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Effects of Chronic Alcohol and Repeated Deprivations on Dopamine D1 and D2 Receptor Levels in the Extended Amygdala of Inbred Alcohol-Preferring Rats

机译:慢性酒精和反复剥夺对近亲偏爱酒精的大鼠扩大杏仁核中多巴胺D1和D2受体水平的影响

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摘要

BackgroundDopaminergic (DA) activity in the extended amygdala (EA) has been known to play a pivotal role in mediating drug and alcohol addiction. Alterations of DA activity within the EA after chronic exposure to alcohol or substances of abuse are considered a major mechanism for the development of alcoholism and addiction. To date, it is not clear how different patterns of chronic alcohol drinking affect DA receptor levels. Therefore, the current studies investigated the effects of chronic ethanol consumption, with or without deprivations, on D1 and D2 receptor densities within the EA.MethodsInbred alcohol-preferring (iP) rats were divided into 3 groups with the following treatments: (1) water for 14 weeks; (2) continuous alcohol (C-Alc) for 14 weeks [24-hour concurrent access to 15 and 30% (v/v) ethanol]; or (3) repeatedly deprived of alcohol (RD-Alc) (24-hour concurrent access to 15 and 30% ethanol for 6 weeks, followed by 2 cycles of 2 weeks of deprivation of and 2 weeks of reexposure to ethanol access). At the end of 14 weeks, the rats were killed for autoradiographic labeling of D1 and D2 receptors.ResultsCompared with the water control group, both the C-Alc and the RD-Alc groups displayed increases in D1 receptor binding density in the anterior region of the Acb core, whereas the RD-Alc group displayed additional increases in D1 receptor binding density in anterior regions of the lateral and intercalated nuclei of the amygdala. Additionally, both C-Alc and RD-Alc rats displayed increases in D2 receptor binding density in anterior regions of the Acb shell and core, whereas RDAlc rats displayed additional increases in D2 receptor binding density in the dorsal striatum.ConclusionThe results of this study indicate that 14-week extended alcohol drinking with continuous chronic or repeated deprivations increase binding sites of D1 and D2 receptors in specific regions of the EA with greater sensitivity in the anterior regions. The repeated deprivation has greater effect on altering D1 and D2 receptor binding sites in the Acb, dorsal striatum, and subamygdala regions. The current result indicates that the two drinking paradigms may have common as well as differential mechanisms on alteration of dopamine receptor–binding sites in specific regions of the EA.
机译:背景技术已知杏仁核(EA)中的多巴胺能(DA)活性在介导药物和酒精成瘾中起关键作用。长期接触酒精或滥用药物后,EA中DA活动的改变被认为是酗酒和成瘾的主要机制。迄今为止,尚不清楚慢性饮酒的不同方式如何影响DA受体水平。因此,目前的研究调查了长期摄入或不剥夺乙醇对EA内D1和D2受体密度的影响。方法将近交偏爱酒精的大鼠(iP)分为3组,采用以下治疗方法:(1)水持续14周; (2)连续饮酒(C-Alc)14周[24小时同时使用15和30%(v / v)乙醇];或(3)反复剥夺酒精(RD-Alc)(24小时同时使用15%和30%乙醇,持续6周,然后进行2个循环,每次剥夺2周,再暴露于乙醇中2周)。 14周后,处死大鼠进行放射自显影标记D1和D2受体。结果与水对照组相比,C-Alc和RD-Alc组在D1和D2受体前区的D1受体结合密度均增加。 Acb核心,而RD-Alc组在杏仁核的外侧和插入核的前部区域显示D1受体结合密度的额外增加。此外,C-Alc和RD-Alc大鼠在Acb壳和核的前部区域均显示D2受体结合密度增加,而RDAlc大鼠在背侧纹状体中显示D2受体结合密度进一步增加。连续连续慢性或反复剥夺的14周长时间饮酒会增加EA特定区域中D1和D2受体的结合位点,并在前部区域具有更高的敏感性。重复剥夺对改变Acb,背侧纹状体和杏仁核下区域的D1和D2受体结合位点具有更大的影响。目前的结果表明,这两种饮酒范例可能在EA特定区域改变多巴胺受体结合位点方面具有共同的和不同的机制。

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