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.
The effects of dipyridamole on TXA2 formation by horse platelet microsomes.
Prostaglandins, leukotrienes, and medicine    February 1, 1983   Volume 10, Issue 2 179-185 doi: 10.1016/s0262-1746(83)80008-0
Katano Y, Imai S.The effects of dipyridamole on thromboxane A2 formation by horse platelet microsomes were studied in comparison with those of imidazole, a prototype inhibitor of TXA2 synthetase and nifedipine, a calcium antagonistic vasodilator. Thromboxane A2 was synthesized by incubating PGH2 with horse platelet microsomes and was assayed on the superfused rabbit aorta. Dipyridamole induced as strong an inhibition of TXA2 synthesis as imidazole, while nifedipine was without effects. The possible beneficial clinical outcomes of this effect of dipyridamole are discussed.
Difference in sizes of human compared to murine alpha-subunits of the glycoprotein hormones arises by four-codon gene deletion or insertion.
Endocrinology    February 1, 1983   Volume 112, Issue 2 482-485 doi: 10.1210/endo-112-2-482
Chin WW, Maizel JV, Habener JF.The sizes of the human and subhuman alpha-subunits of the glycoprotein hormones differ by four amino acids (hCG alpha, 92 amino acids; murine, equine, bovine, and ovine alpha, 96 amino acids). The shortening of the human alpha-subunit has been attributed to posttranslational proteolysis. We have recently determined the nucleotide sequences of the mRNAs encoding the precursors of the alpha-subunit of mouse TSH and rat gonadotropins using recombinant DNA techniques. In this report, we have compared these nucleotide sequences and their deduced amino acid sequences with those of the pre- alpha-sub...
Platelet-activating factor stimulates metabolism of phosphoinositides in horse platelets: possible relationship to Ca2+ mobilization during stimulation.
Proceedings of the National Academy of Sciences of the United States of America    February 1, 1983   Volume 80, Issue 4 965-968 doi: 10.1073/pnas.80.4.965
Billah MM, Lapetina EG.Stimulation of horse platelets with platelet-activating factor (PAF) induces a rapid degradation of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2]. Addition of 0.1 microM PAF for 5 sec to platelets prelabeled with 32P induces a 50% loss of [32P]PtdIns(4,5)P2. 32P-Labeled phosphatidylinositol 4-monophosphate (PtdIns4P) and [32P]phosphatidylinositol (PtdIns) also are decreased, albeit at a slower rate. Loss of 32P radioactivity correlates with a net loss of fatty acids from both polyphosphoinositides. Stimulation of platelets with PAF also produces formation of [32P]phosphatidic acid and ...
Equine complement activation as a mechanism for equine neutrophil migration in Onchocerca cervicalis infections.
Clinical immunology and immunopathology    February 1, 1983   Volume 26, Issue 2 277-286 doi: 10.1016/0090-1229(83)90146-0
Camp CJ, Leid HW.Extracts of Onchocerca cervicalis, an equine parasite, were incubated with radiolabeled equine neutrophils and neutrophil migration was assessed for factors derived from the parasite itself or for host-derived factors after incubation of these same parasite extracts with equine serum. No stimulus for cell migration was observed in saline extracts of adult worms, uterine microfilariae, or skin microfilariae at any dosage tested. However, after incubation of saline extracts with fresh normal equine sera a marked stimulus for neutrophil migration was observed. Ablation of this biologic activity w...
Pathogenic bacteria and fungi associated with extraocular disease in the horse.
Journal of the American Veterinary Medical Association    February 1, 1983   Volume 182, Issue 3 241-242 
McLaughlin SA, Brightman AH, Helper LC, Manning JP, Tomes JE.In 123 cases of external ocular disease in the horse, pathogenic microorganisms isolated with greatest frequency were Streptococcus sp (43.9%), Staphylococcus sp (24.2%), and Pseudomonas sp (13.8%). Fungi were isolated in 4.8% of the cases. In vitro testing showed that most of the Streptococcus sp isolants were sensitive to ampicillin, cephalothin, and carbenicillin. Most of the Staphylococcus sp isolants were sensitive to gentamicin, cephalothin, and bacitracin. Most of the Pseudomonas sp isolants were sensitive to polymyxin B and gentamicin.
Fine structure of Babesia equi Laveran, 1901 within lymphocytes and erythrocytes of horses: an in vivo and in vitro study.
The Journal of parasitology    February 1, 1983   Volume 69, Issue 1 111-120 
Moltmann UG, Mehlhorn H, Schein E, Rehbein G, Voigt WP, Zweygarth E.The development of Babesia equi (Piroplasmia) in the vertebrate host was studied by electron microscopy. The tick-borne sporozoites initiated an exoerythrocytic schizogony in lymphocytes in vivo and in vitro. In lymphocyte cultures the schizonts of B. equi lay as fissured bodies directly within the host cell forming numerous cytomeres. These cytomeres were bordered by a single membrane and contained polymorphous nuclei. Merozoite differentiation was initiated at several places by protrusions appearing at the periphery of the cytomeres. The cytoplasm of the schizont merged progressively into th...
Effects of common radioiodination procedures on the binding of glycoproteins to immobilized lectins.
Biochemical and biophysical research communications    January 14, 1983   Volume 110, Issue 1 103-107 doi: 10.1016/0006-291x(83)91266-4
Montelaro RC, West M, Ivey M.Representative glycoproteins including fetuin, protein A, ovalbumin, alpha 1 acid glycoprotein, and the major glycoprotein of equine infectious anemia virus were labelled with 125I by the chloramine-T or Bolton-Hunter procedure and their binding to immobilized Con A or lentil lectin compared to untreated samples of each glycoprotein. Glycoprotein modification was no greater than one substituted residue per protein molecule. Yet the radioiodinated glycoproteins typically displayed only 0-50% of the lectin binding observed with untreated samples. These results indicate that lectin glycoprotein b...
Identification of the second alpha-2-antiprotease of equine serum as antithrombin III.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 7 917-922 doi: 10.1016/0020-711x(83)90167-2
Pellegrini A, Zweifel HR, von Fellenberg R.The alpha-2-protease inhibitor, of 65,000 daltons molecular weight, described by several authors in horse plasma and also present as a contaminant in alpha-1-isoinhibitor isolates previously described by us (Pellegrini & von Fellenberg (1980) Biochim. biophys. Acta 616, 351-361) has now been isolated to purity and identified as antithrombin III. The inhibitor is composed of a single polypeptide chain as judged by SDS polyacrylamide gel electrophoresis. The inhibitor was effective only against trypsin and thrombin. Serological cross-reaction existed between the inhibitor and the antiserum t...
Infectious center assay of intracellular virus and infective virus titer for equine mononuclear cells infected in vivo and in vitro with equine herpesviruses.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    January 1, 1983   Volume 47, Issue 1 64-69 
Dutta SK, Myrup AC.A novel, simple method of infectious center assay was developed to detect and quantitate the intracellular existence of equine herpesvirus 1 and equine herpesvirus 2 in peripheral blood mononuclear cells infected in vivo and in vitro with the viruses by cocultivation of these cells with a permissive equine cell culture. The infectious center titers were correlated with the infectious virus titers. In vivo equine herpesvirus 1-infected mononuclear cells obtained from ponies experimentally infected with the virus and equine herpesvirus 2-infected mononuclear cells obtained from selected naturall...
Isolation and characterization of horse alpha 2-macroglobulin protease inhibitor.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 8 1003-1011 doi: 10.1016/0020-711x(83)90036-8
Pellegrini A, Zweifel HR, von Fellenberg R.Several publications have described in the past properties of partly purified horse alpha 2-macroglobulin (alpha 2M) which are strikingly different from the human alpha 2M. Horse alpha 2M was therefore isolated to purity by classical procedures, i.e. affinity chromatography, ion exchange chromatography and gel filtration, and its properties are compared with those of its human counterpart. The molecular weight of the native protein and its subunits, the isoelectrofocusing pattern and the change in electrophoretic mobility caused by interaction with protease were similar to those of human alpha...
Immunochemical studies of infectious mononucleosis–XI. comparison of heterophile antibody inhibitors from the erythrocyte membranes of four mammalian species.
Molecular immunology    January 1, 1983   Volume 20, Issue 1 1-10 doi: 10.1016/0161-5890(83)90099-8
Latif ZA, Fletcher MA.Immunochemical comparisons were made of the reactivity of membrane glycoproteins from horse, bovine, sheep and goat erythrocytes with heterophile antibodies of infectious mononucleosis. The four receptors were tested as competitive inhibitors of a sandwich-type solid-phase radioimmunoassay and of agglutination of glycoprotein-latex reagents by infectious mononucleosis serum. The results of this study showed that the bovine glycoprotein had a superior reactivity with this heterophile antibody system and sheep erythrocyte glycoprotein was the least reactive. The latter had negligible ability to ...
Pyrimidine metabolism in peripheral and phytohemagglutinin-stimulated mammalian lymphocytes.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 1 51-55 doi: 10.1016/0020-711x(83)90010-1
Peters GJ, Oosterhof A, Veerkamp JH.1. Activity of uridine kinase was very low in ovine lymphocytes and in those of some pigs. Lymphocytes of other pigs showed a significantly higher activity of this enzyme. Activity of uridine kinase in lymphocytes of man, horse and cattle was intermediate. 2. Activity of uridine phosphorylase was higher than that of uridine kinase with lymphocytes of all species. 3. Activity of uridine kinase in equine lymphocytes increases at PHA-stimulation and also in porcine lymphocytes with a low activity at the start of the culture. Activity of uridine kinase decreased in porcine lymphocytes with a high ...
Streptokinase-dependent delayed activation of horse plasminogen.
Biochimica et biophysica acta    December 6, 1982   Volume 709, Issue 1 19-27 doi: 10.1016/0167-4838(82)90416-2
Marcum JA, Highsmith RF, Kline DL.Complete activation of purified horse plasminogen to plasmin was obtained with a 1:10 molar ratio of streptokinase to plasminogen after 5 min of incubation at 37 degrees C. At a 1:1 molar ratio, maximal activity did not appear until 15-30 min, while at a ratio of 6:1 complete activation was delayed for 120-180 min. Gel filtration studies of isotopically labeled streptokinase and horse plasminogen suggest that the delay was due to impaired formation of a streptokinase-plasminogen complex. The predominant streptokinase moiety within the streptokinase-plasmin complex which forms from the streptok...
Effect of Mycoplasma orale on growth of equine arteritis virus in Vero cells.
Nihon juigaku zasshi. The Japanese journal of veterinary science    December 1, 1982   Volume 44, Issue 6 989-991 doi: 10.1292/jvms1939.44.989
Tsukamoto K, Konishi S, Ogata M.No abstract available
In vitro blastogenesis of equine lymphocytes by inactivated equine adenovirus type 1 antigen.
American journal of veterinary research    November 1, 1982   Volume 43, Issue 11 1922-1925 
Campbell TM, Studdert MJ.An inactivated equine adenovirus type 1 (EAdV1) vaccine was administered to 4 horses. The horses had virus-neutralizing (VN) antibody titers before they were vaccinated, but developed higher VN antibody titers in response to vaccination. Nonvaccinated control horses did not show increases in VN antibody during the study, indicating that any increase in antibody titer in vaccinated horses was a result of vaccination and not due to an EAdV1 epizootic during the study. Specific EAdV1 in vitro lymphocyte blastogenesis (LB) was evaluated, using lymphocytes from 4 vaccinated and 2 control horses. Ho...
Isolation of equine neutrophils and analysis of functional characteristics by chemiluminescence and bacterial assays.
American journal of veterinary research    November 1, 1982   Volume 43, Issue 11 1912-1916 
Jacobsen K, Gintz T, Reed SM, Newbry J, Bayly WM, Perryman LE, Leid RW.Equine neutrophils (PMN) were isolated to greater than 99% purity by isopyknic sedimentation on coated colloidal silica particles. A cell recovery of 84.7 +/- 4.0%, with a viability of greater than 99%, was observed with this method. The isolated PMN were compared with mixed population of equine peripheral leukocytes with respect to functional integrity by chemiluminescence and bactericidal assays. There was no significant difference (P less than 0.01) observed in either assay between the isolated equine PMN and the mixed-cell populations. The methods used in both the isolation as well as the ...
The uptake of mepacrine by horse polymorphonuclear leucocytes in vitro.
The Journal of pharmacy and pharmacology    November 1, 1982   Volume 34, Issue 11 711-714 doi: 10.1111/j.2042-7158.1982.tb06205.x
Read NG, Trist DG.The uptake of mepacrine by isolated horse polymorphonuclear leucocytes (PMN) was measured using spectrophotofluorimetry. Two phases of uptake were observed, the first, rapid fraction, essentially complete by 10 min, and a second, slow fraction, which was still proceeding after 60 min. The appearance of mepacrine within the PMN was also visualized by fluorescence microscopy. Discrete yellow points of fluorescence were observed in the cytoplasm of PMN within 30 s. These discrete points corresponded both in size and number to the PMN granules. After 5 min, the nuclei showed faint fluorescence whi...
Reactivity of equine tracheal smooth muscle to adenosine and some phosphorylated derivatives.
Journal of veterinary pharmacology and therapeutics    September 1, 1982   Volume 5, Issue 3 199-201 doi: 10.1111/j.1365-2885.1982.tb00432.x
Norris AA, Eyre P.No abstract available
Phagocytosis and intracellular killing of the contagious equine metritis organism by equine neutrophils in serum.
Infection and immunity    September 1, 1982   Volume 37, Issue 3 1241-1247 doi: 10.1128/iai.37.3.1241-1247.1982
Bertram TA, Coignoul FL, Jensen AE.Equine neutrophils were combined with Haemophilus equigenitalis (contagious equine metritis organism; CEMO) or Escherichia coli in low- and high-antibody-titer serum to evaluate the neutrophils ability to phagocytize and kill these bacteria. More E. coli than CEMO were phagocytized at each time period. After 120 min in low-antibody-titer serum, 56.3% of the E. coli and 34.3% of the CEMO were phagocytized. A total of 45% of CEMO and 74.9% of E. coli were phagocytized by 120 min when neutrophils were in high-antibody-titer serum. More than 75% of the ingested E. coli and 90% of the ingested CEMO...
[Some physicochemical properties of native and polymerized glutaraldehyde-treated horse heart cytochrome c].
Ukrainskii biokhimicheskii zhurnal (1978)    September 1, 1982   Volume 54, Issue 5 497-501 
Skok MV, Denisiuk PV, Komissarenko SV.Glutaraldehyde treatment does not change the absorption of cytochrome c either in the visible or in UV spectra. It brings about the formation of dimers, trimers and high-polymeric forms of cytochrome c and shifts the pI of all cytochrome c isoelectric fractions to more acid pH. Polymerization also results in changes of kinetic parameters of cytochrome c benzidine reaction increasing its affinity to 3,3-diaminobenzidine with a simultaneous decrease in the effectiveness of H2O2 binding. These biochemical changes can be related to immunochemical differences of native and glutaraldehyde-treated cy...
Morphometry of equine neutrophils isolated at different temperatures.
Veterinary pathology    September 1, 1982   Volume 19, Issue 5 534-543 doi: 10.1177/030098588201900508
Bertram TA, Coignoul FL.Equine neutrophils were evaluated ultrastructurally and by morphometric analysis. Homogeneous populations of neutrophils were isolated from peripheral blood at 4 degrees and 22 degrees C by centrifugation on two sequential Ficoll-Hypaque density gradients. Isolation procedures at both temperatures resulted in neutrophil degranulation but not cell swelling. Degranulation was more extensive in cells isolated at 22 degrees C. Isolation temperature affected the neutrophil content of secondary granules more than primary granules. A granule similar to immature specific granules of human neutrophils ...
Virulence and in vitro growth of a cell-adapted strain of equine infectious anemia virus after serial passage in ponies.
American journal of veterinary research    September 1, 1982   Volume 43, Issue 9 1556-1560 
Orrego A, Issel CJ, Montelaro RC, Adams WV.Five serial passages of a cell-adapted strain of equine infectious anemia (EIA) virus were conducted in Shetland ponies. The 13 recipient ponies became agar-gel immunodiffusion test-positive by 25 days after they were inoculated. The virulence of the cell-adapted strain of EIA virus markedly increased through 3 serial passages, although individual variation within passages was high. The 1st serial-passage recipient remained afebrile through 200 days, whereas a febrile episode occurred about every 185, 44, 35, and 33 days in the 2nd, 3rd, 4th, and 5th serial-passage recipients, respectively. Se...
Purification and identification of horse serum IgA.
Nihon juigaku zasshi. The Japanese journal of veterinary science    August 1, 1982   Volume 44, Issue 4 661-668 doi: 10.1292/jvms1939.44.661
Kurimoto T, Ikeda A, Tanaka K.ウマ分泌型IgA (初乳, 涙) の分離精製については, すでに報告されているが, ウマ血清IgAの分離精製に関する明確な手法を示した報告は見あたらない. われわれは, ウマ血清を脱塩, 硫安塩析し, ついでDEAEセルロース, 免疫吸着体のカラム操作により, 抗原性および分子サイズにおいて, IgG, IgG(T), IgM とは明らかに区別される免疫グロブリンを分離精製した. この免疫グロブリンは抗イヌIgAとの交差反応性により, IgAと同定された. さらに作製した抗分泌型...
Pilar neurocristic hamartoma: its relationship to blue nevus and equine melanotic disease.
Archives of dermatology    August 1, 1982   Volume 118, Issue 8 592-596 doi: 10.1001/archderm.118.8.592
Tuthill RJ, Clark WH, Levene A.A unique pigmented lesion, judged to be a hamartoma of neural crest origin, occurring in a female patient, is compared with equine melanotic disease, The characteristic perifollicular arrangement of pigment-laden spindle cells is remarkably similar in both. Previously described patch- and plaque-like blue nevi in humans are also closely related. Light and ultrastructural features showed differentiation toward both nevus cells and Schwann cells, and it is proposed that the lesion be termed pilar neurocristic hamartoma.
Identification of a transforming retrovirus from cultured equine dermal fibrosarcoma.
Virology    July 30, 1982   Volume 120, Issue 2 490-494 doi: 10.1016/0042-6822(82)90050-2
Fatemi-Nainie S, Anderson LW, Cheevers WP.No abstract available
Specific fragmentation of natural inhibitor of mitochondrial ATPase by thrombin.
Biochemical and biophysical research communications    July 30, 1982   Volume 107, Issue 2 435-441 doi: 10.1016/0006-291x(82)91510-8
Dianoux AC, Freyssinet JM.No abstract available
Immunological studies on equine phycomycosis.
Australian veterinary journal    June 1, 1982   Volume 58, Issue 6 227-231 doi: 10.1111/j.1751-0813.1982.tb00682.x
Miller RI, Campbell RS.One in vivo and 2 in vitro tests were developed to study immunological aspects of phycomycosis in clinically infected, recovered and normal in-contact horses. Serum from all infected horses gave positive readings in an agar-gel double diffusion test; serum from normal and recovered horses did not react. A complement fixation test detected antibody against Hyphomyces destruens in 82% clinical cases at an average titre of 20. Serum from recovered and in-contact horses reacted sporadically at positive titre. An intradermal hypersensitivity test (Heaf test) was used to detect evidence of cellular ...
Effects of amikacin sulfate on the motility of stallion and bull spermatozoa at different temperatures and intervals of storage.
Journal of animal science    June 1, 1982   Volume 54, Issue 6 1105-1110 doi: 10.2527/jas1982.5461105x
Arriola J, Foote RH.Because microfloral content of stallion semen tends to be high, and strains may be resistant to commonly used antibiotics, amikacin was tested with stallion semen and compared with bull semen. Nine ejaculates to stallion semen were incubated at 37 C in egg yolk-tris extender for 0, 2, 4, 6, 8 and 10 h in the presence of amikacin concentrations of 0, 50, 100, 250, 500, 1,000 and 10,000 microgram/ml, with penicillin and penicillin-streptomycin as controls. Averaged over all incubations, spermatozoal motility was 44, 48, 49, 46, 45, 45 and 19%, for increasing concentrations of amikacin, compared ...
The enzymic reduction and kinetics of oxidation of cytochrome b-245 of neutrophils.
The Biochemical journal    May 15, 1982   Volume 204, Issue 2 479-485 doi: 10.1042/bj2040479
Cross AR, Higson FK, Jones OT, Harper AM, Segal AW.1. The absorption coefficient of human neutrophil plasma-membrane reduced-minus-oxidized cytochrome b-245 was determined [delta epsilon (mM; 559-540 nm) = 21.6 cm-1]. 2. Neutrophil polymorphonuclear leucocytes (neutrophils) were prepared from human, ox, horse and pig blood. In each case plasma-membrane fractions were found to contain low-potential cytochrome b. When membranes from horse neutrophils were incubated anaerobically with either NADH or NADPH the cytochrome b became reduced. Prior stimulation of the cells with phorbol myristate acetate did not increase the rate or extent of cytochrom...
Stimulation by phytohaemagglutinin of peripheral blood lymphocytes from horse, pig, sheep and man.
Veterinary immunology and immunopathology    May 1, 1982   Volume 3, Issue 3 295-300 doi: 10.1016/0165-2427(82)90003-4
Peters GJ, Veerkamp JH.Optimal conditions for stimulation by phytohaemagglutinin (PHA) were established for equine, porcine, ovine and human lymphocytes in MEMS medium. Optimal thymidine concentration was determined for assay of cell transformation. With all species tested horse serum gave highest thymidine incorporation. Homologous serum was not more appropriate for lymphocytes of man, pig and sheep. Optimal stimulation was achieved at 20, 0.5-5, 5, and 10-40 micrograms PHA per 10(6) cells for human, equine, porcine and ovine lymphocytes, respectively.