Suppressive effects of cannabidiol on antigen-specific antibody production and functional activity of splenocytes in ovalbumin-sensitized BALB/c mice

被引:53
作者
Jan, Tong-Rong
Su, Shu-Ting
Wu, Hsin-Ying
Liao, Mei-Hsiu
机构
[1] Natl Taiwan Univ, Dept Vet Med, Taipei 106, Taiwan
[2] Inst Nucl Energy Res, Div Isotope Applicat, Tao Yuan, Taiwan
关键词
cannabidiol; ovalbumin; antibody production; splenocyte; cytokine;
D O I
10.1016/j.intimp.2007.01.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cannabidiol (CBD) and cannabis-based medicines are potential therapeutic agents. Because the immune system has been widely demonstrated to be affected by psychoactive cannabinoids, such as Delta(9)-tetrahydrocannabinol, the objective of the present studies is to investigate the immunomodulatory effect of CBD, the major non-psychoactive cannabinoid in marijuana. BALB/c mice were intraperitoneally administered with a single dose of CBD (5-20 mg/kg) prior to ovalbumin (OVA) sensitization, and the serum production of antigen-specific antibodies was measured 7 days post OVA sensitization. The serum level of OVA-specific IgM was significantly attenuated by a high dose of CBD (20 mg/kg), and OVA-specific IgG(1) and IgG(2a) by all 3 doses of CBD. Concordantly, splenocytes of mice administered with CBD (5 or 20 mg/kg) produced less IL-2, IL-4 and IFN-gamma than those of vehicle-treated controls, upon ex vivo stimulation with phorbol ester plus calcium ionophore. Likewise, T-cell mitogen (concanavalin A)-induced proliferation of splenocytes was also markedly suppressed in mice administered with CBD. Furthermore, the observed ex vivo effects of CBD on cytokine production and T-cell proliferation were confirmed in splenocytes directly exposed to CBD (1-8 mu M) in vitro, indicating a direct effect by CBD. Taken together, the results demonstrated that CBD markedly suppressed antigen-specific antibody production in OVA-sensitized mice, and suggest that CBD-mediated suppression of Immoral immunity could be mediated by the impaired functions of splenocytes. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:773 / 780
页数:8
相关论文
共 43 条
[1]   EFFECTS OF DELTA-9-TETRAHYDROCANNABINOL, CANNABINOL AND CANNABIDIOL ON THE IMMUNE-SYSTEM IN MICE .1. INVIVO INVESTIGATION OF THE PRIMARY AND SECONDARY IMMUNE-RESPONSE [J].
BACZYNSKY, WOT ;
ZIMMERMAN, AM .
PHARMACOLOGY, 1983, 26 (01) :1-11
[2]   EFFECTS OF DELTA-9-TETRAHYDROCANNABINOL, CANNABINOL AND CANNABIDIOL ON THE IMMUNE-SYSTEM IN MICE .2. INVITRO INVESTIGATION USING CULTURED MOUSE SPLENOCYTES [J].
BACZYNSKY, WOT ;
ZIMMERMAN, AM .
PHARMACOLOGY, 1983, 26 (01) :12-19
[3]   THE POLYCLONAL AND ANTIGEN-SPECIFIC IGE AND IGG SUBCLASS RESPONSE OF MICE INJECTED WITH OVALBUMIN IN ALUM OR COMPLETE FREUND ADJUVANT [J].
BECK, L ;
SPIEGELBERG, HL .
CELLULAR IMMUNOLOGY, 1989, 123 (01) :1-8
[4]   Nonclassical and endogenous cannabinoids: Effects on the ordering of brain membranes [J].
Bloom, AS ;
Edgemond, WS ;
Moldvan, JC .
NEUROCHEMICAL RESEARCH, 1997, 22 (05) :563-568
[5]  
Cabral GA, 2005, HANDB EXP PHARMACOL, V168, P385
[6]   Inhibition of an equilibrative nucleoside transporter by cannabidiol: A mechanism of cannabinoid immunosuppression [J].
Carrier, Erica J. ;
Auchampach, John A. ;
Hillard, Cecilia J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (20) :7895-7900
[7]   Effect of cannabinoid ingestion (in the form of bhang) on the immune system of high school and university students [J].
EL-Gohary, M ;
Eid, MA .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2004, 23 (03) :149-156
[8]  
FINKELMAN FD, 1990, ANNU REV IMMUNOL, V8, P303, DOI 10.1146/annurev.iy.08.040190.001511
[9]   Inhibition of the cyclic AMP signaling cascade and nuclear factor binding to CRE and κB elements by cannabinol, a minimally CNS-Active cannabinoid [J].
Herring, AC ;
Koh, WS ;
Kaminski, NE .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (07) :1013-1023
[10]   Cannabinol enhancement of interleukin-2 (IL-2) expression by T cells is associated with an increase in IL-2 distal nuclear factor of activated T cell activity [J].
Jan, TR ;
Rao, GK ;
Kaminski, NE .
MOLECULAR PHARMACOLOGY, 2002, 61 (02) :446-454