Increased numbers of motor activity peaks during light cycle are associated with reductions in adrenergic α2-receptor levels in a transgenic Huntington's disease rat model

被引:28
作者
Bode, Felix J. [2 ,3 ]
Stephan, Michael [2 ,4 ]
Wiehager, Sara
Nguyen, Huu Phuc [5 ]
Bjorkqvist, Maria [6 ]
von Hoersten, Stephan [7 ]
Bauer, Andreas [8 ,9 ]
Petersen, Asa [1 ]
机构
[1] Lund Univ, Dept Expt Med Sci, Translat Neuroendocrine Res Unit, S-22184 Lund, Sweden
[2] Hannover Med Sch, Inst Funct & Appl Anat, D-30625 Hannover, Germany
[3] Univ Bonn, Dept Neurol, D-53105 Bonn, Germany
[4] Hannover Med Sch, Clin Psychosomat & Psychotherapy, D-30625 Hannover, Germany
[5] Univ Tubingen, Dept Med Genet, D-72076 Tubingen, Germany
[6] Lund Univ, Dept Expt Med Sci, Neuronal Survival Unit, S-22184 Lund, Sweden
[7] Univ Erlangen Nurnberg, Franz Penzoldt Ctr, D-91054 Erlangen, Germany
[8] Res Ctr Juelich, Inst Neurosci & Med INM 2, D-52425 Julich, Germany
[9] Univ Dusseldorf, Dept Neurol, D-40001 Dusseldorf, Germany
基金
瑞典研究理事会;
关键词
Circadian rhythm; Huntington's disease; Sleep; Hypothalamus; Basal forebrain; Adrenergic alpha(2)-receptor; Orexin; Leptin; LATERAL TUBERAL NUCLEUS; HYPOTHALAMIC REGULATION; BASAL FOREBRAIN; SLEEP; NEURONS; HYPOCRETINS; RECEPTORS; LEPTIN; MOUSE; CATECHOLAMINES;
D O I
10.1016/j.bbr.2009.06.031
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Huntington's disease (HID) is a neurodegenerative disorder caused by a CAG repeat expansion in the HD gene. Besides psychiatric, motor and cognitive symptoms, HD patients suffer from sleep disturbances. In order to screen a rat model transgenic for HD (tgHD rats) for sleep-wake cycle dysregulation, we monitored their circadian activity peaks in the present study. TgHD rats of both sexes showed hyperactivity during the dark cycle and more frequent light cycle activity peaks indicative for a disturbed sleep-wake cycle. Focusing on males at the age of 4 and 14 months, analyses of receptor levels in the hypothalamus and the basal forebrain revealed that 5-HT2A- and adrenergic alpha(2)-receptor densities in these regions were significantly altered in tgHD rats compared to their wild-type littermates. Adrenergic receptor densities correlated negatively with the light cycle hyperactivity peaks at later stages of the disease in male tgHD rats. Furthermore, reduced leptin levels, a feature associated with circadian misalignment, were present. Our study demonstrates that the male tgHD rat is a suitable model to investigate HD associated sleep alterations. Further studies are warranted to elucidate the role of adrenergic- and 5-HT2A- receptors as therapeutic targets for dysregulation of the circadian activity in HD. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 182
页数:8
相关论文
共 55 条
[1]   The hypocretins as sensors for metabolism and arousal [J].
Adamantidis, Antoine ;
de Lecea, Luis .
JOURNAL OF PHYSIOLOGY-LONDON, 2009, 587 (01) :33-40
[2]   Rapid eye movement sleep disturbances in Huntington disease [J].
Arnulf, Isabelle ;
Nielsen, Jorgen ;
Lohmann, Ebba ;
Schieffer, Johannes ;
Wild, Edward ;
Jennum, Poul ;
Konofal, Eric ;
Walker, Matthew ;
Oudiette, Delphine ;
Tabrizi, Sarah ;
Durr, Alexandra .
ARCHIVES OF NEUROLOGY, 2008, 65 (04) :482-488
[3]   Sleep disturbances in Parkinsonism [J].
Askenasy, JJM .
JOURNAL OF NEURAL TRANSMISSION, 2003, 110 (02) :125-150
[4]   Hypocretin and melanin-concentrating hormone in patients with Huntington disease [J].
Aziz, Ahmad ;
Fronczek, Rolf ;
Maat-Schieman, Marion ;
Unmehopa, Unga ;
Roelandse, Freek ;
Overeem, Sebastiaan ;
van Duinen, Sjoerd ;
Lammers, Gert-Jan ;
Swaab, Dick ;
Roos, Raymund .
BRAIN PATHOLOGY, 2008, 18 (04) :474-483
[5]   Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation [J].
Bauer, A ;
Zilles, K ;
Matusch, A ;
Holzmann, C ;
Riess, O ;
von Hörsten, S .
JOURNAL OF NEUROCHEMISTRY, 2005, 94 (03) :639-650
[6]   Hypocretins (orexins) and sleep-wake disorders [J].
Baumann, CR ;
Bassetti, CL .
LANCET NEUROLOGY, 2005, 4 (10) :673-682
[7]   Cerebrospinal fluid levels of orexin-A are not a clinically useful biomarker for Huntington disease [J].
Bjorkqvist, M. ;
Petersen, A. ;
Carroll, J. ;
Nielsen, J. ;
Ecker, D. ;
Mulder, H. ;
Hayden, M. R. ;
Landwehrmeyer, B. ;
Brundin, P. ;
Leavitt, B. R. .
CLINICAL GENETICS, 2006, 70 (01) :78-79
[8]   Sex differences in a transgenic rat model of Huntington's disease:: decreased 17β-estradiol levels correlate with reduced numbers of DARPP32+ neurons in males [J].
Bode, Felix J. ;
Stephan, Michael ;
Suhling, Hendrik ;
Pabst, Reinhard ;
Straub, Rainer H. ;
Raber, Kerstin A. ;
Bonin, Michael ;
Nguyen, Huu Phuc ;
Riess, Olaf ;
Bauer, Andreas ;
Sjoberg, Charlotte ;
Petersen, Asa ;
von Hoersten, Stephan .
HUMAN MOLECULAR GENETICS, 2008, 17 (17) :2595-2609
[9]   Postnatal lipopolysaccharide-induced illness predisposes to periodontal disease in adulthood [J].
Breivik, T ;
Stephan, M ;
Brabant, GE ;
Straub, RH ;
Pabst, R ;
von Hörsten, S .
BRAIN BEHAVIOR AND IMMUNITY, 2002, 16 (04) :421-438
[10]   The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity [J].
De Lecea, L ;
Kilduff, TS ;
Peyron, C ;
Gao, XB ;
Foye, PE ;
Danielson, PE ;
Fukuhara, C ;
Battenberg, ELF ;
Gautvik, VT ;
Bartlett, FS ;
Frankel, WN ;
van den Pol, AN ;
Bloom, FE ;
Gautvik, KM ;
Sutcliffe, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :322-327