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Serotonin-3 Receptors in the Posterior Ventral Tegmental Area Regulate Ethanol Self-Administration of Alcohol-Preferring (P) Rats

机译:后腹侧被盖区的5-羟色胺3受体调节乙醇(P)大鼠的乙醇自我管理。

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摘要

Several studies indicated the involvement of serotonin-3 (5-HT3) receptors in regulating alcohol-drinking behavior. The objective of this study was to determine the involvement of 5-HT3 receptors within the ventral tegmental area (VTA) in regulating ethanol self-administration by alcohol-preferring (P) rats. Standard two-lever operant chambers were used to examine the effects of 7 consecutive bilateral micro-infusions of ICS205-930 (ICS), a 5-HT3 receptor antagonist, directly into the posterior VTA on the acquisition and maintenance of 15% (v/v) ethanol self-administration. P rats readily acquired ethanol self-administration by the 4th session. The three highest doses (0.125, 0.25 and 1.25 ug) of ICS prevented acquisition of ethanol self-administration. During the acquisition post-injection period, all rats treated with ICS demonstrated higher responding on the ethanol lever, with the highest dose producing the greatest effect. In contrast, during the maintenance phase, the 3 highest doses (0.75, 1.0 and 1.25 ug) of ICS significantly increased responding on the ethanol lever; following the 7-day dosing regimen, responding on the ethanol lever returned to control levels. Micro-infusion of ICS into the posterior VTA did not alter the low responding on the water lever, and did not alter saccharin (0.0125% w/v) self-administration.. Micro-infusion of ICS into the anterior VTA did not alter ethanol self-administration. Overall, the results of this study suggest that 5-HT3 receptors in the posterior VTA of the P rat may be involved in regulating ethanol self-administration. In addition, chronic operant ethanol self-administration, and/or repeated treatments with a 5-HT3 receptor antagonist may alter neuronal circuitry within the posterior VTA.
机译:几项研究表明,血清素3(5-HT3)受体参与调节饮酒行为。这项研究的目的是确定腹侧被盖区(VTA)中的5-HT3受体在调节酒精偏爱(P)大鼠的乙醇自我给药中的作用。使用标准的两杆手术室检查连续5次直接向后VTA输注5-HT3受体拮抗剂ICS205-930(ICS)的7次双向双边微注对15%(v / v)乙醇自我管理。到第4次实验时,P大鼠很容易获得乙醇的自我管理。 ICS的三种最高剂量(0.125、0.25和1.25 ug)阻止了乙醇的自我给药。在注射后的采集期间,所有接受ICS治疗的大鼠均表现出对乙醇杠杆的更高响应,最高剂量产生最大的作用。相反,在维持阶段,ICS的3种最高剂量(0.75、1.0和1.25 ug)显着增加了对乙醇杠杆的响应。在为期7天的给药方案后,对乙醇杠杆的响应恢复到控制水平。将ICS微量注入后VTA不会改变水杠杆的低响应性,也不会改变糖精(0.0125%w / v)的自我给药。.将ICS微量注入前VTA不会改变乙醇自我管理。总体而言,这项研究的结果表明,P大鼠后VTA中的5-HT3受体可能参与调节乙醇的自我给药。另外,慢性操作性乙醇自我给药和/或用5-HT3受体拮抗剂反复治疗可能会改变后VTA内的神经元回路。

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