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Their small size makes them ideal for large-scale drug discovery screens. However, the extent that sapje mimic the muscle dysfunction of higher vertebrate models of DMD is unclear. We used an optical birefringence assay to differentiate affected dystrophic sapje larvae from their unaffected siblings and then studied trunk muscle contractility at 4\u20137 days postfertilization. Preparation cross-sectional area (CSA) was similar for affected and unaffected larvae, yet tetanic forces of affected preparations were only 30\u201360% of normal. ANCOVA indicated that the linear relationship observed between tetanic force and CSA for unaffected preparations was absent in the affected population. Consequently, the average force\/CSA of affected larvae was depressed 30\u201370%. Disproportionate reductions in twitch vs. tetanic force, and a slowing of twitch tension development and relaxation, indicated that the myofibrillar disorganization evident in the birefringence assay could not explain the entire force loss. Single eccentric contractions, in which activated preparations were lengthened 5\u201310%, resulted in tetanic force deficits in both groups of larvae. However, deficits of affected preparations were three- to fivefold greater at all strains and ages, even after accounting for any recovery. Based on these functional assessments, we conclude that the sapje mutant zebrafish is a phenotypically severe model of DMD. The severe contractile deficits of sapje larvae represent novel physiological endpoints for therapeutic drug screening.<\/jats:p>","DOI":"10.1152\/physiolgenomics.00088.2016","type":"journal-article","created":{"date-parts":[[2016,10,8]],"date-time":"2016-10-08T03:23:10Z","timestamp":1475896990000},"page":"850-860","source":"Crossref","is-referenced-by-count":38,"title":["Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy"],"prefix":"10.1152","volume":"48","author":[{"given":"Jeffrey J.","family":"Widrick","sequence":"first","affiliation":[{"name":"Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts;"},{"name":"Department of Pediatrics and Genetics, Harvard Medical School, Boston, Massachusetts;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthew S.","family":"Alexander","sequence":"additional","affiliation":[{"name":"Division of Genetics and Genomics, Boston Children's Hospital, Boston, 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