Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.6.99.1 (NADPH-diaphorase)
3,903 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Morphological and histochemical investigations of the activity of succinate, malate, lactate, isocitrate, and glucoso-6-phosphate dehydrogenases, and NAD-diaphorase in the central, marginal, borderline and perifocal zones of ischemic brain infarctions were carried out. Deep changes in the activity of the enzymes listed, and peculiarities of this activity in various brain structures and tissues were revealed. A connection between the activity of the enzymes, the duration of the infarction, and the structural and biochemical peculiarities of the affected brain part is demonstrated. A suggestion is made on the pathogenesis of the ischemic infarctions and on the possibility of using histochemical data for the purposes of the pathoanatomic diagnosis.
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PMID:[Morphologo-histochemical characteristics of ischemic cerebral infarcts in the acute stage of the stroke in patients with atherosclerosis]. 689 83

The article deals with the results of histochemical study of some redox and proteolytic enzymes (SDH, MDH, NAD-diaphorase, LDH, and acid and alkaline phosphatase) in experiments on animals in various periods after infliction of a craniocerebral injury and on autopsy material, i.e. the brain of patients who had died from severe craniocerebral injury incompatible with life. It is shown that the activity of all enzymes decreases (SDH, MDH, NAD-diaphorase, and alkaline phosphatase) or increases (LDH, acid phosphatase) in various periods after the injury. The results were compared with the findings of morphological examination of the same brain areas performed by means of neurohistological methods.
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PMID:[Redox and proteolytic enzymes in brain tissue after a concussion]. 689 60

A new enzymatic fluorimetric assay for the determination of total serum bile acids is described. The enzyme 3 alpha-idroxysteroid NAD oxireductase by oxydising the free OH in position 3 alpha of bile acid molecule, reduce NAD previously added. Afterwards the hydrogen of the generated NADH is transferred by a diaphorase to resazurin to yield the fluorophore resorufin proportionally to the amount of bile acids in the sample. The assay is simple, accurate, without bilirubin's influence and useful for a routine use because the analysis time is not different from the more common laboratory tests.
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PMID:[Spectrophotofluorimetric enzymatic determination of total serum bile acids]. 692 10

In the early stages of experiments there was a structural-metabolic reconstruction in the adrenal cortex, manifest by changes in interzonal relations and dissociation of the activity of enzymes responsible for energy supply and synthesis of steroid hormones. Analogous changes were also seen later on. However, in the early stages that process was a response to the pancreas injury, whereas in the later period it preceded the emergence of repeated lesions in the gland. In animals with experimental pancreatitis, administration of metapyrone caused an activation of NAD-diaphorase in the glomerular and reticular zones and concurrent potentiation of the activity of glucose-6-phosphate dehydrogenase in all 3 zones of the adrenal cortex.
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PMID:[Histoenzymological characteristics of the adrenal cortical reaction in variants of experimental pancreatitis]. 695 49

Results of histochemical study of testicular tissue in 31 patients, aged 2.5 to 31 years, suffering from dysgenesia syndrome of the testis are presented. Enzymes and lipids furnishing synthesis of steroid hormones (3-beta-oxysteroid dehydrogenase, alcohol dehydrogenase, glucose-6-phosphate dehydrogenase. NAD- and NADP-diaphorase, cholesterol and its esters) were revealed in Leydig's cells of pubertal-juvenile and adult patients, in Leydig's cells precursors in children, and also in Sertoli's cells of all these patients. All these cellular elements possessed high activity of the enzymes under study. It is suggested that Sertoli cells and Leydig's cells precursors, along with mature Leydig's cells, provide a sufficiently high functional activity of the gonads in patients with dysgenesia of the testis.
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PMID:[Functional activity of gonadal glandular cells in patients with testicular dysgenesis]. 699 Apr 2

A series of straight chain N-alkymaleimides was shown to simultaneously inactivate the reductase, transhydrogenase and diaphorase activities of yeast glutathione reductase (NAD(P)H: oxidized-glutathione oxidoreductase, EC 1.6.4.2.) at pH 7.5 and 25 degrees C. Apparent second-order rate constants for the inactivation of all enzyme activities exhibited parallel increases with increasing chainlength from C-2 through C-7 of the alkyl substituent of the enhanced binding of maleimides through nonpolar interactions with the enzyme. Reduction of the active site disulfide with NADPH was required prior to addition of maleimide for inactivation to occur. NADP, AcPyADP, SNADP, AADP, and oxidized glutathione all protected the enzyme from inactivation. 2'AMP, 3' AMP, 2'-phospho-5' AMP, 2'-phospho5'-ADP and 2'-phospho-ADP-ribose although all coenzyme-competitive inhibitors failed to protect the enzyme from N-ethylmaleimide inactivation. N-Phenyl and N-alkylmaleimides covalently modified two, of six available sulfhydryl groups per subunit. No other amino acid residues were modified. The reactivity of these sulfhydryl groups was at least two orders of magnitude higher than any reported for the N-ethylmaleimide reaction with many other 'essential sulfhydryl' enzymes. No change in the charge transfer band of the reduced enzyme was observed upon complete inactivation by N-ethyl, N-heptyl or N-phenylmaleimide. The retention of the charge transfer band after selective modification of two sulfhydryl groups suggests the involvement of a third reactive sulfhydryl group in the functioning of the yeast enzyme. No inactivation was observed when coenzymatically reduced enzyme was incubated with the site-specific sulfhydryl reagent, diazotized AADP.
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PMID:Simultaneous inactivation of the catalytic activities of yeast glutathione reductase by N-alkylmaleimides. 701 85

The investigation was carried out on 86 white non-inbred male rats. Hypokinesia was produced by putting the animals into pencil-boxes for 1,2 and 4 weeks. The changes in specific volumes of various hepatic microvessels under hypokinesia and under hypokinesia combined with metyrapone administration were studied sterologically. NAD-diaphorase activity in hepatocytes and in the interlobular connective tissue was estimated photometrically. hypokinesia produces certain changes in the specific volume of all the hepatic microvessels studied, but the degree and character of the volumetric relations revealed between these microvessels are different. At metyrapone administration, the volumetric changes in various microvessels occur with greater regularity. The changes in NAD-diaphorase activity under the same conditions occur slower and by the end of the experiment the enzymatic activity returns to the initial level.
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PMID:[Functional and morphological characteristics of rat liver microvessels in hypokinesia]. 709 90

The purification by affinity chromatography up to homogeneity and the properties of NAD-reductase from purple sulfur bacterium Thiocapsa roseopersicina, strain BBS, are described. The molecular weight of NAD-reductase is about 80000; pI is 3.9. The enzyme consists of two subunits. According to the stabilizing effect of FAD at preparative electrophoresis and the inhibitory effect of atebrine NAD-reductase is a flavoprotein. The bulk of the enzyme (about 75%) is localized in the cell periplasmic space. NAD-reductase is less thermostable and has a lower O2 stability as compared to the NADP-reductase from the same organism. The enzyme is specific to NADH ane catalyzes the menadione-reductase reaction, diaphorase reaction of benzyl viologen and methyl viologen reductions. In the presence of NADH NAD-reductase reduces cytochromes c552 and "c3" from T. roseopersicina and forms a complex with spinach ferredoxin.
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PMID:[Purification and properties of NAD-reductase from phototrophic bacterium Thiocapsa roseopersicina]. 723 99

1-Methoxy-5-methylphenazinium methyl sulfate (1-methoxyPMS) is a photochemically stable electron mediator between NAD(P)H and tetrazolium dyes. We have examined the efficiency of 1-methoxyPMS as an electron mediator in the assay of human lactate dehydrogenase (LDH, EC 1.1.1.27) and the activity staining of LDH isozymes after electrophoresis. The turnover number of 1-methoxyPMS as an electron mediator between NADH and nitrotetrazolium blue was 10--12 s-1, which is a value equal to that of PMS. Correlation coefficient between the estimated LDH activities of human sera obtained with 1-methoxyPMS and those obtained with diaphorase was 0.998. 1-MethoxyPMS successfully substituted for the unstable PMS in the activity staining of LDH isozymes of human serum, giving less background staining. We conclude that 1-methoxyPMS will be useful for routine methods of activity assay and activity staining of enzymes of diagnostic importance.
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PMID:Use of 1-methoxy-5-methylphenazinium methyl sulfate (1-methoxyPMS) in the assay of some enzymes of diagnostic importance. 735 52

Examination of macrophages, polymorphonuclear leukocytes (PMNL) and lymphocytes of the trachea, PMNL and blood lymphocytes, of the condition of pulmonary tissue in the time course of the process (1st day--l months) revealed an association between the developing cellular and tissue changes. The development of alterations in the lungs with predominant anabolic changes and moderate exudation are characterized by a decrease in the content of nucleoproteins (deoxyribonucleoproteins, ribonucleoproteins), and activity of NAD-diaphorase and alkaline phosphatase, an increase in the activity of acid phosphatase in the above-mentioned cells of the trachea and blood as well as by increased permeability of lysosomal membranes and degeneration of macrophages, PMNL and lymphocytes of the trachea. The above cellular changes in combination with increased permeability of PMNL and blood lymphocyte lysosomal membranes correspond to the development in the lungs of catabolic alterative lesions, marked exudation, and suppurative-necrotic processes. The increase in the content of nucleoproteins and NAD-diaphorase and alkaline phosphatase activity and the decrease in the acid phosphatase activity are accompanied by activation of proliferation in the lungs.
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PMID:[Cyto-histochemical study of morphogenesis of experimental nonspecific pneumonia]. 741 96


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