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RAPID NEUROADAPTATION IN THE NUCLEUS ACCUMBENS AND BED NUCLEUS OF THE STRIA TERMINALIS MEDIATES SUPPRESSION OF OPERANT RESPONDING DURING WITHDRAWAL FROM ACUTE OPIOID DEPENDENCE

机译:纹状体末梢核伏核和床状核的快速神经适应介导了急性鸦片依赖引起的拔除操作员反应

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摘要

Single injections of morphine induce a state of acute opioid dependence in humans and animals, measured as precipitated withdrawal when an antagonist is administered 4–24 hours after morphine. Additional morphine exposure at daily or weekly intervals results in further increases in withdrawal severity, suggesting that acute opioid dependence reflects the early stages in the development of a chronic state of dependence. The current study evaluated the role of the nucleus accumbens (NAC), bed nucleus of stria terminalis (BNST), interstitial nucleus of posterior limb of the anterior commissure (IPAC), and central amygdala (CeA) in the expression of antagonist-precipitated suppression of operant responding for food as a measure of withdrawal from acute opioid dependence. Rats trained on an FR15 schedule received one or four daily injections, with the lipophobic opioid antagonist methylnaloxonium (16–2000 ng) infused into one of the brain regions or the lateral ventricle (ICV) 4 hr after the final morphine injection. After acute morphine methylnaloxonium was more potent upon infusion into the NAC (17.9-fold potency shift), BNST (6.8-fold) and CeA (5.5-fold) than it was upon ICV administration. Following repeat morphine the NAC and BNST but not CeA continued to show greater sensitivity relative to ICV infusion (12.9- and 8.7-, and 3.2-fold potency shifts, respectively). The IPAC was insensitive to methylnaloxonium after acute or repeat morphine at doses that reliably suppressed responding upon ICV infusion (125–500 ng). Thus, among the components of extended amygdala examined in this study, rapid neuroadaptation within the nucleus accumbens and bed nucleus of the stria terminalis appear to play the most prominent role in antagonist-precipitated suppression of operant responding during the early stages in the development of opioid dependence.
机译:单次注射吗啡会在人和动物中引起急性阿片类药物依赖状态,以吗啡注射后4-24小时给予拮抗剂时的沉淀戒断来衡量。每天或每周额外的吗啡暴露导致戒断严重程度进一步增加,这表明急性阿片类药物依赖反映了慢性依赖状态发展的早期阶段。本研究评估伏隔核(NAC),纹状体床床核(BNST),前连合后肢间质核(IPAC)和中央杏仁核(CeA)在拮抗剂沉淀抑制表达中的作用操作员对食物的反应,作为从急性阿片类药物依赖中撤退的一种措施。按FR15时间表训练的大鼠每天注射一或四次,最后一次吗啡注射后4小时,将疏脂阿片拮抗剂甲基纳络酮(16–2000 ng)注入大脑区域之一或侧脑室(ICV)。急性吗啡甲基纳络酮在输注NAC时(效价变化17.9倍),BNST(6.8倍)和CeA(5.5倍)比ICV给药更有效。重复吗啡后,相对于ICV输注,NAC和BNST而不是CeA继续显示出更高的敏感性(分别为12.9和8.7以及3.2倍的效能变化)。在急性或重复吗啡给药后,IPAC对甲基纳洛酮不敏感,剂量可靠地抑制了对ICV输注的反应(125-500 ng)。因此,在本研究中研究的延伸杏仁核的成分中,纹状体终末伏伏核和床核内的快速神经适应似乎在阿片样物质发展的早期阶段拮抗拮抗剂抑制的操作员应答中起着最重要的作用。依赖。

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