Literature DB >> 2372235

Pharmacokinetics and metabolism of a single subneurotoxic oral dose of tri-o-cresyl phosphate in hens.

E Suwita1, M B Abou-Donia.   

Abstract

Hens were given a single oral dose of 50 mg (4.6 microCi)/kg [14C] tri-o-cresyl phosphate (TOCP). Four groups of three hens each were killed after 0.5, 1, 2, and 5 days. The half-life of 14C in plasma was 2 days. TOCP and its metabolites in the plasma, liver, kidneys, and lungs were analyzed by high-performance liquid chromatography and liquid scintillation counting. TOCP reached its highest concentration in plasma between 0.5 and 1 day after administration. Under these experimental conditions, the disappearance of TOCP from the plasma followed monoexponential kinetics with a half-life of 2.2 days. Appreciable concentrations of saligenin cyclic-o-tolyl phosphate, the active neurotoxic metabolite, were detected in the plasma as well as in the liver, kidneys, and lungs at all time points and had half-lives of 2.06, 1.36, 1.11 and 4.44 days, respectively. The presence of this active metabolite of TOCP might contribute to the sensitivity of the hen to TOCP-induced delayed neurotoxicity. Other hydrolytic and oxidative products of TOCP were also identified in tissues.

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Year:  1990        PMID: 2372235     DOI: 10.1007/bf02010730

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


  17 in total

1.  EFFECTS OF CERTAIN METABOLICALLY ACTIVE DRUGS AND OXIMES ON TRI-O-CRESYL PHOSPHATE TOXICITY.

Authors:  M J BLEIBERG; H JOHNSON
Journal:  Toxicol Appl Pharmacol       Date:  1965-03       Impact factor: 4.219

2.  Biological activity of a trio-cresyl phosphate metabolite.

Authors:  J E CASIDA; M ETO; R L BARON
Journal:  Nature       Date:  1961-09-30       Impact factor: 49.962

3.  Non-ionic diffusion and the excretion of weak acids and bases.

Authors:  M D MILNE; B H SCRIBNER; M A CRAWFORD
Journal:  Am J Med       Date:  1958-05       Impact factor: 4.965

4.  The role of pharmacokinetics and metabolism in species sensitivity to neurotoxic agents.

Authors:  M B Abou-Donia; A A Nomeir
Journal:  Fundam Appl Toxicol       Date:  1986-02

5.  Absorption, distribution, and elimination of a single oral dose of [14C]tri-o-cresyl phosphate in hens.

Authors:  M B Abou-Donia; E Suwita; A A Nomeir
Journal:  Toxicology       Date:  1990-03-30       Impact factor: 4.221

6.  Time related disposition of tri-O-tolyl phosphate (TOTP) and metabolites in chicken.

Authors:  R P Sharma; P G Watanabe
Journal:  Pharmacol Res Commun       Date:  1974-10

Review 7.  Toxicokinetics and metabolism of delayed neurotoxic organophosphorus esters.

Authors:  M B Abou-Donia
Journal:  Neurotoxicology       Date:  1983       Impact factor: 4.294

Review 8.  Organophosphorus ester-induced delayed neurotoxicity.

Authors:  M B Abou-Donia
Journal:  Annu Rev Pharmacol Toxicol       Date:  1981       Impact factor: 13.820

9.  Evidence for the presence of 2-(o-cresyl)-4H-1:3:2-benzodioxaphosphoran-2-one in cat intestine following tri-o-cresyl phosphate administration.

Authors:  J D Taylor; H S Buttar
Journal:  Toxicol Appl Pharmacol       Date:  1967-11       Impact factor: 4.219

10.  Effect of tri-o-cresyl phosphate, tri-o-cresyl thiophosphate and 2-(o-cresyl)-4H :1:3:2 benzodioxaphosphoran-2-one on pentobarbital induced sleeping time in mice.

Authors:  H S Buttar; D L Tyrrell; J D Taylor
Journal:  Arch Int Pharmacodyn Ther       Date:  1968-04
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  2 in total

1.  Disposition, elimination, and metabolism of tri-o-cresyl phosphate following daily oral administration in Fischer 344 male rats.

Authors:  S G Somkuti; M B Abou-Donia
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

Review 2.  Sarin (GB, O-isopropyl methylphosphonofluoridate) neurotoxicity: critical review.

Authors:  Mohamed B Abou-Donia; Briana Siracuse; Natasha Gupta; Ashly Sobel Sokol
Journal:  Crit Rev Toxicol       Date:  2016-10-05       Impact factor: 5.635

  2 in total

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