首页> 外文期刊>Neuropharmacology >The 5-HT(6) serotonin receptor antagonist SB-271046 attenuates the development and expression of nicotine-induced locomotor sensitisation in Wistar rats.
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The 5-HT(6) serotonin receptor antagonist SB-271046 attenuates the development and expression of nicotine-induced locomotor sensitisation in Wistar rats.

机译:5-HT(6)血清素受体拮抗剂SB-271046减弱了Wistar大鼠中尼古丁引起的运动敏化的发展和表达。

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摘要

5-HT(6) receptors are almost exclusively expressed in the central nervous system, particularly in areas relevant for addictive behaviour. Based on this, together with other data, this receptor may be a viable target for the control of drug abuse. The present study tested the ability of the 5-HT(6) receptor antagonist SB-271046 to attenuate the development and expression of nicotine-induced behavioural sensitisation. Rats were habituated to the test apparatus prior to experimentation (day 0) and locomotor activity recorded. On days 1 and 5, animals were placed in locomotor test apparatus and after 30 min injected with SB-271046 (1, 3, and 6 mg/kg, intraperitoneally IP) or vehicle. Thirty minutes later, nicotine (0.4 mg/kg, subcutaneously SC) or saline were administered and activity recorded for 60 min. On days 2, 3 and 4 treatments were performed in the home cage. After 17 days of withdrawal (day 23), a challenge test was performed with nicotine (0.4 mg/kg SC) or saline. In a separate experiment of similar design the effects of SB-271046 (1, 3, and 6 mg/kg IP) was tested for its ability to reduce the expression of behavioural sensitisation (day 23). SB-271046 dose dependently reduced the development and expression of nicotine sensitisation vs respective controls. In conclusion, the 5-HT(6) receptor antagonist SB-271046 reduced both the development and expression of nicotine sensitisation, suggesting that the 5-HT(6) receptor may be a viable target for the control of nicotine abuse. Further studies are warranted to substantiate this conclusion and further understand the role of 5-HT(6) receptors in addiction.
机译:5-HT(6)受体几乎只在中枢神经系统中表达,特别是在与成瘾行为有关的区域中。基于此,连同其他数据,该受体可能是控制药物滥用的可行目标。本研究测试了5-HT(6)受体拮抗剂SB-271046减弱尼古丁诱导的行为敏化的发展和表达的能力。实验前(第0天)使大鼠习惯于测试设备,并记录运动活动。在第1和第5天,将动物置于运动测试仪中,并在30分钟后注射SB-271046(1、3和6 mg / kg,腹膜内腹膜内注射)或媒介物。 30分钟后,给予尼古丁(0.4mg / kg,皮下SC)或盐水,并记录60分钟的活性。在第2、3和4天在笼中进行治疗。戒断17天(第23天)后,用尼古丁(0.4 mg / kg SC)或生理盐水进行攻击试验。在类似设计的另一个实验中,测试了SB-271046(1、3和6 mg / kg IP)的效果,可降低其行为敏化的表达(第23天)。与相应的对照相比,SB-271046剂量依赖性地减少了尼古丁致敏的发生和表达。总之,5-HT(6)受体拮抗剂SB-271046减少了尼古丁致敏的发展和表达,表明5-HT(6)受体可能是控制尼古丁滥用的可行靶标。必须进行进一步的研究以证实这一结论,并进一步了解5-HT(6)受体在成瘾中的作用。

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