Literature DB >> 4310059

Studies in vitro on the effects of 1H,2H,4H(5H)-octafluorocyclohexane and 1H,4H(2H)-nonafluorocyclohexane on enzymes and organelles.

J Nath, H G Bray.   

Abstract

A comparison has been made of the effect of 1H,2H,4H(5H)-octafluorocyclohexane, which is highly toxic (LD(50) 17mg./kg. in rats), and of 1H,4H(2H)-nonafluorocyclohexane, which is relatively non-toxic (LD(50)>440mg./kg. in rats), on the respiration of rat liver homogenates and mitochondria in vitro. 1H,2H,4H(5H)-Octafluorocyclohexane strongly inhibited the respiration of both homogenates and mitochondria, but neither compound had any significant effect on glycolysis or on glutamate dehydrogenase or NADH-cytochrome c reductase activity. 1H,2H,4H(5H)-Octafluorocyclohexane, however, caused a very marked inhibition of cytochrome oxidase activity, causing an almost complete lesion in this region of the respiratory chain. 1H,4H(2H)-Nonafluorocyclohexane was without effect in this respect. A marked decrease in turbidity of mitochondrial suspensions at 520nm. was caused by addition of both compounds, the effect being greater with 1H,2H,4H(5H)-octafluorocyclohexane. ATP, Mg(2+) and bovine serum albumin did not reverse these changes. Mitochondrial adenosine triphosphatase activity was increased twofold by the toxic compound, but only slightly by the non-toxic compound. Electron-microscopic examination of mitochondria treated with 1H,2H,4H(5H)-octafluorocyclohexane revealed gross morphological damage, whereas the effect of 1H,4H(2H)-nonafluorocyclohexane appeared to be merely to cause swelling. The results obtained account, to some extent at any rate, for the toxic effects of 1H,2H,4H(5H)-octafluorocyclohexane.

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Year:  1969        PMID: 4310059      PMCID: PMC1184965          DOI: 10.1042/bj1140785

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  10 in total

1.  On the mechanism of oxidative phosphorylation. IV. Mitochondrial swelling caused by arsenite in combination with 2,3-dimercaptopropanol and by cadmium ion.

Authors:  A L FLUHARTY; D R SANADI
Journal:  Biochemistry       Date:  1962-03       Impact factor: 3.162

2.  Studies of the electron transport system. XXXV. Purification and properties of cytochrome oxidase.

Authors:  D E GRIFFITHS; D C WHARTON
Journal:  J Biol Chem       Date:  1961-06       Impact factor: 5.157

3.  The stimulation of adenosine triphosphatase in submitochondrial particles by sulfhydryl reagents.

Authors:  C COOPER
Journal:  J Biol Chem       Date:  1960-06       Impact factor: 5.157

4.  The enzymic hydrolysis of adenosine triphosphate by liver mitochondria. I. Activities at different pH values.

Authors:  D K MYERS; E C SLATER
Journal:  Biochem J       Date:  1957-12       Impact factor: 3.857

5.  The catalytic effect of 2,4-dinitrophenol on adenosinetriphosphate hydrolysis by cell particles and soluble enzymes.

Authors:  H A LARDY; H WELLMAN
Journal:  J Biol Chem       Date:  1953-03       Impact factor: 5.157

6.  The measurement of the cytochrome oxidase activity of enzyme preparations.

Authors:  E C Slater
Journal:  Biochem J       Date:  1949       Impact factor: 3.857

7.  Latent adenosinetriphosphatase activity in resting rat liver mitochondria.

Authors:  V R POTTER; P SIEKEVITZ; H C SIMONSON
Journal:  J Biol Chem       Date:  1953-12       Impact factor: 5.157

8.  Water uptake and extrusion by mitochondria in relation to oxidative phosphorylation.

Authors:  A L LEHNINGER
Journal:  Physiol Rev       Date:  1962-07       Impact factor: 37.312

9.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

10.  A METHOD FOR THE COLORIMETRIC DETERMINATION OF PHOSPHORUS.

Authors:  J B Sumner
Journal:  Science       Date:  1944-11-03       Impact factor: 47.728

  10 in total

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