Ridley R M, Pugh P, Maclean C J, Baker H F
MRC Comparative Cognition Team, Department of Experimental Psychology, Downing Street, Cambridge CB2 3EB, UK.
Brain Res. 1999 Jul 31;836(1-2):120-38. doi: 10.1016/s0006-8993(99)01641-8.
Monkeys with immunotoxic lesions of both the basal nucleus of Meynert and the vertical limb of the diagonal band of Broca (NBM+VDB) lost cholinergic innervation throughout the cortex and hippocampus. They were impaired at learning discriminations between objects differing in either few, or many, attributes and at learning visuospatial conditional discriminations. Monkeys with immunotoxic lesions of the NBM lost cholinergic innervation of the neocortex only. Initially, they were unable to learn a simple visual discrimination where the stimuli differed in a limited number of attributes but they were unimpaired at learning discriminations between objects that differed in more attributes. They were mildly impaired at learning a visuospatial conditional task. The impairment exhibited by monkeys with lesions of the NBM alone ameliorated with time but that following NBM+VDB lesions did not. Previous experiments have shown that monkeys with immunotoxic lesions of the VDB alone are impaired at learning visuospatial conditional discriminations but are unimpaired at learning simple visual discriminations. When monkeys with NBM lesions were given excitotoxic lesions of the CA1 field of the hippocampus the learning impairment on discriminations between objects which differed in few attributes was reinstated. Pretreatment with a cholinergic agonist improved learning ability on visual discrimination learning in all monkeys but this improvement was significantly greater in monkeys with lesions of the NBM. On conditional discrimination learning, which is particularly sensitive to hippocampal damage, pilocarpine produced a significant improvement in monkeys with NBM+VDB lesions (where the hippocampal dysfunction was cholinergic) but not in monkeys with NBM+CA1 lesions (where the hippocampal damage was structural).
双侧迈内特基底核和布罗卡斜角带垂直支(NBM+VDB)出现免疫毒性损伤的猴子,其整个皮层和海马体的胆碱能神经支配丧失。它们在学习区分具有少量或许多属性差异的物体时以及学习视觉空间条件辨别时均受损。仅NBM出现免疫毒性损伤的猴子,仅新皮层的胆碱能神经支配丧失。最初,它们无法学习一种简单的视觉辨别任务,即刺激在有限数量的属性上存在差异,但在学习区分具有更多属性差异的物体时未受损。它们在学习视觉空间条件任务时轻度受损。仅NBM损伤的猴子所表现出的损伤会随时间改善,但NBM+VDB损伤后的损伤则不会。先前的实验表明,仅VDB出现免疫毒性损伤的猴子在学习视觉空间条件辨别时受损,但在学习简单视觉辨别时未受损。当给NBM损伤的猴子海马体CA1区施加兴奋性毒性损伤时,在区分具有少量属性差异的物体时的学习损伤会再次出现。用胆碱能激动剂进行预处理可提高所有猴子在视觉辨别学习上的学习能力,但这种改善在NBM损伤的猴子中明显更大。在对海马损伤特别敏感的条件辨别学习中,毛果芸香碱使NBM+VDB损伤的猴子(海马功能障碍为胆碱能性)有显著改善,但对NBM+CA1损伤的猴子(海马损伤为结构性)则无改善。