Behavioral phenotyping of minipigs transgenic for the Huntington gene

被引:13
作者
Schramke, Sarah [1 ,2 ]
Schuldenzucker, Verena [1 ]
Schubert, Robin [1 ]
Frank, Frauke [1 ,3 ]
Wirsig, Maike [1 ]
Ott, Stefanie [1 ]
Motlik, Jan [3 ]
Fels, Michaela [2 ]
Kemper, Nicole [2 ]
Hoelzner, Eva [1 ]
Reilmann, Ralf [1 ,4 ,5 ,6 ,7 ]
机构
[1] George Huntington Inst, Technol Pk Muenster,Johann Krane Weg 27, D-48149 Munster, Germany
[2] Univ Vet Med Hannover, Inst Anim Hyg Anim Welf & Farm Anim Behav, Bischofsholer Damm 15, D-30173 Hannover, Germany
[3] AS CR, Vvi, Inst Anim Physiol & Genet, Lab Cell Regenerat & Plast, Libechov, Czech Republic
[4] Univ Klinikum Muenster, Dept Radiol, Albert Schweitzer Campus 1, D-48149 Munster, Germany
[5] Dept Neurol Muenster, Munster, Germany
[6] Univ Tubingen, Dept Neurodegenerat Dis, Hoppe Seyler Str 3, D-72076 Tubingen, Germany
[7] Univ Tubingen, Hertie Inst Clin Brain Res, Hoppe Seyler Str 3, D-72076 Tubingen, Germany
关键词
Animal models; Minipig; Phenotyping; Behavioral; Motor; Cognitive; Preclinical research; ANIMAL-MODELS; CLINICAL-TRIALS; TRACK-HD; DISEASE; PREMANIFEST; MOTOR; TRANSLATION; IMPAIRMENTS; PREDICTORS; ONSET;
D O I
10.1016/j.jneumeth.2015.11.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: While several novel therapeutic approaches for HD are in development, resources to conduct clinical trials are limited. Large animal models have been proposed to improve assessment of safety, tolerability and especially to increase translational reliability of efficacy signals obtained in preclinical studies. They may thus help to select candidates for translation to human studies. We here introduce a battery of novel tests designed to assess the motor, cognitive and behavioral phenotype of a transgenic (tg) HD minipig model. New methods: A group of tgHD and wildtype (wt) Libechov minipigs (n = 36) was available for assessment with (1) a gait test using the GAITRite (R) automated acquisition system, (2) a hurdle-test, (3) a tongue coordination test, (4) a color discrimination test, (5) a startbox back and forth test and (6) a dominance test. Performance of all tests and definition of measures obtained is presented. Results: Minipigs were able to learn performance of all tests. All tests were safe, well tolerated and feasible. Exploratory between group comparisons showed no differences between groups of tgHD and wt minipigs assessed, but low variability within and between groups. Comparison with existing method(s): So far there are no established or validated assessments to test minipigs in the domains described. Conclusions: The data shows that the tests presented are safe, well tolerated and all measures defined can be assessed. Prospective longitudinal application of these tests is warranted to determine their test retest reliability, sensitivity and validity in assessing motor, cognitive and behavioral features of tg and wt minipigs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 45
页数:12
相关论文
共 53 条
[1]  
[Anonymous], TEACHING FILM VIDEO
[2]   Regional Atrophy Associated with Cognitive and Motor Function in Prodromal Huntington Disease [J].
Aylward, Elizabeth H. ;
Harrington, Deborah L. ;
Mills, James A. ;
Nopoulos, Peggy C. ;
Ross, Christopher A. ;
Long, Jeffrey D. ;
Liu, Dawei ;
Westervelt, Holly K. ;
Paulsen, Jane S. .
JOURNAL OF HUNTINGTONS DISEASE, 2013, 2 (04) :477-489
[3]   A Transgenic Minipig Model of Huntington's Disease [J].
Baxa, Monika ;
Hruska-Plochan, Marian ;
Juhas, Stefan ;
Vodicka, Petr ;
Pavlok, Antonin ;
Juhasova, Jana ;
Miyanohara, Atsushi ;
Nejime, Tetsuya ;
Klima, Jiri ;
Macakova, Monika ;
Marsala, Silvia ;
Weiss, Andreas ;
Kubickova, Svatava ;
Musilova, Petra ;
Vrtel, Radek ;
Sontag, Emily M. ;
Thompson, Leslie M. ;
Schier, Jan ;
Hansikova, Hana ;
Howland, David S. ;
Cattaneo, Elena ;
DiFiglia, Marian ;
Marsala, Martin ;
Motlik, Jan .
JOURNAL OF HUNTINGTONS DISEASE, 2013, 2 (01) :47-68
[4]   Tapping linked to function and structure in premanifest and symptomatic Huntington disease [J].
Bechtel, N. ;
Scahill, R. I. ;
Rosas, H. D. ;
Acharya, T. ;
van den Bogaard, S. J. A. ;
Jauffret, C. ;
Say, M. J. ;
Sturrock, A. ;
Johnson, H. ;
Onorato, C. E. ;
Salat, D. H. ;
Durr, A. ;
Leavitt, B. R. ;
Roos, R. A. C. ;
Landwehrmeyer, G. B. ;
Langbehn, D. R. ;
Stout, J. C. ;
Tabrizi, S. J. ;
Reilmann, R. .
NEUROLOGY, 2010, 75 (24) :2150-2160
[5]  
Bohlen S, 2012, EUR J NEUROL, P10
[6]   Cognitive Reserve and Brain Reserve in Prodromal Huntington's Disease [J].
Bonner-Jackson, Aaron ;
Long, Jeffrey D. ;
Westervelt, Holly ;
Tremont, Geoffrey ;
Aylward, Elizabeth ;
Paulsen, Jane S. .
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 2013, 19 (07) :739-750
[7]   Transgenic animal models for study of the pathogenesis of Huntington's disease and therapy [J].
Chang, Renbao ;
Liu, Xudong ;
Li, Shihua ;
Li, Xiao-Jiang .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2015, 9 :2179-2188
[8]  
Craufurd D, 2001, NEUROPSY NEUROPSY BE, V14, P219
[9]   Huntington's Disease: Can Mice Lead the Way to Treatment? [J].
Crook, Zachary R. ;
Housman, David .
NEURON, 2011, 69 (03) :423-435
[10]   Pig Models of Neurodegenerative Disorders: Utilization in Cell Replacement-Based Preclinical Safety and Efficacy Studies [J].
Dolezalova, Dasa ;
Hruska-Plochan, Marian ;
Bjarkam, Carsten R. ;
Rensen, Jens Christian H. S. ;
Cunningham, Miles ;
Weingarten, David ;
Ciacci, Joseph D. ;
Juhas, Stefan ;
Juhasova, Jana ;
Motlik, Jan ;
Hefferan, Michael P. ;
Hazel, Tom ;
Johe, Karl ;
Carromeu, Cassiano ;
Muotri, Alysson ;
Bui, Jack ;
Strnadel, Jan ;
Marsala, Martin .
JOURNAL OF COMPARATIVE NEUROLOGY, 2014, 522 (12) :2784-2801