Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/44932
Title: Physiological pathways involved in nutritional muscle dystrophy and healing in European sea bass (Dicentrarchus labrax) larvae
Authors: Betancor, Mónica B.
Izquierdo, Marisol 
Terova, Genciana
Preziosa, Elena
Saleh, Reda
Montero, Daniel 
Hernández-Cruz, Carmen María 
Caballero, M. José 
UNESCO Clasification: 251092 Acuicultura marina
Keywords: Sea bass larvae
Oxidative stress
DHA
Muscle
Histology
Issue Date: 2013
Project: Mecanismos Fisiologicos Implicados en la Actuación de Lagunos Nutrientes Relacionados Con la Oxidación Lipidica y Sus Repercursiones en El Desarrollo Larvario de Los Peces Marinos. 
Journal: Comparative biochemistry and physiology. Part A, Molecular & integrative physiology 
Abstract: The potential muscle regeneration after nutritional dystrophy caused by high dietary DHA contents in fish and the physiological pathways involved are still unknown. To better understand this process, an experiment was conducted for 3 weeks in 14 day-old European sea bass larvae using different DHA ratios (1 or 5%). After this period, part of the larvae fed 5% DHA diet was switched to 1% DHA diet (“wash-out”) for another 2 weeks. Larvae fed 5% DHA diet showed altered oxidative status as indicated by the highest TBARS values, antioxidant enzymes (AOE) expression and incidence of muscular lesions. Accordingly, “washed-out” larvae showed lower dry weight and α-TOH content. IGF-I gene expression was elevated in 5% DHA larvae at 35 dph, suggesting increased muscle mitogenesis that was corroborated by the increase in myosin heavy chain expression. It can be concluded that high dietary DHA contents alter the oxidative status and cause muscular lesions in European sea bass larvae, with morphological and molecular aspects of mammalians muscular degenerative disease.
URI: http://hdl.handle.net/10553/44932
ISSN: 1095-6433
DOI: 10.1016/j.cbpa.2012.11.017
Source: Comparative Biochemistry and Physiology. Part A, Molecular and Integrative Physiology [ISSN 1095-6433], v. 164 (2), p. 399-409
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