Chao Owen Y, Nikolaus Susanne, Huston Joseph P, de Souza Silva Maria A
Center for Behavioral Neuroscience, Institute of Experimental Psychology, University of Düsseldorf, Universitätsstr. 1, 40225 Düsseldorf, Germany.
Clinic of Nuclear Medicine, University Hospital Düsseldorf, Moorenstr. 5, 40225 Düsseldorf, Germany.
Neurobiol Learn Mem. 2014 Oct;114:178-85. doi: 10.1016/j.nlm.2014.06.009. Epub 2014 Jun 24.
Senktide, a potent neurokinin-3 receptor (NK3-R) agonist, has been shown to have promnestic effects in adult and aged rodents and to facilitate episodic-like memory (ELM) in mice when administrated before the learning trial. In the present study we assessed the effects of senktide on memory consolidation by administering it post-trial (after the learning trial) in adult rats. We applied an ELM test, based on the integrated memory for object, place and temporal order, which we developed (Kart-Teke, de Souza Silva, Huston, & Dere, 2006). This test involves two learning trials and one test trial. We examined intervals of 1h and 23 h between the learning and test trials (experiment 1) in untreated animals and found that they exhibited intact ELM after a delay of 1 h, but not 23 h. In another test for ELM performed 7 days later, vehicle or senktide (0.2 mg/kg, s.c.) was applied immediately after the second learning trial and the test was conducted 23 h later (experiment 2). Senktide treatment recovered components of ELM (memory for place and object) compared with vehicle-treated animals. After one more week, vehicle or senktide (0.2 mg/kg, s.c.) was applied post-trial and the test conducted 6h later (experiment 3). The senktide-treated group exhibited intact ELM, unlike the vehicle-treated group. Finally, animals received post-trial treatment with either vehicle or SR142801, a selective NK3-R antagonist (6 mg/kg, i.p.), 1 min before senktide injection (0.2 mg/kg, s.c.) in the ELM paradigm and were tested 6h later (experiment 4). The vehicle+senktide group showed intact ELM, while the SR142801+senktide group did not. The results indicate that senktide facilitated the consolidation or the expression of ELM and that the senktide effect was NK3-R dependent.
森克肽是一种强效神经激肽-3受体(NK3-R)激动剂,已被证明在成年和老年啮齿动物中具有促记忆作用,并且在学习试验前给药时可促进小鼠的情景样记忆(ELM)。在本研究中,我们通过在成年大鼠试验后(学习试验后)给予森克肽来评估其对记忆巩固的影响。我们应用了一种基于对物体、位置和时间顺序的综合记忆的ELM测试,该测试由我们开发(Kart-Teke、de Souza Silva、Huston和Dere,2006年)。该测试包括两次学习试验和一次测试试验。我们在未处理的动物中检查了学习试验和测试试验之间1小时和23小时的间隔(实验1),发现它们在延迟1小时后表现出完整的ELM,但延迟23小时后则没有。在7天后进行的另一项ELM测试中,在第二次学习试验后立即给予溶剂或森克肽(0.2mg/kg,皮下注射),并在23小时后进行测试(实验2)。与溶剂处理的动物相比,森克肽处理恢复了ELM的组成部分(对位置和物体的记忆)。再过一周后,试验后给予溶剂或森克肽(0.2mg/kg,皮下注射),并在6小时后进行测试(实验3)。与溶剂处理组不同,森克肽处理组表现出完整的ELM。最后,在ELM范式中,动物在注射森克肽(0.2mg/kg,皮下注射)前1分钟接受溶剂或选择性NK3-R拮抗剂SR142801(6mg/kg,腹腔注射)的试验后处理,并在6小时后进行测试(实验4)。溶剂+森克肽组表现出完整的ELM,而SR142801+森克肽组则没有。结果表明,森克肽促进了ELM的巩固或表达,并且森克肽的作用是依赖于NK3-R的。