enterohepatic

Due to the effect of enterohepatic circulation a second peak is seen several hours later.

This is interpreted by the authors as evidence that no enterohepatic circulation takes place.

Some of it is recycled through the enterohepatic circulation.

This replaced bile acid loss from the enterohepatic circulation.

This process is known as enterohepatic circulation.

Such migratory route is known as enterohepatic pulmonar larval migration.

Drugs may remain in the enterohepatic circulation for a prolonged period of time as a result of this recycling process.

By doing so, they bind bile acids and sequester them from enterohepatic circulation.

Also known as the enterohepatic circulation.

This enterohepatic circulation contributes to maintaining estradiol levels.

It is classified as a second generation sulfonylurea, which means that it undergoes enterohepatic circulation.

It is uncertain whether repeated administration of activated charcoal is effective, in theory interrupting enterohepatic cycling.

This constitutes the normal "enterohepatic urobilinogen cycle".

In normal animals, this negative feedback mechanism keeps the enterohepatic bile acid pool in equilibrium.

Next, charcoal adsorbs drugs that are secreted in bile, thereby preventing their enterohepatic recirculation.

This mechanism might facilitate bile salt absorption into the enterohepatic circulation by slowing intestinal transit time.

By inhibiting the enterohepatic circulation, more L-thyroxine will be lost through defecation, thus lowering body thyroxine levels.

It interrupts the enterohepatic and enteroenteric circulation of some drugs/toxins and their metabolites.

It undergoes enterohepatic circulation.

Nitrate toxicosis can occur through enterohepatic metabolism of nitrate to nitrite being an intermediate.

Enterohepatic circulation also means that some molecules which would not otherwise be very toxic can become extremely hepatotoxic as they reach unexpectedly high hepatic concentrations.

NPHS encompass two (gastric and enterohepatic) groups, showing different organ specificity.

Repeated doses of activated carbon may be helpful by absorbing any toxins that are returned to the gastrointestinal tract following enterohepatic circulation.

This input mimics the case of an intestinally absorbed solute that is excreted by the liver and then reabsorbed (enterohepatic circulation).