Matsuoka N, Yamazaki M, Yamaguchi I
Basic Research Group, Tsukuba Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Ibaraki, Japan.
Neuroscience. 1995 Jun;66(3):617-26. doi: 10.1016/0306-4522(94)00628-i.
To clarify the functional role of the brain somatostatinergic system in cognitive processes, changes in the performance in passive avoidance and water maze tasks and in brain somatostatin contents were comparatively investigated in young Fischer rats subjected to brain cholinergic and somatostatinergic depletion, and in aged Fischer rats. Lesioning of the nucleus basalis magnocellularis and administration of cysteamine (200 mg/kg, s.c.), a depletor of somatostatin, resulted in significant deficits in passive avoidance, but complete transection of the fimbria-fornix hardly affected the performance in the task. When cognitive performance was assessed in the Morris water maze, lesions of the nucleus basalis magnocellularis and the fimbria-fornix, and administration of cysteamine, significantly impaired the acquisition of navigatory spatial memories of rats. On the other hand, aged rats (24-27 months) showed severe impairments of memory acquisition in both tasks. Neurochemistry measurements showed that lesions of the nucleus basalis magnocellularis produced a selective reduction both in the cortical cholinergic marker choline acetyltransferase and in striatal somatostatin level, whereas lesioning of the fimbria-fornix caused a marked loss of choline acetyltransferase in the hippocampus and posterior cortex, and a significant reduction in hippocampal somatostatin. On the other hand, treatment with cysteamine significantly reduced the contents of somatostatin in all the brain regions examined, but minimally affected choline acetyltransferase activity. However, significant reduction in the striatal choline acetyltransferase activity and elevation in somatostatin content in the frontal cortex were found in aged rats compared with young rats. Taken together, these results strongly suggest that changes in the brain somatostatinergic transmission are involved in the cognitive deficits in the experimental animal models of dementia presently employed. Furthermore, the present comparative study further implies that there are differences in the relative involvement of the cholinergic and somatostatinergic systems in the performance of rats on two different tests of mnemonic function.
为阐明大脑生长抑素能系统在认知过程中的功能作用,对接受大脑胆碱能和生长抑素能耗竭的幼年Fischer大鼠以及老年Fischer大鼠在被动回避和水迷宫任务中的表现变化以及大脑生长抑素含量进行了比较研究。损毁基底大细胞核并给予生长抑素耗竭剂半胱胺(200mg/kg,皮下注射)导致被动回避出现显著缺陷,但穹窿海马伞完全横断对该任务的表现几乎没有影响。当在莫里斯水迷宫中评估认知表现时,基底大细胞核和穹窿海马伞的损伤以及半胱胺的给药显著损害了大鼠的导航空间记忆获取。另一方面,老年大鼠(24 - 27个月)在这两项任务中均表现出严重的记忆获取障碍。神经化学测量表明,基底大细胞核损伤导致皮质胆碱能标志物胆碱乙酰转移酶以及纹状体生长抑素水平选择性降低,而穹窿海马伞损伤导致海马和后皮质中胆碱乙酰转移酶显著丧失,海马生长抑素显著减少。另一方面,半胱胺治疗显著降低了所有检测脑区的生长抑素含量,但对胆碱乙酰转移酶活性影响极小。然而,与幼年大鼠相比,老年大鼠纹状体胆碱乙酰转移酶活性显著降低,额叶皮质生长抑素含量升高。综上所述,这些结果强烈表明,大脑生长抑素能传递的变化参与了目前所采用的痴呆实验动物模型中的认知缺陷。此外,本比较研究进一步表明,胆碱能和生长抑素能系统在大鼠两项不同记忆功能测试表现中的相对参与程度存在差异。