Literature DB >> 3128272

Mechanism of inhibition of cyclo-oxygenase in human blood platelets by carbamate insecticides.

H F Krug1, U Hamm, J Berndt.   

Abstract

Carbamates are a widely used class of insecticides and herbicides. They were tested for their ability to affect human blood platelet aggregation and arachidonic acid metabolism in platelets. (1) The herbicides of the carbamate type have no, or only little, influence up to a concentration of 100 microM; the carbamate insecticides, however, inhibit both aggregation and arachidonic acid metabolism in a dose- and time-dependent manner. (2) Carbaryl, the most effective compound, inhibits platelet aggregation and cyclo-oxygenase activity completely at 10 microM. The liberation of arachidonic acid from phospholipids and the lipoxygenase pathway are not affected, whereas the products of the cyclo-oxygenase pathway are drastically decreased. (3) By using [14C]carbaryl labelled in the carbamyl or in the ring moiety, it could be proved that the carbamyl residue binds covalently to platelet proteins. In contrast with acetylsalicylic acid, which acetylates only one protein, carbaryl carbamylates a multitude of platelet proteins. (4) One of the carbamylated proteins was found to be the platelet cyclo-oxygenase, indicating that carbaryl resembles in this respect acetylsalicylic acid, which is known to inhibit this enzyme specifically by acetylation.

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Year:  1988        PMID: 3128272      PMCID: PMC1148821          DOI: 10.1042/bj2500103

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


  34 in total

1.  Inhibition of prostaglandin synthesis in mouse 3T3 fibroblasts and human platelets by substituted phenols.

Authors:  J A Lindgren; H E Claesson; S Hammarström
Journal:  Prostaglandins       Date:  1977-06

2.  The inhibition of the fatty acid oxygenase of sheep vesicular gland by antioxidants.

Authors:  J Y Vanderhoek; W E Lands
Journal:  Biochim Biophys Acta       Date:  1973-02-14

3.  A rapid spectrophotometric assay for prostaglandin synthetase: application to the study of non-steroidal antiinflammatory agents.

Authors:  C Takeguchi; C J Sih
Journal:  Prostaglandins       Date:  1972-09

4.  The nature of the reaction of organophosphorus compounds and carbamates with esterases.

Authors:  W N Aldridge
Journal:  Bull World Health Organ       Date:  1971       Impact factor: 9.408

5.  The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis.

Authors:  K Weber; M Osborn
Journal:  J Biol Chem       Date:  1969-08-25       Impact factor: 5.157

6.  Drugs which inhibit prostaglandin biosynthesis.

Authors:  R J Flower
Journal:  Pharmacol Rev       Date:  1974-03       Impact factor: 25.468

7.  Aspirin as a quantitative acetylating reagent for the fatty acid oxygenase that forms prostaglandins.

Authors:  L H Rome; W E Lands; G J Roth; P W Majerus
Journal:  Prostaglandins       Date:  1976-01

8.  The mechanism of the effect of aspirin on human platelets. I. Acetylation of a particulate fraction protein.

Authors:  G J Roth; P W Majerus
Journal:  J Clin Invest       Date:  1975-09       Impact factor: 14.808

9.  Stimulation of arachidonic acid metabolism via phospholipase A2 by triethyl lead.

Authors:  H Krug; J Berndt
Journal:  Eur J Biochem       Date:  1987-01-15

10.  Acetylation of prostaglandin synthase by aspirin.

Authors:  G J Roth; N Stanford; P W Majerus
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

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  1 in total

1.  A study of the effects of p,p'-DDE and other related chlorinated hydrocarbons on inhibition of platelet aggregation.

Authors:  C E Lundholm; M Bartonek
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

  1 in total

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