Kitamura Y, Ohnuki T, Nomura Y
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Jpn J Pharmacol. 1991 Jun;56(2):231-5. doi: 10.1254/jjp.56.231.
Senescence-accelerated mouse (SAM-P/8) is known as a murine model of aging and memory dysfunction, compared with control mouse (SAM-R/1). In the hippocampus of 9-month-old SAM-P/8, the Bmax of [3H]QNB binding was decreased compared with that of SAM-R/1 at the same age. Single and repeated administrations of bifemelane to SAM-P/8 induced an increase in the Bmax of [3H]QNB binding in the hippocampus. From these results, bifemelane seems to exert pharmacological effects through possible activation of the cholinergic system in the hippocampus of SAM.
与对照小鼠(SAM-R/1)相比,衰老加速小鼠(SAM-P/8)被认为是衰老和记忆功能障碍的小鼠模型。在9个月大的SAM-P/8小鼠的海马体中,[3H]QNB结合的最大结合量(Bmax)与同年龄的SAM-R/1相比有所降低。对SAM-P/8单次和重复给予比芬美兰可诱导海马体中[3H]QNB结合的Bmax增加。从这些结果来看,比芬美兰似乎通过可能激活SAM小鼠海马体中的胆碱能系统而发挥药理作用。