Effects of donepezil, nicotine and haloperidol on the central serotonergic system in mice: Implications for Tourette's syndrome

被引:33
作者
Hayslett, RL [1 ]
Tizabi, Y [1 ]
机构
[1] Howard Univ, Coll Med, Dept Pharmacol, Washington, DC 20059 USA
关键词
donepezil; aricept; nicotine; haloperidol; 5-HT receptors; 5-HT mRNA; cortex; Tourette's syndrome;
D O I
10.1016/j.pbb.2005.06.010
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
We have previously reported that acute and chronic donepezil and nicotine administration significantly attenuate DOI-induced head twitch response (HTR) in mice. This behavior, primarily mediated by stimulation of 5-HT2A receptors, has been proposed to model tic symptoms seen in Tourette ' s syndrome (TS). Haloperidol, a drug widely used to treat symptoms of TS, has also been reported to reduce DOI-induced head shakes in rodents when administered acutely. These findings suggest an inhibitory interaction of these drugs with 5-HT2A receptors. To test this hypothesis, we evaluated the effects of chronic donepezil, nicotine and haloperidol on expression levels of 5-HT2A mRNA and 5HT(2A) receptor density in select brain regions. Initially, we established a dose-response relationship for the acute and chronic haloperidol and DOI-induced HTR. Male ICR mice were treated twice daily with donepezil (0.1 mg/kg), nicotine (0.5 mg/kg), and once daily with haloperidol (0.4 mg g) for 14 days and were sacrificed 16-18 h after the last injection. These drug regimens were chosen because of their CA significant effects on DOI-induced HTR. Donepezil significantly increased 5-HT2A mRNA level, but not the receptor density in the striatum. In the midbrain, donepezil significantly decreased the receptor density without affecting the 5-HT2A MRNA level. In the frontal cortex, only haloperidol significantly reduced the 5-HT2A receptor density. The cortex was the only area where donepezil, nicotine and haloperidol significantly reduced the 5-HT2A receptor density. The results suggest that the anti-tic properties of donepezil, nicotine and haloperidol in this paradigm might be due to antagonism of cortical 5-HT2A receptors. Thus, further investigation of involvement of cortical 5-HT2A receptors in TS as well as evaluation of selective 5-HT2A receptor antagonists in this disorder is warranted. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:879 / 886
页数:8
相关论文
共 63 条
[1]  
Aloyo VJ, 2001, J PHARMACOL EXP THER, V299, P1066
[2]   DIFFERENTIAL EFFECT OF SUBCHRONIC TREATMENT WITH VARIOUS NEUROLEPTIC AGENTS ON SEROTONIN2 RECEPTORS IN RAT CEREBRAL-CORTEX [J].
ANDREE, TH ;
MIKUNI, M ;
TONG, CY ;
KOENIG, JI ;
MELTZER, HY .
JOURNAL OF NEUROCHEMISTRY, 1986, 46 (01) :191-197
[3]  
[Anonymous], 1999, Am J Hum Genet, V65, P1428
[4]  
ARNT J, 1984, ACTA PHARMACOL TOX, V55, P363
[5]   NEUROCHEMICAL AND SOME RELATED PSYCHOPHARMACOLOGICAL ASPECTS OF TOURETTES-SYNDROME - AN UPDATE [J].
BAKER, GB ;
CHOKKA, PR ;
BORNSTEIN, RA .
JOURNAL OF PSYCHOPHARMACOLOGY, 1995, 9 (03) :273-280
[6]   ACUTE AND CHRONIC EFFECTS OF SEROTONIN (5HT) ANTAGONISTS ON SEROTONIN BINDING-SITES [J].
BLACKSHEAR, MA ;
FRIEDMAN, RL ;
SANDERSBUSH, E .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1983, 324 (02) :125-129
[7]  
BLACKSHEAR MA, 1982, J PHARMACOL EXP THER, V221, P303
[8]   ADAPTIVE-CHANGES IN THE 5-HT2 BINDING-SITE AFTER CHRONIC ADMINISTRATION OF AGONISTS AND ANTAGONISTS [J].
BLACKSHEAR, MA ;
MARTIN, LL ;
SANDERSBUSH, E .
NEUROPHARMACOLOGY, 1986, 25 (11) :1267-1271
[9]  
BLISS J, 1980, ARCH GEN PSYCHIAT, V37, P1343
[10]   The effects of antipsychotic drugs on the mRNA levels of serotonin 5HT(2A) and 5HT(2C) receptors [J].
Buckland, PR ;
DSouza, U ;
Maher, NA ;
McGuffin, P .
MOLECULAR BRAIN RESEARCH, 1997, 48 (01) :45-52