Schneider Piper, Goldbaum Danielle, Agarwal Ansh, Taylor Ashton, Sundberg Peyton, Gardner Eliot L, Ranaldi Robert, You Zhi-Bing, Galaj Ewa
Department of Psychological and Brain Sciences, Colgate University, Hamilton, NY, USA.
Neuropsychopharmacology Section, National Institute on Drug Abuse Intramural Research Program, Baltimore, MD, USA.
Pharmacol Biochem Behav. 2025 Feb;247:173931. doi: 10.1016/j.pbb.2024.173931. Epub 2024 Dec 1.
While stress increases vulnerability to development of addiction, the recruitment of corticotropin releasing factor (CRF) with excessive drug use heightens the risk of stress-induced relapse. CRF signaling is transmitted via CRF1 and CRF2 receptors, but the roles of these receptors in heroin self-administration and related neuroadaptations of the CRF system within mesolimbic brain loci are not well understood. In this study, we first investigated the causal role of CRF1 and CRF2 receptors in heroin self-administration. Intracerebroventricular (ICV) microinjections of antalarmin (a CRF1 antagonist) or astressin-2B (a CRF2 antagonist) caused brief, dose-dependent reductions in heroin self-administration in female rats, suggesting that these receptors play a critical role in heroin-motivated behaviors. We then used western blotting to examine neuroadaptive changes to CRF1 and CRF2 receptor expression in key forebrain and midbrain regions associated with opioid addiction. Female Long Evans rats treated with escalating doses of heroin for 16 days demonstrated significantly higher naloxone-precipitated withdrawal symptoms than saline-treated rats. Heroin-treated rats showed a significant decrease in CRF1 receptor protein expression in the ventral tegmental area (VTA) and an increase in the nucleus accumbens (NAc) but no changes in the prefrontal cortex (PFC), insula, dorsal striatum (dSTR), dorsal hippocampus (dHippo), anterior hypothalamus (HYPTH), amygdala, or substantia nigra (SN) as compared to saline-treated rats. After chronic heroin exposure, CRF2 receptor expression was significantly downregulated in the dHippo, VTA and HYPTH but not in the other brain regions we investigated. The results of this study suggest that: (1) CRF1 and CRF2 receptors play an important role in self-administration and (2) heroin exposure may lead to region-specific neuroadaptation of CRF1 and CRF2 receptors. Such neuroadaptations might in part contribute to the continuation of drug use and stress-induced relapse.
虽然压力会增加成瘾易感性,但过度使用药物时促肾上腺皮质激素释放因子(CRF)的募集会增加应激诱导复吸的风险。CRF信号通过CRF1和CRF2受体传递,但这些受体在海洛因自我给药及中脑边缘脑区CRF系统相关神经适应性变化中的作用尚未完全明确。在本研究中,我们首先探究了CRF1和CRF2受体在海洛因自我给药中的因果作用。向雌性大鼠脑室内(ICV)微量注射安他拉明(一种CRF1拮抗剂)或阿斯特辛 - 2B(一种CRF2拮抗剂)会导致海洛因自我给药出现短暂的、剂量依赖性降低,这表明这些受体在海洛因驱动的行为中起关键作用。然后我们使用蛋白质免疫印迹法来检测与阿片类成瘾相关的关键前脑和中脑区域中CRF1和CRF2受体表达的神经适应性变化。用递增剂量海洛因处理16天的雌性Long Evans大鼠表现出比用生理盐水处理的大鼠明显更高的纳洛酮诱发戒断症状。与生理盐水处理的大鼠相比,海洛因处理的大鼠腹侧被盖区(VTA)中CRF1受体蛋白表达显著降低,伏隔核(NAc)中表达增加,但前额叶皮质(PFC)、岛叶、背侧纹状体(dSTR)、背侧海马(dHippo)、下丘脑前部(HYPTH)、杏仁核或黑质(SN)中无变化。慢性海洛因暴露后,dHippo、VTA和HYPTH中的CRF2受体表达显著下调,但在我们研究的其他脑区中未下调。本研究结果表明:(1)CRF1和CRF2受体在自我给药中起重要作用;(2)海洛因暴露可能导致CRF1和CRF2受体的区域特异性神经适应性变化。这种神经适应性变化可能部分促成了药物使用的持续及应激诱导的复吸。