Circadian rhythm and suprachiasmatic nucleus alterations in the mouse model of mucopolysaccharidosis IIIB

被引:24
作者
Canal, Maria M. [1 ]
Wilkinson, Fiona L. [2 ]
Cooper, Jonathan D. [3 ]
Wraith, J. Ed [4 ]
Wynn, Rob [5 ]
Bigger, Brian W. [2 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Fac Med & Human Sci, MPS Stem Cell Res Grp, Manchester M13 9PT, Lancs, England
[3] Kings Coll London, Inst Psychiat, Pediat Storage Disorders Lab, Dept Neurosci,Ctr Cellular Basis Behav, London SE5 9NU, England
[4] Royal Manchester Childrens Hosp, Bone Marrow Transplant Unit, Manchester M27 1HA, Lancs, England
[5] Royal Manchester Childrens Hosp, Willink Biochem Genet Unit, Manchester M27 1HA, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
Mucopolysaccharidosis; Sanfilippo; Lysosomal storage disease; Circadian rhythm; Behaviour; Synaptic loss; Neurodegenerative disease; MPSIIIB; Suprachiasmatic nucleus; ADAPTIVE IMMUNE ACTIVATION; SANFILIPPO-SYNDROME; FUNCTIONAL-ANALYSIS; SLEEP DISTURBANCE; NOCTURNAL RODENTS; BRAIN; NEURODEGENERATION; SYNAPTOPHYSIN; PACEMAKERS; CHILDREN;
D O I
10.1016/j.bbr.2010.01.045
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
Mucopolysaccharidosis IIIB (MPSIIIB) is a lysosomal storage disease characterised by progressive central nervous system degeneration in patients, with death usually in the late teens. Serious behavioural problems have been reported in children at the early stages of the disease, such as hyperactivity and severe sleep disturbances, which suggest alterations in circadian rhythms. We investigated the circadian rhythm of locomotor activity of young and old MPSIIIB mice, under a 24-h light-dark (LD) cycle and under constant darkness (DD), and also examined neuropeptide expression in the suprachiasmatic nucleus (SCN), site of the principal biological pacemaker. We show that MPSIIIB mice have higher activity levels during the light (resting) phase of the LD cycle, together with weaker circadian rhythms, and a longer active phase due to a late peak of activity, in both LD and DD. In addition, young MPSIIIB mice showed shorter phase delays in response to a light pulse in DD. Increased lysosomal storage, neuroinflammation and changes in the expression of Arginine Vasopressin and Vasointestinal Polypeptide, two circadian neuropeptides, were observed in the SCN, which may be in part responsible for the changes in circadian behaviour observed in MPSIIIB mice. These findings suggest an alteration of the circadian system in MPSIIIB mice, and may inform better clinical management of circadian, sleep and behavioural disturbances in patients with MPSIII. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:212 / 220
页数:9
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