Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
Behav Brain Res. 2021 Sep 24;414:113450. doi: 10.1016/j.bbr.2021.113450. Epub 2021 Jul 12.
Investigations have shown that the circadian rhythm can affect the mechanisms associated with drug dependence. In this regard, we sought to assess the negative consequence of morphine withdrawal syndrome on conditioned place aversion (CPA) and lateral paragigantocellularis (LPGi) neuronal activity in morphine-dependent rats during light (8:00-12:00) and dark (20:00-24:00) cycles. Male Wistar rats (250-300 g) were received 10 mg/kg morphine or its vehicle (Saline, 2 mL/kg/12 h, s.c.) in 13 consecutive days for behavioral assessment tests. Then, naloxone-induced conditioned place aversion and physical signs of withdrawal syndrome were evaluated during light and dark cycles. In contrast to the behavioral part, we performed in vivo extracellular single-unit recording for investigating the neural response of LPGi to naloxone in morphine-dependent rats on day 10 of morphine/saline exposure. Results showed that naloxone induced conditioned place aversion in both light and dark cycles, but the CPA score during the light cycle was larger. Moreover, the intensity of physical signs of morphine withdrawal syndrome was more severe during the light cycle (rest phase) compare to the dark one. In electrophysiological experiments, results indicated that naloxone evoked both excitatory and inhibitory responses in LPGi neurons and the incremental effect of naloxone on LPGi activity was stronger in the light cycle. Also, the neurons with the excitatory response exhibited higher baseline activity in the dark cycle, but the neurons with the inhibitory response showed higher baseline activity in the light cycle. Interestingly, the baseline firing rate of neurons recorded in the light cycle was significantly different in response (excitatory/inhibitory) -dependent manner. We concluded that naloxone-induced changes in LPGi cellular activity and behaviors of morphine-dependent rats can be affected by circadian rhythm and the internal clock.
研究表明,生物钟节律会影响与药物依赖相关的机制。在这方面,我们试图评估吗啡戒断综合征对吗啡依赖大鼠条件性位置厌恶(CPA)和外侧旁巨细胞区(LPGi)神经元活动的负面影响,分别在光(8:00-12:00)和暗(20:00-24:00)周期。雄性 Wistar 大鼠(250-300 g)连续 13 天接受 10 mg/kg 吗啡或其载体(生理盐水,2 mL/kg/12 h,皮下注射),进行行为评估测试。然后,在光和暗周期评估纳洛酮诱导的条件性位置厌恶和戒断综合征的身体迹象。与行为部分相反,我们进行了体内细胞外单单位记录,以研究在吗啡/生理盐水暴露的第 10 天,吗啡依赖大鼠 LPGi 对纳洛酮的神经反应。结果表明,纳洛酮在光和暗周期都诱导了条件性位置厌恶,但在光周期的 CPA 评分更大。此外,在光周期(休息期),与暗周期相比,吗啡戒断综合征的身体迹象的强度更为严重。在电生理实验中,结果表明,纳洛酮在 LPGi 神经元中诱发了兴奋性和抑制性反应,纳洛酮对 LPGi 活性的递增效应在光周期更强。此外,具有兴奋性反应的神经元在暗周期的基线活动较高,但具有抑制性反应的神经元在光周期的基线活动较高。有趣的是,在光周期记录的神经元的基线放电率在响应(兴奋性/抑制性)依赖性方式上有显著差异。我们得出结论,纳洛酮诱导的吗啡依赖大鼠 LPGi 细胞活动和行为的变化可能受昼夜节律和生物钟的影响。