Mohammad Ahmadi Soleimani S, Azizi Hossein, Pachenari Narges, Mirnajafi-Zadeh Javad, Semnanian Saeed
Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Neuropeptides. 2017 Jun;63:28-36. doi: 10.1016/j.npep.2017.03.004. Epub 2017 Mar 23.
Opioids have always been used in clinical practice for pain management. However, development of tolerance to their effects following long term administration, seriously restricts further clinical use of these drugs. In this regard, μ-opioid receptor (MOR) desensitization, as an initial step in development of opioid tolerance, is of particular significance. Previous studies support the involvement of orexinergic system in development of opioid tolerance. Locus coeruleus (LC) nucleus has been shown to modulate pain and development of tolerance. Opioid receptors (particularly μ) are densely expressed within the LC. Moreover, it receives widespread orexinergic inputs and orexin type 1 receptors (OX1Rs) are also highly expressed in this brain region. In the present study, the effect of orexin-A (OXA) on met-enkephalin (ME)-induced MOR desensitization was investigated in locus coeruleus neurons of male Wistar rats (2-3weeks of age). ME (30μM), as a potent MOR agonist, was applied for 10min and the outward K current was recorded using whole cell patch clamp recording. The percentage of decrease in ME-induced K current was considered as the degree of MOR desensitization. Results indicated that OXA (100nM) enhances ME-induced MOR desensitization via affecting OX1Rs in rat locus coeruleus neurons and this effect is mediated by a protein kinase C dependent mechanism within the LC. The activity of orexinergic system might potentiate the signaling pathways underlying opioid-induced receptor desensitization.
阿片类药物一直被用于临床实践中的疼痛管理。然而,长期给药后对其效果产生耐受性,严重限制了这些药物的进一步临床应用。在这方面,μ-阿片受体(MOR)脱敏作为阿片类药物耐受性发展的初始步骤,具有特别重要的意义。先前的研究支持食欲素能系统参与阿片类药物耐受性的发展。蓝斑(LC)核已被证明可调节疼痛和耐受性的发展。阿片受体(特别是μ受体)在LC中密集表达。此外,它接受广泛的食欲素能输入,并且食欲素1型受体(OX1Rs)在该脑区也高度表达。在本研究中,研究了食欲素A(OXA)对雄性Wistar大鼠(2 - 3周龄)蓝斑神经元中脑啡肽(ME)诱导的MOR脱敏的影响。ME(30μM)作为一种有效的MOR激动剂,应用10分钟,并使用全细胞膜片钳记录外向钾电流。ME诱导的钾电流减少的百分比被视为MOR脱敏的程度。结果表明,OXA(100nM)通过影响大鼠蓝斑神经元中的OX1Rs增强ME诱导的MOR脱敏,并且这种作用是由LC内的蛋白激酶C依赖性机制介导的。食欲素能系统的活性可能增强阿片类药物诱导的受体脱敏的信号通路。