Standardization of zebrafish drug testing parameters for muscle diseases

被引:5
作者
Karuppasamy, Muthukumar [1 ,2 ]
English, Katherine G. [1 ,2 ]
Henry, Clarissa A. [3 ,4 ]
Manzini, M. Chiara [5 ,6 ]
Parant, John M. [7 ]
Wright, Melissa A. [8 ]
Ruparelia, Avnika A. [9 ,10 ]
Currie, Peter D. [9 ,10 ,11 ]
Gupta, Vandana A. [12 ,13 ]
Dowling, James J. [14 ,15 ,16 ,17 ]
Maves, Lisa [18 ,19 ]
Alexander, Matthew S. [1 ,2 ,20 ,21 ,22 ,23 ]
机构
[1] Univ Alabama Birmingham, Dept Pediat, Div Neurol, Birmingham, AL 35294 USA
[2] Childrens Alabama, Birmingham, AL 35294 USA
[3] Univ Maine, Grad Sch Biomed Sci & Engn, Orono, ME 04469 USA
[4] Univ Maine, Sch Biol & Ecol, Orono, ME 04469 USA
[5] Rutgers Robert Wood Johnson Med Sch, Child Hlth Inst New Jersey, Rutgers, New Brunswick, NJ 08901 USA
[6] Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, New Brunswick, NJ 08901 USA
[7] Univ Alabama Birmingham, Dept Pharmacol & Toxicol, Heersink Sch Med, Birmingham, AL 35294 USA
[8] Univ Colorado Anschutz Med Campus, Dept Pediat, Sect Child Neurol, Aurora, CO 80045 USA
[9] Univ Melbourne, Fac Med Dent & Hlth Sci, Sch Biomed Sci, Dept Anat & Physiol, Melbourne, Vic 3010, Australia
[10] Univ Melbourne, Ctr Muscle Res, Dept Anat & Physiol, Melbourne, Vic 3010, Australia
[11] Monash Univ, Australian Regenerat Med Inst, Clayton, Vic 3800, Australia
[12] Monash Univ, EMBL Australia, Victorian Node, Clayton, Vic 3800, Australia
[13] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Genet, Boston, MA 02115 USA
[14] Hosp Sick Children, Div Neurol, Toronto, ON M5G 1X8, Canada
[15] Univ Toronto, Dept Paediat, Toronto, ON M5G 1X8, Canada
[16] Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON M5G 0A4, Canada
[17] Univ Toronto, Dept Mol Genet, Toronto, ON M5G 0A4, Canada
[18] Seattle Childrens Res Inst, Ctr Dev Biol & Regenerat Med, Seattle, WA 98101 USA
[19] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[20] Univ Alabama Birmingham, UAB Ctr Exercise Med, Birmingham, AL 35294 USA
[21] Univ Alabama Birmingham, Dept Genet, Birmingham, AL 35294 USA
[22] Univ Alabama Birmingham, Civitan Int Res Ctr, Birmingham, AL 35294 USA
[23] UAB Ctr Neurodegenerat & Expt Therapeut CNET, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
Zebrafish; Drug discovery; Standardization; Drug screening parameters; Drug library; MUSCULAR-DYSTROPHY; IN-VIVO; ADULT ZEBRAFISH; DANIO-RERIO; MODEL; MUTANT; CELLS; TOOL; DIFFERENTIATION; IDENTIFICATION;
D O I
10.1242/dmm.050339
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Skeletal muscular diseases predominantly affect skeletal and cardiac muscle, resulting in muscle weakness, impaired respiratory function and decreased lifespan. These harmful outcomes lead to poor healthrelated quality of life and carry a high healthcare economic burden. The absence of promising treatments and new therapies for muscular disorders requires new methods for candidate drug identification and advancement in animal models. Consequently, the rapid screening of drug compounds in an animal model that mimics features of human muscle disease is warranted. Zebrafish are a versatile model in preclinical studies that support developmental biology and drug discovery programs for novel chemical entities and repurposing of established drugs. Due to several advantages, there is an increasing number of applications of the zebrafish model for high -throughput drug screening for human disorders and developmental studies. Consequently, standardization of key drug screening parameters, such as animal husbandry protocols, drug compound administration and outcome measures, is paramount for the continued advancement of the model and field. Here, we seek to summarize and explore critical drug treatment and drug screening parameters in the zebrafishbased modeling of human muscle diseases. Through improved standardization and harmonization of drug screening parameters and protocols, we aim to promote more effective drug discovery programs.
引用
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页数:14
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