Analyze Diet

Topic:Enzymes

Enzymes are biological catalysts that facilitate biochemical reactions in horses by lowering the activation energy required for these processes. They are involved in various physiological functions, including digestion, metabolism, and cellular repair. Common enzymes in equine biology include amylase, lipase, and lactate dehydrogenase, each playing a specific role in the breakdown of nutrients and energy production. The activity and concentration of these enzymes can vary in response to different physiological and pathological conditions, serving as potential indicators in veterinary diagnostics. This page compiles peer-reviewed research studies and scholarly articles that explore the function, regulation, and clinical implications of enzymes in equine health.
Effects of training on muscle composition in horses.
American journal of veterinary research    January 1, 1986   Volume 47, Issue 1 12-15 
Hodgson DR, Rose RJ, Dimauro J, Allen JR.Biopsy samples were obtained from the middle gluteal muscle of 10 Thoroughbred horses undergoing a commercial race-training program. Samples were obtained before the program began and again after 6 and 12 weeks of training. All horses had raced at least once by the 12th week of training. Serial sections of muscle were examined histochemically for myosin adenosinetriphosphatase after either acid (pH 4.3 and 4.6) or alkaline (pH 10.3) preincubation, and then muscle fibers were identified as types I, IIA, IIB, or IIC. The oxidative capacity of individual fibers was assessed, using the reduced nic...
Lysosomal arylsulfatases A and B from horse blood leukocytes: purification and physico-chemical properties.
Biology of the cell    January 1, 1986   Volume 57, Issue 2 147-152 doi: 10.1111/j.1768-322x.1986.tb00471.x
Wojczyk B.Lysosomal arylsulfatases A and B (aryl-sulfate sulfohydrolases, EC 3.1.6.1) from horse leukocytes were purified about 680-fold and 70-fold, respectively, starting from a crude extract of the azurophil and specific granules of leukocytes, by affinity, ion exchange, and gel filtration chromatography. Purified arylsulfatase A displayed anomalous kinetics, a pH optimum at 5.2, an isoelectric point at 4.3, and a Km value for p-nitrocatechol sulfate (pNCS) of 0.37 mM. This enzyme was found to exist in two association states depending on pH: a high molecular weight form at pH 5.0 and a low molecular ...
[Normal values of the hematological, biochemical and enzymological indices of the donkey].
Veterinarno-meditsinski nauki    January 1, 1986   Volume 23, Issue 10 69-75 
Dinev D, Khubenov KhD.Studied were a total of 85 (33 male and 52 female) donkeys of the Martina Franca breed of the domestic ass, aged from one to twelve years. Stated are the results for the normal values of hemoglobin, hematocrit, ESR, total erythrocyte and leukocyte counts, leukocyte formula, blood sugar, cholesterin, urea, total protein and protein fractions, some micro- and macroelements, and enzymes as tabulated in four diagrams. No differences have been established with regard to sex. It has been found that with young animals the normal values of hemoglobin and erythrocytes are lower than with adult ones. Wi...
DNA polymorphism in the major histocompatibility complex of man and various farm animals.
Animal genetics    January 1, 1986   Volume 17, Issue 2 113-133 doi: 10.1111/j.1365-2052.1986.tb00732.x
Vaiman M, Chardon P, Cohen D.In the past few years it has been possible by combining enzymatic cleavage of genomic DNA and the Southern blot hybridization technique to explore the endonuclease recognition site polymorphism of the MHC. HLA class I and DR and DQ alpha and beta class II specific probes as well as human C4 and Bf class III probes were used. All these probes were shown to cross-hybridize with DNA from pigs, cattle, sheep and horses. Hybridization of human genomic DNA with a class I probe showed 15-25 bands per genome depending on the enzyme used. Distinct endonucleases generated clusters of restriction fragmen...
The interaction between some serine proteinases and horse leucocyte inhibitor.
Folia histochemica et cytobiologica    January 1, 1986   Volume 24, Issue 2 163-168 
Dubin A, Potempa J, Turyna B.Horse blood leucocyte cytosol exhibits a broad inhibitory activity against serine proteinases. The purified inhibitor was exposed to investigated enzymes (trypsin, chymotrypsin, elastases and serine proteinase from S. aureus) for variable time and the products were analyzed by gradient polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulphate. The molar ratio I:E, association rate constants k on and inhibition constants Ki for the enzymes and inhibitor were determined. The examined elastases form stable, stoichiometric complexes with the inhibitor (Ki less than 10(-10) M), ...
Confirmation of pregnancy in mares by enzyme immunoassay of oestrogens in faeces.
Zentralblatt fur Veterinarmedizin. Reihe A    December 1, 1985   Volume 32, Issue 10 760-763 doi: 10.1111/j.1439-0442.1985.tb01997.x
Choi HS, Möstl E, Bamberg E.No abstract available
Comparison of neutrophil elastases and of neutrophil protease inhibitors in the horse and man.
American journal of veterinary research    December 1, 1985   Volume 46, Issue 12 2480-2484 
von Fellenberg R, Kohler L, Grünig G, Pellegrini A.Neutral neutrophil protease, elastase activities, and cytosol protease inhibitors of these enzymes of horses and man were compared. Human neutrophils had 5 times the elastase activity of equine neutrophils, and neutral protease activity was approximately 50% greater in human neutrophils than that in equine neutrophils. Cytosol inhibitors for elastase and neutral proteases were not found in human neutrophils, whereas large amounts were found in equine neutrophils. Using fibrinogen-agarose electrophoresis, 4 cytosol inhibitors of different enzyme specificities were detected. These cytosol inhibi...
Energy metabolism in relation to skeletal muscle fibre properties during treadmill exercise.
Equine veterinary journal    November 1, 1985   Volume 17, Issue 6 439-444 doi: 10.1111/j.2042-3306.1985.tb02551.x
Valberg S, Essén-Gustavsson B, Lindholm A, Persson S.The skeletal muscle metabolism of horses with a wide range of cardiocirculatory capacities was studied during a standardised near-maximal exercise test in relation to muscle fibre composition. Although the same amount of work was performed by all horses the amount of triglycerides and glycogen utilised and lactate accumulated differed widely. Both blood and muscle lactate accumulation were positively related to the amount of glycogen utilised. These factors were in turn positively associated with the percentage of Type IIB fibres and consequently negatively associated with the percentage of Ty...
Preliminary studies on long distance, retrograde transport of horseradish peroxidase in equine peripheral nerves.
Equine veterinary journal    November 1, 1985   Volume 17, Issue 6 453-458 doi: 10.1111/j.2042-3306.1985.tb02554.x
Fubini SL, Cummings JF, Todhunter RJ.As a prelude to studies on retrograde axonal transport of neurotoxin (ie, so-called suicide transport) as a means to prevent post neurectomy neuroma formation, preliminary studies were conducted with an innocuous enzymatic marker, horseradish peroxidase (HRP). The proximal stumps of resected medial and lateral palmar digital nerves in six ponies were injected via a tuberculin syringe and needle with 50 micron 1 of a 30 per cent solution of HRP in order to assess long distance retrograde axonal transport. The dorsal root ganglion of the cervical spinal enlargement (ie, C6, C7, C8, T1, T2) were ...
Horse kidney neutral alpha-D-glucosidase: purification of the detergent-solubilized enzyme; comparison with the proteinase-solubilized forms.
Biochimica et biophysica acta    September 20, 1985   Volume 831, Issue 1 59-66 doi: 10.1016/0167-4838(85)90149-9
Giudicelli J, Boudouard M, Delqué P, Vannier C, Sudaka P.Neutral alpha-D-glucosidase (alpha-D-glucoside glucohydrolase, EC 3.2.1.20) from horse kidney brush-border membranes was solubilized using Emulphogene BC 720 and purified by an affinity chromatography technique. The enzyme preparation (390-fold purified), which was free of other known microvillus hydrolases, exhibited one precipitate line in crossed immunoelectrophoresis and migrated as a single band on sodium dodecyl sulfate polyacrylamide gel electrophoresis. Several criteria (charge-shift crossed immunoelectrophoresis and hydrophobic chromatography) revealed the purified detergent form of t...
Complexities in the denaturation of horse metmyoglobin by guanidine hydrochloride.
The Journal of biological chemistry    September 5, 1985   Volume 260, Issue 19 10458-10460 
Ahmad F.The denaturation of horse metmyoglobin by guanidine hydrochloride was studied at pH 6.4 and 25 degrees C. Measurements of both the peptide circular dichroism and the absorbance in the Soret region suggest that the extent of renaturation strongly depends on the time interval during which the protein is exposed to concentrated solutions of the denaturant. From the equilibrium measurements of the absorption in the Soret region, it is concluded that the unfolding of metmyoglobin is complex. This is further supported by kinetic studies of denaturation which suggest the occurrence of the least four ...
Activities of key enzymes of aerobic and anaerobic metabolism in middle gluteal muscle from trained and untrained horses.
Equine veterinary journal    September 1, 1985   Volume 17, Issue 5 354-356 doi: 10.1111/j.2042-3306.1985.tb02519.x
Cutmore CM, Snow DH, Newsholme EA.The effect of physical training on the in vitro activities of key enzymes that provide quantitative information on the maximum capacities of anaerobic and aerobic metabolism has been investigated in the gluteal muscle of the horse. Training had no effect on the activities of 6-phosphofructokinase or creatine kinase, suggesting that there was no effect on the capacity of anaerobic metabolism in this muscle. However, the activities of hexokinase and citrate synthase were increased, indicating that training increased the capacity of aerobic metabolism. For comparative purposes, muscle fibre compo...
The influence of dietary selenium levels on blood levels of selenium and glutathione peroxidase activity in the horse.
Journal of animal science    September 1, 1985   Volume 61, Issue 3 590-594 doi: 10.2527/jas1985.613590x
Shellow JS, Jackson SG, Baker JP, Cantor AH.Twenty mature geldings, averaging 535 kg, were used to determine the influence of dietary selenium (Se) on the blood levels of Se and Se-dependent glutathione peroxidase (SeGSH-Px) activity in the horse. Horses were randomly assigned within breed to four treatments consisting of five horses each and fed a basal diet containing .06 ppm of naturally occurring Se. Diets were supplemented with .05, .10 and .20 ppm Se, as sodium selenite. Blood was drawn for 2 wk before, and for 12 wk following, the inclusion of supplement Se in the diets. Whole blood and plasma Se concentrations and plasma SeGSH-P...
Kinetic studies of the unfolding-refolding of horse muscle phosphoglycerate kinase induced by guanidine hydrochloride.
Biochemistry    August 13, 1985   Volume 24, Issue 17 4570-4577 doi: 10.1021/bi00338a013
Betton JM, Desmadril M, Mitraki A, Yon JM.The kinetics of the unfolding and refolding of horse muscle phosphoglycerate kinase were studied with three different signals: fluorescence emission intensity at 336 nm (excitation at 292 nm), ellipticity at 220 nm, and enzyme activity. The results corroborate the conclusion on the existence of intermediates in the folding pathway obtained from equilibrium studies. Kinetic studies showed at least two phases of refolding, as revealed by fluorescence as well as by circular dichroism measurements. During the fast phase, an intermediate was formed with a fluorescence intensity higher than that of ...
Purification and characterization of a polymorphic equine muscle carbonic anhydrase.
Nihon juigaku zasshi. The Japanese journal of veterinary science    August 1, 1985   Volume 47, Issue 4 539-547 doi: 10.1292/jvms1939.47.539
Nishita T.No abstract available
Proteinase inhibitors of horse seminal plasma. A high molecular mass, acid-soluble proteinase inhibitor.
Biological chemistry Hoppe-Seyler    August 1, 1985   Volume 366, Issue 8 705-712 doi: 10.1515/bchm3.1985.366.2.705
von Fellenberg R, Zweifel HR, Grünig G, Pellegrini A.Horse seminal plasma does not possess a proteinase inhibitor corresponding to human HUSI-I (human seminal plasma inhibitor). Instead a protein complex of high relative molecular mass (Mr) containing proteinase inhibitory activity was detected, which was called horse seminal plasma protein complex or HSPC. The compound had a broad enzyme-inhibiting spectrum. Its Mr was estimated to be 800 000 and it was composed of 7 different polypeptides with Mr values ranging from 11 000 to 30 000. Its carbohydrate content was between 3.5% and 5%. Despite the high molecular mass, the complex was soluble in d...
Enzyme histochemical features of equine gluteus muscle fibers.
American journal of veterinary research    August 1, 1985   Volume 46, Issue 8 1755-1761 
van den Hoven R, Meijer AE, Wensing T, Breukink HJ.Gluteal muscle specimens were taken from 4 horses. From 1 of the 4 gluteal muscles, serial sections were prepared. Individual muscle fibers were identified and studied, using photomicrographs of sections stained by different enzyme histochemical methods. In specimens in which cytoplasmic soluble enzymes were studied, use was made of the semi-permeable membrane technique to hamper enzyme diffusion into reaction fluids. Enzymes involved in glycogenolysis, glycolysis, the tricarboxylic acid cycle, synthesis of reduced nicotinamide adenine dinucleotide phosphate, the pentose phosphate cycle, the a...
Pre-alpha 2-elastase inhibitor of the horse: a hybrid molecule between alpha 1-proteinase inhibitor and alpha 2-beta 1-glycoprotein.
Biochimica et biophysica acta    July 18, 1985   Volume 830, Issue 1 20-24 doi: 10.1016/0167-4838(85)90125-6
Pellegrini A, von Fellenberg R.Pre-alpha 2-elastase inhibitor of horse plasma has recently been isolated in our laboratory. In this article we demonstrate that the inhibitor is a composite structure built of alpha 1-proteinase inhibitor and alpha 1-beta 1-glycoprotein. The compound inhibitor is biologically active, although it has previously been shown that its enzyme specificity is different from that of free alpha 1-proteinase inhibitor. Our observations are based on immunochemical cross-reactions between pre-alpha 1-elastase inhibitor and antibodies to alpha 2-beta 1-glycoprotein as well as antibodies to alpha 1-proteina...
Effects of a submaximal treadmill training programme on histochemical properties, enzyme activities and glycogen utilisation of skeletal muscle in the horse.
Equine veterinary journal    July 1, 1985   Volume 17, Issue 4 300-305 doi: 10.1111/j.2042-3306.1985.tb02504.x
Hodgson DR, Rose RJ, DiMauro J, Allen JR.The effects of training on skeletal muscle composition were studied in four Standardbred geldings given a seven week submaximal treadmill training programme. Before the start of training, muscle biopsies were collected from the left middle gluteal muscle for the determination of muscle fibre types, oxidative capacity and capillary numbers using histochemical techniques. The concentrations of citrate synthase, 3-hydroxyacyl-CoA dehydrogenase (HAD), lactate dehydrogenase and total muscle glycogen were measured using fluorometric methods. Muscle biopsy samples were repeated after one, three, five...
Enhanced prostacyclin biosynthesis and decreased thromboxane formation by 3-dimethylamino 5-(2′,6′-dichlorobenzylidene) 6-methyl (4H)-pyridazine (PC 89).
Prostaglandins, leukotrienes, and medicine    July 1, 1985   Volume 19, Issue 1 37-49 doi: 10.1016/0262-1746(85)90159-3
Pham HC, Lasserre B, Tronche P, Couquelet J, Dossou-Gbete V, Palhares de Miranda AL.The effects of 3-dimethylamino 5-(2',6'-dichlorobenzylidene) 6-methyl (4H)-pyridazine (PC 89) on the biosynthesis of PG I2 and TX A2 using horse aorta and horse platelet microsomes as sources of enzymes and arachidonic acid as substrate, were investigated. PC 89 (1.10(-6) M- 1.10(-3) M) dose-dependently - enhanced the biosynthesis of PG I2: the AD50 was 6.8 X 10(-6) M +/- 1.2 X 10(-9) M, the Vmax did not vary significantly with concentrations: PC 89 increased the affinity of enzyme for substrate - but inhibited TX A2 biosynthesis (ID50 = 3.31 X 10(-3) M +/- 4.8 X 10(-7) M): this inhibiting act...
Mammalian ribonucleases. The absence of a glycosylated Asn-Pro-Thr sequence in horse ribonuclease and the presence of tryptophan at position 39 in horse and dromedary ribonuclease.
FEBS letters    June 3, 1985   Volume 185, Issue 1 115-120 doi: 10.1016/0014-5793(85)80752-3
Beintema JJ.Parts of the amino acid sequences of horse and dromedary pancreatic ribonuclease were reinvestigated. The sequence of residues 21-25 in horse ribonuclease is Ser-Asn-Pro-Thr-Tyr or Ser-Asn-Ser-Thr-Tyr. The asparagine in the latter sequence is glycosylated. Horse ribonuclease possesses four additional amino acid residues at the C-terminus, like a number of other ribonucleases. Position 39 in horse and dromedary ribonuclease is not deleted but is occupied by tryptophan.
The amino-acid sequence of beta-lactoglobulin II from horse colostrum (Equus caballus, Perissodactyla): beta-lactoglobulins are retinol-binding proteins.
Biological chemistry Hoppe-Seyler    June 1, 1985   Volume 366, Issue 6 601-608 doi: 10.1515/bchm3.1985.366.1.601
Godovac-Zimmermann J, Conti A, Liberatori J, Braunitzer G.beta-Lactoglobulin isolated from horse colostrum is heterogeneous and contains two components: beta-lactoglobulin I and beta-lactoglobulin II. These two proteins are monomeric and show differences in their electrophoretic mobilities, chain lengths and primary structures. The complete amino-acid sequence of beta-lactoglobulin II was determined by automated Edman degradation of the intact protein and of the peptides derived from these by digestion with trypsin or chymotrypsin and by chemical cleavage with cyanogen bromide. Unlike other beta-lactoglobulins which contain 162 amino acids, horse bet...
Failure of superoxide dismutase to alter equine arachidonic acid-induced platelet aggregation, in vitro or ex vivo.
American journal of veterinary research    May 1, 1985   Volume 46, Issue 5 1104-1106 
Clemmons RM, Lee MR, Bliss EL, Asbury AC, Cook D, Brown V.Superoxide dismutase (SOD), a free radical scavenger with anti-inflammatory activity, was administered IM to horses. Ex vivo platelet aggregation in response to arachidonic acid was monitored to determine whether exogenous SOD altered equine platelet prostaglandin metabolism. Preparations of platelet-rich plasma obtained before SOD administration were incubated with different concentrations of SOD and were aggregated with arachidonic acid. Superoxide dismutase did not exert a demonstrable effect, either ex vivo or in vitro. Aspirin abolished arachidonic acid-induced platelet aggregation in vit...
Antigenic determinants of acylphosphatase from porcine skeletal muscle.
Journal of biochemistry    April 1, 1985   Volume 97, Issue 4 1143-1154 doi: 10.1093/oxfordjournals.jbchem.a135159
Kizaki T, Mizuno Y, Takasawa T, Shiokawa H.Analysis of the quantitative precipitin reaction of acylphosphatase from porcine skeletal muscle with rabbit antiserum indicated the presence of at least two antigenic determinants on the porcine enzyme molecule. Immunological cross-reactivities of acylphosphatases from equine and rabbit skeletal muscles were examined. In double immunodiffusion with the antiserum, the precipitin lines of the porcine and equine enzymes completely fused, while the rabbit enzyme gave no precipitin line. The reaction between the 125I-labeled porcine enzyme and its antibody was inhibited to the same extent by the p...
[Hyalurodinase activity of beta-hemolytic streptococci of the Lancefield group C]. Balke E, Weiss R, Seipp A.A total of 110 strains of beta-hemolytic streptococci, belonging to serogroup C (Lancefield), isolated from horses (71 S. zooepidemicus, 27 S. equisimilis and 12 S. equi) as well as 5 reference strains were tested for their ability to produce hyaluronidase. The determinations were carried out in a culture test on agarose gel and in a liquid test system (turbidity test according to DiFerrante). The results of both methods used showed that the three Streptococcus species could be differentiated by the relative quantitative determination of hyaluronidase activity. S. equisimilis strains produce 5...
Inhibition of lipases by proteins. A kinetic study with dicaprin monolayers.
The Journal of biological chemistry    February 25, 1985   Volume 260, Issue 4 2268-2273 
Gargouri Y, Pieroni G, Rivière C, Sugihara A, Sarda L, Verger R.We report further investigations on protein inhibition of pancreatic and microbial lipases carried out with the monolayer technique. When beta-lactoglobulin A, melittin, serum albumin, myoglobin, and a protein inhibiting lipase from soybean were preincubated with a dicaprin film at a surface pressure of 35 dynes/cm, no activity was detected with horse pancreatic or Rhizopus delemar lipases. By contrast, Rhizopus arrhizus and Geotrichum candidum lipase activities were not impaired under the same conditions. Experiments using mixed lipid-protein film transfer clearly show that the inhibition of ...
Native and carboxymethylated horse liver alcohol dehydrogenase: electrostatic fields and the Pauling strain-distortion hypothesis.
Progress in clinical and biological research    January 1, 1985   Volume 174 169-179 
Dunn MF, Dahl KH.No abstract available
Activity of delta(5)3beta-hydroxysteroid dehydrogenase and steroid hormones content in early preimplantation horse embryos.
Folia histochemica et cytobiologica    January 1, 1985   Volume 23, Issue 1-2 81-84 
Paulo E, Tischner M.The activity of delta (5)3 beta-hydroxysteroid dehydrogenase was examined histochemically in 6 to 10 days aged horse blastocysts. A positive reaction was noted in the blastomeres of all embryos incubated in medium with substrate. Measurable amounts of progesterone, androgens and estrogens were found in blastocysts on day 8th. The presence of enzyme and hormones suggests that steroid hormone production takes place in very early preimplantation horse embryos.
[Clinical signs, enzyme activity and antibody formation in experimental sarcosporidia infections of horses]. Schnieder T, Zimmermann U, Matuschka FR, Bürger HJ, Rommel M.No abstract available
Influence of several perturbants on the rate of autoxidation of horse heart ferrocytochrome c.
The International journal of biochemistry    January 1, 1985   Volume 17, Issue 1 119-122 doi: 10.1016/0020-711x(85)90095-3
Harrington JP, Carrier TL.The effect of several different types of perturbants and pH on the rate of autoxidation of horse heart ferrocytochrome c was investigated. The kinetic behavior is unique to each perturbant used. Rates of autoxidation followed first-order kinetics over the time span (0-180 min) studied. The Cl- and Br- anions exhibit an initial increase in the rate of autoxidation up to 100 mM, followed by a decrease in kinetics at 500 mM anion concentration. The ClO4- anion exhibits only an increase in the rate of autoxidation with increasing ionic strength, where as, propylurea, a hydrophobic perturbant, is n...
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