Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:1.1.1.37 (malate dehydrogenase)
 4,591 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The method of enzyme-electrophoresis in agar gel according to Wieme (1959) was used for the study of lactate dehydrogenase (LDH) and malate dehydrogenase (MDH) isoenzymes of 24-hour and 48-hour Salmonella cultures exposed to a 0.02% solution of potassium dichloroisocyanurate (PDIC). Severe repression of LDH and MDH isoenzymes was observed immediately after the exposure of the culture to the disinfectant solution. A significant decrease in the content of the isoenzyme LDH1 and of the cytoplasmic fraction (C1) of MDH simultaneously with the appearance of the fractions LDH4, LDH1a and LDH1b were established in the strains cultured on MPA in the course of 24 hours following the exposure. A tendency to a decrease in the LDH1 content was preserved in the experimental cultures after 48 hours, but the spectrum of MDH isoenzymes showed almost no differences in comparison with that of MDH isoenzymes in 48-hour cultures of the control strains.
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PMID:Changes in lactate and malate dehydrogenase isoenzymes in salmonella under the effect of potassium dichloroisocyanurate. 56 70

Activities of lactate dehydrogenase (LDH) and NAD-dependent malate dehydrogenase (MDH) were considerably increased in blood serum of healthy children within the first 10 hrs after their birth. Content of LDH4 and LDH5 isoenzymes was increased, along with a decrease in LDH1 content, in blood serum. Differences in LDH isozyme spectra between blood serum and hemolysate in healthy newborns became more distinct within the perinatal period. In blood serum of newborns with hemolytic disease high activity of LDH and MDH was found immediately after birth. As distinct from healthy children, high content of LDH1 and very low concentrations of LDH4 and LDH5 were observed in blood serum of the impaired children within the perinatal period. The dissimilarity in LDH spectra became less distinct in blood serum and hemolysate of children with hemolytic disease. The composition of MDH isoenzymes was not distinctly altered in blood serum and hemolysate of both healthy and impaired newborn children within the perinatal period.
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PMID:[Activity and isoenzyme composition of lactate dehydrogenase and malate dehydrogenase in the blood and erythrocytes of newborn children with hemolytic disease]. 57 Jul 58

Isoenzyme spectra of lactate and malate dehydrogenases were studied by means of polyacrylamide gel disc electrophoresis in heart muscle and liver tissue of rabbits with thyreoidin toxicosis. Under conditions of thyreotoxicosis in liver tissue content of isoenzymes LDH4 and LDH5, which slowly moved to anode, was decreased; in heart muscle content of LDH2-LDH5 was also decreased. In liver tissue the relative predominance of LDH1-LDH2 was observed, in heart muscle of LDH1. Activity and isoenzyme pattern of MDH were shown to be unaltered in homogenates of the tissues in thyreotoxicosis. An aerobisation of the LDH isoenzyme spectrum together with normal content of MDH suggested that intensive aerobic oxidation of substrates of glycolytic pathway occurred in heart muscle and liver tissue of rabbits with thyreoidin toxicosis.
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PMID:[Lactate dehydrogenase and malate dehydrogenase isoenzymes in the myocardium and liver of rabbits with thyrotoxicosis]. 111 10

The genetic structure of two Chukot Evens subpopulations (314 individuals) for electrophoretic protein systems and taste sensitivity to PTC was studied. 17 of the 39 loci were polymorphic (43.59%). The following systems were completely monomorphic: diaphorase NAD H (Dia); glucose-6-phosphate dehydrogenase (G-6-PD); glutamatoxalate transaminase (GOT); carbonic anhydrase (Ca-1); catalase (Ct), lactate dehydrogenase (loci LDH-A and LDH-B); leucine aminopeptidase (Lap); malate dehydrogenase (MDH); purine nucleoside phosphorylase (PNP); superoxide phosphorylase (PNP); superoxide dismutase (SOD); phosphoglucomutase-2 (PGM2); cholinesterase (locus E1); red cell esterase (4 loci); albumin (Alb); hemoglobin (Hb A and B); ceruloplasmin (Cp); and blood, gren, using the standard method. The following systems were polymorphic: red cell acid phosphatase (AcP); phosphoglucomutase-1 (PGM1); 6-phosphogluconate dehydrogenase (PGD); glutamatepyruvate transaminase (GPT); glyoxalase-1 (GLO-1); esterase (EsD); adenilatkinase (AK); alkaline phosphatase (Pp); cholinesterase (locus E2); haptoglobin (Hp); transferrin (Tf); group-specific component (Gc) and ABO, MN, Lewis, P blood groups and taste sensitivity to PTC. The following allele frequencies for polymorphic loci have been detected: AKI = 0.994; GLO = 1I = 0.082; GPT1 = 0.653; AcPA = 0.400; AcPB = 0.599; AcPC = 0.001; PGDA = 0.944; PGM1(1) = 0.906; EsD1 = 0.897; E2+ = 0.048; HpI = 0.394; GcI = 0,919; Tfc = 0.987; r(O) = 0.669; p(A) = 0.184; q(B) = 0.146; M = 0.711; Le = 0.411; P1+ = 0.521; t = 0.295. The genetic structure of Chukot Evens population is significantly nearer to that of the other ethnic groups of the North-East, in comparison with the genetic structure of Evenks of the Middle Siberia.
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PMID:[Genetic structure of the populations of native inhabitants in the northeastern USSR. V. The Chukot Evens]. 293 99

Plasma CPK activity and the activity of isoenzymes MDH, AST and LDH were assessed in 60 patients with myocardial infarction of different severity, with reference to the time since the onset of the attack. The peaks of CPK and MDH-C activity were reached sooner than those of LDH-M and AST-C, while the CPK and MDH-C curves were similar. The severity of the disease showed correlation to later onset of enzyme peaks and markedly delayed decrease in the respective values. Increased activity of mitochondrial isoenzymes and blood LDH-M provided additional information on the severity of the disease. Delayed normalization of these activities was associated with a poor diagnosis.
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PMID:[Malate dehydrogenase isoenzymes in myocardial infarction]. 323 Jul 77

The ontogenetic trends in the expression of 25 isozymes in liver, gizzard, heart, and pectoralis muscle of White Leghorn chickens were examined using starch gel electrophoresis. Little change in expression during development was evident in liver S-AAT-A, GPI-A, S-ICDH-A, S-MDH-A and M-MDH-A, in gizzard S-ACON-A, ADH-A, GPI-A, HK-1, HK-3, ME-A PEP-1, and PGM-A, in heart ADH-A, HK-1, HK-3, ME-A, PEP-2, PGM-A, and LDH-A, in pectoralis M-ACON-A, S-ACON-A, ADH-A, HK-1, HK-3, ME-A, PEP-2, and PGM-A, and in liver, gizzard, and heart M-ACON-A, ALD-A, CK-A, G3PDH-A, HK-1, and PGDH-A. Increasing levels of activity were demonstrated in liver ADH-A, ME-A, and PEP-2, in heart M-MDH-A, S-ICDH-A, M-ICDH, and M-AAT-A, and in pectoralis LDH-A, LDH-B, G3PDH-3, ALD-A, CK-A, HK-2, and PGM-B. There was a decrease in the activity of HK-1 in liver and in PEP-1 and PGDH-A in pectoralis muscle throughout development. While CK-C is active in the embryonic pectoralis, CK-A is restricted to later developmental stages. Isozyme expressions in regions of the pectoralis containing fast and slow muscle fibers in 7-month-posthatch individuals were noted and found to be identical. The results underscore the need to use similar developmental stages and tissue samples in comparative electrophoretic studies of birds.
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PMID:A survey of tissue-specific isozyme expressions during chicken ontogeny. 360 63

Schistosoma mansoni was isolated by hatching eggs obtained from a naturally infected Rat in Grand Etang, Guadeloupe; fifty Biomphalaria glabrata were exposed to five miracidia each. The resulting cercariae were used to infect laboratory mice which were later sacrificed to provide worms for enzyme analyses and eggs for further infections. Seven enzymes in extracts of individual worms were examined by isoelectric focusing in polyacrylamide gels: AcP, G6PDH, PGM, GPI and HK showed no variation, whereas MDH and LDH proved to be polymorphic. Two MDH loci were recognised, MDH-2 was invariant whereas two alleles were assumed at the MDH-1 locus. It was not possible to make a genetic interpretation of the complex banding pattern of LDH, although 4 types (LDH-A, -B, -C, -D) were observed. Of the snail infections, one batch of snails was exposed to 5 miracidia per snail in the normal way whereas other snails were each exposed to a single miracidium. The latter were sacrificed to provide sporocysts to transplant into further groups of recipient snails. Cercariae from the recipient snails were used to infect mice and the adult worms were analysed and compared with the normally passaged material. In this way, three lines, defined by the possession of particular MDH and LDH types, were selected from the originally polymorphic population; two were identical. The combination of single miracidium infections and enzyme typing has illustrated the possibility of selecting parasite lines of known genotype; transplantation of sporocysts from snail to snail has demonstrated that such lines can be maintained exclusively in the intermediate host.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[Selection of genotypes of Schistosoma mansoni and their maintenance by sporocyst transplantation]. 643 12

The isozyme patterns and activities of six enzymes were determined in surgical biopsy samples of lung tumors and non-neoplastic pulmonary areas. Fetal lungs were also examined. No tissue differences were found in the isozyme pattern of hexokinase or alkaline phosphatase; small differences in pyruvate kinase isozyme proportions were observed. The tumors exhibited significant deviations with respect to the lactate dehydrogenase (LDH) and malate dehydrogenase (MDH) isozyme patterns. Despite the diversity of cell types, the proportions of the M-subunit of LDH in each tumor and that of the mitochondrial isozyme of MDH in all but one tumor were higher than in control samples from the same lung. In contrast, the normal fetal lung showed a higher LDH-H proportion than did adult lung and a mature MDH isozyme pattern. The alpha-glycerophosphate dehydrogenase and adenylate kinase activities of the tumors were about one-tenth and one-fourth, respectively, of those of nonneoplastic adult lung. These lower activities (evident also in normal fetal lung) were accompanied by 3- to 5-fold increases in the LDH, MDH, pyruvate kinase, and hexokinase activities of the tumors; fetal lungs had lesser increases (2- to 3-fold) for the first 3 enzymes. The common features of tumors with different cell types and histological grade identified here point to several enzymes the quantitation or isozyme analysis of which may be of practical use in distinguishing cancerous from nonneoplastic human lung samples. A combination of different indicators, such as opposite changes in LDH and alpha-glycerophosphate dehydrogenase activity, coupled with elevated proportions of LDH-M, may be used to diagnose neoplasia most reliably.
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PMID:Enzyme activities and isozyme patterns in human lung tumors. 669 92

Twelve different enzyme activities, which are listed and explained in greater detail in Table 2, were determined statistically secured, and discussed, following a three-year study into arterial plasma of 118 female and 124 male minks, aged between six and seven months and kept under anaesthesia. Simply normally distributed or logarithmically distributed plasma enzyme activities were found to differ primarily by sex, with other experimental conditions being identical and regular. The enzyme activities of ICDH, active CPK, and total LDH (the latter only with females) were normally distributed, whereas all the other enzymes activities tested, except for gamma-GT and SDH, were of Gaussian distribution only after logarithmic transformation of the individual values. The plasma enzyme activities of GPT, LAP, ChE, LDH1, MDH, and AP differed from those of GOT, gamma-GT, SDH, total LDH and active CPK, in that they usually exhibited highly significant sex-related differences. All minks were tranquilised and kept under general anaesthesia, using neuroleptanalgesia, but all their enzyme activities were found to vary just as widely as those reported elsewhere in literature, in the context of minks without anaesthesia. The latter result was experimentally confirmed by means of a model experiment in which enzyme activities were recorded from nine male ferrets, prior to, during, and after neuroleptanalgesia.
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PMID:[Morphology and biochemistry of blood of various mustelids. 3. Enzymographic studies of arterial plasma of mink (Mustela vison Schreber, 1777)]. 701 Dec 44

The effects of insulin and tyroxin on the activities of pyruvate kinase, pyruvate dehydrogenase, ATP-citrate-lyase, NADP-malate dehydrogenase (decarboxylase), lactate dehydrogenase and on that of pyruvate carrier in rat liver were investigated. Insulin increased the activities of all the enzymes tested. The total activity of lactate dehydrogenase was not altered thereby; however, a redistribution of isoenzymes towards an increase in LDH1 and a decrease of LDH4 was observed. No increase of the pyruvate kinase, ATP-citrate-lyase and NADP-malate dehydrogenase activities took place, when actinomycin D was injected simultaneously with insulin. Tyroxin decreased the activities of pyruvate kinase, pyruvate dehydrogenase and ATP-citrate-lyase and increased that of NADP-malate dehydrogenase. The role of induction by insulin and inhibition by tyroxin of the enzyme activity in the citrate-pyruvate system of CoASA transport in lipogenesis control in rat liver is discussed. It is assumed that when lipogenesis is stimulated by insulin, the malate oxidized by the malate dehydrogenase reaction is formed in the cytoplasm, while under tyroxin action it is produced by the mitochondria.
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PMID:[Control of lipogenesis in rat liver by changing the enzyme activity of the citrate-pyruvate system of acetyl coenzyme A transport]. 703 8


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