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CJAP ›› 2016, Vol. 32 ›› Issue (6): 567-570.doi: 10.13459/j.cnki.cjap.2016.06.018

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Dual co-agonist CI-1206 antagonizes Aβ1-42-induced impairments in spatial learning and memory in mice

YANG Ju, ZHANG Jun, YUAN Li, QU Xue-song, QI Jin-shun   

  1. Department of Physiology, Shanxi Medical University, Taiyuan 030001, China
  • Online:2016-11-28 Published:2018-06-19
  • Contact: 祁金顺,Tel:0351-4135091;E-mail:jinshunqi2009@163.com E-mail:jinshunqi2009@163.com
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Abstract: Objective: To study the neuroprotective effects of a novel GIP/GLP-1 receptor dual agonist CI-1206 against Aβ1-42-induced impairments in spatial working memory and long term memory in mice. Methods: C57 mice, after receiving intracerebralventricular (i.c.v.) injection of Aβ1-42 and intraperitoneal injection of CI-1206, were divided into the following groups:saline+D-PBS, Aβ1-42+saline, CI-1206+D-PBS and Aβ1-42+CI-1206 group (n=12). Y maze spontaneous alternation of mice was tested to assess short term working memory, and Morris water maze task was used to assess long term reference memory. Results: ①The percentage of right alternation of mice in Aβ1-42+saline group was significantly decreased, while the percentage in Aβ1-42+CI-1206 group was significantly larger than that in Aβ1-42 alone group (P<0.05). ②In Morris water maze test, the escape latency of mice in Aβ1-42+saline group showed a significant increase, with a significant decline in swimming time in target quadrant. Treatment with CI-1206 significantly antagonized these detrimental effects induced by Aβ1-42. ③Aβ1-42 and CI-1206 did not affect the motor ability and vision of mice. Conclusion: I.C.V. administration of Aβ1-42 impaired the short term and long term spatial memory of mice, while CI-1206 could effectively antagonize the detrimental effects.

Key words: CI-1206, Amyloid &beta, protein, Y-maze, Morris water maze, spatial learning and memory, mouse

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