Effect of diethyl maleate pretreatment on biliary excretion and choleretic action of sulfobromophthalein in rats. 1986

M J Aza, and J Gonzalez, and A Esteller

The effect of intraperitoneal administration of diethyl maleate on biliary excretion and choleretic action of sulfobromophthalein (BSP) was investigated in rats. Diethyl maleate was injected 60 min prior to the administration of the dye to avoid interferences with the organic anion transport system. The glutathione content of the liver was decreased by 75% following diethyl maleate treatment. Diethyl maleate had no influence on the biliary excretion of BSP after injection of its conjugate with glutathione, though there was a significant reduction after free BSP administration, with a lowered percentage of the conjugate in bile. The choleretic effect of the dye was not changed after conjugated BSP, but a marked cholestasis appeared following free BSP injection. These results confirm that diethyl maleate decreases the hepatic transport of BSP by reducing the conjugation of the dye and that free BSP induces an inhibitory effect on bile flow.

UI MeSH Term Description Entries
D007274 Injections, Intraperitoneal Forceful administration into the peritoneal cavity of liquid medication, nutrient, or other fluid through a hollow needle piercing the abdominal wall. Intraperitoneal Injections,Injection, Intraperitoneal,Intraperitoneal Injection
D007275 Injections, Intravenous Injections made into a vein for therapeutic or experimental purposes. Intravenous Injections,Injection, Intravenous,Intravenous Injection
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008297 Male Males
D008298 Maleates Derivatives of maleic acid (the structural formula (COO-)-C
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002756 Cholagogues and Choleretics Gastrointestinal agents that stimulate the flow of bile into the duodenum (cholagogues) or stimulate the production of bile by the liver (choleretic). Choleretics,Cholagogues,Cholagogues, Choleretics,Choleretics and Cholagogues,Hydrocholeretics
D005978 Glutathione A tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides. Reduced Glutathione,gamma-L-Glu-L-Cys-Gly,gamma-L-Glutamyl-L-Cysteinylglycine,Glutathione, Reduced,gamma L Glu L Cys Gly,gamma L Glutamyl L Cysteinylglycine
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001646 Bile An emulsifying agent produced in the LIVER and secreted into the DUODENUM. Its composition includes BILE ACIDS AND SALTS; CHOLESTEROL; and ELECTROLYTES. It aids DIGESTION of fats in the duodenum. Biliary Sludge,Sludge, Biliary

Related Publications

M J Aza, and J Gonzalez, and A Esteller
August 1982, Biochemical pharmacology,
M J Aza, and J Gonzalez, and A Esteller
January 1987, European journal of drug metabolism and pharmacokinetics,
M J Aza, and J Gonzalez, and A Esteller
November 1989, Antimicrobial agents and chemotherapy,
M J Aza, and J Gonzalez, and A Esteller
August 1976, Canadian journal of physiology and pharmacology,
M J Aza, and J Gonzalez, and A Esteller
January 1980, Drug metabolism and disposition: the biological fate of chemicals,
M J Aza, and J Gonzalez, and A Esteller
January 1971, Journal de physiologie,
M J Aza, and J Gonzalez, and A Esteller
May 1984, Biochemical pharmacology,
M J Aza, and J Gonzalez, and A Esteller
October 1980, Toxicology letters,
Copied contents to your clipboard!