Evidence that the effect of 5-HT2 receptor stimulation on temporal differentiation is not mediated by receptors in the dorsal striatum

被引:16
作者
Body, S
Asgari, K
Cheung, THC
Bezzina, G
Fone, KFC
Glennon, JC
Bradshaw, CM
Szabadi, E
机构
[1] Univ Nottingham, Queens Med Ctr, Div Psychiat, Psychopharmacol Sect,Med Sch, Nottingham NG7 2UH, England
[2] Univ Nottingham, Sch Biomed Sci, Nottingham NG7 2RD, England
[3] Solvay Pharmaceut, Weesp, Netherlands
基金
英国生物技术与生命科学研究理事会;
关键词
free-operant psychophysical procedure; temporal differentiation; 5-HT2; receptors; corpus striatum; DOI; MDL-100907; RS-102221;
D O I
10.1016/j.beproc.2005.10.004
中图分类号
B84 [心理学];
学科分类号
04 [教育学]; 0402 [心理学];
摘要
5-HT2 receptor stimulation alters temporal differentiation in free-operant timing schedules. The anatomical location of the receptor population responsible for this effect is unknown. We examined the effect of a 5-HT2 receptor agonist and antagonists, injected systemically and into the dorsal striatum, a region that is believed to play a major role in interval timing. Rats were trained under the free-operant psychophysical procedure to press levers A and Bin 50 s trials in which reinforcement was provided intermittently for responding on A in the first half, and Bin the second half of the trial. Percent responding on B (%B) was recorded in successive 5 s epochs of the trials; logistic functions were fitted to the data from each rat to derive timing indices (T-50: time corresponding to %B = 50; Weber :fraction: [T-75 - T-25]/2T(50), where T-75 and T-25 are the times corresponding to %B = 75 and %B = 25). Systemic treatment with the 5-HT2A/2C receptor agonist 2,5,-dimethoxy-4-iodo-amphetamine (DOI) (0.25 mg/kg, s.c.) reduced T-50; the 5-HT2A receptor antagonist MDL-100907 (0.5 mg/kg, i.p.) did not affect performance, but completely blocked the effect of DOI. DOI (1 and 3 mu g) injected bilaterally into the dorsal striatum did not alter T-50. The effect of systemic treatment with DOI (0.25 mg/kg, s.c.) was not altered by intra-striatal injection of MDL-100907 (0.3 mu g) or the 5-HT2C receptor antagonist RS-102221 (0.15 mu g). The ability of systemically administered MDL-100907 to reverse DOI's effect on T-50 confirms the sensitivity of temporal differentiation to 5-HT2A receptor stimulation. The failure of intra-striatal MDL-100907 to antagonize the effects of DOI suggests that 5-HT2A receptors in the dorsal striatum are unlikely to be primarily responsible for DOI's effects on timing. Furthermore, the results provide no evidence for a role of striatal 5-HT2C receptors in DOI's effect on timing. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 267
页数:10
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