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.
Affinity chromatographic purification of horse muscle acylphosphatase: evidence of the existence of multiple molecular forms.
Archives of biochemistry and biophysics    October 15, 1983   Volume 226, Issue 2 414-424 doi: 10.1016/0003-9861(83)90310-7
Manao G, Camici G, Stefani M, Berti A, Cappugi G, Liguri G, Nassi P, Ramponi G.Acylphosphatase was purified from horse muscle by a new procedure involving an affinity chromatography step and subsequent ion-exchange chromatography. This procedure was considerably milder than the preceding one, gave an overall yield of about 60% of activity and permitted isolation of three molecular forms with acylphosphatase activity. All these enzymatic forms are tightly bound to Sepharose 4B-linked anti-horse muscle acylphosphatase antibodies. Two of these forms (Ho1 and Ho3) are present in larger amounts: Ho1 corresponds to the enzyme purified according to the older procedure; this enz...
Automated serum chemical analysis in the foal.
Journal of the American Veterinary Medical Association    October 1, 1983   Volume 183, Issue 7 769-772 
Rumbaugh GE, Adamson PJ.Blood was collected from healthy Quarter Horse and Appaloosa foals at birth and at intervals until 18 weeks of age and then was processed in an automated system for serum chemical analysis, grouping the results by age. The test values were markedly different from those normally expected in adult horses. The greatest differences were in alkaline phosphatase, lactate dehydrogenase, glucose, and total bilirubin measurements. It was concluded that serum biochemical test results be compared with age-specific normal values before diagnoses are made in cases of illness.
Glutathione peroxidase activity in the blood of healthy horses given different selenium supplementation.
Nordisk veterinaermedicin    October 1, 1983   Volume 35, Issue 10 337-345 
Ronéus B, Lindholm A.Glutathione peroxidase (GSH-px) activity in the blood is correlated to the amount of selenium which was given to the horse. Currently recommended doses of selenium seem to be sufficient in order to prevent selenium deficiency. The blood GSH-px in foals reflects the amount of selenium given to the mare during pregnancy.
Comparison of pyrimidine 5’nucleotidase activity in erythrocytes of sheep, dogs, cats, horses, calves, and Mongolian gerbils.
American journal of veterinary research    October 1, 1983   Volume 44, Issue 10 1968-1970 
George JW, Duncan JR, Mahaffey EA.Pyrimidine 5'nucleotidase (P5N) activities of erythrocytes for Mongolian gerbils, cats, dogs, sheep, horses, and calves were measured, using a radiometric technique with [14C]cytidine monophosphate as the substrate. Erythrocytes of gerbils had the highest activity [1,177.1 +/- 133.6 mU/g of hemoglobin (Hb)]. Feline erythrocytes had 327.4 +/- 204.4 mU/g of Hb. Canine erythrocytes had 148.0 +/- 19.8 mU/g of Hb. Ovine erythrocytes (44.3 +/- 20.9 mU/g of Hb), equine erythrocytes (30.0 +/- 15.9 mU/g of Hb), and bovine erythrocytes (14.1 +/- 6.9) had relatively low P5N activity. The P5N activity was...
High-performance liquid affinity chromatography on silica-bound alcohol dehydrogenase.
Analytical biochemistry    October 1, 1983   Volume 134, Issue 1 60-72 doi: 10.1016/0003-2697(83)90264-6
Nilsson K, Larsson PO.Horse liver alcohol dehydrogenase was immobilized on glycerylpropyl-silica (10 micron, 1000-A pores) activated with 2,2,2-trifluoroethanesulfonyl chloride (tresyl chloride). The coupling and activity yield was almost 100%. The coenzyme-binding sites were equivalent and virtually unaffected by the immobilization process, as judged from Scatchard plots and active-site titrations. The silica-bound enzyme, packed in steel columns, was integrated with HPLC equipment and then successfully used for chromatography of adenine nucleosides, adenine nucleotides, and triazine dyes. Dissociation constants w...
Release of 3H2O from 1 beta,2 beta[3H]androstenedione by equine granulosa cells.
Acta endocrinologica    October 1, 1983   Volume 104, Issue 2 227-232 doi: 10.1530/acta.0.1040227
YoungLai EV, Jarrell JF.Granulosa cells were harvested from mares at various stages of the oestrous cycle and incubated in Krebs-Ringer bicarbonate buffer with 1 beta,2 beta[3H]androstenedione as substrate. The release of 3H2O expressed as CPM/h/mg protein varied from 44000 to 768000 in follicles from 7 mares. The release of 3H2O was not significantly altered by luteinizing hormone, follicle stimulating hormone or pregnant mare's serum gonadotrophin. There was a significant negative correlation between the release of 3H2O and the concentration of progesterone in the follicular fluid. Based on the assumption that the ...
Enzymatic trimethylation of lysine-72 in cytochrome c.
European journal of biochemistry    September 15, 1983   Volume 135, Issue 2 259-262 doi: 10.1111/j.1432-1033.1983.tb07646.x
Paik WK, Farooqui J, Gupta A, Smith HT, Millett F.The present observations are the continuation of our earlier study on the physicochemical mechanism of protein-lysine methylation. In this paper the electrophoretic behaviour (pI values) of two chemically modified horse heart cytochromes c at lysine-72 with trifluoromethylphenylcarbamoyl (neutral group) or carboxydinitrophenyl (acidic group) is compared with the enzymatically methylated cytochrome c. The results indicate that although both chemically modified cytochromes c have lower pI values than the unmodified cytochrome c, the enzymatic methylation appears to be much more efficient in lowe...
Measurement of superoxide dismutase, diamine oxidase and caeruloplasmin oxidase in the blood of thoroughbreds.
Research in veterinary science    September 1, 1983   Volume 35, Issue 2 160-164 
Smith P, Stubley D, Blackmore DJ.Methods were developed for the measurement of superoxide dismutase (SOD), diamine oxidase (DAO) and caeruloplasmin oxidase in the blood of thoroughbred horses. These enzymes were measured in 178 normal thoroughbreds stabled throughout the United Kingdom. The relationships between the activities of SOD, DAO and caeruloplasmin oxidase and the blood concentrations of their associated trace metals (copper, zinc and manganese) were studied in 52 of the thoroughbreds. Trace metals were measured by electrothermal atomic absorption spectrophotometry. No relationships were found between the activities ...
Sodium and potassium ion-dependent change in oligomerization of Na,K-ATPase in C12E8 detected by low-angle laser light scattering technique in combination with high performance porous silica-gel chromatography.
Journal of biochemistry    September 1, 1983   Volume 94, Issue 3 689-697 doi: 10.1093/oxfordjournals.jbchem.a134408
Nakao T, Ohno-Fujitani T, Nakao M.Approximate molecular weights and the subunit structures of Na,K-ATPase from horse kidney were estimated by means of the combination of porous silica gel chromatography, laser light scattering (LS) and refractive index (RI) measurements in C12E8. When the enzymes were eluted with NaCl- or KCl-containing solution, 3 or 4 protein peaks, respectively were detected except that of low molecular weight range. These peaks were tentatively named Na-1, Na-2, Na-2', Na-3 (NaCl-containing eluents), K-1, K-2, K-3 (KCl-containing eluents), respectively. Na,K-ATPase and K-p-nitrophenylphosphatase activities...
Linkage of the equine serum esterase (Es) and mitochondrial glutamate oxaloacetate transaminase (GOTM) loci. A horse-mouse homology.
The Journal of heredity    September 1, 1983   Volume 74, Issue 5 361-364 doi: 10.1093/oxfordjournals.jhered.a109811
Andersson L, Sandberg K, Adalsteinsson S, Gunnarsson E.Three previously described electrophoretic phenotypes of mitochondrial glutamate oxaloacetate transaminase (GOTM) in horse leukocytes are shown to be controlled by two codominant alleles at a single autosomal locus. The GOTM locus is linked to the serum esterase locus (Es), as no recombination between these loci was observed among 16 informative offspring in one sire family. The results assign GOTM to equine linkage group (LG) II. The hypothesis that a part of LG II (e-Es) shares homologies with mouse chromosome 8 is thus confirmed, as the murine homologue of GOTM is located within the cluster...
Unfolding pathway of myoglobin. Evidence for a multistate process.
Biochemistry    August 30, 1983   Volume 22, Issue 18 4165-4170 doi: 10.1021/bi00287a001
Bismuto E, Colonna G, Irace G.The free energy of unfolding of horse myoglobin has been calculated from the denaturation pattern induced by guanidine hydrochloride as well as by acid. The delta GH2O, i.e., the value in the absence of denaturant obtained by using the two-state transition model, was found to be 25% lower than that determined from the acid denaturation pattern, i.e., 12.0 kcal/mol, although the extent of protein denaturation produced by acid was much lower. The amount of helical structure surviving the acid-induced conformational change was estimated to be 50% of that present in the native protein, and it coul...
Interspecies activation of lecithin-cholesterol acyltransferase by apolipoprotein A-I isolated from the plasma of humans, horses, sheep, goats and rabbits.
Biochimica et biophysica acta    August 29, 1983   Volume 753, Issue 1 40-46 doi: 10.1016/0005-2760(83)90095-4
Chen CH, Albers JJ.The abilities of apolipoprotein A-I species isolated from humans, horses, sheep, goats and rabbits to activate purified human lecithin-cholesterol acyltransferase and the enzyme from homologous plasmas and plasma of other mammalian species were compared. Each purified apolipoprotein A-I species was individually incorporated into phosphatidylcholine/cholesterol vesicles by the cholate dialysis method to form proteoliposome common substrates (apolipoprotein A-I/phosphatidylcholine/cholesterol molar ratio of 1:250:12.5) for the enzyme activity assay. All apolipoprotein A-I species tested had the ...
Properties and distribution of phosphatidylinositol-specific phospholipase C in human and horse platelets.
Biochimica et biophysica acta    July 12, 1983   Volume 752, Issue 2 329-338 doi: 10.1016/0005-2760(83)90131-5
Siess W, Lapetina EG.Phospholipase C has been studied in homogenates, total particulate and soluble fractions of horse and human platelets. This enzyme, assayed with exogenous L-3-phosphatidyl[14C]inositol, is predominantly localized in the soluble fraction and its distribution parallels that of lactate dehydrogenase. A small percentage of activity present in the particulate fraction seems to be due to contamination with soluble enzyme. Enzyme from horse and human platelets appears identical, having a Km of 0.10-0.15 mM, acid pH optimum (pH 5.5) and showing Ca2+-dependency and weak inhibition by deoxycholate. Anal...
Effects of extensive resection of the small intestine in the pony.
American journal of veterinary research    July 1, 1983   Volume 44, Issue 7 1187-1191 
Tate LP, Ralston SL, Koch CM, Everitt JI.Small intestinal resection (SIR) is not uncommonly done in surgical treatment of equine colic, but little is known about the long-term effects of SIR on horses and ponies. Twelve ponies, fed maintenance amounts of pelleted feed, were divided randomly into 4 treatment groups. D-Xylose absorption curves were recorded for each pony before surgical treatments were performed. Treatments consisted of control (ileal bypass) and 40%, 60%, or 80% SIR. D-Xylose absorption, serum electrolyte, and enzyme profiles for each animal were recorded once every 30 days for 180 days after surgical treatment, and t...
[Study of conformational changes in alcohol dehydrogenase during its interaction with silochrome adsorbent by the EPR spectroscopy method].
Biokhimiia (Moscow, Russia)    June 1, 1983   Volume 48, Issue 6 970-974 
Kharakhonycheva NV, Likhtenshteĭn GI, Shkileva EA, Adamenkova MD.The possible use of EPR spectroscopy (spin labelling) for the study of horse liver alcohol dehydrogenase with a silochrome adsorbent is discussed. The rotatory diffusion of nitroxyl labels chemically linked to the enzyme was studied with reference to the time of the enzyme incubation with the adsorbent and the degree of its accumulation on the adsorbent surface. The mobility of nitroxyl radicals attached to the protein globules was shown to increase with time. It was concluded that the conformation of the enzyme molecules changes during their interaction with the adsorbent.
Localization of the second calcium ion binding site in porcine and equine phospholipase A2.
Biochemistry    May 10, 1983   Volume 22, Issue 10 2470-2478 doi: 10.1021/bi00279a025
Donné-Op den Kelder GM, de Haas GH, Egmond MR.At alkaline pH porcine pancreatic phospholipase A2 is known to bind two Ca2+ ions per protein molecule. One Ca2+ ion is strongly bound to the active site and is essential for enzyme activity. A second Ca2+ ion binds more weakly to the protein and improves the affinity of the enzyme for lipid-water interfaces severalfold at high pH values. A group having a pK around 6 controls enzyme binding to lipid-water interfaces in the absence of Ca2+. By use of proton titration techniques this group is now identified to be a carboxylate having an abnormally high pK. Its pK shifts to a value around 4.5 in ...
A study on the possible role of chymotrypsin in the aetiology of equine chronic obstructive pulmonary disease (COPD).
Veterinary immunology and immunopathology    April 1, 1983   Volume 4, Issue 3 387-395 doi: 10.1016/0165-2427(83)90048-x
Thomson JR, McPherson EA, Lawson GH, Wooding P, Brown R.The chymotrypsin activity of seven batches of Micropolyspora faeni and of five batches of Aspergillus fumigatus culture extracts, prepared for inhalation challenge in horses, was assayed and was found to range between 0.29 and 1.45 units/mg protein and 0.02 and 0.20 units/mg protein respectively. Horses affected with chronic obstructive pulmonary disease (COPD) were challenged with two batches of each antigen which had different chymotrypsin activities and no significant correlations were found between the degree of response to challenge and the chymotrypsin activity of the antigens. Inhalatio...
Use of procainamide gels in the purification of human and horse serum cholinesterases.
The Biochemical journal    April 1, 1983   Volume 211, Issue 1 243-250 doi: 10.1042/bj2110243
Ralston JS, Main AR, Kilpatrick BF, Chasson AL.Two large-scale methods based primarily on the use of procainamide-Sepharose gels were developed for the purification of horse and human serum non-specific cholinesterases. With method I, the procainamide-Sepharose 4B gel was used in the first step to handle large volumes of serum. With method II, the procainamide-Sepharose 4B gel was used in the final step to obtain pure enzyme. Although both methods gave electrophoretically pure cholinesterase preparations in good yields, they were significantly more efficient at purifying the horse enzyme than the human enzyme. To study this problem, the re...
Examination of the origin of increased equine serum alkaline phosphatase concentrations.
The Canadian veterinary journal = La revue veterinaire canadienne    April 1, 1983   Volume 24, Issue 4 108-111 
Trueman KF, Lumsden JH, McSherry BJ.Serum alkaline phosphatase activity was found to be increased in 32.6% of equine samples analyzed at the Ontario Veterinary College over an 18 month period. An attempt was made using sensitivity to L-phenylalanine and heat to identify the origin of increased serum alkaline phosphatase isoenzymes present in 44 clinical cases. No difference in sensitivity to either procedure was observed for serum alkaline phosphatase from groups of foals and horses representing different clinical problems. Alkaline phosphatase of osseous tissue origin appeared to be the major source of activity for each group o...
A comparative study of the effect of triazine herbicides on alcohol dehydrogenases isolated from various sources.
Environmental research    April 1, 1983   Volume 30, Issue 2 389-392 doi: 10.1016/0013-9351(83)90224-4
Leblová S, Galociová J, Cerovská N.The studied herbicides (terbutylazine, simazine) inhibit the activity of plant, animal, and yeast alcohol dehydrogenases. The inhibition constant Ki for alcohol dehydrogenase (ADH) isolated from peas and bakers' yeast equals approximately 10(-4) M, and that for ADH isolated from horse liver is of the order of 10(-5) M. The character of inhibition for all the herbicides studied for the reaction catalyzed by pea, liver, and yeast ADH is always noncompetitive toward ethanol and competitive with respect to NAD. The inhibition constants for the enzyme isolated from peas are pH independent. The inte...
Gamma Glutamyl Transferase in domestic animals.
Veterinary research communications    March 1, 1983   Volume 6, Issue 2 77-90 doi: 10.1007/BF02214900
Braun JP, Benard P, Burgat V, Rico AG.In domestic animals, Gamma Glutamyl Transferase is mainly in the kidneys, the pancreas and the intestine; its liver activity is relatively high in cows, horses, sheep and goats and very low in dogs, cats and birds. The use of plasma reference values can help to interpret the variations of serum GGT mainly in hepatobiliary diseases of cattle, sheep, goats and cholestatic disorders of dogs. Urinary GGT is a good test of kidney toxic damage.
Dansylarginine N-(3-ethyl-1.5-pentanediyl)amide. A potent and selective fluorescent inhibitor of butyrylcholinesterase.
Biochemical pharmacology    February 15, 1983   Volume 32, Issue 4 699-706 doi: 10.1016/0006-2952(83)90495-1
Brimijoin S, Mintz KP, Prendergast FG.Interactions between dansylarginine N-(3-ethyl-1,5-pentanediyl)amide (DAPA) and the cholinesterases were examined by the techniques of enzyme kinetics and fluorescence spectroscopy. When tested with partially purified enzyme preparations, DAPA was a potent inhibitor of butyrylcholinesterase (IC50 = 2 x 10(-7) M) but not of acetylcholinesterase (IC50 = 4 x 10(-4) M). For a detailed study of the effects of DAPA on butyrylcholinesterase (BuChE), the enzyme was purified to homogeneity from horse serum, with the aid of affinity chromatography on N-methyl acridinium. The kinetics of the inhibition o...
Intestinal alkaline phosphatase-like properties of horse kidney alkaline phosphatase.
Enzyme    January 1, 1983   Volume 30, Issue 4 269-272 doi: 10.1159/000469588
Hoffmann WE, Dorner JL, Morris H.Two isoenzymes of alkaline phosphatase from horse kidney were identified by cellulose acetate electrophoresis. Horse kidney alkaline phosphatase was similar to horse intestinal alkaline phosphatase, in regard to both antigenicity and response to levamisole inhibition, but different from horse liver alkaline phosphatase. This study suggests that horse kidney alkaline phosphatase is an expression of the intestinal gene locus and not the hepatic gene locus.
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...
S-adenosylhomocysteine hydrolase activity in horses, Equus cabalus, with severe combined immunodeficiency.
Comparative biochemistry and physiology. B, Comparative biochemistry    January 1, 1983   Volume 75, Issue 1 113-117 doi: 10.1016/0305-0491(83)90047-0
Magnuson NS, Decker DM, Perryman LE.1. Activities of S-adenosylhomocysteine (AdoHcy) hydrolase were measured in tissues of horses with severe combined immunodeficiency. No decrease in activity of the enzyme was detected. 2. The activity in erythrocytes was 14.2 ± 9.2 nmol AdoHcy formed/min/g hemoglobin and in fibroblasts it was 28.0 ± 7.9 nmol AdoHcy formed/min/108 cells. 3. Km values were obtained for hemolysates (0.77 μM) and for fibroblast lysates (0.59 μM). 4. Effects of 2′-deoxyadenosine on enzyme inactivation were studied.
The effect of exercise on blood parameters in standardbred and Finnish-bred horses.
Acta veterinaria Scandinavica    January 1, 1983   Volume 24, Issue 2 170-184 doi: 10.1186/BF03546745
Pösö AR, Soveri T, Oksanen HE.Serum enzyme activities, albumin, protein, urea, cholesterol, triglyceride, free fatty acid, glucose and lactate concentrations as well as hematocrit values were measured in standardbred and Finnish-bred horses at rest and after (i) a short controlled exercise and (ii) a trotting competition. There were no breed differences in the enzyme activities at rest and the 2 breeds responded in the same manner to the exercise. Only after the race proper significant increases in the enzyme activities were found. The activities rose more in the standardbred horses than in the Finnish-bred horses. Urea an...
Subcellular localization and properties of the NAD(P)H oxidase from equine polymorphonuclear leukocytes.
Enzyme    January 1, 1983   Volume 29, Issue 3 198-207 doi: 10.1159/000469633
Heyneman RA.The subcellular distribution of the superoxide-forming enzyme in horse polymorphonuclear leukocytes was investigated. After activation of the cells with sodium oleate, a relatively stable and NAD(P)H-dependent oxygen consumption and superoxide production was found in association with the plasma membranes. The pH dependence displayed an optimum near neutrality. The apparent Km values were 38 x 10(-6) mol/l for NADPH and 1,560 x 10(-6) mol/l for NADH, suggesting that NADPH is the physiological donor. The rates of oxygen uptake, O2- production, and NADP consumption were consistent with the stoich...
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...
Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes    January 1, 1983   Volume 18, Issue 1 29-63 doi: 10.1080/03601238309372357
Main AR.The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric ...
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 ...
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