Nash Family Department of Neuroscience, Department of Pharmacological Sciences, and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Boston University Chobanian and Avedisian School of Medicine, Boston, MA, USA.
Nat Neurosci. 2023 Jul;26(7):1229-1244. doi: 10.1038/s41593-023-01350-3. Epub 2023 Jun 8.
The development of physical dependence and addiction disorders due to misuse of opioid analgesics is a major concern with pain therapeutics. We developed a mouse model of oxycodone exposure and subsequent withdrawal in the presence or absence of chronic neuropathic pain. Oxycodone withdrawal alone triggered robust gene expression adaptations in the nucleus accumbens, medial prefrontal cortex and ventral tegmental area, with numerous genes and pathways selectively affected by oxycodone withdrawal in mice with peripheral nerve injury. Pathway analysis predicted that histone deacetylase (HDAC) 1 is a top upstream regulator in opioid withdrawal in nucleus accumbens and medial prefrontal cortex. The novel HDAC1/HDAC2 inhibitor, Regenacy Brain Class I HDAC Inhibitor (RBC1HI), attenuated behavioral manifestations of oxycodone withdrawal, especially in mice with neuropathic pain. These findings suggest that inhibition of HDAC1/HDAC2 may provide an avenue for patients with chronic pain who are dependent on opioids to transition to non-opioid analgesics.
由于阿片类镇痛药的滥用而导致身体依赖和成瘾障碍的发展是疼痛治疗的一个主要关注点。我们开发了一种在存在或不存在慢性神经病理性疼痛的情况下暴露于羟考酮和随后戒断的小鼠模型。羟考酮单独戒断会在伏隔核、内侧前额叶皮层和腹侧被盖区引发强烈的基因表达适应性,在外周神经损伤的小鼠中,许多基因和途径会被羟考酮戒断特异性地影响。通路分析预测组蛋白去乙酰化酶 (HDAC)1 是伏隔核和内侧前额叶皮层阿片类戒断的顶级上游调节剂。新型 HDAC1/HDAC2 抑制剂,Regenacy Brain Class I HDAC Inhibitor (RBC1HI),减轻了羟考酮戒断的行为表现,特别是在有神经病理性疼痛的小鼠中。这些发现表明,抑制 HDAC1/HDAC2 可能为依赖阿片类药物的慢性疼痛患者提供一种途径,使他们能够过渡到非阿片类镇痛药。