Sandin J, Nylander I, Georgieva J, Schött P A, Ogren S O, Terenius L
Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
Neuroscience. 1998 Jul;85(2):375-82. doi: 10.1016/s0306-4522(97)00605-2.
The hippocampus plays a central role in the acquisition and storage of information. Long-term potentiation in the mossy fibre pathway to the CA3 region in the hippocampus, an animal model of memory acquisition, is modulated by dynorphin peptides. This study investigated the possible role of hippocampal dynorphin in spatial learning. Male rats were trained in the Morris Water Task after microinjection with different doses of dynorphin B (1, 3.3 or 10 nmol/rat) or artificial cerebrospinal fluid (as control) into the CA3 region of the dorsal hippocampus. Dynorphin B was found to impair spatial learning at all tested doses. The synthetic kappa1-selective opiate receptor antagonist nor-binaltorphimine (2 nmol) also given into the hippocampus fully blocked the acquisition impairment caused by dynorphin B (10 nmol), while nor-binaltorphimine alone did not affect learning performance. These findings suggest that dynorphin peptides could play a modulatory role in hippocampal plasticity by acting on hippocampal kappa-receptors and thereby impair spatial learning.
海马体在信息获取和存储中起着核心作用。海马体中通向CA3区的苔藓纤维通路的长时程增强是记忆获取的动物模型,它受强啡肽调节。本研究调查了海马体强啡肽在空间学习中的可能作用。雄性大鼠在向背侧海马体CA3区微量注射不同剂量的强啡肽B(1、3.3或10 nmol/只大鼠)或人工脑脊液(作为对照)后,接受莫里斯水迷宫任务训练。结果发现,所有测试剂量的强啡肽B均损害空间学习能力。同样注入海马体的合成κ1选择性阿片受体拮抗剂诺-纳曲酮(2 nmol)完全阻断了强啡肽B(10 nmol)引起的学习障碍,而单独使用诺-纳曲酮并不影响学习表现。这些发现表明,强啡肽可能通过作用于海马体κ受体在海马体可塑性中发挥调节作用,从而损害空间学习能力。