Chronic treatment with the endocannabinoid anandamide increases cytochrome P450 metabolizing system in the rat

被引:7
作者
Costa, B
Parolaro, D
Colleoni, M [1 ]
机构
[1] Univ Milan, Dipartimento Farmacol Chemioterapia & Tossicol Me, I-20129 Milan, Italy
[2] Univ Milano Bicocca, Fac Sci, Dipartimento Biotecnol & Biosci, I-20126 Milan, Italy
[3] Univ Insubria Varese, Dipartimento Biol Strutturale & Funzionale, Sez Farmacol, I-21052 Busto Arsizio, Italy
关键词
cannabinoid; anandamide; tolerance; cytochrome P450; liver; rat; brain;
D O I
10.1016/S0014-2999(02)01994-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this work was to investigate the effects of single and repeated administration of the endogenous cannabinoid anandamide (20 mg/kg i.p.) on cytochrome P450-mediated biotransformation in the rat. In liver microsomes from chronically treated rats, an increase in cytochrome P450 content and in the activity and immunoreactivity of cytochrome P450 reductase was detected. Immunoblot analysis of the hepatic microsomal proteins revealed an increase in the relative level of cytochrome P450 2B1/2 and 3A2. The activity of monooxygenase enzymes linked to specific cytochrome P450 isoforms was significantly enhanced. This increase in the content and activity of the cytochrome P450 system was also seen in liver microsomes from acutely treated rats; however, these increases were smaller than those seen after prolonged treatment. After acute treatment, the brain cytochrome P450 and b(5) content was increased, whereas after chronic treatment, only that of b5 was enhanced. Cytochrome P450 reductase activity and its relative abundance were increased only in the brains of chronically treated rats. The present findings demonstrate that anandamide administration increased the metabolic activity of the cytochrome P450 system in rat liver and brain. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 46 条
[1]   RAT-BRAIN CYTOCHROMES P-450 - CATALYTIC, IMMUNOCHEMICAL PROPERTIES AND INDUCIBILITY OF MULTIPLE FORMS [J].
ANANDATHEERTHAVARADA, HK ;
SHANKAR, SK ;
RAVINDRANATH, V .
BRAIN RESEARCH, 1990, 536 (1-2) :339-343
[2]   THE CHRONIC ADMINISTRATION OF NICOTINE INDUCES CYTOCHROME-P450 IN RAT-BRAIN [J].
ANANDATHEERTHAVARADA, HK ;
WILLIAMS, JF ;
WECKER, L .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (05) :1941-1944
[3]   Biosynthesis and degradation of bioactive fatty acid amides in human breast cancer and rat pheochromocytoma cells - Implications for cell proliferation and differentiation [J].
Bisogno, T ;
Katayama, K ;
Melck, D ;
Ueda, N ;
De Petrocellis, L ;
Yamamoto, S ;
Di Marzo, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 254 (03) :634-642
[4]   MICROSOMAL CYTOCHROME P450-MEDIATED LIVER AND BRAIN ANANDAMIDE METABOLISM [J].
BORNHEIM, LM ;
KIM, KY ;
CHEN, BL ;
CORREIA, MA .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (05) :677-686
[5]   THE EFFECT OF CANNABIDIOL ON MOUSE HEPATIC-MICROSOMAL CYTOCHROME P450-DEPENDENT ANANDAMIDE METABOLISM [J].
BORNHEIM, LM ;
KIM, KY ;
CHEN, BL ;
CORREIA, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (02) :740-746
[6]  
BORNHEIM LM, 1991, MOL PHARMACOL, V40, P228
[7]  
BORNHEIM LM, 1989, MOL PHARMACOL, V36, P377
[8]   INDUCTION AND GENETIC-REGULATION OF MOUSE HEPATIC CYTOCHROME-P450 BY CANNABIDIOL [J].
BORNHEIM, LM ;
EVERHART, ET ;
LI, JM ;
CORREIA, MA .
BIOCHEMICAL PHARMACOLOGY, 1994, 48 (01) :161-171
[9]   ETHOXYPHENOXAZONES, PENTOXYPHENOXAZONES, AND BENZYLOXYPHENOXAZONES AND HOMOLOGS - A SERIES OF SUBSTRATES TO DISTINGUISH BETWEEN DIFFERENT INDUCED CYTOCHROMES-P-450 [J].
BURKE, MD ;
THOMPSON, S ;
ELCOMBE, CR ;
HALPERT, J ;
HAAPARANTA, T ;
MAYER, RT .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (18) :3337-3345
[10]   CYTOCHROME-P450 AND THE ARACHIDONATE CASCADE [J].
CAPDEVILA, JH ;
FALCK, JR ;
ESTABROOK, RW .
FASEB JOURNAL, 1992, 6 (02) :731-736