Marichal-Cancino Bruno A, Fajardo-Valdez Alfonso, Ruiz-Contreras Alejandra E, Méndez-Díaz Mónica, Prospéro-García Oscar
Departamento de Fisiología y Farmacología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Ciudad Universitaria, Aguascalientes, México,
Grupo de Neurociencias, Laboratorio de Cannabinoides, Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, México.
Acta Neurobiol Exp (Wars). 2018;78(1):41-50.
Endocannabinoids (eCBs) are involved in the hippocampal mechanisms of spatial learning and memory in rats. Although eCBs exert many of their actions on spatial learning and memory via CB1 receptors, the putative cannabinoid receptor GPR55 (expressed in the hippocampus, cortex, forebrain, cerebellum and striatum) seems to be also involved. To investigate the potential role of GPR55 in spatial learning and memory, Wistar rats received bilateral infusions of lysophosphatidylinositol (LPI, GPR55‑agonist) into the hippocampus 5‑minutes before training‑phase in the Barnes‑maze (BM). This manipulation increased the use of serial navigation while preventing the learning of spatial navigation strategy and decreasing the use of random activity to find the escape‑tunnel in the BM. In contrast, CID16020046 (GPR55‑antagonist) increased the use of random activity at the expense of spatial and serial navigation strategies. Finally, CID16020046 significantly reduced the time spent in the target zone during a retention test. Our results suggest: (i) a potential role of GPR55 in developing navigation strategies; (ii) a prospective function for LPI acting in hippocampal CA1 (probably via GPR55) to perform a serial navigation strategy; and (iii) a potential role of GPR55 in the mechanisms involved in spatial memory (object placement memory).
内源性大麻素(eCBs)参与大鼠空间学习和记忆的海马机制。尽管eCBs通过CB1受体对空间学习和记忆发挥多种作用,但假定的大麻素受体GPR55(在海马体、皮质、前脑、小脑和纹状体中表达)似乎也参与其中。为了研究GPR55在空间学习和记忆中的潜在作用,Wistar大鼠在巴恩斯迷宫(BM)训练阶段前5分钟接受双侧海马内注射溶血磷脂酰肌醇(LPI,GPR55激动剂)。这种操作增加了序列导航的使用,同时阻止了空间导航策略的学习,并减少了在BM中寻找逃生通道时随机活动的使用。相比之下,CID16020046(GPR55拮抗剂)以牺牲空间和序列导航策略为代价增加了随机活动的使用。最后,CID16020046在保留测试期间显著减少了在目标区域花费的时间。我们的结果表明:(i)GPR55在制定导航策略中的潜在作用;(ii)LPI作用于海马CA1(可能通过GPR55)执行序列导航策略的预期功能;以及(iii)GPR55在空间记忆(物体位置记忆)相关机制中的潜在作用。