Department of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Neuropsychopharmacology and Neurotoxicology Program, College of Pharmacy, Kangwon National University, Chunchon, Republic of Korea.
Neurochem Int. 2018 Dec;121:1-7. doi: 10.1016/j.neuint.2018.10.009. Epub 2018 Oct 4.
Opioid addiction is a growing problem for public health, and opioids have correspondingly become more heavily regulated over time. We have previously shown that TRPV1 plays a critical role in morphine addiction using a self-administration paradigm in rats, and the current study evaluates the effects of the TRPV1 signaling pathway on morphine self-administration (SA). We found that treatment with a selective TRPV1 antagonist, SB366791, significantly decreased the morphine SA-induced activation of Ca2/calmodulin-dependent protein kinase II (CaMKII), Akt and the cAMP response element binding protein (CREB) in the nucleus accumbens (NAc). In addition, phospho-PKA and phospho-PKC expression levels were significantly increased in the NAc of the morphine-SA groups, regardless of SB366791 treatment. Finally, local microinjection of SB366791 into the NAc significantly suppressed the maintenance of morphine SA. Taken together, our findings highlight that TRPV1 plays an important role in morphine addiction, likely via activation of the CaMKII-CREB pathway in the NAc.
阿片类药物成瘾是公共卫生领域日益严重的问题,相应地,阿片类药物的管制也越来越严格。我们之前已经使用大鼠自我给药范式表明 TRPV1 在吗啡成瘾中起着关键作用,本研究评估了 TRPV1 信号通路对吗啡自我给药(SA)的影响。我们发现,使用选择性 TRPV1 拮抗剂 SB366791 处理可显著降低伏隔核(NAc)中吗啡 SA 诱导的 Ca2+/钙调蛋白依赖性蛋白激酶 II(CaMKII)、Akt 和 cAMP 反应元件结合蛋白(CREB)的激活。此外,无论是否用 SB366791 处理,吗啡-SA 组 NAc 中的磷酸化-PKA 和磷酸化-PKC 表达水平均显著增加。最后,将 SB366791 局部微注射到 NAc 中可显著抑制吗啡 SA 的维持。综上所述,我们的研究结果表明 TRPV1 在吗啡成瘾中起重要作用,可能通过 NAc 中的 CaMKII-CREB 通路激活来实现。