Davoudi Mahnaz, Azizi Hossein, Mirnajafi-Zadeh Javad, Semnanian Saeed
Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
J Physiol Sci. 2019 Mar;69(2):281-293. doi: 10.1007/s12576-018-0645-1. Epub 2018 Nov 7.
Acute opioid withdrawal syndrome is a series of neurological symptoms caused by the abrupt cessation of the chronic administration of opioids such as morphine. The locus coeruleus (LC) in the brain stem receives a dense projection of orexinergic fibers from the hypothalamus and is a candidate site for the expression of the somatic aspects of morphine withdrawal. Previous studies have shown that orexin-A contributes to the behavioral symptoms of naloxone-induced morphine withdrawal, partly by reducing the activity of GABAergic neurons, suggesting that orexin-A may negatively modulate fast GABAergic neurotransmission during morphine withdrawal. We used whole-cell patch-clamp recordings of LC neurons in brainstem slices to investigate the effect of orexin-A on bicuculline-sensitive GABAergic inhibitory postsynaptic currents (IPSCs) during naloxone-induced morphine withdrawal. Male Wistar rats (P14-P21) were given morphine (20 mg/kg, i.p.) daily for seven consecutive days to create dependency on the drug. The application of naloxone (1 µM) to brain slices of morphine-treated rats reduced the amplitude of evoked IPSCs (eIPSCs) as well as spontaneous IPSCs (sIPSCs) frequency but did not change sIPSCs amplitude. Orexin-A (100 nM) significantly enhanced the suppressive effect of naloxone on eIPSCs amplitude and sIPSCs frequency but had no effect on the presence of the orexin type 1 receptor (OX1R) antagonist, SB-334867. Orexin-A alone had no significant effect on eIPSCs and sIPSCs in the absence of naloxone. In summary, our results show that orexin-A, via OX1R, potentiates the suppressive effect of naloxone on GABAergic IPSCs of LC neurons in morphine-treated rats. We conclude that orexins may have a critical role in regulating GABAergic neurotransmission to LC neurons during naloxone-induced morphine withdrawal.
急性阿片类药物戒断综合征是由突然停止长期使用吗啡等阿片类药物引起的一系列神经症状。脑干中的蓝斑核(LC)接受来自下丘脑的密集的食欲素能纤维投射,是吗啡戒断躯体症状表达的候选部位。先前的研究表明,食欲素A部分通过降低GABA能神经元的活性,促成纳洛酮诱导的吗啡戒断的行为症状,这表明食欲素A可能在吗啡戒断期间对快速GABA能神经传递产生负调节作用。我们使用脑干切片中LC神经元的全细胞膜片钳记录,来研究在纳洛酮诱导的吗啡戒断期间,食欲素A对荷包牡丹碱敏感的GABA能抑制性突触后电流(IPSCs)的影响。雄性Wistar大鼠(P14 - P21)连续7天每天腹腔注射吗啡(20 mg/kg)以建立对该药物的依赖性。将纳洛酮(1 μM)应用于吗啡处理大鼠的脑切片,可降低诱发IPSCs(eIPSCs)的幅度以及自发性IPSCs(sIPSCs)的频率,但不改变sIPSCs的幅度。食欲素A(100 nM)显著增强了纳洛酮对eIPSCs幅度和sIPSCs频率的抑制作用,但对1型食欲素受体(OX1R)拮抗剂SB - 334867的存在没有影响。在没有纳洛酮的情况下,食欲素A单独对eIPSCs和sIPSCs没有显著影响。总之,我们的结果表明,食欲素A通过OX1R增强了纳洛酮对吗啡处理大鼠中LC神经元GABA能IPSCs的抑制作用。我们得出结论,在纳洛酮诱导的吗啡戒断期间,食欲素可能在调节向LC神经元的GABA能神经传递中起关键作用。