Vestibular loss causes hippocampal atrophy and impaired spatial memory in humans

被引:443
作者
Brandt, T
Schautzer, F
Hamilton, DA
Brüning, R
Markowitsch, HJ
Kalla, R
Darlington, C
Smith, P
Strupp, M
机构
[1] Univ Munich, Dept Neurol, D-81377 Munich, Germany
[2] LKH Villach, Dept Neurol & Psychosomat, Villach, Austria
[3] Univ New Mexico, Dept Psychol, Albuquerque, NM 87131 USA
[4] Univ Munich, Dept Neuroradiol, Munich, Germany
[5] Univ Bielefeld, D-4800 Bielefeld, Germany
[6] Univ Otago, Sch Med, Sch Med Sci, Dept Pharmacol & Toxicol, Dunedin, New Zealand
关键词
hippocampus; bilateral vestibular failure; spatial memory; navigation;
D O I
10.1093/brain/awh617
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The human hippocampal formation plays a crucial role in various aspects of memory processing. Most literature on the human hippocampus stresses its non-spatial memory functions, but older work in rodents and some other species emphasized the role of the hippocampus in spatial learning and memory as well. A few human studies also point to a direct relation between hippocampal size, navigation and spatial memory. Conversely, the importance of the vestibular system for navigation and spatial memory was until now convincingly demonstrated only in animals. Using magnetic resonance imaging volumetry, we found that patients (n = 10) with acquired chronic bilateral vestibular loss (BVL) develop a significant selective atrophy of the hippocampus (16.9% decrease relative to controls). When tested with a virtual variant (on a PC) of the Morris water task these patients exhibited significant spatial memory and navigation deficits that closely matched the pattern of hippocampal atrophy. These spatial memory deficits were not associated with general memory deficits. The current data on BVL patients and bilateral hippocampal atrophy revive the idea that a major-and probably phylogenetically ancient-function of the archicortical hippocampal tissue is still evident in spatial aspects of memory processing for navigation. Furthermore, these data demonstrate for the first time in humans that spatial navigation critically depends on preserved vestibular function, even when the subjects are stationary, e.g. without any actual vestibular or somatosensory stimulation.
引用
收藏
页码:2732 / 2741
页数:10
相关论文
共 75 条
[31]   The well-worn route and the path less traveled: Distinct neural bases of route following and wayfinding in humans [J].
Hartley, T ;
Maguire, EA ;
Spiers, HJ ;
Burgess, N .
NEURON, 2003, 37 (05) :877-888
[32]   Vestibular influences on CA1 neurons in the rat hippocampus: an electrophysiological study in vivo [J].
Horii, A ;
Russell, NA ;
Smith, PF ;
Darlington, CL ;
Bilkey, DK .
EXPERIMENTAL BRAIN RESEARCH, 2004, 155 (02) :245-250
[33]  
Iaria G, 2003, J NEUROSCI, V23, P5945
[34]  
Insausti R, 1998, AM J NEURORADIOL, V19, P659
[35]   Brain activation patterns during imagined stance and locomotion in functional magnetic resonance imaging [J].
Jahn, K ;
Deutschländer, A ;
Stephan, T ;
Strupp, M ;
Wiesmann, M ;
Brandt, T .
NEUROIMAGE, 2004, 22 (04) :1722-1731
[36]   ON THE ROLE OF THE HIPPOCAMPUS IN LEARNING AND MEMORY IN THE RAT [J].
JARRARD, LE .
BEHAVIORAL AND NEURAL BIOLOGY, 1993, 60 (01) :9-26
[37]   Spatial memory deficits in patients after unilateral selective amygdalohippocampectomy [J].
Kessels, RPC ;
Hendriks, MPH ;
Schouten, J ;
Van Asselen, M ;
Postma, A .
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 2004, 10 (06) :907-912
[38]   Varieties of human spatial memory: a meta-analysis on the effects of hippocampal lesions [J].
Kessels, RPC ;
de Haan, EHF ;
Kappelle, LJ ;
Postma, A .
BRAIN RESEARCH REVIEWS, 2001, 35 (03) :295-303
[39]   Influence of a sensorimotor conflict on the memorization of a path traveled in virtual reality [J].
Lambrey, S ;
Viaud-Delmon, I ;
Berthoz, A .
COGNITIVE BRAIN RESEARCH, 2002, 14 (01) :177-186
[40]   Cytosolic glucocorticoid receptor expression in the rat vestibular nucleus and hippocampus following unilateral vestibular deafferentation [J].
Lindsay, L ;
Liu, P ;
Gliddon, C ;
Zheng, YW ;
Smith, PF ;
Darlington, CL .
EXPERIMENTAL BRAIN RESEARCH, 2005, 162 (03) :309-314