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grapefruit$32552$ - ترجمة إلى اليونانية

DRUG INTERACTIONS WITH GRAPEFRUIT JUICE
Grapefruit juice effect; Grapefruit effect; List of drugs affected by grapefruit; Grapefruit drug interactions; Grapefruit-drug interactions; Citrus-drug interactions
  •  pmc=4817432 }}</ref> Fucomarin production has been inherited by some hybrid [[cultivars]]; others have not inherited the fucomarin-producing genes.
  • 500px

grapefruit      
n. κίτρο, φράπα, γκρέιπφρούτ
grapefruit juice         
  • Chopped pink grapefruit
FRUIT JUICE FROM GRAPEFRUITS
Grapefruit Juice
χυμός γκρέιπφρουτ

تعريف

grapefruit
(grapefruit, or grapefruits)
A grapefruit is a large, round, yellow fruit, similar to an orange, that has a sharp, slightly bitter taste.
N-VAR

ويكيبيديا

Grapefruit–drug interactions

Some fruit juices and fruits can interact with numerous drugs, in many cases causing adverse effects. The effect is most studied with grapefruit and grapefruit juice, but similar effects have been observed with certain other citrus fruits.

The effect was first discovered accidentally in 1991, when a test of drug interactions with alcohol used grapefruit juice to hide the taste of the ethanol. A 2005 medical review advised patients to avoid all citrus juices until further research clarifies the risks. It was reported in 2008 that similar effects had been observed with apple juice.

One whole grapefruit, or a small glass (200 mL, 6.8 US fl oz) of grapefruit juice, can cause drug overdose toxicity. Fruit consumed three days before the medicine can still have an effect. The relative risks of different types of citrus fruit have not been systematically studied. Affected drugs typically have an auxiliary label saying "Do not take with grapefruit" on the container, and the interaction is elaborated upon in the package insert. People are also advised to ask their physician or pharmacist about drug interactions.

The effects are caused by furanocoumarins (and, to a lesser extent, flavonoids). These chemicals inhibit key drug metabolizing enzymes, such as cytochrome P450 3A4 (CYP3A4). CYP3A4 is a metabolizing enzyme for almost 50% of drugs, and is found in the liver and small intestinal epithelial cells. As a result, many drugs are affected. Inhibition of enzymes can have two different effects, depending on whether the drug is either

  1. metabolized by the enzyme to an inactive metabolite, or
  2. activated by the enzyme to an active metabolite.

In the first instance, inhibition of drug-metabolizing enzymes results in elevated concentrations of an active drug in the body, which may cause adverse effects. Conversely, if the medication is a prodrug, it needs to be metabolised to be converted to the active drug. Compromising its metabolism lowers concentrations of the active drug, reducing its therapeutic effect, and risking therapeutic failure.

Low drug concentrations can also be caused when the fruit suppresses drug absorption from the intestine.