What does cytochrome P450 reductase do?

Abstract. Cytochrome P450 reductases (CPRs) are diflavin oxidoreductases that supply electrons to type II cytochrome P450 monooxygenases (CYPs). In addition, it can also reduce other proteins and molecules, including cytochrome c, ferricyanide, and different drugs.

How do cytochrome P450 enzymes work?

Cytochrome P450 monooxygenases catalyze the oxidation and metabolism of a large number of xenobiotics and endogenous compounds. CYP450 enzymes evolved as the primary defense against xenobiotics and in this process are also responsible for the bioactivation of drugs and toxicants to more reactive intermediates.

What happens when cytochrome P450 is inhibited?

IRREVERSIBLE INHIBITION In some cases, CYP450 inhibition is irreversible. The formation of a stable complex, between a drug and the metabolizing enzyme, is one mechanism that can result in irreversible inhibition. The inhibitor can be a drug or one of its metabolites.

What is the function of cytochrome P450 in phase I metabolism?

Cytochrome P450 (CYP) enzymes are a group of enzymes encoded by P450 genes and are expressed as membrane bound proteins mostly found in the endoplasmic reticulum of the liver. CYP enzymes function as monoxygenases and effect oxidation by transfer of one oxygen atom through a number of steps.

Is cytochrome P450 NADPH dependent?

The NADPH-dependent cytochrome P450 reductase (CPR) is a key electron donor to eucaryotic cytochromes P450 (CYPs). CPR shuttles electrons from NADPH through the FAD and FMN-coenzymes into the iron of the prosthetic heme-group of the CYP.

How does cytochrome P450 detoxify?

The Cytochrome P450 family 2 is specifically involved in detoxification of xenobiotic compounds by mono-oxygenation or hydroxylation, thereby inactivating potential bioactive compounds which have been ingested35.

How do cytochromes work?

cytochrome, any of a group of hemoprotein cell components that, by readily undergoing reduction and oxidation (gain and loss of electrons) with the aid of enzymes, serve a vital function in the transfer of energy within cells. Hemoproteins are proteins linked to a nonprotein, iron-bearing component.

How does cytochrome P450 affect drug metabolism?

Cytochrome P450 enzymes can be inhibited or induced by drugs, resulting in clinically significant drug-drug interactions that can cause unanticipated adverse reactions or therapeutic failures. Interactions with warfarin, antidepressants, antiepileptic drugs, and statins often involve the cytochrome P450 enzymes.

What is the role of cytochromes?

Is Nadph a cytochrome?

The systematic name of this enzyme class is NADPH:ferricytochrome-c2 oxidoreductase. Other names in common use include cytochrome c2 reductase (reduced nicotinamide adenine dinucleotide, phosphate), cytochrome c2 reductase (reduced nicotinamide adenine dinucleotide, and phosphate, NADPH).