Planta Med 2007; 73(8): 742-747
DOI: 10.1055/s-2007-981548
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Effect of Chrysin and Natural Coumarins on UGT1A1 and 1A6 Activities in Rat and Human Hepatocytes in Primary Culture

Amina Chlouchi1 , Corinne Girard1 , Alexandre Bonet2 , Catherine Viollon-Abadie2 , 3 , 4 , Bruno Heyd3 , Georges Mantion3 , Hélène Martin2 , Lysiane Richert2 , 3 , 4
  • 1Laboratoire de Pharmacognosie, EA 3921 ”Optimisation Métabolique et Cellulaire”, IFR 133, UFR des Sciences Médicales et Pharmaceutiques, Besançon, France
  • 2Laboratoire de Biologie Cellulaire, EA 3921 ”Optimisation Métabolique et Cellulaire”, IFR 133, UFR des Sciences Médicales et Pharmaceutiques, Besançon, France
  • 3Service de Chirurgie Digestive et Vasculaire, CHU Jean Minjoz, EA 3921 ”Optimisation Métabolique et Cellulaire”, IFR 133, UFR des Sciences Médicales et Pharmaceutiques, Besançon, France
  • 4KaLy-Cell, Besançon, France
Weitere Informationen

Publikationsverlauf

Received: June 8, 2006 Revised: May 9, 2007

Accepted: May 16, 2007

Publikationsdatum:
28. Juni 2007 (online)

Preview

Abstract

Flavonoids and coumarins are naturally occurring compounds that are widely distributed in vegetables and have a broad pharmacological activity. Inducibility of UDP-glucuronosyltransferases (UGTs) by xenobiotics is well documented and can be considered beneficial for health. In particular, UGT1A1-dependent bilirubin conjugation plays a critical role in the detoxification of neurotoxic bilirubin and phenobarbital-mediated UGT1A1 induction therapy is commonly used in the treatment of unconjugated hyperbilirubinemic diseases such as Crigler-Najjar type II disease. In the present study, the effects of the flavone chrysin and six natural coumarins isolated from various Rutaceous plants on UGT1A6-dependent p-nitrophenol and/or UGT1A1-dependent bilirubin glucuronoconjugation activities were evaluated in cultured rat and human hepatocytes and compared to those of the prototypical UGT1A inducers β-naphthoflavone, phenobarbital and clofibric acid. After 3 days of treatment at a concentration of 25 μM, the pyranocoumarins avicennin and cis-avicennol, and the furocoumarins bergapten and imperatorin, increased by 2-fold UGT1A1-dependent activity, equivalent to the increases obtained with chrysin at 25 μM, whereas in the presence of the simple coumarins such as coumarin or umbelliferone, UGT1A1-dependent activity was not modified. In terms of structural requirements for UGT1A1 induction, the present study suggests that the B-ring (phenyl) for chrysin and the furan or pyran rings for coumarins are essential for the biological activity.

Abbreviations

BCA:bicinchoninic acid

Bili:biliribin

BSA:bovine serum albumin

CLO:clofibric acid

FCS:foetal calf serum

HBSS:Hank’s buffered salt solution

HEPES:4-(2-hydroxyethyl)piperazine-1-ethane sulfonic acid

NF:β-naphthoflavone

PB:Phenobarbital

PBS:phosphate buffered saline

PNP:p-nitrophenol

UDPGA:Uridine 5′-diphosphoglucuronic acid

UGTs:UD-glucuronosyltransferases

References

Dr. Corinne Girard

Laboratoire de Pharmacognosie

EA 3921 ”Optimisation Métabolique et Cellulaire”

UFR des Sciences Médicales et Pharmaceutiques

Place Saint-Jacques

25030 Besançon cedex

France

Telefon: +33-3-8166-5559

Fax: +33-3-8166-5568

eMail: corinne.girard@univ-fcomte.fr