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Mechanism of inhibition of cyclo-oxygenase in human blood platelets by carbamate insecticides.
Krug, H F; Hamm, U; Berndt, J.
Afiliação
  • Krug HF; Gesellschaft für Strahlen- und Umweltforschung, Institut für Toxikologie und Biochemie, München, Federal Republic of Germany.
Biochem J ; 250(1): 103-10, 1988 Feb 15.
Article em En | MEDLINE | ID: mdl-3128272
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plaquetas / Inibidores de Ciclo-Oxigenase / Fenilcarbamatos / Inseticidas Limite: Humans Idioma: En Revista: Biochem J Ano de publicação: 1988 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plaquetas / Inibidores de Ciclo-Oxigenase / Fenilcarbamatos / Inseticidas Limite: Humans Idioma: En Revista: Biochem J Ano de publicação: 1988 Tipo de documento: Article