Amanzade Aysan, Khakpai Fatemeh, Zarrindast Mohammad-Reza
Department of Pharmacology and Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Department of Physiology, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Psychopharmacology (Berl). 2024 Apr;241(4):753-766. doi: 10.1007/s00213-023-06507-3. Epub 2024 Feb 21.
The endocannabinoid system plays a key role in the control of many emotional-correlated reactions such as stress, depressed mood, and anxiety. Moreover, citicoline has neuroprotective properties and indicates beneficial effects in the treatment of depressive problems. Acute restraint stress (ARS) is an experimental model used for the induction of rodent models of depression.
This research was designed to assess the effects of intracerebroventricular (i.c.v.) injection of cannabinoid CB1 receptor agents on citicoline-induced response to depression-like behaviors in the non-acute restraint stress (NARS) and ARS mice.
For i.c.v. microinjection, a guide cannula was implanted in the left lateral ventricle of male mice. The ARS model was carried out by movement restraint for 4 h. Depression-related behaviors were assessed by forced swimming test (FST), tail suspension test (TST), and splash test.
The results exhibited that the ARS mice showed depressive-like responses. I.c.v. infusion of ACPA (1 μg/mouse) induced an antidepressant-like effect in the NARS and ARS mice by reduction of immobility time in the FST and TST as well as enhancement of grooming activity time in the splash test. On the other hand, i.c.v. microinjection of AM251 dose-dependently (0.5 and 1 μg/mouse) induced a depressant-like effect in the NARS mice. I.p. injection of citicoline (80 mg/kg) induced an antidepressant-like response in the NARS and ARS mice. Furthermore, ACPA (0.25 μg/mouse, i.c.v.) potentiated the antidepressant-like response induced by citicoline (20 mg/kg, i.p.) in the NARS and ARS mice. However, AM251 (0.25 μg/mouse, i.c.v.) reversed the antidepressant-like effect produced by the citicoline (80 mg/kg, i.p.) in the NARS and ARS mice. Interestingly, our results indicated a synergistic effect between citicoline and ACPA based on the induction of an antidepressant-like effect in the NARS and ARS mice.
These results suggested an interaction between citicoline and cannabinoid CB1 receptors on the modulation of depression-like behaviors in the NARS and ARS mice.
内源性大麻素系统在控制许多与情绪相关的反应(如应激、抑郁情绪和焦虑)中起关键作用。此外,胞磷胆碱具有神经保护特性,并在治疗抑郁问题方面显示出有益效果。急性束缚应激(ARS)是一种用于诱导啮齿动物抑郁模型的实验模型。
本研究旨在评估脑室内(i.c.v.)注射大麻素CB1受体激动剂对胞磷胆碱诱导的非急性束缚应激(NARS)和ARS小鼠抑郁样行为反应的影响。
对于i.c.v.微量注射,将引导套管植入雄性小鼠的左侧脑室。通过移动束缚4小时建立ARS模型。通过强迫游泳试验(FST)、悬尾试验(TST)和溅水试验评估与抑郁相关的行为。
结果显示,ARS小鼠表现出抑郁样反应。i.c.v.注入ACPA(1μg/小鼠)通过减少FST和TST中的不动时间以及增加溅水试验中的梳理活动时间,在NARS和ARS小鼠中诱导出抗抑郁样效应。另一方面,i.c.v.微量注射AM251(0.5和1μg/小鼠)剂量依赖性地在NARS小鼠中诱导出抑郁样效应。腹腔注射胞磷胆碱(80mg/kg)在NARS和ARS小鼠中诱导出抗抑郁样反应。此外,ACPA(0.25μg/小鼠,i.c.v.)增强了胞磷胆碱(20mg/kg,腹腔注射)在NARS和ARS小鼠中诱导的抗抑郁样反应。然而,AM251(0.25μg/小鼠,i.c.v.)逆转了胞磷胆碱(80mg/kg,腹腔注射)在NARS和ARS小鼠中产生的抗抑郁样效应。有趣的是,我们的结果表明,基于在NARS和ARS小鼠中诱导出抗抑郁样效应,胞磷胆碱和ACPA之间存在协同作用。
这些结果表明,胞磷胆碱与大麻素CB1受体之间在调节NARS和ARS小鼠的抑郁样行为方面存在相互作用。