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猴子的基底前脑损伤会扰乱注意力,但不会影响学习和记忆。

Basal forebrain lesions in monkeys disrupt attention but not learning and memory.

作者信息

Voytko M L, Olton D S, Richardson R T, Gorman L K, Tobin J R, Price D L

机构信息

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2196.

出版信息

J Neurosci. 1994 Jan;14(1):167-86. doi: 10.1523/JNEUROSCI.14-01-00167.1994.

Abstract

Cognitive impairments in humans and animals have been linked to dysfunction of neurons in the basal forebrain cholinergic system (BFCS). Degeneration of these cells may be, in part, responsible for some of the cognitive deficits observed in Alzheimer's disease (AD). Although memory deficits are associated with lesions of the BFCS in rats, impairments in memory have been more subtle following similar lesions in monkeys. To evaluate the effects of BFCS lesions on cognitive processes in monkeys, we have systematically investigated the behavioral effects of ibotenic acid injections in the medial septum, nucleus of the diagonal band of Broca, and nucleus basalis of Meynert in cynomolgus monkeys, using a large series of cognitive tasks that examined different mnemonic and attentional abilities. These lesions did not impair accuracy in delayed nonmatching-to-sample, delayed response, simple or concurrent visual discriminations, spatial discriminations, or discrimination reversals. However, these lesions disrupted attentional focusing. Similar impairments in attention have been noted in patients with AD. BFCS lesions increased sensitivity to injections of the cholinergic antagonist scopolamine in a delayed nonmatching-to-sample task, indicating that the central cholinergic system was compromised in these monkeys. In concert, the results of this study suggest that the primate basal forebrain may be more involved in attentional than mnemonic processes, and that degeneration of neurons in the BFCS in cases of AD may contribute to the attention deficits observed in these individuals.

摘要

人类和动物的认知障碍与基底前脑胆碱能系统(BFCS)中神经元的功能障碍有关。这些细胞的退化可能部分导致了在阿尔茨海默病(AD)中观察到的一些认知缺陷。尽管记忆缺陷与大鼠BFCS的损伤有关,但在猴子身上进行类似损伤后,记忆障碍更为微妙。为了评估BFCS损伤对猴子认知过程的影响,我们系统地研究了在食蟹猴的内侧隔核、布罗卡斜角带核和迈内特基底核注射鹅膏蕈氨酸的行为影响,使用了一系列检查不同记忆和注意力能力的认知任务。这些损伤并没有损害延迟非匹配样本、延迟反应、简单或同时进行的视觉辨别、空间辨别或辨别逆转的准确性。然而,这些损伤破坏了注意力集中。在AD患者中也注意到了类似的注意力损伤。在延迟非匹配样本任务中,BFCS损伤增加了对胆碱能拮抗剂东莨菪碱注射的敏感性,表明这些猴子的中枢胆碱能系统受到了损害。总之,这项研究的结果表明,灵长类动物的基底前脑可能更多地参与注意力而非记忆过程,并且在AD病例中BFCS中神经元的退化可能导致这些个体出现注意力缺陷。

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