Clofibrate and clofibric acid: comparison of the metabolic disposition in rats and dogs. 1977

M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik

In rats, equimolar oral doses of [14C]clofibrate and [14c]clofibric acid produced essentially the same profiles of blood levels, tissue distribution and excretion of radioactivity. Both compounds were completely absorbed, and all radioactivity found in the serum was due to clofibric acid (CPIB). Tissues contained readily detectable radioactivity levels, but the concentration was generally lower than in serum. A large proportion of CPIB in liver, heart, kidney, fat and muscle was associated with intracellular space. In rat urine, CPIB was present both free and conjugated with glucuronic acid. Approximately 97% of the serum CPIB was not conjugated. Identical decreases in serum lipids and hepatic cholesterol synthesis were observed in rats treated for 1 week with either compound. In dogs, the serum contained 40% more radioactivity after [14C]clofibric acid than after an equimolar oral dose of [14C]clofibrate; approximately 88% of the serum radioactivity was due to CPIB. Some biliary excretion was detected. The extent of binding to serum protein varied with concentration of CPIB and with the species; the affinity was in the order man greater than dog greater than rat. The results demonstrate that clofibric acid and clofibrate are metabolically and pharmacologically equivalent in rats, but not in dogs. The data are in accordance with the view that the pharmacological activity of clofibrate is due to clofibric acid.

UI MeSH Term Description Entries
D007408 Intestinal Absorption Uptake of substances through the lining of the INTESTINES. Absorption, Intestinal
D008297 Male Males
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D002994 Clofibrate A fibric acid derivative used in the treatment of HYPERLIPOPROTEINEMIA TYPE III and severe HYPERTRIGLYCERIDEMIA. (From Martindale, The Extra Pharmacopoeia, 30th ed, p986) Athromidin,Atromid,Atromid S,Clofibric Acid, Ethyl Ester,Ethyl Chlorophenoxyisobutyrate,Miscleron,Miskleron,Chlorophenoxyisobutyrate, Ethyl
D004285 Dogs The domestic dog, Canis familiaris, comprising about 400 breeds, of the carnivore family CANIDAE. They are worldwide in distribution and live in association with people. (Walker's Mammals of the World, 5th ed, p1065) Canis familiaris,Dog
D006207 Half-Life The time it takes for a substance (drug, radioactive nuclide, or other) to lose half of its pharmacologic, physiologic, or radiologic activity. Halflife,Half Life,Half-Lifes,Halflifes
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
D013045 Species Specificity The restriction of a characteristic behavior, anatomical structure or physical system, such as immune response; metabolic response, or gene or gene variant to the members of one species. It refers to that property which differentiates one species from another but it is also used for phylogenetic levels higher or lower than the species. Species Specificities,Specificities, Species,Specificity, Species
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
March 1985, Journal of pharmaceutical sciences,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
January 1983, Drug metabolism and disposition: the biological fate of chemicals,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
March 1977, Xenobiotica; the fate of foreign compounds in biological systems,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
May 1982, Zeitschrift fur arztliche Fortbildung,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
January 1980, Journal of pharmaceutical sciences,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
July 1993, Biological & pharmaceutical bulletin,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
March 1989, The Journal of nutrition,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
August 2007, Xenobiotica; the fate of foreign compounds in biological systems,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
December 1975, Die Medizinische Welt,
M N Cayen, and E S Ferdinandi, and E Greselin, and W T Robinson, and D Dvornik
June 1977, Xenobiotica; the fate of foreign compounds in biological systems,
Copied contents to your clipboard!