Analyze Diet

Topic:Biochemistry

The study of biochemistry in horses encompasses the chemical processes and substances that occur within equine organisms. This field investigates the molecular interactions and pathways that are fundamental to horse physiology, including metabolism, enzyme activity, and genetic expression. Key areas of interest include the examination of metabolic disorders, nutrient absorption, and the biochemical basis of muscle function and energy production. Researchers utilize biochemical analysis to understand health and disease mechanisms in horses, contributing to the development of diagnostic tools and therapeutic strategies. This page gathers peer-reviewed studies and scholarly articles that explore various biochemical processes and their implications for equine health and performance.
A comparison of techniques for the quantitative analysis of hyaluronic acid in equine synovial fluid.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    April 1, 1976   Volume 40, Issue 2 202-208 
Marsh JA, Hallett FR, Owen RR.A comparison of methods of preparing the hyaluronic acid of equine synovial fluid for quantitative spectrophotographic analysis is presented. A new method is proposed which appears superior to the previous methods.
Structural studies on horse spleen apoferritin.
Archives internationales de physiologie et de biochimie    April 1, 1976   Volume 84, Issue 2 380-381 
Collet-Cassart D, Crichton RR.No abstract available
Horse-liver alcohol dehydrogenase and Pseudomonas testosteroni 3(17)beta-hydroxysteroid dehydrogenase transfer epimeric hydrogens from NADH to 17beta-hydroxy-5alpha-androstan-3-one. An exception to one of the Alworth-Bentley rules.
European journal of biochemistry    April 1, 1976   Volume 63, Issue 2 427-429 doi: 10.1111/j.1432-1033.1976.tb10244.x
Groman EV, Schultz RM, Engel LL, Orr JC.In the reduction of 17beta-hydroxy-5alpha-androstan-3-one to the 3beta-alcohol, horse liver alcohol dehydrogenase utilizes the 4-pro-R hydrogen of NADH whereas the 3(17)beta-hydroxysteroid dehydrogenase of Pseudomonas testosteroni utulized the 4-pro-S hydrogen. These observations provide an exception to the rule proposed by Alworth and Bentley that with regard to the paired methylene hydrogens at C-4 of NADH and NADPH "the stereospecificity of a particular reaction is fixed and does not vary with the source of the enzyme preparation". It is also apparent that for these two enzymes, the selecti...
Mefanamic acid blood and urine levels in the horse determined by derivative gas-liquid chromatography-electron capture.
Journal of chromatographic science    April 1, 1976   Volume 14, Issue 4 201-203 doi: 10.1093/chromsci/14.4.201
Bland SA, Blake JW, Ray RS.Mefenamic acid is extracted from biological fluids and is acylated with pentafluoropropionic anhydride to form a derivative possessing high electron affinity. The derivative is analyzed by gas-liquid chromatography with an electron capture detector. The method is particularly valuable for determining drug levels in blood where small sample and/or drug concentrations are available.
Effects of ovariectomy and season on plasma luteinizing hormone in mares.
Endocrinology    April 1, 1976   Volume 98, Issue 4 958-962 doi: 10.1210/endo-98-4-958
Garcia MC, Ginther OJ.Six pony mares were ovariectomized (OVX) on day 16 of diestrus during June and July, 1972, to study short term changes in plasma luteinizing hormone (LH) concentrations. Plasma LH was higher (P less than .05) 3 days after OVX (1.76 ng/ml) than the day after OVX (1.01 ng/ml), and a gradual increase occurred over the first 2 weeks. Elevated plasma LH concentrations similar to mid-estrus levels were present from the 2nd to 11th week post-OVX. In another experiment, the same 6 OVX mares were bled once a month from February, 1973, to January, 1974, to study long-term changes in plasma LH in relatio...
Three-dimensional structure of horse liver alcohol dehydrogenase at 2-4 A resolution.
Journal of molecular biology    March 25, 1976   Volume 102, Issue 1 27-59 doi: 10.1016/0022-2836(76)90072-3
Eklund H, Nordström B, Zeppezauer E, Söderlund G, Ohlsson I, Boiwe T, Söderberg BO, Tapia O, Brändén CI, Akeson A.No abstract available
Characterization of protein phosphokinase activities in horse thyroid nuclei.
Biochimica et biophysica acta    March 11, 1976   Volume 429, Issue 1 163-172 doi: 10.1016/0005-2744(76)90038-3
Verhaegen M, Sand G.The distribution of protein phosphokinase (EC 2.7.1.37) activities has been established in horse thyroid nuclei. The presence of several enzyme activities has been demonstrated, two of which are clearly distinct. The first one acts on histone as substrate and is activated by cyclic AMP. Physico-chemical properties of this nuclear cyclic AMP-dependent histone kinase and of the cytosol histone kinase are different, demonstrating the absence of a contamination from the cytosol. The second enzyme acts on casein as substrate and is not stimulated by cyclic AMP POR CYCLIC GMP. The findings are consi...
Inactivation of horse liver alcohol dehydrogenase by modification of cysteine residue 174 with diazonium-1H-tetrazole.
Biochemistry    March 9, 1976   Volume 15, Issue 5 1087-1093 doi: 10.1021/bi00650a021
Sogin DC, Plapp BV.Diazonium-1H-tetrazole was tested as a potential active-site-directed reagent for amino acid residues involved in catalysis by alcohol dehydrogenase. In a novel reaction with a protein, diazonium-1H-tetrazole inactivated the enzyme selectively, and almost stoichiometrically, but reacting with the sulfur of a cysteine residue, Cys-174. As a model compound, the tetrazole adduct of free cysteine was prepared. Elementary and spectral analyses of the adduct were consistent with the structure 5-tetrazoleazo-S-cysteine. The adduct absorbs light with a maximun at 316 nm, and is destroyed by irradiatio...
Effects of training on biochemical values in standardbred horses.
American journal of veterinary research    March 1, 1976   Volume 37, Issue 3 285-290 
Milne DW, Skarda RT, Gabel AA, Smith LG, Ault K.Effects of training at a regular, fixed, standard exercise load on venous lactic acid, mixed venous and arterial blood gases and pH, and serum muscle enzymes were determined on previously unconditioned, healthy, adult, Standardbred horses. Arterial and mixed venous blood gases, pH, and serum muscle enzymes did not change in a consistent manner during training. Venous lactic acid concentrations did increase significantly with training and may be of value for the biochemical evaluation of fitness in horses.
Proceedings: Potassium content and turnover of lymphocytes and granulocytes isolated from human and from horse blood.
The Journal of physiology    March 1, 1976   Volume 256, Issue 1 4P 
Baker DJ, Trist DG, Weatherall M.No abstract available
Chemical mediators of anaphylaxis (histamine, 5-HT, and SRS-A) released from horse lung and leukocytes in vitro.
Research communications in chemical pathology and pharmacology    March 1, 1976   Volume 13, Issue 3 379-388 
Burka JF, Deline TR, Holroyde MC, Eyre P.Horses were sensitized to bovine plasma in Freund's complete adjuvant. Leukocytes, separated from venous blood, yielded histamine upon incubation with bovine plasma. Ioslated lung fragments incubated with bovine plasma liberated histamine and 5-HT, but not SRS-A. Pulmonary veins obtained from the same animals contracted to histamine, 5-HT and to antigen (Schultz-Dale reaction). Histamine and 5-HT probably contribute to immediate-type hypersensitivity in horses whereas the role of SRS-A is not proved.
The effect of exercise on the lactic dehydrogenase and creatine kinase isoenzyme composition of horse serum.
Research in veterinary science    March 1, 1976   Volume 20, Issue 2 191-196 
Anderson MG.The distribution of lactic dehydrogenase, aldolase and creatine kinase in various horse tissues was determined. Using polyacrylamide gel electrophoresis the lactic dehydrogenase and creatine kinase isoenzyme composition of horse serum, taken before and after exercise, was studied. Horse tissue isoenzyme patterns were also obtained. By comparing tissue and serum patterns, skeletal muscle was found to be the tissue of origin of the increase in serum lactic dehydrogenase and creatine kinase observed after exercise.
Some assay restrictions on inferences made from determining hormones in horses, cows, and their fetuses.
Journal of toxicology and environmental health    March 1, 1976   Volume 1, Issue 4 669-679 doi: 10.1080/15287397609529365
Hafs HD.Often in developing hormone assays, hormones that may interfere with the assay by cross-reaction are not available for testing the validity of the assay. For example, horse TSH was unavailable to test for cross-reaction in an LH radioimmunoassay (RIA). The authors devised an indirect means of accomplishing the same goal, and the evidence from the indirect test of cross-reaction was at least as persuasive as a direct test might have been. Other examples are given of experiments where extensive effort was devoted to validation of steroid RIA, but there were substantial quantitative differences i...
Plasma bile acid elevation following CCI4 induced liver damage in dogs, sheep, calves and ponies.
Research in veterinary science    March 1, 1976   Volume 20, Issue 2 127-130 
Anwer MS, Engelking LR, Gronwall R, Klentz RD.Plasma bile acid concentration was determined in normal dogs,sheep, calves and ponies for three days before and six days after liver damage, induced by carbon tetrachloride. In all species, a significant increase in plasma bile acid concentration was associated with a concomitant significant increase in plasma sorbitol dehydrogenase and transferase activity. Plasma bilirubin also significantly increased in all animals except the dogs. Results suggested that plasma bile acid levels could be used to test liver function in domestic animals.
Evaluation of adenosine deaminase and other purine salvage pathway enzymes in horses with combined immunodeficiency.
Infection and immunity    March 1, 1976   Volume 13, Issue 3 995-997 doi: 10.1128/iai.13.3.995-997.1976
McGuire TC, Pollara B, Moore JJ, Poppie MJ.Foals with combined immunodeficiency had normal levels of purine salvage pathway enzymes, including adenosine deaminase, nucleoside phosphorylase, and xanthine oxidase.
Studies on metabolism and effects of estrogen on pituitary prolactin and LH secretion.
Journal of toxicology and environmental health    March 1, 1976   Volume 1, Issue 4 641-655 doi: 10.1080/15287397609529363
Chen CL, Pattison ML, Engleking LR, Gronwall RR.The effect of a subcutaneous injection of estradiol on the secretion of pituitary prolactin in the rat and the relationship between serum estradiol level and luteinizing hormone (LH) secretion in mare were reviewed. In addition, the effect of estradiol injection on LH secretion and the metabolism of [14C] estradiol in intact and bile duct fistulated pony mares were studied. Low (0.1 mug/day/rat) to moderate dose (5 mug/day/rat) of estradiol benzoate injected subcutaneously to mature or immature rats significantly increased pituitary content of prolactin and serum prolactin level five- to tenfo...
Isolation and some molecular parameters of elastase-like normal proteinases from horse blood leucocytes.
The Biochemical journal    February 1, 1976   Volume 153, Issue 2 389-396 doi: 10.1042/bj1530389
Dubin A, Koj A, Chudzik J.Cytoplasmic granules were isolated from horse blood polymorphonuclear leucocytes by the heparin method and extracted with 0.9% NaCl by repeated freezing. Soluble proteins were separated on a column of Sephadex G-75 followed by chromatography on a column of CM-Sephadex with a NaCl gradient. Gel filtration, density-gradient centrifugation, isoelectric focusing and 0.1% sodium dodecyl sulphate/polyacrylamide-gel electrophoresis at pH 7.0 and at pH 4.5 were used to determine molecular parameters of proteinases. Three enzymes hydrolysing both casein and N-benzyloxycarbonyl-L-alanine nitrophenyl est...
Substrate specificity and modifications of the active centre of elastase-like neutral proteinases from horse blood leucocytes.
The Biochemical journal    February 1, 1976   Volume 153, Issue 2 397-402 doi: 10.1042/bj1530397
Koj A, Chudzik J, Dubin A.Two proteinases (2A and 2B) purified from the granular fraction of horse blood leucocytes degrade casein (Km values 12.8 and 6mg/ml respectively) with maximum activity at pH 7.4 and in the presence of 2m-urea. Urea-denatured haemoglobin, fibrinogen, albumin and resorcin/fuchsin-stained elastin are digested at a slower rate. The enzymes hydrolyse synthetic substrates of elastase, N-benzyloxycarbonyl-L-alanine 4-nitrophenyl ester (Km 0.114 and 0.178 mM) and N-acetyl-tri-L-alanine methyl ester (Km 5.55 and 0.98 mM), but they do not hydrolyse synthetic substrates of trypsin, chymotrypsin and throm...
Immunochemical studies on blood groups. Structures and immunochemical properties of nine oligosaccharides from B-active and non-B-active blood group substances of horse gastric mucosae.
Archives of biochemistry and biophysics    February 1, 1976   Volume 172, Issue 2 353 
Newman W, Kabat EA.No abstract available
Concentration of prostaglandins F in uterine venous plasma of anesthetized mares during the estrous cycle and early pregnancy.
Prostaglandins    February 1, 1976   Volume 11, Issue 2 251-260 doi: 10.1016/0090-6980(76)90148-9
Douglas RH, Ginther OJ.Prostaglandins F were quantitated by radioimmunoassay in uterine venous plasma of anesthetized mares on day 7 of estrus, days 2, 6, 10, 14 or 18 of diestrus and days 10, 14 or 18 of pregnancy. The PGF concentration was greater (P less than .01) at day 14 of diestrus than at all other days studied. The concentrations at days 10 and 18 of diestrus and at days 10, 14 and 18 of pregnancy were greater (P less than .05) than at day 7 of estrus and days 2 and 6 of diestrus. PGF concentrations at days 10 and 14 were greater (P less than .01) for diestrous than for pregnant mares.
Immunochemical studies on blood groups. Purification, chemical and immunochemical properties of blood group-active glycoproteins from horse gastric mucosae.
Archives of biochemistry and biophysics    February 1, 1976   Volume 172, Issue 2 510-523 doi: 10.1016/0003-9861(76)90104-1
Newman W, Kabat EA.No abstract available
Cell-free synthesis of equine herpesvirus type 3 nucleocapsid polypeptides.
Virology    February 1, 1976   Volume 69, Issue 2 751-762 doi: 10.1016/0042-6822(76)90503-1
Allen GP, Bryans JT.No abstract available
Immunochemical studies on blood groups. Immunochemical properties of B-active and non-B-active blood group substances from horse gastric mucosae and the relative size distributions of oligosaccharides liberated by base-borohydride.
Archives of biochemistry and biophysics    February 1, 1976   Volume 172, Issue 2 524-534 doi: 10.1016/0003-9861(76)90105-3
Newman W, Kabat EA.No abstract available
Fiber types and size in equine skeletal muscle.
American journal of veterinary research    February 1, 1976   Volume 37, Issue 2 145-148 
Aberle ED, Judge MD, Kirkham WW, Page EH, Crawford BH.Frozen sections of equine musculus semitendinosus were examined for myosin adenosine triphosphatase (ATPase) and reduced nicotinamide adenine dinucleotide-tetrazolium reductase (NADH-TR), using standard histochemical procedures, and the proportions of the various fiber types and average fiber sectional size were determined. With ATPase staining, approximately 70% of the fibers were classified as alpha fibers (ATPase positive), and 30%, as beta fibers (ATPase negative). In addition, 2 populations of alpha fibers could be readily distinguished on the basis of the intensity of the ATPase reaction...
Primary structure determination of two cytochromes c2: close similarity to functionally unrelated mitochondrial cytochrome C.
Proceedings of the National Academy of Sciences of the United States of America    February 1, 1976   Volume 73, Issue 2 472-475 doi: 10.1073/pnas.73.2.472
Ambler RP, Meyer TE, Kamen MD.The amino-acid sequences of the cytochromes c2 from the photosynthetic non-sulfur purple bacteria Rhodomicrobium vannielii and Rhodopseudomonas viridis have been determined. Only a single residue deletion (at position 11 in horse cytochrome c) is necessary to align the sequences with those of mitochondrial cytochromes c. The overall sequence similarity between these cytochromes c2 and mitochondrial cytochromes c is closer than that between mitochondrial cytochromes c and the other cytochromes c2 of known sequence, and in the latter multiple insertions and deletions must be postulated before a ...
Oxidation of human and animal haemoglobins with ascorbate, acetylphenylhydrazine, nitrite, and hydrogen peroxide.
British journal of haematology    February 1, 1976   Volume 32, Issue 2 193-203 doi: 10.1111/j.1365-2141.1976.tb00922.x
Harvey JW, Kaneko JJ.Partially purified haemoglobin solutions of man, horse, car and dog were oxidized with ascorbate, acetylphenylhydrazine, nitrite, and H2O2 at 25 degrees C and with ascorbate and acetylphenylhydrazine at 37 degrees C. Haemoglobins of the carnivores were more easily oxidized with ascorbate, nitrite, and H2O2 than equine and human haemoglobins. Feline haemoglobin, in general, appeared more susceptible to oxidation, particularly oxidative denaturation, than those of the other species. In addition, results of the incubations at 37 degrees C suggest that feline haemoglobin B might be more susceptibl...
Characterization of human, bovine, and horse antithrombin III.
Biochemistry    January 27, 1976   Volume 15, Issue 2 368-373 doi: 10.1021/bi00647a020
Kurachi K, Schmer G, Hermodson MA, Teller DC, Davie EW.A comparison of the physical-chemical properties of human, bovine, and horse antithrombin III has been made. These three plasma proteins are strong inhibitors of bovine factor Xa and form a 1:1 molar complex with this coagulation enzyme. Human, bovine, and horse antithrombin III are glycoproteins containing hexose, hexosamine, and neuraminic acid. The total carbohydrate was 9, 12, and 16% for human, bovine, and horse antithrombin III, respectively. These proteins have a similar amino acid composition, although some monor variations were noted. Each antithrombin III is composed of a single poly...
Chemical modification as a probe of the topography and reactivity of horse-spleen apoferritin.
European journal of biochemistry    January 15, 1976   Volume 61, Issue 2 545-550 doi: 10.1111/j.1432-1033.1976.tb10049.x
Wetz K, Crichton RR.In apoferritin, but not in ferritin, 1.0 +/- 0.1 cysteine residue per subunit can be modified. In ferritin 3.3 +/- 0.3 lysine residues and 7.1 +/- 0.7 carboxyl groups per subunit can be modified, whilst the corresponding values for apoferritin are 4.4 +/- 0.4 lysine residues and 11.0 +/- 0.4 carboxyl groups per subunit. Modification of lysine residues which maleic anhydride and carboxyl groups with glycineamide in apoferritin which has been dissociated and denatured in guanidine hydrochloride leads to the introduction of 9.1 +/- 0.5 maleyl groups per subunit and 22.0 +/- 0.9 glycineamide resid...
Ligand binding properties of horse hemoglobins containing deutero- and mesoheme.
The Journal of biological chemistry    January 10, 1976   Volume 251, Issue 1 45-52 
Seybert DW, Moffat K, Gibson QH.The reactions of horse globin reconstituted with proto-, deutero-, and mesoheme have been examined by equilibrium and kinetic methods. In virtually all reactions studied, mesohemoglobin displays the more extreme functional behavior, whereas deuterohemoglobin exhibits behavior which is either very similar to native hemoglobin or intermediate between the two. Our kinetic and equilibrium results indicate that the primary effect of heme modification on the functional properties of hemoglobin is to alter the intrinsic reactivities of the deoxy and liganded conformations. Heme modification does not,...
[Values of acid-base equilibrium in the blood of various species of domestic animals].
Veterinarni medicina    January 1, 1976   Volume 21, Issue 1 51-59 
Komárek J, Stros K, Sýkora I, Kynclová I, Jadrný L, Selinger P.By means of the Astrup equilibration method the values of the acid-base balance of the blood were determined in 104 cows, 99 horses, 100 pigs, 15 sheep, 20 goats, and in 101 dogs. The pH values of the blood, the partial pressure of CO2, the base excess, the base buffer, the standard bicarbonate, the actual bicarbonate, and the total CO2 were processed statistically and are presented in tables.