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. 2024 Jun 9;25(12):6388. doi: 10.3390/ijms25126388

Table 4.

Effects and mechanisms of drug–herb interaction.

Herb Drug Effect Mechanism
Green tea lisinopril plasma concentration ↓
nadolol plasma concentration ↓ OATP1A2 and OATP2B1 inhibition, ↓ absorbtion, (OATP)1A2-mediated uptake ↓
amlodipine cytochrome P450 system inhibition
Garlic nifedipine intestinal metabolism ↑, plasma concentration ↑
valsartan and losartan intestinal absorption ↓, plasma concentration ↓ intestinal transporters↓
carvedilol LDH ↓, CK-MB ↓, antioxidant ↑
atenolol cardiac workload↓ oxidative stress↓
propranolol SBP ↓, cholesterol, tryglicerides, glucose ↓
Aloe vera general effect intestinal transit time ↓, intestinal absorption ↓
Ginkgo biloba losartan/ EXP3174 plasma concentration ↑/plasma concentration ↓
talinolol plasma concentration ↑
Berberine losartan/ EXP3174 plasma concentration ↑/plasma concentration ↓ inhibition of CYP2D6, CYP3A4 and CYP2C9
irbesartan plasma concentration ↑
Ginseng fimasartan/amlodipine/hydrochlorothiazide no interaction
furosemide resistance
Celery (Apium graveolens) non no interaction
Nigella sativa amlodipine HR ↓
losartan plasma concentration ↑ inhibition of CYP3A4 and CYP2C9 enzyme activity
metoprolol enhancing effect
Cinnamon nicotine time-dependent inhibition of CYP2A6
Wild thyme non no interaction
Ginger amlodipine enhancing effect
losartan plasma concentration ↑ inhibition of CYP enzymes
clopidogrel competitive inhibitory effect on CYP2C19 enzyme

Abbreviations: (OATP)1A2/2B2: human organic anion-transporting polypeptide 1A2/2B2; LDH: lactate dehydrogenase; CK-MB: creatine kinase muscle–brain; SBP: systolic blood pressure; HR: heart rate; CYP2D6: cytochrome P 450, family 2, subfamily D, member 6; CYP3A4: cytochrome P 450, family 3, subfamily A, member 4; CYP2C9: cytochrome P 450, family 2, subfamily C, member 9; CYP2A6: cytochrome P 450, family 2, subfamily A, member 6; CYP2C19: cytochrome P 450, family 2, subfamily C, member 19; CYP: cytochrome P 450; EXP3174: losartan carboxylic acid. Symbols ↑ and ↓ represent the stimulating or inhibiting effect of the substance on the presented drugs metabolization and bioavailability.