecipitin techniques. These antibodies could be used to study aspects of the muscle acylphosphatase structure, localization and other biological properties.
[Purification of alpha-1,4 leads to 1,4-glucosyltransferase from horse blood serum].
Polskie archiwum weterynaryjne    January 1, 1982   Volume 23, Issue 3 65-72 
Kotoński B.The purification of alpha-1,4-1,4-glucosyltransferase from the equine serum is presented. Ion-exchange chromatography on DE-11, DE-32 and CM-32 celluloses was applied in the successive steps of isolation. Gel-filtration on Bio-Gel P-200 was the last step of purification; it gave the protein which was homogeneous on disc polyacrylamide gel electrophoresis. The purification degree was of the order 2100 at about 40% yield.
[Properties of alpha-1,4 leads to -glucosyltransferase from the muscles and blood serum of horses].
Polskie archiwum weterynaryjne    January 1, 1982   Volume 23, Issue 3 73-85 
Dzongowska-Dzongu T, Kotoński B, Hutny J.Alpha-1,4 leads to 1,4-glucosyltransferase preparations from horse muscles and serum were studied. The enzyme proteins from both tissues are very similar. Both proteins have a molecular weight of 240 000 and consist of four subunits of 60 000 daltons each. pH 5,0 is optimal for the activity. Only substrates with alpha-1, 4-linkages can serve as glucosyl donors for transferase reactions. Km values for both enzymes differ very slightly. At low substrate concentrations the hydrolytic activity can be found in addition to transferase reactions. At the concentration of the substrate higher than 40 m...
Isolation and some properties of equine alpha 1-antitrypsin.
The International journal of biochemistry    January 1, 1982   Volume 14, Issue 4 327-334 doi: 10.1016/0020-711x(82)90094-5
Laegreid WW, Breeze RG, Counts DF.1. Equine alpha 1-antitrypsin was isolated from horse plasma by a combination of ammonium sulfate and acidification precipitation followed by ion-exchange chromatography on DEAE-cellulose, molecular sieve chromatography on Sephadex G-200 and affinity chromatography on Cibacron Blue-agarose. 2. The purified protein showed a single precipitin arc on immunoelectrophoresis in agarose but gave two bands on discontinuous polyacrylamide gel electrophoresis (PAGE). 3. Both bands appeared to interact equally with trypsin and were thought to represent two isoinhibitors of equine alpha 1-AT.
Some aspects of equine embryo transfer.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 405-408 
Douglas RH.The number of successful embryo recoveries was 56.0% in experimental mares with no history of breeding problems but in barren mares only 34.3% of embryo recovery attempts were successful. When a recovery attempt was successful, the incidence of twin embryos was 10.7% in experimental mares and 16.7% in barren mares. Maintenance of embryos in vitro for greater than 6 h before non-surgical transfer significantly reduced pregnancy rates compared to maintenance for less than 3 h. The pregnancy rate in recipients at 100 days after ovulation was lower (P less than 0.05) than those at 24 and 30 days a...
Effects of adenosine and deoxyadenosine on PHA-stimulation of lymphocytes of man, horse and pig.
The International journal of biochemistry    January 1, 1982   Volume 14, Issue 5 377-385 doi: 10.1016/0020-711x(82)90023-4
Peters GJ, Oosterhof A, Veerkamp JH.1. Adenosine inhibits thymidine and uridine incorporation of PHA-stimulated lymphocytes of man and horse at concentrations higher than 50 and 10 microM, respectively. Deoxyadenosine is inhibitory at concentrations higher than 100 microM. Thymidine and uridine incorporation of porcine lymphocytes are elevated 5-7-fold by 25-100 microM adenosine, deoxyadenosine, inosine and hypoxanthine. Leucine incorporation of PHA-stimulated lymphocytes was affected by adenosine and deoxyadenosine in the same way, but to a lower extent. 2. Effects of adenosine and deoxyadenosine were more pronounced at shorter...
Radioimmunoassay and in-vitro bioassay of serum LH throughout the equine oestrous cycle.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 253-260 
Alexander S, Irvine CH.Mares were bled once daily throughout a cycle, or 3 times daily from the first day of oestrus to the 2nd day after ovulation. LH was measured by heterologous radioimmunoassay and by an in-vitro bioassay based on LH-stimulated testosterone production by mouse Leydig cells. The patterns of bio- and immuno-active LH during the oestrous cycle were similar but not identical, so that in both groups of mares the ratio of biological: immunological (B:I) activity during the LH surge was significantly higher before than after ovulation (P less than 0 . 001). Considerable individual variation in cycle me...
Effect of pregnancy and collection technique on prostaglandin F in the uterine lumen of Pony mares.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 335-341 
Berglund LA, Sharp DC, Vernon MW, Thatcher WW.Uterine flushings were obtained through the cervix (Method A) and through the wall of the uterus after hysterectomy (Method B) of ovariectomized Pony mares after s.c. injection of oestrogen for 1 week and progesterone for 2 weeks (Exp. 1). Non-pregnant and pregnant mares were flushed by Method A on Day 14 after ovulation and the flushings compared with those of non-pregnant mares injected i.v. with flunixen meglumine, a prostaglandin synthetase inhibitor, shortly before flushing (Exp. 3). Uterine flushings were also collected by Methods A and B from non-pregnant and pregnant Pony mares on Day ...