Jokara Zahra, Khatamsaz Saeed, Alaei HojjatAllah, Shariati Mehrdad
Department of Biology, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Iran J Basic Med Sci. 2022 May;25(5):604-610. doi: 10.22038/IJBMS.2022.62133.13751.
The central nucleus of the amygdala (CeA) is one of the most important areas for the morphine reward system. This study investigated the effect of electrical stimulation of CeA on morphine conditioned place preference (CPP) in male rats.
After anesthetizing male Wistar rats, both electrode and cannula were implanted into CeA for stimulating (low intensity: 25 μA, and high intensity: 150 μA) and injecting (lidocaine and dopamine D2 receptor antagonist), respectively. Then, CPP induced by effective (5 mg/kg) and ineffective (0.5 mg/kg) doses of morphine was evaluated for five consecutive days (n = 6 / group).
The low electrical stimulation intensity of 25 μA suppressed both acquisition and expression phases, but the high intensity of 150 µA attenuated only the expression phase. On the other hand, intra-CeA administration of dopamine D2 receptor antagonist, eticlopride (2 µg/rat), with the effective dose of morphine, decreased CPP. In addition, infusion of lidocaine into the CeA inhibited morphine-induced CPP in both acquisition and expression phases with the effective dose of morphine.
Electrical stimulation of the CeA may play an important role in attenuating morphine induced CPP via possible changes in neurotransmitters involved in the reward system such as dopamine (DA) and gamma-aminobutyric acid (GABA).
杏仁核中央核(CeA)是吗啡奖赏系统最重要的区域之一。本研究调查了电刺激CeA对雄性大鼠吗啡条件性位置偏爱(CPP)的影响。
对雄性Wistar大鼠进行麻醉后,将电极和套管分别植入CeA用于刺激(低强度:25 μA,高强度:150 μA)和注射(利多卡因和多巴胺D2受体拮抗剂)。然后,连续五天评估有效剂量(5 mg/kg)和无效剂量(0.5 mg/kg)吗啡诱导的CPP(每组n = 6)。
25 μA的低电刺激强度抑制了获得期和表达期,但150 μA的高强度仅减弱了表达期。另一方面,在给予有效剂量吗啡的同时,向CeA内注射多巴胺D2受体拮抗剂依托必利(2 μg/大鼠)可降低CPP。此外,在给予有效剂量吗啡的情况下,向CeA内注入利多卡因在获得期和表达期均抑制了吗啡诱导的CPP。
电刺激CeA可能通过奖赏系统中涉及的神经递质如多巴胺(DA)和γ-氨基丁酸(GABA)的可能变化,在减弱吗啡诱导的CPP中发挥重要作用。