Literature DB >> 7334020

Generation of hydrogen peroxide on oxidation of NADH by hepatic plasma membranes.

T Ramasarma, A Swaroop, W MacKellar, F L Crane.   

Abstract

The oxidation of NADH by mouse liver plasma membranes was shown to be accompanied by the formation of H2O2. The rate of H2O2 formation was less than one-tenth the rate of oxygen uptake and much slower than the rate of reduction of artificial electron acceptors. The optimum pH for this reaction was 7.0 and the Km value for NADH was found to be 3 X 10(-6) M. The H2O2-generating system of plasma membranes was inhibited by quinacrine and azide, thus distinguishing it from similar activities in endoplasmic reticulum and mitochondria. Both NADH and NADPH served as substrates for plasma membrane H2O2 generation. Superoxide dismutase and adriamycin inhibited the reaction. Vanadate, known to stimulate the oxidation of NADH by plasma membranes, did not increase the formation of H2O2. In view of the growing evidence that H2O2 can be involved in metabolic control, the formation of H2O2 by a plasma membrane NAD(P)H oxidase system may be pertinent to control sites at the plasma membrane.

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Year:  1981        PMID: 7334020     DOI: 10.1007/bf00743203

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  31 in total

1.  The oxidation of drugs by liver microsomes: on the role of TPNH and oxygen.

Authors:  J R GILLETTE; B B BRODIE; B N LA DU
Journal:  J Pharmacol Exp Ther       Date:  1957-04       Impact factor: 4.030

2.  Evaluation of the horseradish peroxidase-scopoletin method for the measurement of hydrogen peroxide formation in biological systems.

Authors:  A Boveris; E Martino; A O Stoppani
Journal:  Anal Biochem       Date:  1977-05-15       Impact factor: 3.365

3.  Dependence of plasmodial glutathione metabolism on the host cell.

Authors:  J R Eckman; J W Eaton
Journal:  Nature       Date:  1979-04-19       Impact factor: 49.962

4.  Oxidative metabolism of the human eosinophil.

Authors:  L R DeChatelet; P S Shirley; L C McPhail; C C Huntley; H B Muss; D A Bass
Journal:  Blood       Date:  1977-09       Impact factor: 22.113

5.  A rapid and reproducible homogenization procedure for the isolation of plasma membranes from rat liver.

Authors:  W N Yunghans; D J Morré
Journal:  Prep Biochem       Date:  1973

6.  Hexose transport in isolated brown fat cells. A model system for investigating insulin action on membrane transport.

Authors:  M P Czech; J C Lawrence; W S Lynn
Journal:  J Biol Chem       Date:  1974-09-10       Impact factor: 5.157

7.  Vanadate inhibits mevalonate synthesis and activates NADH oxidation in microsomes.

Authors:  A S Menon; M Rau; T Ramasarma; F L Crane
Journal:  FEBS Lett       Date:  1980-05-19       Impact factor: 4.124

8.  Characterisation of the enzyme defect in chronic granulomatous disease.

Authors:  A W Segal; T J Peters
Journal:  Lancet       Date:  1976-06-26       Impact factor: 79.321

9.  Insulin-stimulated intracellular hydrogen peroxide production in rat epididymal fat cells.

Authors:  J M May; C de Haën
Journal:  J Biol Chem       Date:  1979-04-10       Impact factor: 5.157

10.  Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria.

Authors:  J F Turrens; A Boveris
Journal:  Biochem J       Date:  1980-11-01       Impact factor: 3.857

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  5 in total

Review 1.  Electron and proton transport across the plasma membrane.

Authors:  F L Crane; I L Sun; R Barr; H Löw
Journal:  J Bioenerg Biomembr       Date:  1991-10       Impact factor: 2.945

2.  A vanadate-stimulated NADH oxidase in erythrocyte membrane generates hydrogen peroxide.

Authors:  S Vijaya; F L Crane; T Ramasarma
Journal:  Mol Cell Biochem       Date:  1984-06       Impact factor: 3.396

Review 3.  NADH oxidase of plasma membranes.

Authors:  D J Morré; A O Brightman
Journal:  J Bioenerg Biomembr       Date:  1991-06       Impact factor: 2.945

4.  The oxidative function of diferric transferrin.

Authors:  Frederick L Crane; Hans Löw
Journal:  Biochem Res Int       Date:  2012-02-09

5.  CYP450 Mediates Reactive Oxygen Species Production in a Mouse Model of β-Thalassemia through an Increase in 20-HETE Activity.

Authors:  Rayan Bou-Fakhredin; Batoul Dia; Hilda E Ghadieh; Stefano Rivella; Maria Domenica Cappellini; Assaad A Eid; Ali T Taher
Journal:  Int J Mol Sci       Date:  2021-01-23       Impact factor: 5.923

  5 in total

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