DeNoble V J
Pharmacol Biochem Behav. 1987 Jan;26(1):183-6. doi: 10.1016/0091-3057(87)90552-1.
Vinpocetine, vincamine, apovincaminic acid, vinconate, aniracetam, Hydergine, and pemoline were evaluated for their ability to enhance retrieval of a step-through passive avoidance response in rats. The percentage of rats performing the avoidance response was found to decrease as a function of the number of days between training and retention testing (Day 1, 100%; Day 2, 65%; Day 3, 23%; Days 4 and 5, 0%). Vinpocetine administered 60 minutes prior to testing for retention significantly increased the number of rats performing the passive avoidance response. Retrieval enhancement was dose-related in an inverted U-shaped function with the effective doses at 18 and 30 mg/kg PO. In contrast, apovincaminic acid (1-400 mg/kg PO), vincamine (1-200 mg/kg PO), vinconate (1-200 mg/kg PO), aniracetam (1-300 mg/kg PO), Hydergine (0.1-10 mg/kg PO), and pemoline (1-30 mg/kg PO) were not effective. These data support the view that vinpocetine has cognition-activating abilities as defined in an animal model of memory retrieval.
对长春西汀、长春胺、阿朴长春胺酸、长春乙酯、茴拉西坦、喜得镇和匹莫林增强大鼠穿梭箱被动回避反应记忆恢复的能力进行了评估。发现执行回避反应的大鼠百分比随训练与记忆测试之间的天数增加而降低(第1天,100%;第2天,65%;第3天,23%;第4天和第5天,0%)。在进行记忆测试前60分钟给予长春西汀,显著增加了执行被动回避反应的大鼠数量。记忆恢复增强与剂量相关,呈倒U形函数,有效剂量为18和30mg/kg口服。相比之下,阿朴长春胺酸(1 - 400mg/kg口服)、长春胺(1 - 200mg/kg口服)、长春乙酯(1 - 200mg/kg口服)、茴拉西坦(1 - 300mg/kg口服)、喜得镇(0.1 - 10mg/kg口服)和匹莫林(1 - 30mg/kg口服)均无效。这些数据支持了长春西汀具有在记忆恢复动物模型中所定义的认知激活能力这一观点。