Literature DB >> 4026577

Structure-acute toxicity relationship of dinitriles in mice.

H Tanii, K Hashimoto.   

Abstract

Acute toxicity and metabolism of seven dinitriles in mice was studied in relation to the chemical structures. The oral LD50 for each nitrile was determined under different conditions for mice pretreated with either carbon tetrachloride (CCl4) or olive oil. All test nitriles were metabolized into cyanide in vivo and in vitro. The cyanide level was variable among the compounds (0.35-0.74 micrograms CN/g brain) at death in the brains of mice, the level for malono- and adiponitrile being comparable to that found in mice killed by dosing with potassium cyanide. After receiving each nitrile, the mean survival time of mice pretreated with CCl4 was prolonged and their brain cyanide level decreased when compared with the corresponding control. With malononitrile, the former did not significantly change and the latter decreased slightly. Brain cyanide levels of control mice at death showed a peak at the lower log P region, while those of CCl4-pretreated animals remained lower independently of log P, with the exception of malononitrile. Microsomal metabolism of nitriles to cyanide was greatly inhibited when microsomes were prepared from livers of mice pretreated with CCl4. The relationship between log (1/LD50-CCl4), LD50 in mice pretreated with CCl4, and log P fits a parabolic plot.

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Year:  1985        PMID: 4026577     DOI: 10.1007/bf00343116

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  18 in total

1.  Critical role of lipid peroxidation in carbon tetrachloride-induced loss of aminopyrine demethylase, cytochrome P-450 and glucose 6-phosphatase.

Authors:  E A Glende; A M Hruszkewycz; R O Recknagel
Journal:  Biochem Pharmacol       Date:  1976-10-01       Impact factor: 5.858

2.  Cumulative excretion of succinonitrile in mice.

Authors:  S H Curry
Journal:  Biochem Pharmacol       Date:  1975-02-01       Impact factor: 5.858

3.  The effects and the fate of malononitrile and related compounds in animals tissues.

Authors:  J STERN; H WEIL-MALHERBE; R H GREEN
Journal:  Biochem J       Date:  1952-09       Impact factor: 3.857

4.  Liberation of cyanide from succinonitrile.

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

5.  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

6.  Studies on the destruction of liver microsomal cytochrome P-450 by carbon tetrachloride administration.

Authors:  H A Sasame; J A Castro; J R Gillette
Journal:  Biochem Pharmacol       Date:  1968-09       Impact factor: 5.858

7.  The role of cyanide liberation in the acute toxicity of aliphatic nitriles.

Authors:  C C Willhite; R P Smith
Journal:  Toxicol Appl Pharmacol       Date:  1981-07       Impact factor: 4.219

8.  Structure-toxicity relationship of acrylates and methacrylates.

Authors:  H Tanii; K Hashimoto
Journal:  Toxicol Lett       Date:  1982-04       Impact factor: 4.372

9.  Inhibition of rat liver aldehyde dehydrogenase by carbon tetrachloride.

Authors:  J J Hjelle; J H Grubbs; D G Beer; D R Petersen
Journal:  J Pharmacol Exp Ther       Date:  1981-12       Impact factor: 4.030

10.  Studies on in vitro metabolism of acrylamide and related compounds.

Authors:  H Tanii; K Hashimoto
Journal:  Arch Toxicol       Date:  1981-09       Impact factor: 5.153

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  1 in total

1.  Influence of ethanol on the in vivo and in vitro metabolism of nitriles in mice.

Authors:  H Tanii; K Hashimoto
Journal:  Arch Toxicol       Date:  1986-02       Impact factor: 5.153

  1 in total

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