Evaluation of Neurodegeneration in a Mouse Model of Infantile Batten Disease by Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy

被引:10
作者
Munasinghe, Jeeva [2 ]
Zhang, Zhongjian [1 ]
Kong, Eryan [1 ]
Heffer, Alison [1 ]
Mukherjee, Anil B. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Dev Endocrinol & Genet, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Neurol Disorders & Stroke, In Vivo NMR Ctr HNQ2 3, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
Neurodegeneration; Neuronal ceroid lipofuscinosis; Infantile neuronal ceroid lipofuscinosis; Infantile batten disease; Magnetic resonance imaging; Magnetic resonance spectroscopy; NEURONAL CEROID-LIPOFUSCINOSIS; PALMITOYL-PROTEIN THIOESTERASE; CEREBRAL BLOOD-VOLUME; APPARENT DIFFUSION-COEFFICIENT; RAT-BRAIN; APOPTOSIS; MICE; INCL; MRI; DISRUPTION;
D O I
10.1159/000334838
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuronal ceroid lipofuscinoses (NCLs) represent a group of common hereditary childhood neurodegenerative storage disorders that have no effective treatment. Mutations in eight different genes cause various forms of NCLs. Infantile NCL (INCL), the most lethal disease, is caused by inactivating mutations in the palmitoyl-protein thioesterase-1 (PPT1) gene. The availability of Ppt1-knockout (Ppt1-KO) mice, which recapitulate virtually all clinical and pathological features of INCL, provides an opportunity to test the effectiveness of novel therapeutic strategies in vivo. However, such studies will require noninvasive methods that can be used to perform serial evaluations of the same animal receiving an experimental therapy. Thus, the development of noninvasive method(s) of evaluation is urgently needed. Here, we report our evaluation of the progression of neurodegeneration in Ppt1-KO mice starting at 3 months of age by MRI and MR spectroscopy (MRS) and repeating these tests using the same mice at 4, 5 and 6 months of age. Our results showed progressive cerebral atrophy, which was associated with histological loss of neuronal content and increase in astroglia. Remarkably, while the brain volumes in Ppt1-KO mice progressively declined with advancing age, the MRS signals, which were significantly lower than those of their wild-type littermates, remained virtually unchanged from 3 to 6 months of age. In addition, our results also showed an abnormality in cerebral blood flow in these mice, which showed progression with age. Our findings provide methods to serially examine the brains of mouse models of neurodegenerative diseases (e.g. Ppt1-KO mice) using noninvasive and non-lethal procedures such as MRI and MRS. These methods may be useful in studies to understand the progression of neuropathology in animal models of neurodegenerative diseases as they allow repeated evaluations of the same animal in which experimental therapies are tested. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:159 / 169
页数:11
相关论文
共 46 条
  • [1] Palmitoylation cycles and regulation of protein function (Review)
    Baekkeskov, Steinnunn
    Kanaani, Jamil
    [J]. MOLECULAR MEMBRANE BIOLOGY, 2009, 26 (1-2) : 42 - 54
  • [2] Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis
    Bible, E
    Gupta, P
    Hofmann, SL
    Cooper, JD
    [J]. NEUROBIOLOGY OF DISEASE, 2004, 16 (02) : 346 - 359
  • [3] Blamire AM, 2000, J NEUROSCI, V20, P8153
  • [4] CAMP LA, 1993, J BIOL CHEM, V268, P22566
  • [5] CAMP LA, 1994, J BIOL CHEM, V269, P23212
  • [6] Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis
    Cooper, Jonathan D.
    Russell, Claire
    Mitchison, Hannah M.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2006, 1762 (10): : 873 - 889
  • [7] Recent advances in iron oxide nanocrystal technology for medical imaging
    Corot, Claire
    Robert, Philippe
    Idee, Jean-Marc
    Port, Marc
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (14) : 1471 - 1504
  • [8] A cytoplasmic acyl-protein thioesterase that removes palmitate from G protein α subunits and p21RAS
    Duncan, JA
    Gilman, AG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) : 15830 - 15837
  • [9] Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations
    Erichsen, A. K.
    Server, A.
    Landro, N. I.
    Sandvik, L.
    Tallaksen, C. M. E.
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 277 (1-2) : 124 - 129
  • [10] Current state of clinical and morphological features in human NCL
    Goebel, HH
    Wisniewski, KE
    [J]. BRAIN PATHOLOGY, 2004, 14 (01) : 61 - 69