Cytochrome P450 Flashcards
Many of the major pharmacokinetics interaction between drugs are due to hepatic ________
Cytochrome P450
Isoenzymes are a group of heme-containing enzyme embedded primarily and the lipid bilayer of the endoplasmic reticulum of hepatocytes it takes a part of metabolism of many drugs, steroids and carcinogens
Cytochrome P450
Drug interaction involving the p450 isoforms generally are the two types
Enzyme induction or enzyme inhibition
______Reduce metabolism were as ________ can increase it.
Enzyme inhibition
Enzyme induction
As have been shown in a recent death caused by dysrhythmia or bone marrow (haematopoetic) inhibition due to combine administration of
Terfenadine and ketoconazole, erythromycin and intraconazole, and sorivudine and flouropyrimidines
What are the six main enzyme attributed by p450 enzyme
CYP 1A2, 2C9, 2C19, 2D6, 2E1 AND 3A4
This enzymes are most significant cyp enzyme in terms of quantity
CYP3A4 and CYP2D6
This enzyme is found not only in the liver but also in the gut wall, where it may serve as a primary defense mechanism
CYP3A4
CYP1A consist of two enzymes
1A1 AND 1A2
Is not significantly expressed in the liver. It is found mainly in the lungs, mammary glands, placenta and lymphocytes.
CYP1A1
it is an enzyme involved in the inactivation of procarcinogens and is highly induced by polycystic aromatic hydrocarbon ( PAHs) which are found in cigarette smoke.
CYP1A1
Is expressed mainly in the liver and is induced by cigarette smoking. It is also induced by the indigestion of some food stuff such as cruciferous vegetables as well as barbecued or charboiled food
CYP1A2
Some drugs such as ____ may induce CYP 1A2 activity
Omeprazole
Drugs which are known to be metabolized by CYP1A2 include:
Theophylline, caffiene, imipramine, and phenacitin
Previously known as couramin hydroxylase
CYP2 FAMILY