Distinct roles of basal forebrain cholinergic neurons in spatial and object recognition memory

被引:48
|
作者
Okada, Kana [1 ]
Nishizawa, Kayo [2 ]
Kobayashi, Tomoko [2 ]
Sakata, Shogo [1 ]
Kobayashi, Kazuto [2 ,3 ]
机构
[1] Hiroshima Univ, Grad Sch Integrated Arts & Sci, Dept Behav Sci, Higashihiroshima 7398521, Japan
[2] Fukushima Med Univ, Sch Med, Inst Biomed Sci, Dept Mol Genet, Fukushima 9601295, Japan
[3] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
日本科学技术振兴机构;
关键词
192; IGG-SAPORIN; MEDIAL PREFRONTAL CORTEX; SERIAL REACTION-TIME; PERIRHINAL CORTEX; NUCLEUS BASALIS; SELECTIVE IMMUNOLESIONS; WORKING-MEMORY; DOUBLE DISSOCIATION; ALZHEIMERS-DISEASE; PLACE NAVIGATION;
D O I
10.1038/srep13158
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recognition memory requires processing of various types of information such as objects and locations. Impairment in recognition memory is a prominent feature of amnesia and a symptom of Alzheimer's disease (AD). Basal forebrain cholinergic neurons contain two major groups, one localized in the medial septum (MS)/vertical diagonal band of Broca (vDB), and the other in the nucleus basalis magnocellularis (NBM). The roles of these cell groups in recognition memory have been debated, and it remains unclear how they contribute to it. We use a genetic cell targeting technique to selectively eliminate cholinergic cell groups and then test spatial and object recognition memory through different behavioural tasks. Eliminating MS/vDB neurons impairs spatial but not object recognition memory in the reference and working memory tasks, whereas NBM elimination undermines only object recognition memory in the working memory task. These impairments are restored by treatment with acetylcholinesterase inhibitors, anti- dementia drugs for AD. Our results highlight that MS/vDB and NBM cholinergic neurons are not only implicated in recognition memory but also have essential roles in different types of recognition memory.
引用
收藏
页数:13
相关论文
共 50 条
  • [31] TIME OF ORIGIN OF CHOLINERGIC NEURONS IN THE RAT BASAL FOREBRAIN
    SEMBA, K
    FIBIGER, HC
    JOURNAL OF COMPARATIVE NEUROLOGY, 1988, 269 (01) : 87 - 95
  • [32] Cholinergic neurons in the basal forebrain of aged female mice
    Kalesnykas, G
    Puoliväli, J
    Sirviö, J
    Miettinen, R
    BRAIN RESEARCH, 2004, 1022 (1-2) : 148 - 156
  • [33] Cholinergic Neurons Excite Cortically Projecting Basal Forebrain GABAergic Neurons
    Yang, Chun
    McKenna, James T.
    Zant, Janneke C.
    Winston, Stuart
    Basheer, Radhika
    Brown, Ritchie E.
    JOURNAL OF NEUROSCIENCE, 2014, 34 (08): : 2832 - 2844
  • [34] Basal forebrain regulation of cortical activity and sleep-wake states: Roles of cholinergic and non-cholinergic neurons
    Deurveilher, Samueel
    Semba, Kazue
    SLEEP AND BIOLOGICAL RHYTHMS, 2011, 9 : 65 - 70
  • [35] Basal forebrain regulation of cortical activity and sleep-wake states: Roles of cholinergic and non-cholinergic neurons
    Samüel Deurveilher
    Kazue Semba
    Sleep and Biological Rhythms, 2011, 9 : 65 - 70
  • [36] Spatial memory impairments following imunotoxic lesion of GABAergic neurons of the basal forebrain
    Kruashvili, L.
    Burjanadze, M.
    Dashniani, M.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2020, 31 : S38 - S39
  • [38] Adolescent Intermittent Alcohol Exposure: Deficits in Object Recognition Memory and Forebrain Cholinergic Markers
    Swartzwelder, H. Scott
    Acheson, Shawn K.
    Miller, Kelsey M.
    Sexton, Hannah G.
    Liu, Wen
    Crews, Fulton T.
    Risher, Mary-Louise
    PLOS ONE, 2015, 10 (11):
  • [39] Neurotrophic factors rescue basal forebrain cholinergic neurons and improve performance on a spatial learning test
    Lee, Yu-Shang
    Danandeh, Andalib
    Baratta, Janie
    Lin, Ching-Yi
    Yu, Jen
    Robertson, Richard T.
    EXPERIMENTAL NEUROLOGY, 2013, 249 : 178 - 186
  • [40] DEMENTIA PUGILISTICA - LOSS OF BASAL FOREBRAIN CHOLINERGIC NEURONS AND CORTICAL CHOLINERGIC MARKERS
    UHL, GR
    MCKINNEY, M
    HEDREEN, JC
    WHITE, CL
    COYLE, JT
    WHITEHOUSE, PJ
    PRICE, DL
    ANNALS OF NEUROLOGY, 1982, 12 (01) : 99 - 99