Yıl: 2013 Cilt: 28 Sayı: 4 Sayfa Aralığı: 164 - 170 Metin Dili: Türkçe İndeks Tarihi: 29-07-2022

Bitkiler ve ilaç etkileşimleri

Öz:
Bitkiler ve bitkisel tıp, sık rastlanan birçok hastalığın tedavisinde özellikle Doğu ülkelerinde çok eski dönemlerden beri kullanılmaktadır. Genellikle insanlar, terapatik ve koruyucu amaçlar ile bitkileri doğal kaynaklı olması nedeni ile güvenilir görmekte ve bitkisel ürünleri bu nedenle kullanmaktadır,ancak bitkisel ürünlerin toksikolojik ve farmakolojik etkileri ile ilgili bilimsel kanıtlar yetersizdir. Bazı çalışmalarda, Ginkgo Biloba, Ginseng, Kava, Sarımsak, Ekinezya, Valerian, St. Johns worth gibi bitkilerin terapatik ilaçlar ile etkileştiğine dair kanıtlar bulunmaktadır. Genel olarak bitkisel ürünler faz 1 ve faz 2 yolları ile metabolize olur ve çeşitli taşıyıcılar içinsubstrat görevi yaparlar. P-glikoprotein ve sitokrom P450 3A4 enzimleri oral olarak emilen ilaçlar üzerinde bariyer etki yaparlar. Yapılan in vitro çalışmalar, bitkisel bileşiklerin, ilaçları metabolize eden enzim ve taşıyıcıları indükleyebildiğini ve inhibe edebildiğini göstermektedir. Taşıyıcı ve enzimlerle etkileşim nedeniyle bitkisel besinlerin varlığında ilaçları metabolize eden enzim ve taşıyıcıların aktivitesi değişmektedir. Yapılan literatür çalışmaları, klinik raporlar ve in vitro çalışmalar, birçok ilacın ve bitkisel aktif bileşenlerin hem P-glikoproteinin hem de sitokrom P450 3A4 enziminin subs-tratı olduğunu göstermektedir.
Anahtar Kelime:

Konular: Genel ve Dahili Tıp

Herbs and drug interactions

Öz:
Herbal medicines have been frequently used for thousands of years in the East in the hope of treatment of some diseases. Patients who self-medicate with herbs for preventive and the- rapeutic purposes may assume that these products are safe because they are natural but some products cause adverse effects or have the potential to interact with prescription medi- cations despite their mechanisms of action being generally unknown, the lack of evidence of efficacy, and inadequate toxi- cological data.There are some evidence that herbs such as ginkgo biloba, ginseng, kava, garlic, echinacea,valerian, st. john s worth have been reported to interact with drugs leading to clinically relevant adverse drug reactions. Herbal products contain several chemicals that are metabolized by phase 1 and phase 2 pathways and also serve as substrates for certain transporters. P-glycoprotein and cytochrome P450 3A4 toget- her constitute a highly efficient barrier for many orally absorbed drugs. Induction and inhibition of drug metabolizing enzymes and transporters by herbal component has been documented in several in vitro studies. Due to their interaction with these enzymes and transporters there is a potential for alteration in the activity of drug metabolizing enzymes and transporters the presence of herbal components Available literature studies, clinical reports and in vitro studies indicate that many drugs and active herbal constituents are substrates for both P-glycoprotein and cytochrome P450 3A4.
Anahtar Kelime:

Konular: Genel ve Dahili Tıp
Belge Türü: Makale Makale Türü: Derleme Erişim Türü: Erişime Açık
  • 1.Eisenberg DM, Davis RB, Ettner SL, et al. Trends in alternative medicine use in the United States, 1990-1997: results of a follow-up national survey. JAMA 1998;280:1569-1575. http://dx.doi.org/10.1001/jama.280.18.1569
  • 2.Kaufman DW, Kelly JP, Rosenberg L, et al. Recent pat- terns of medication use in the ambulatory adult population of the United States: the Slone survey. JAMA 2002;287:337- 344. http://dx.doi.org/10.1001/jama.287.3.337
  • 3.EMEA Commitee on Herbal Medicinal Products (HMPC). Guideline on the assessment of clinical safety and efficacy in the preparation of community herbal monographs for well- estabilished and of community herbal monographs/entries to the community list for traditional harbal medicinal pro- ducts/substances/preparations. 2006. Avaible from: http:// www.emea.europa.eu/pdfs/human/hmpc/10461305en.pdf Accessed on:December 15, 2012.
  • 4.Lazarou J, Pomeranz BH, Corey PN. Incidence of adver- se drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA 1998;279:1200-5. http://dx.doi.org/10.1001/jama.279.15.1200
  • 5.Ajayi FO, Sun H, Perry J. Adverse drug reactions: a re- view of relevant factors. J Clin Pharmacol 2000;40:1093- 101.
  • 6.Ernst E. Herbal medicines: balancing benefits and risks. Novartis Found Symp 2007;282:154-72, 212-218. http://dx.doi.org/10.1002/9780470319444.ch11
  • 7.Schilter B, Andersson C, Anton R, et al. Guidance for the safety assessment of botanicals and botanical preparations for use in food and food supplements. Food Chem Toxicol 2003;41:1625-49. http://dx.doi.org/10.1016/S0278-6915(03)00221-7
  • 8.U.S. Department of Health and Human Services, Office of Inspector General. Adverse event reporting for dietary supplements: an inadequate safety valve 2001 Avaible from: http://oig.hhs.gov/oei/reports/oei-01-00-00180.pdf Accessed on:December 12, 2012.
  • 9.Barnes J, Mills SY, Abbot NC, et al. Different standards for reporting ADRs to herbal remedies and conventional OTC medicines: faceto- face interviews with 515 users of herbal remedies. Br J Clin Pharmacol 1998;45:496-500. http://dx.doi.org/10.1046/j.1365-2125.1998.00715.x
  • 10.Bacchini M, Cuzzolin L, Camerlengo T, et al. Phytothe- rapic compounds: the consumer-pharmacist relationship. Drug Saf 2008;31(5):424-7. http://dx.doi.org/10.2165/00002018-200831050-00008
  • 11.Brazier NC, Mitchell AH, Levine MD. Understanding drug-herb interaction. Pharmacoepidemiol Drug Saf 2003;12:427-30. http://dx.doi.org/10.1002/pds.870
  • 12.Fugh-Berman A. Herb-drug interactions. Lancet 2000;355:134-8. http://dx.doi.org/10.1016/S0140-6736(99)06457-0
  • 13.Rendic S. Summary of information on human CYP enz- ymes: Human P450 metabolism data. Drug Metab Rev 2002;34:83-448. http://dx.doi.org/10.1081/DMR-120001392
  • 14.Venkataramanan R, Komoroski B, Strom S. In vitro and in vivo assessment of herb drug interactions 2006;78:2105- 2115.
  • 15.Allen SW, Mueller L, Williams SN, et al. The use of a high-volume screening procedure to assess the effects of dietary flavonoids on human CYP1A1 expression DMD, 2001;29:1074-1079.
  • 16.Goodwin B, Redinbo MR, Kliewer SA. Regulation of CYP3A gene transcription by the pregnane X receptor. Pharmacol Toxicol 2002;42:1-23.
  • 17.Aruna D, Naidu MU. Pharmacodynamic interaction studies of Ginkgo biloba with cilostazol and clopidogrel in healthy human subjects. Br J Clin Pharmacol 2007;63:333-338. http://dx.doi.org/10.1111/j.1365-2125.2006.02759.x
  • 18.Matic M, Mahns A, Tsoli M, et al. Pregnane X recep- tor: promiscuous regulator of detoxification pathways 2007;39:478-483.
  • 19.Kaufman DW, Kelly JP, Rosenberg L, et al. Recent pat- terns of medication use in the ambulatory adult population of the United States: the Slone survey. JAMA 2002;287:337- 344. http://dx.doi.org/10.1001/jama.287.3.337
  • 20.Tovar RT, Petzel RM. Herbal Toxicity 2009;55:592-641.
  • 21.Görün MS, Süzer Ö. Bitkisel İlaçlar. Süzer Farmakoloji, Klinisyen Tıp Kitapevleri (3. Baskı), İstanbul; 2004;533- 539.
  • 22.Aydos R. Hoşgörüyle Gelen Felaket: Bitkisel Ürün-İlaç Etkileşmeleri. Türk Farmakoloji Derneği Klinik Farmakoloji Çalışma Grubu 2011;54.
  • 23.Engdal S, Klepp O, Nilsen OG. Identification and explo- ration of herb-drug combinations used by cancer patients. Integr Cancer Ther 2009;8:29-36. http://dx.doi.org/10.1177/1534735408330202
  • 24.Mills E, Montori VM, Wu P, et al. Interaction of St John’s Wort with conventional drugs: systematic review of clinical trials. BMJ 2004;329:27-30. http://dx.doi.org/10.1136/bmj.329.7456.27
  • 25. Dannawi M. Possible serotonin syndrome after combina- tion of buspirone and St John’s Wort. J Psychopharmacol 2002;16:401. http://dx.doi.org/10.1177/026988110201600420
  • 26.Block KI, Gyllenhaal C, Mead MN. Safety and efficacy of herbal sedatives in cancer care. Integr Cancer Ther 2004; 3:128–148. http://dx.doi.org/10.1177/1534735404265003
  • 27.Mathews JM, Etheridge AS, Black SR. Inhibition of hu- man cytochrome P450 activities by kava extract and kavalactones. Drug Metab Dispos 2002;30:1153-1157. http://dx.doi.org/10.1124/dmd.30.11.1153
  • 28.Sridar C, Goosen TC, Kent UM, et al. Silybin inactivates cytochromes P450 3A4 and 2C9 and inhibits major hepatic glucuronosyltransferases. Drug Metab Dispos 2004;32:587- 594. http://dx.doi.org/10.1124/dmd.32.6.587
  • 29.Han Y, Guo D, Chen Y, et al. Effect of silymarin on the pharmacokinetics of losartan and its active metabolite E-3174 in healthy Chinese volunteers. Eur J Clin Pharma- col 2009;65:585-591. http://dx.doi.org/10.1007/s00228-009-0624-9
  • 30.Pal D, Mitra AK. MDR- and CYP3A4-mediated drug- herbal interactions. Life Sciences 2006;78:2131-2145. http://dx.doi.org/10.1016/j.lfs.2005.12.010
  • 31.Huang SH, Duke RK, Chebib M et al. Ginkgolides, diterpene trilactones of Ginkgo biloba, as antagonists at recombinant alpha1beta2gamma2L GABA receptors. Eur J Pharmacol 2004; 28:494(2-3):131-8.
  • 32.Vaes LP, Chyka PA. Interactions of warfarin with garlic, ginger, ginkgo, or ginseng: nature of the evidence. Ann- Pharmacother 2000;34:1478-82. http://dx.doi.org/10.1345/1542-6270(2000)034_____1478:IO WWGG>2.0.CO;2
  • 33.Vuksan V, Sievenpiper JL, Xu Z et al. Konjac-Mannan and American ginsing: emerging alternative therapies for type 2 diabetes mellitus. J Am Coll Nutr 2001;20:370-380. http://dx.doi.org/10.1080/07315724.2001.10719170
  • 34.Upton R, Romm A. Guidelines for Herbal Medicine Use. American Herbalists Guild 2001; 75-96.
  • 35.Houghton PJ. The scientific basis for the reputed activity of valerian. J Pharm Pharmacol 1999; 51:505–512. http://dx.doi.org/10.1211/0022357991772772
  • 36.Hellum BH, Hu Z, Nilsen OG. The Induction of CYP1A2, CYP2D6 andCYP3A4 by six trade herbal products in cultured primary human hepatocytes. Basic Clin Pharmacol Toxicol 2006;100:23-30. http://dx.doi.org/10.1111/j.1742-7843.2007.00011.x
  • 37.Gonzalez FJ. Role of cytochromes P450 in chemical toxicity and oxidative stress: studies with CYP2E1. Mutat Res 2005;569:101-110. http://dx.doi.org/10.1016/j.mrfmmm.2004.04.021
  • 38.Blumenthal M. The ABC Clinical Guide to Herbs.American Botanical Council, (Senior Ed.) Austin, TX, 90,200.
  • 39.Gorski JC, Huang SM, Pinto A, et al. The effect of echinacea (Echinacea purpurea root) on cytochrome P450 activity in vivo. Clinical Pharmacology and Therapeutics 2004;75(1):89-100. http://dx.doi.org/10.1016/j.clpt.2003.09.013
  • 40.Rose KD, Croissant PD, Parliament CF, et al. Spontaneous spinal epidural hematoma with associated platelet dysfunction from excessive garlic ingestion: a case report. Neurosurgery 1990;26(5):880-882. http://dx.doi.org/10.1227/00006123-199005000-00026
  • 41.Burnham BE. Garlic as a possible risk for postoperative bleeding. Plastic and Reconstructive Surgery 1995;95(1):213. http://dx.doi.org/10.1097/00006534-199501000-00060
  • 42.German K, Kumar U, Blackford HN. Garlic and the risk of TRUP bleeding. British Journal of Urology 1995;76(4):518. http://dx.doi.org/10.1111/j.1464-410X.1995.tb07766.x
  • 43.Ariga T, Tsuj K, Seki T, et al. Antithrombotic and antine- oplastic effects of phyto-organosulfur compounds. Biofactors 2000;13(1-4):251-255. http://dx.doi.org/10.1002/biof.5520130138
  • 44.Briggs WH, Xiao H, Parkin KL, et al. Differential in- hibition of human platelet aggregation by selected allium thiosulfinates. Journal of Agricultural and Food Chemistry 2000;48(11):5731-5735. http://dx.doi.org/10.1021/jf0004412
  • 45.Rahman K, Billington D. Dietary supplementation with aged garlic extract inhibits adp-induced platelet aggregation in humans. Journal of Nutrition 2000;130(11):2662-2665.
  • 46.Steiner M, Li W. Aged garlic extract, a modulator of cardiovascular risk factors: a dose-finding study on the effects of age on platelet functions. Journal of Nutrition 2001;131(3):980-984.
  • 47.Piscitelli SC, Burstein AH, Welden N, et al. The effect of garlic supplements on the pharmacokinetics of saquinavir. Clinical Infectious Diseases 2002;34(2):234-238. http://dx.doi.org/10.1086/324351
  • 48.Ang-Lee MK, Moss J, Yuan CS. Herbal medicines and perioperative care. JAMA 2001;286(2):208-16. http://dx.doi.org/10.1001/jama.286.2.208
  • 49.Fugh-Berman A, Ernst E. Herb-drug interactions: review and assessment of report reliability. British Journal of Clinical Pharmacology 2001;52(5):587-595. http://dx.doi.org/10.1046/j.0306-5251.2001.01469.x
  • 50.Mary LC, Melanie AJ, Pedro I. Evidence-based drug-herbal interactions. Life Sciences 2006;78:2146-2157. http://dx.doi.org/10.1016/j.lfs.2005.12.009
APA Gezmen Karadağ M, TÜRKÖZÜ D, KAPUCU TOPAĞAÇ D (2013). Bitkiler ve ilaç etkileşimleri. , 164 - 170.
Chicago Gezmen Karadağ Makbule,TÜRKÖZÜ Duygu,KAPUCU TOPAĞAÇ Didem Bitkiler ve ilaç etkileşimleri. (2013): 164 - 170.
MLA Gezmen Karadağ Makbule,TÜRKÖZÜ Duygu,KAPUCU TOPAĞAÇ Didem Bitkiler ve ilaç etkileşimleri. , 2013, ss.164 - 170.
AMA Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D Bitkiler ve ilaç etkileşimleri. . 2013; 164 - 170.
Vancouver Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D Bitkiler ve ilaç etkileşimleri. . 2013; 164 - 170.
IEEE Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D "Bitkiler ve ilaç etkileşimleri." , ss.164 - 170, 2013.
ISNAD Gezmen Karadağ, Makbule vd. "Bitkiler ve ilaç etkileşimleri". (2013), 164-170.
APA Gezmen Karadağ M, TÜRKÖZÜ D, KAPUCU TOPAĞAÇ D (2013). Bitkiler ve ilaç etkileşimleri. Göztepe Tıp Dergisi, 28(4), 164 - 170.
Chicago Gezmen Karadağ Makbule,TÜRKÖZÜ Duygu,KAPUCU TOPAĞAÇ Didem Bitkiler ve ilaç etkileşimleri. Göztepe Tıp Dergisi 28, no.4 (2013): 164 - 170.
MLA Gezmen Karadağ Makbule,TÜRKÖZÜ Duygu,KAPUCU TOPAĞAÇ Didem Bitkiler ve ilaç etkileşimleri. Göztepe Tıp Dergisi, vol.28, no.4, 2013, ss.164 - 170.
AMA Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D Bitkiler ve ilaç etkileşimleri. Göztepe Tıp Dergisi. 2013; 28(4): 164 - 170.
Vancouver Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D Bitkiler ve ilaç etkileşimleri. Göztepe Tıp Dergisi. 2013; 28(4): 164 - 170.
IEEE Gezmen Karadağ M,TÜRKÖZÜ D,KAPUCU TOPAĞAÇ D "Bitkiler ve ilaç etkileşimleri." Göztepe Tıp Dergisi, 28, ss.164 - 170, 2013.
ISNAD Gezmen Karadağ, Makbule vd. "Bitkiler ve ilaç etkileşimleri". Göztepe Tıp Dergisi 28/4 (2013), 164-170.