Cannabidiol, a safe and non-psychotropic ingredient of the marijuana plant Cannabis sativa, is protective in a murine model of colitis

被引:152
作者
Borrelli, Francesca [1 ]
Aviello, Gabriella [1 ]
Romano, Barbara [1 ]
Orlando, Pierangelo [4 ]
Capasso, Raffaele [1 ]
Maiello, Francesco [2 ]
Guadagno, Federico [3 ]
Petrosino, Stefania [3 ]
Capasso, Francesco [1 ]
Di Marzo, Vincenzo [3 ]
Izzo, Angelo A. [1 ]
机构
[1] Univ Naples Federico II, Dept Expt Pharmacol, I-80131 Naples, Italy
[2] Osped Pellegrini, Dept Diagnost Serv, Anat & Pathol Histol Serv, ASL 1, Naples, Italy
[3] CNR, Inst Biomol Chem, Pozzuoli, NA, Italy
[4] CNR, Inst Prot Biochem, Naples, Italy
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2009年 / 87卷 / 11期
关键词
Cannabinoids; Colitis; Inflammatory bowel disease; Gastroenterology; INFLAMMATORY-BOWEL-DISEASE; ACID AMIDE HYDROLASE; INTESTINAL INFLAMMATION; ANTITUMOR-ACTIVITY; OXIDATIVE STRESS; CB2; RECEPTORS; NITRIC-OXIDE; IN-VIVO; ANANDAMIDE; CELLS;
D O I
10.1007/s00109-009-0512-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Inflammatory bowel disease affects millions of individuals; nevertheless, pharmacological treatment is disappointingly unsatisfactory. Cannabidiol, a safe and non-psychotropic ingredient of marijuana, exerts pharmacological effects (e.g., antioxidant) and mechanisms (e.g., inhibition of endocannabinoids enzymatic degradation) potentially beneficial for the inflamed gut. Thus, we investigated the effect of cannabidiol in a murine model of colitis. Colitis was induced in mice by intracolonic administration of dinitrobenzene sulfonic acid. Inflammation was assessed both macroscopically and histologically. In the inflamed colon, cyclooxygenase-2 and inducible nitric oxide synthase (iNOS) were evaluated by Western blot, interleukin-1 beta and interleukin-10 by ELISA, and endocannabinoids by isotope dilution liquid chromatography-mass spectrometry. Human colon adenocarcinoma (Caco-2) cells were used to evaluate the effect of cannabidiol on oxidative stress. Cannabidiol reduced colon injury, inducible iNOS (but not cyclooxygenase-2) expression, and interleukin-1 beta, interleukin-10, and endocannabinoid changes associated with 2,4,6-dinitrobenzene sulfonic acid administration. In Caco-2 cells, cannabidiol reduced reactive oxygen species production and lipid peroxidation. In conclusion, cannabidiol, a likely safe compound, prevents experimental colitis in mice.
引用
收藏
页码:1111 / 1121
页数:11
相关论文
共 46 条
[1]   Interleukin 10 gene transfer prevents experimental colitis in rats [J].
Barbara, G ;
Xing, Z ;
Hogaboam, CM ;
Gauldie, J ;
Collins, SM .
GUT, 2000, 46 (03) :344-349
[2]   Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide [J].
Bisogno, T ;
Hanus, L ;
De Petrocellis, L ;
Tchilibon, S ;
Ponde, DE ;
Brandi, I ;
Moriello, AS ;
Davis, JB ;
Mechoulam, R ;
Di Marzo, V .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (04) :845-852
[3]   Cannabidiol, extracted from Cannabis sativa, selectively inhibits inflammatory hypermotility in mice [J].
Capasso, R. ;
Borrelli, F. ;
Aviello, G. ;
Romano, B. ;
Scalisi, C. ;
Capasso, F. ;
Izzo, A. A. .
BRITISH JOURNAL OF PHARMACOLOGY, 2008, 154 (05) :1001-1008
[4]   Fatty acid amide hydrolase controls mouse intestinal motility in vivo [J].
Capasso, R ;
Matias, I ;
Lutz, B ;
Borrelli, F ;
Capasso, F ;
Marsicano, G ;
Mascolo, N ;
Petrosino, S ;
Monory, K ;
Valenti, M ;
Di Marzo, V ;
Izzo, AA .
GASTROENTEROLOGY, 2005, 129 (03) :941-951
[5]   The 10 remaining mysteries of inflammatory bowel disease [J].
Colombel, Jean-Frederic ;
Watson, Alastair J. M. ;
Neurath, Markus F. .
GUT, 2008, 57 (04) :429-433
[6]   RECOMBINANT INTERLEUKIN-1 RECEPTOR ANTAGONIST BLOCKS THE PROINFLAMMATORY ACTIVITY OF ENDOGENEOUS INTERLEUKIN-1 IN RABBIT IMMUNE COLITIS [J].
COMINELLI, F ;
NAST, CC ;
DUCHINI, A ;
LEE, M .
GASTROENTEROLOGY, 1992, 103 (01) :65-71
[7]   The non-psychoactive cannabis constituent cannabidiol is an orally effective therapeutic agent in rat chronic inflammatory and neuropathic pain [J].
Costa, Barbara ;
Trovato, Anna Elisa ;
Comelli, Francesca ;
Giagnoni, Gabriella ;
Colleoni, Mariapia .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 556 (1-3) :75-83
[8]   CHRONIC ADMINISTRATION OF CANNABIDIOL TO HEALTHY-VOLUNTEERS AND EPILEPTIC PATIENTS [J].
CUNHA, JM ;
CARLINI, EA ;
PEREIRA, AE ;
RAMOS, OL ;
PIMENTEL, C ;
GAGLIARDI, R ;
SANVITO, WL ;
LANDER, N ;
MECHOULAM, R .
PHARMACOLOGY, 1980, 21 (03) :175-185
[9]   Up-regulation of anandamide levels as an endogenous mechanism and a pharmacological strategy to limit colon inflammation [J].
D'Argenio, G ;
Valenti, M ;
Scaglione, G ;
Cosenza, V ;
Sorrentini, I ;
Di Marzo, V .
FASEB JOURNAL, 2006, 20 (01) :568-+
[10]   Effect of cannabidiol on sepsis-induced motility disturbances in mice:: involvement of CB1 receptors and fatty acid amide hydrolase [J].
De Filippis, D. ;
Iuvone, T. ;
D'Amico, A. ;
Esposito, G. ;
Steardo, L. ;
Herman, A. G. ;
Pelckmans, P. A. ;
De Winter, B. Y. ;
De Man, J. G. .
NEUROGASTROENTEROLOGY AND MOTILITY, 2008, 20 (08) :919-927