Literature DB >> 7274308

Metabolism of succinonitrile in liver: studies on the systems involved in cyanide release.

M Floreani, F Carpenedo, R Santi, A R Contessa.   

Abstract

The liberation of cyanide from succinonitrile has been studied to obtain information on the cellular systems responsible for the release of this metabolite. 1) Using isolated endoplasmic reticulum preparations a complex between succinonitrile and cyt. P 450 has been detected. This finding together with the inhibition of cyanide liberation by SKF-525A in liver slices indicates that the endoplasmic reticulum is involved in the early stages of succinonitrile metabolism. 2) The decreased metabolism of succinonitrile which was observed after addition of inhibitors of oxidative phosphorylation indicates that an energy-dependent mitochondrial step might be involved in the subsequent steps. 3) It is concluded that cyanide liberation from succinonitrile is a multistep process in which the mitochondrial membrane and the endoplasmic reticulum are involved. The requirement for cellular integrity in order to accomplish the process of succinonitrile metabolism suggests other components or equilibria that are difficult to reproduce in in vitro experiments.

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Year:  1981        PMID: 7274308     DOI: 10.1007/BF03189480

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  17 in total

1.  EFFECTS OF ETHANOL ON MITOCHONDRIAL OXIDATIONS.

Authors:  B O CHRISTOPHERSEN
Journal:  Biochim Biophys Acta       Date:  1964-04-04

2.  The intracellular distribution of glycolytic and other enzymes in rat-brain homogenates and mitochondrial preparations.

Authors:  M K JOHNSON
Journal:  Biochem J       Date:  1960-12       Impact factor: 3.857

3.  Arginase, adenosinepyrophosphatase, and rhodanese levels in the liver of rats.

Authors:  O ROSENTHAL; C S ROGERS; H M VARS; C C FERGUSON
Journal:  J Biol Chem       Date:  1950-08       Impact factor: 5.157

4.  Spectral studies of drug interaction with hepatic microsomal cytochrome.

Authors:  J B Schenkman; H Remmer; R W Estabrook
Journal:  Mol Pharmacol       Date:  1967-03       Impact factor: 4.436

5.  Substrate interaction with hydroxylase system in liver microsomes.

Authors:  Y Imai; R Sato
Journal:  Biochem Biophys Res Commun       Date:  1966-03-22       Impact factor: 3.575

6.  Evidence for biochemically different types of vesicles in the hepatic microsomal fraction.

Authors:  Y Imai; A Ito; R Sato
Journal:  J Biochem       Date:  1966-10       Impact factor: 3.387

7.  Liberation of cyanide from succinonitrile.

Authors:  A R Contessa; R Santi
Journal:  Biochem Pharmacol       Date:  1973-04-01       Impact factor: 5.858

8.  Fate of succinonitrile-1- 14 C in the mouse.

Authors:  R Cavanna; F Pocchiari
Journal:  Biochem Pharmacol       Date:  1972-09-15       Impact factor: 5.858

9.  Induction and inhibition of hepatic microsomal and mitochondrial enzymes by ethanol.

Authors:  E Rubin; P Bacchin; H Gang; C S Lieber
Journal:  Lab Invest       Date:  1970-06       Impact factor: 5.662

10.  Liberation of cyanide from succinonitrile. 2. The effect of ethanol.

Authors:  A R Contessa; M Floreani; A C Bonetti; R Santi
Journal:  Biochem Pharmacol       Date:  1978       Impact factor: 5.858

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