Department of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Department of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran; Research Center for Cognitive and Behavioral Sciences, Tehran University of Medical Sciences, Tehran, Iran; Iranian National Center for Addiction Studies (INCAS), Tehran University of Medical Sciences, Tehran, Iran.
Drug Alcohol Depend. 2019 Dec 1;205:107638. doi: 10.1016/j.drugalcdep.2019.107638. Epub 2019 Nov 2.
The dynorphin (DYN)/kappa opioid receptor (KOR) system plays an important role in the development of addiction, and dysregulation of this system could lead to abnormal activity in the reward pathway. It has been reported that the expression state of the neurotransmitters and their receptors in the brain is reflected in peripheral blood lymphocytes (PBLs).
We have evaluated the PBLs and plasma samples of four groups: 1) subjects with severe opioid use disorder (SOD), 2) methadone-maintenance treated (MMT) individuals, 3) long-term abstinent subjects having former SOD, and 4) healthy control subjects (n = 20 in each group). The mRNA expression level of preprodynorphin (pPDYN) and KOR in PBLs has been evaluated by real-time PCR. Peptide expression of PDYN in PBLs has been studied by western blot, and DYN concentration in plasma has been measured by ELISA.
The relative expression level of the pPDYN mRNA and PDYN peptide in PBLs were significantly up-regulated in SOD, MMT, and abstinent groups compared to control subjects. No significant difference was found in the plasma DYN concentration between study groups. The expression level of the KOR mRNA in PBLs was significantly decreased in all three study groups compared to the control subjects.
the expression changes in the DYN/KOR system after chronic exposure to opioids, including methadone, seems to be stable and does not return to normal levels even after 12 months abstinence. These long-time and permanent changes in PBLs may serve as a biomarker and footprint of SOD development in the periphery.
强啡肽(DYN)/κ 阿片受体(KOR)系统在成瘾的发展中起着重要作用,该系统的失调可能导致奖励途径的异常活动。据报道,大脑中神经递质及其受体的表达状态反映在外周血淋巴细胞(PBL)中。
我们评估了四组的 PBL 和血浆样本:1)有严重阿片类药物使用障碍(SOD)的受试者,2)接受美沙酮维持治疗(MMT)的个体,3)有 former SOD 的长期禁欲受试者,和 4)健康对照受试者(每组 20 名)。通过实时 PCR 评估了 PBL 中前强啡肽原(pPDYN)和 KOR 的 mRNA 表达水平。通过 Western blot 研究了 PBL 中 PDYN 的肽表达,通过 ELISA 测量了血浆中 DYN 的浓度。
与对照组相比,SOD、MMT 和禁欲组 PBL 中 pPDYN mRNA 和 PDYN 肽的相对表达水平显着上调。研究组之间血浆 DYN 浓度无显着差异。与对照组相比,所有三组 PBL 中 KOR mRNA 的表达水平均显着降低。
在慢性暴露于阿片类药物(包括美沙酮)后,DYN/KOR 系统的表达变化似乎是稳定的,即使在 12 个月禁欲后也不会恢复到正常水平。这些在外周血淋巴细胞中的长期和永久性变化可能作为 SOD 发展的生物标志物和痕迹。