Egashira Nobuaki, Tanoue Akito, Higashihara Fuminori, Mishima Kenichi, Fukue Yoshihiko, Takano Yukio, Tsujimoto Gozoh, Iwasaki Katsunori, Fujiwara Michihiro
Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1, Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
Neurosci Lett. 2004 Feb 19;356(3):195-8. doi: 10.1016/j.neulet.2003.11.050.
In this study, we examined the performance of vasopressin V1a receptor (V1aR) and vasopressin V1b receptor (V1bR) knockout (KO) mice compared to wild-type (WT) mice in an eight-arm radial maze. V1aR KO mice exhibited an impairment of spatial memory in comparison to WT mice. By contrast, we did not observe any significant differences between the V1bR KO mice and the WT mice in the eight-arm radial maze. Moreover, OPC-21268, a selective V1aR antagonist, impaired spatial memory in the eight-arm radial maze in WT mice characterized by an increased number of errors. These results suggest that the V1aR controls spatial memory in mice.
在本研究中,我们检测了血管加压素V1a受体(V1aR)和血管加压素V1b受体(V1bR)基因敲除(KO)小鼠与野生型(WT)小鼠在八臂辐射状迷宫中的表现。与WT小鼠相比,V1aR基因敲除小鼠表现出空间记忆受损。相比之下,我们在八臂辐射状迷宫中未观察到V1bR基因敲除小鼠与WT小鼠之间存在任何显著差异。此外,选择性V1aR拮抗剂OPC-21268损害了WT小鼠在八臂辐射状迷宫中的空间记忆,其特征为错误数量增加。这些结果表明,V1aR控制小鼠的空间记忆。