Abstract
We examined two commercially available St. John's wort extracts and some of their constituents for their potential in inducing rat cytochrome P450 (CYP450) enzyme activities after oral administration. None of the extracts or pure constituents tested enhanced the hepatic cytochrome content or the activity of cytochrome P450 isozymes in rat liver microsomes. Our results demonstrated that the reported interactions between St. John's Wort and various other drugs are not mediated by CYP 450 isoforms present in rat liver.
MeSH terms
-
Animals
-
Anthracenes
-
Antidepressive Agents / pharmacology
-
Bridged Bicyclo Compounds
-
Cytochrome P-450 Enzyme System / metabolism*
-
Ethanol
-
Excitatory Amino Acid Antagonists / pharmacology
-
Female
-
Hypericum*
-
Liver / metabolism*
-
Male
-
Methanol
-
Microsomes / drug effects*
-
Microsomes / metabolism
-
Perylene / analogs & derivatives*
-
Perylene / pharmacology
-
Phenobarbital / pharmacology
-
Phloroglucinol / analogs & derivatives
-
Plant Extracts / pharmacology*
-
Quercetin / analogs & derivatives*
-
Quercetin / pharmacology
-
Rats
-
Rats, Sprague-Dawley
-
Sex Factors
-
Solvents
-
Terpenes / pharmacology
Substances
-
Anthracenes
-
Antidepressive Agents
-
Bridged Bicyclo Compounds
-
Excitatory Amino Acid Antagonists
-
Plant Extracts
-
Solvents
-
Terpenes
-
Ethanol
-
Perylene
-
hypericin
-
hyperoside
-
Cytochrome P-450 Enzyme System
-
Quercetin
-
Phloroglucinol
-
pseudohypericin
-
hyperforin
-
Methanol
-
Phenobarbital