Nordihydroguaiaretic acid: hepatotoxicity and detoxification in the mouse

被引:65
作者
Lambert, JD [1 ]
Zhao, D
Meyers, RO
Kuester, RK
Timmermann, BN
Dorr, RT
机构
[1] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
关键词
nordihydroguaiaretic acid; hepatotoxicity; polyphenols; glucuronidation;
D O I
10.1016/S0041-0101(02)00203-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Larrea tridentata (Moc & Sess) Cov. (Zygophyllaceae) is an ethnobotanically important plant found in the American Southwest and northern Mexico. Although numerous beneficial effects have been attributed to this plant, several case reports have demonstrated high doses of Larrea-containing herbals induce hepatotoxicity and nephrotoxicity in humans. Nordihydriguaiaretic acid (NDGA) is a lignan found in high amounts (up to 10% by dry weight) in the leaves and twigs of L. tridentata. Previously, NDGA has been shown to induce cystic nephropathy in the rat, however, no reports have been made concerning this compound's hepatotoxic potential. Here, we report that intraperitoneal adminstration of NDGA is lethal in the mouse (LD50 = 75 mg/kg). Administration is associated with a time and dose-dependent increase in serum alanine aminotransferase levels, which suggest liver damage. Indeed, freshly isolated mouse hepatocytes are more sensitive to NDGA than human melanoma cells. Furthermore, we have identified glucuronidation as a potential detoxification mechanism for NDGA. Both mono and diglucuronide conjugates of NDGA are formed after intravenous dosing. The monoglucuronide is also formed after incubation of NDGA with human hepatic microsomes; suggesting that glucuronide conjugation is important in the metabolism of NDGA by humans. In summary, this report indicates that NDGA may contribute to the hepatotoxicity of L. tridentata and provides preliminary information on NDGA metabolism. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1701 / 1708
页数:8
相关论文
共 25 条
[1]  
[Anonymous], 1977, Creosote bush: biology and chemistry of Larrea in New World deserts
[2]  
[Anonymous], J GERIATRIC DERMATOL
[3]   INHIBITION OF BENZOYL PEROXIDE-MEDIATED TUMOR PROMOTION IN 7,12-DIMETHYLBENZ(A)ANTHRACENE-INITIATED SKIN OF SENCAR MICE BY ANTIOXIDANTS NORDIHYDROGUAIARETIC ACID AND DIALLYL SULFIDE [J].
ATHAR, M ;
RAZA, H ;
BICKERS, DR ;
MUKHTAR, H .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (02) :162-165
[4]   Growth control of lung cancer by interruption of 5-lipoxygenase-mediated growth factor signaling [J].
Avis, IM ;
Jett, M ;
Boyle, T ;
Vos, MD ;
Moody, T ;
Treston, AM ;
Martinez, A ;
Mulshine, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :806-813
[5]   Glutathione oxidation and mitochondrial depolarization as mechanisms of nordihydroguaiaretic acid-induced apoptosis in lipoxygenase-deficient FL5.12 cells [J].
Biswal, SS ;
Datta, K ;
Shaw, SD ;
Feng, X ;
Robertson, JD ;
Kehrer, JP .
TOXICOLOGICAL SCIENCES, 2000, 53 (01) :77-83
[6]   Antiviral activities of methylated nordihydroguaiaretic acids.: 2.: Targeting herpes simplex virus replication by the mutation insensitive transcription inhibitor tetra-O-methyl-NDGA [J].
Chen, HS ;
Teng, L ;
Li, JN ;
Park, R ;
Mold, DE ;
Gnabre, J ;
Hwu, JR ;
Tseng, WN ;
Huang, RCC .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (16) :3001-3007
[7]   Conjugation position of quercetin glucuronides and effect on biological activity [J].
Day, AJ ;
Bao, YP ;
Morgan, MRA ;
Williamson, G .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (12) :1234-1243
[8]  
DORRR RT, 1994, CANC CHEMOTHERAPY HD, P1020
[9]   NEPHRON OBSTRUCTION IN NORDIHYDROGUAIARETIC ACID-INDUCED RENAL CYSTIC-DISEASE [J].
EVAN, AP ;
GARDNER, KD .
KIDNEY INTERNATIONAL, 1979, 15 (01) :7-19
[10]   ENDOTOXIN PROVOCATION OF EXPERIMENTAL RENAL CYSTIC-DISEASE [J].
GARDNER, KD ;
REED, WP ;
EVAN, AP ;
ZEDALIS, J ;
HYLARIDES, MD ;
LEON, AA .
KIDNEY INTERNATIONAL, 1987, 32 (03) :329-334