Analyze Diet

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.
Comparison of the interaction of equine LH and human chorionic gonadotrophin to equine testicular receptors.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 113-121 
Evans JW, Roser JF, Mikuckis GM.Human chorionic gonadotrophin (hCG) can be used to study horse luteinizing hormone (LH) receptors in stallion testicular tissue. hCG was more stable than horse LH during radioiodination when compared by their abilities to bind to testicular receptor sites. During incubation, neither hormone lost binding activity at 4 degrees C. Horse LH lost binding activity during incubation at 25 degrees C and both hormones lost binding activity at 37 degrees C. Both hormones bound to the same receptor sites which are specific for the hormones. The receptor sites were not degraded when incubated at 4 degrees...
Lymphocyte stimulation response in horses against phytohaemagglutinin and M protein of Streptococcus equi using whole blood.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    January 1, 1982   Volume 46, Issue 1 51-56 
Srivastava SK, Barnum DA.Lymphocyte stimulation was observed in whole equine blood in the presence of phytohaemagglutinin and M protein extracted from a typical strain of Streptococcus equi. Blood samples were collected from several healthy horses and horse and pony foals and cultured in vitro with varying concentrations of phytohaemagglutinin and M protein for several days. Phytohaemagglutinin was found to induce lymphocyte stimulation in these animals. Highest mean stimulation indices in horse foals (49.3 +/- 24.4) and pony foals (54.7 +/- 32.0) were observed with 0.625 and 1.25 micrograms/mL phytohaemagglutinin, re...
Titration of antiserum to South American rattlesnake (Crotalus durissus terrificus) venom by measuring inhibition of phospholipase A2 activity.
Toxicon : official journal of the International Society on Toxinology    January 1, 1982   Volume 20, Issue 3 563-569 doi: 10.1016/0041-0101(82)90050-2
da Silva MH, Bier OG.Horse antiserum to the venom of Crotalus durissus terrificus, A South American rattlesnake, inhibits the phospholipase activity of the crude venom. There is a close relationship between this inhibitory property and the neutralizing potency of the antiserum in vivo. This may provide the basis for a rigorous standardization of anticrotalid venom in vitro.
Influence of bacterial products on the motility of stallion spermatozoa.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 35-40 
Rideout MI, Burns SJ, Simpson RB.Sterile filtrates were prepared from equine isolates of Klebsiella pneumoniae (genitalium), Proteus mirabilis, Pseudomonas aeruginosa, Escherichia coli, Streptococcus zooepidemicus, Streptococcus equisimilis, Actinobacillus equuli, and Corynebacterium equi and mixed individually with extended stallion semen. When diluted in the extended semen the filtrates represented bacterial populations of 0.5 x 10(6), 1 x 10(6), 2 x 10(6) and 4 x 10(6) cells/ml. pH values were recorded for each filtrate. Specimens were monitored for percentage motile spermatozoa at 30-min intervals until they reached 10% o...
The interaction of Corynebacterium equi and equine alveolar macrophages in vitro.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 491-496 
Zink MC, Johnson JA, Prescot JF, Pascoe PJ.The in-vitro interaction of Corynebacterium equi and foal alveolar macrophages was examined qualitatively and quantitatively using cells collected by sequential bronchoalveolar lavage at 2-week intervals from birth until 14 weeks of age. Total and differential counts were performed on the recovered cells. Macrophages were identified using the non-specific esterase strain. Cultures of the alveolar macrophages were challenged with C. equi suspensions and the process and extent of ingestion was examined by light and electron microscopy. Few macrophages were recovered from the lungs of foals less ...
Preliminary characterization of equine interferons and their antiviral activities on bovine, ovine, and human cells.
Journal of interferon research    January 1, 1982   Volume 2, Issue 3 363-370 doi: 10.1089/jir.1982.2.363
Yilma T, McGuire TC, Perryman LE.Equine dermal cells induced with poly I:C + DEAE-dextran produced low levels of interferon tentatively classified as equine interferon beta (EqIFN-beta). In contrast, dermal cells initially primed with EqIFN-beta and then superinduced with poly I:C + DEAE-dextran in the presence of cycloheximide and actinomycin D produced greater than 100-fold EqIFN-beta. Equine blood mononuclear cells induced with Newcastle disease virus and phytohemagglutinin produced high levels of interferons tentatively classified as equine interferon alpha (EqIFN-alpha) and equine interferon gamma (EqIFN-gamma), respecti...
Immune recognition of Echinococcus granulosus. 1. Parasite-activated, primary transformation by normal murine lymph node cells.
Parasite immunology    January 1, 1982   Volume 4, Issue 1 33-45 doi: 10.1111/j.1365-3024.1982.tb00418.x
Dixon JB, Jenkins P, Allan D.Culture of murine lymph node cells together with living protoscolices of Echinococcus granulosus is described. The presence of the parasite induced potent blastic transformation in lymphocytes of unimmunized mice as indicated by tritiated thymidine incorporation. The response was markedly reduced by killing the parasite immediately prior to culture. No blastogenic activity was detectable in supernatants from living parasites cultured alone. Protoscolices from artificially infected syngeneic mice were effective stimuli, as were protoscolices from naturally infected horse and sheep. Stimulation ...
Cibacron Blue-induced modification of neutral proteinase from horse blood leukocytes.
Acta biologica et medica Germanica    January 1, 1982   Volume 41, Issue 1 47-52 
Potempa J.The proteolytic activity of the elastase-like proteinase from granules of horse blood leukocytes is retained on a column of Cibacron Blue-Sepharose and can be eluted with 0.5 M KSCN. During this procedure its mol. wt. is reduced from 49000 to 30000 and isoelectric point is shifted towards higher pH. The inactive protein not adsorbed on Cibacron Blue-Sepharose is strongly acidic and shows a mol. wt. of 20000. Upon mixing this protein with the modified enzyme the native proteinase is reconstituted as shown by polyacrylamide gel electrophoresis at pH 8.3 and isoelectric focusing in a sucrose grad...
Inhibition of sperm binding to porcine ova by antibodies to equine zonae pellucidae.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 315-318 
Shivers CA, Liu IK.Sera and follicular fluid from mares previously determined as having antibodies to the zona pellucida were exposed to porcine ovarian oocytes before insemination with boar spermatozoa in vitro. There was a dramatic decline in the number of spermatozoa bound to zonae compared to treatments with sera and follicular fluid from mares negative for zona antibodies. These data suggest that antibodies reactive with the zona pellucida may be responsible for reduced or even complete infertility in some mares. In a group of 50 randomly selected mares tested for antizona antibodies, 2 pregnant mares were ...
Limited trypsinolysis of porcine and equine colipases. Spectroscopic and kinetic studies.
Biochimica et biophysica acta    December 29, 1981   Volume 671, Issue 2 155-163 doi: 10.1016/0005-2795(81)90129-x
Rathelot J, Canioni P, Bosc-Bierne I, Sarda L, Kamoun A, Kaptein R, Cozzone PJ.Porcine and equine colipases have been submitted to mild tryptic digestion. Proteolysis occurs at the Arg5-Gly6 bond with the loss of the N-terminal pentapeptide. Studies of native and trypsin-treated colipases by circular dichroism and laser chemically induced dynamic nuclear polarization indicate that proteolysis induces conformational changes in the region of the tyrosine cluster. Experiments in the presence of phospholipid provide further evidence showing that these residues are in or close to the region of the protein interacting with aggregated lipids. Kinetic studies of the reaction of ...
Babesia equi (Laveran 1901) 1. Development in horses and in lymphocyte culture.
Tropenmedizin und Parasitologie    December 1, 1981   Volume 32, Issue 4 223-227 
Schein E, Rehbein G, Voigt WP, Zweygarth E.The vertebrate development of Babesia equi from infected Hyalomma marginatum in Morocco was investigated in vitro and in vivo. It was demonstrated that the sporozoites of B. equi initiate a phase of exo-erythrocytic schizogony in lymphocytes both in vitro and in vivo. On the other hand, sporozoites did not invade erythrocytes in vitro. The complete vertebrate life cycle of B. equi was simulated in vitro, from the invasion of lymphocytes by sporozoites, to the development of macro- and microschizonts, the invasion of erythrocytes by merozoites, and the subsequent intra-erythrocytic schizogony. ...
Isolation of equine muscle carbonic anhydrase in crystalline form.
Biochemical and biophysical research communications    November 30, 1981   Volume 103, Issue 2 573-580 doi: 10.1016/0006-291x(81)90490-3
Nishita T, Deutsch HF.No abstract available
Collection and cultivation in vitro of equine mammary macrophages.
American journal of veterinary research    November 1, 1981   Volume 42, Issue 11 1956-1958 
Anderson LW, Banks KL.Equine macrophages were obtained from female Shetland ponies by injection of Escherichia coli lipopolysaccharide through the lactiferous ducts of the mammary gland. After 6 to 11 days, balanced salt solution was injected into the mammary gland to wash out accumulated cells. Harvested cells contained a mixture of macrophages, lymphocytes, and neutrophils, with the majority of the cells of mononuclear type. In culture, cells adherent after 24 hours were characterized as macrophages by morphologic features, nonspecific esterase staining, and by the presence of complement and immunoglobulin recept...
Molecular cloning of equine herpesvirus type 1 DNA: analysis of standard and defective viral genomes and viral sequences in oncogenically transformed cells.
Proceedings of the National Academy of Sciences of the United States of America    November 1, 1981   Volume 78, Issue 11 6684-6688 doi: 10.1073/pnas.78.11.6684
Robinson RA, Tucker PW, Dauenhauer SA, O'Callaghan DJ.Genomic DNA sequences of equine herpesvirus type 1 (EHV-1) have been cloned as BamHI and EcoRI restriction fragments into the plasmid pBR322 and propagated in Escherichia coli. With the exception of two EcoRI restriction fragments that reside in the S region of the viral genome, all of the cloned fragments demonstrated the same electrophoretic mobilities, restriction cleavage sites, and blot-hybridization patterns as did the parent fragments produced by BamHI or EcoRI digestion of virion DNA. The EcoRI J fragment and the BamHI E fragment of the L-region terminus were cloned after the addition ...
Circular dichroism study of horse colipase interaction with bile salt.
Biochimica et biophysica acta    October 28, 1981   Volume 670, Issue 3 305-311 doi: 10.1016/0005-2795(81)90101-x
Canioni P, Julien R, Romanetti R, Cozzone P, Sarda L.No abstract available
Primary structure of 3-phosphoglycerate kinase from horse muscle. I. Purification of cyanogen bromide peptides and amino acid sequence of peptide CB5 (104 residues).
The Journal of biological chemistry    October 25, 1981   Volume 256, Issue 20 10284-10292 
Hardy GW, Darbre A, Merrett M.3-Phosphoglycerate kinase was isolated from horse muscle and subjected to the action of cyanogen bromide. The resulting peptides were separated using gel filtration combined with either ion exchange chromatography on phosphocellulose in 6 M urea or high voltage paper electrophoresis. The sequence of the largest peptide, CB5, has been determined by a combination of automated and manual Edman degradation carried out on the intact peptide and derivatives obtained by proteolytic digestion. The isolation of two peptides derived from CB5 by cleavage of the bond between Asp109 and Pro110 facilitated ...
Ineffectiveness of isoniazid against three equine pathogens.
Journal of the American Veterinary Medical Association    October 15, 1981   Volume 179, Issue 8 806-808 
Hietala S, Knight HD.No abstract available
Analysis of the potentiometric titration of reduced horse heart cytochrome c.
Biopolymers    October 1, 1981   Volume 20, Issue 10 2243-2252 doi: 10.1002/bip.1981.360201016
Marini MA, Martin CJ, Forlani L.No abstract available
Effects of cytotoxic drugs on cultured equine cells in vitro.
Equine veterinary journal    October 1, 1981   Volume 13, Issue 4 251-253 doi: 10.1111/j.2042-3306.1981.tb03509.x
Doyle A, Owen LN.Sixteen cytotoxic drugs used in cancer chemotherapy in man were studied for cytopathic effect on equine fibrosarcoma, melanoma and normal equine lung cells in vitro. Three drugs, vincristine, melphalan and methotrexate, produced cytopathic effect
Rat lymphocyte proliferative in vitro response to horse spleen ferritin.
Journal of the Reticuloendothelial Society    September 1, 1981   Volume 30, Issue 3 227-234 
Lause DB, Houston JA, Bockman DE.No abstract available
Effects of in vitro hemolysis on equine serum chemical values.
American journal of veterinary research    September 1, 1981   Volume 42, Issue 9 1519-1522 
Dorner JL, Hoffmann WE, Lock TF.No abstract available
The interaction of equine platelet tropomyosin with skeletal muscle actin.
The Journal of biological chemistry    July 25, 1981   Volume 256, Issue 14 7257-7261 
Côté GP, Smillie LB.Whereas skeletal muscle tropomyosin binds strongly to muscle F-actin in a buffer containing 30 mM KCl and 1-2 mM free Mg2+, equine platelet tropomyosin only binds stoichiometrically (1 tropomyosin molecule per 6 actin monomers) at higher Mg2+ concentrations (7-8 mM free Mg2+). At low free Mg2+ concentrations (1.5 mM) the binding of the platelet protein is only marginally increased by raising the KCl concentration to an optimal value (0.10-0.20 M). This weaker binding can be attributed to the relatively poor head-to-tail polymerization of platelet tropomyosin and its fewer actin-binding sites. ...
Biological functions and receptor binding activities of equine chorionic gonadotrophins.
Journal of reproduction and fertility    July 1, 1981   Volume 62, Issue 2 527-536 doi: 10.1530/jrf.0.0620527
Stewart F, Allen WR.The role of equine chorionic gonadotrophin (CG, formerly termed Pregnant Mare serum Gonadotrophin, PMSG) in maintaining equine pregnancy was investigated by examining the effects of this hormone on the maternal ovaries during early gestation and relating these findings to the receptor binding activities of CG in vitro. Measurement of plasma progestagen profiles in mares and donkeys carrying horse, donkey, mule ( female horse X male donkey) and hinny (female donkey X male horse) conceptuses confirmed that CG induced several secondary ovulations and thus maintained maternal progestagen concentra...
Electron transfer between horse heart and Candida krusei cytochromes c in the free and bound states.
Biochimica et biophysica acta    July 1, 1981   Volume 636, Issue 2 129-135 doi: 10.1016/0005-2728(81)90085-2
Yoshimura T, Sogabe T, Aki K.Electron transfer between horse heart and Candida krusei cytochromes c in the free and phosvitin-bound states was examined by difference spectrum and stopped-flow methods. The difference spectra in the wavelength range of 540-560 nm demonstrated that electrons are exchangeable between the cytochromes c of the two species. The equilibrium constants of the electron transfer reaction for the free and phosvitin-bound forms, estimated from these difference spectra, were close to unity at 20 degrees C in 20 mM Tris-HCl buffer (pH 7.4). The electron transfer rate for free cytochrome c was (2-3).10(4)...
Nucleic acid-protein interactions. Degradation of double-stranded RNA by glycosylated ribonucleases.
Biochimica et biophysica acta    June 26, 1981   Volume 654, Issue 1 77-85 doi: 10.1016/0005-2787(81)90138-6
Carsana A, Furia A, Gallo A, Beintema JJ, Libonati M.1. Extensively glycosylated ribonucleases, like the enzymes from pig and horse pancreas, show a much higher activity on double-stranded RNAs than similarly charged, carbohydrate-free RNAases under stranded assay conditions (relatively high salt concentrations). Glycosylated pig and horse pancreas RNAases also show a larger destabilizing effect on double-stranded poly[d(A-T)] X poly[d(A-T)], than that displayed by bovine RNAase A under these conditions. Both activities show a similar dependence on the ionic strength of the medium. 2. A partial enzymic removal of the heterosaccharide side chains...
Relationship of sialic acid residues to in vitro biological and immunological activities of equine gonadotropins.
Biology of reproduction    June 1, 1981   Volume 24, Issue 5 1082-1087 
Aggarwal BB, Papkoff H.No abstract available
Effects of dilution rates, animal species and instruments on the spectrophotometric determination of sperm counts.
Revue canadienne de biologie    June 1, 1981   Volume 40, Issue 2 173-180 
Rondeau M, Rouleau M.Using semen from bull, boar and stallion as well as different spectrophotometers, we established the calibration curves relating the optical density of a sperm sample to the sperm count obtained on the hemacytometer. The results show that, for a given spectrophotometer, the calibration curve is not characteristic of the animal species we studied. The differences in size of the spermatozoa are probably too small to account for the anticipated specificity of the calibration curve. Furthermore, the fact that different dilution rates must be used, because of the vastly different concentrations of ...
Hydrolysis by horse muscle acylphosphatase of (Ca2+ + Mg2+)-ATPase phosphorylated intermediate.
Archives of biochemistry and biophysics    April 15, 1981   Volume 208, Issue 1 37-41 doi: 10.1016/0003-9861(81)90120-x
Stefani M, Liguri G, Berti A, Nassi P, Ramponi G.No abstract available
Isolation of cellulolytic phycomycete fungi from the caecum of the horse.
Journal of general microbiology    April 1, 1981   Volume 123, Issue 2 287-296 doi: 10.1099/00221287-123-2-287
Orpin CG.Microscopic examination of horse caecum contents revealed vegetative growth of phycomycete fungi on particles of digesta, and uniflagellated cells similar to fungal zoospores in the liquid phase. Three morphologically distinct isolates of strictly anaerobic phycomycete fungi were obtained from the caecum contents and cultured in vitro. Two of the isolates were able to utilize a wide range of plant carbohydrates for growth, including alpha-cellulose, xylan and particulate starch, and extensively digested water-insoluble plant tissues.
Method for the automation of equine differential leucocyte counts.
Equine veterinary journal    April 1, 1981   Volume 13, Issue 2 115-118 doi: 10.1111/j.2042-3306.1981.tb04133.x
Allen BV.A technique for automating equine differential leucocyte counts by analysis of volume distribution curves using the Coulter Channelyzer has been developed and evaluated. A comparison between the results obtained by this method and standard microscopic techniques showed good agreement in most cases. Blood samples can be analysed for both differential and total leucocyte counts at a rate of 25/h. For each sample an average 16,000 leucocytes are classified by the Channelyzer. The method of volume analysis is suitable for the precise counting of polymorphonuclear neutrophils, lymphocytes and eosin...