Chegini Hamid-Reza, Nasehi Mohammad, Zarrindast Mohammad-Reza
Institute for Cognitive Science Studies (ICSS), Tehran, Iran.
Institute for Cognitive Science Studies (ICSS), Tehran, Iran; Department of Biology, Faculty of Basic Sciences, Garmsar Branch, Islamic Azad University, Garmsar, P.O. Box 13145-784, Iran.
Behav Brain Res. 2014 Mar 15;261:114-26. doi: 10.1016/j.bbr.2013.12.007. Epub 2013 Dec 12.
The critical role of cannabinoidergic and serotonergic systems of the amygdala in modulation of anxiety-like behaviors and emotional memory has already been demonstrated. The present study aimed to investigate the possible role of the basolateral amygdala (BLA) 5-HT3 and 5-HT4 serotonergic systems upon ACPA (CB1 cannabinoid receptor agonist)-induced anxiolytic-like behaviors and emotional memory impairment using the elevated plus-maze (EPM) test-retest paradigm in male mice.
bilateral guide-cannulae were implanted to allow intra-BLA microinjection of serotonergic agents.
the intraperitoneal injection of ACPA could induce anxiolytic-like behaviors and reduce the emotional memory formation. Intra-BLA injection of M-Chlorophenylbiguanide (M-Chl, a 5-HT3 serotonin receptor agonist) neither altered the anxiety-like behaviors nor the emotional memory formation by itself, while the higher dose of Y-25130 (a 5-HT3 serotonin receptor antagonist) reduced the emotional memory formation and locomotor activity but not the anxiety-like behaviors. Furthermore, injection of a higher dose of RS67333 and RS23597 (as 5-HT4 serotonin receptor agonist and antagonist, respectively) did not alter the anxiety-like behaviors, while reduced the emotional memory formation. In addition, the intra-BLA injection of M-Chl but not Y-25130 and RS67333 restored the ACPA-induced anxiolytic-like behaviors and emotional memory deficit, while a higher dose of RS67333 decreased the locomotor activity. Moreover, the intra-BLA microinjection of RS23597 could restore the ACPA-induced anxiolytic-like behaviors but not the emotional memory deficit.
based on our findings, ACPA seems to induce its anxiolytic-like behaviors and emotional memory formation deficits via activation and deactivation of the BLA 5-HT4 and 5-HT3 serotonin receptors.
杏仁核的大麻素能和5-羟色胺能系统在调节焦虑样行为和情绪记忆方面的关键作用已得到证实。本研究旨在利用高架十字迷宫(EPM)重测范式,研究基底外侧杏仁核(BLA)的5-HT3和5-HT4 5-羟色胺能系统在ACPA(CB1大麻素受体激动剂)诱导的抗焦虑样行为和情绪记忆损害中可能发挥的作用。
植入双侧引导套管,以便在BLA内微量注射5-羟色胺能药物。
腹腔注射ACPA可诱导抗焦虑样行为并减少情绪记忆形成。BLA内注射M-氯苯双胍(M-Chl,一种5-HT3 5-羟色胺受体激动剂)本身既不改变焦虑样行为,也不改变情绪记忆形成,而高剂量的Y-25130(一种5-HT3 5-羟色胺受体拮抗剂)可减少情绪记忆形成和运动活动,但不改变焦虑样行为。此外,注射高剂量的RS67333和RS23597(分别作为5-HT4 5-羟色胺受体激动剂和拮抗剂)不改变焦虑样行为,但可减少情绪记忆形成。此外,BLA内注射M-Chl而非Y-25130和RS67333可恢复ACPA诱导的抗焦虑样行为和情绪记忆缺陷,而高剂量的RS67333可降低运动活动。此外,BLA内微量注射RS23597可恢复ACPA诱导的抗焦虑样行为,但不能恢复情绪记忆缺陷。
基于我们的研究结果,ACPA似乎通过激活和失活BLA的5-HT4和5-HT3 5-羟色胺受体来诱导其抗焦虑样行为和情绪记忆形成缺陷。