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- Andrade, Carlos A. P., et al.
(författare)
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Allometric Growth in Red Porgy Larvae : Developing Morphological Indices for Mesocosm Semi-Intensive Culture
- 2013
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Ingår i: North American Journal of Aquaculture. - : Wiley. - 1522-2055 .- 1548-8454. ; 75:1, s. 42-49
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Tidskriftsartikel (refereegranskat)abstract
- We studied the morphological development, allometric growth, and cannibalistic behavior of Red Porgy Pagrus pagrus reared in mesocosm semi-intensive culture. The study was conducted from hatching to 32 d after hatching (DAH). Red porgy ontogeny was characterized by strong positive allometric growth of body depth at anus (BDA) to 6.7mm total length (TL) at about 2122 DAH. The BDA combined with standard length (SL) in a morphometric index was found to be better correlated with dry weight than TL and provided an improved method to estimate larval growth. Mouth size also exhibited strong positive allometric growth at early larval stages that, together with inflation of the swim bladder, may have contributed to improve feeding ability, in preparation for the high energy demands of metamorphosis. A predictive regression model developed for cannibalism underestimated prey size. Cannibalism coincided with the development of acidic digestion and was first evident at 27 DAH as larvae reached about 23% of their maximum size variation. We hypothesize that cannibalism is associated with larval size and condition, but is prompted by physiological and energetic factors. The bivariate morphometric index developed in this study can be used to mitigate cannibalism by controlling larval size variation and improving feed supply. The morphological measurements and morphometric indices that result from this study provide important tools for improving red porgy larvae culture. Received December 13, 2011; accepted July 12, 2012
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| 2. |
- Andrade, Carlos A. P., et al.
(författare)
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Red Porgy, Pagrus pagrus, Larvae Performance and Nutritional Condition in Response to Different Weaning Regimes
- 2012
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Ingår i: Journal of the World Aquaculture Society. - : Wiley. - 0893-8849 .- 1749-7345. ; 43:3, s. 321-334
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Tidskriftsartikel (refereegranskat)abstract
- Red porgy, Pagrus pagrus, is a candidate species for aquaculture diversification. The aim of this work was to assess whether an early supply of enriched Artemia (D1) or a direct step to dry diets (D3) would be advantageous weaning strategies for red porgy larvae, compared to a later supply of Artemia followed by dry diets (D2). Direct weaning to dry diet resulted in significantly lower growth, survival, pancreatic (trypsin and lipase), and intestinal (alkaline phosphatase) enzyme-specific activity, with the exception of leucine-alanine peptidase. The direct weaning strategy presented severe nutritional restrictions from early weaning stages with an associated delay of the maturation of digestive system. The two-step strategy presented in D1 and D2 resulted in comparable results in most parameters, including survival. Weaning using enriched Artemia as an intermediate step is confirmed as the most adequate strategy for red porgy larvae. Digestive enzymes and selected fatty acids correlated well with performance responses to dietary regimes, thereby supporting the use of these parameters as sensitive and reliable indicators of red porgy nutritional or physiological status during larval stages.
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| 3. |
- Garcia, Juliana, et al.
(författare)
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A breakthrough on Amanita phalloides poisoning : an effective antidotal effect by polymyxin B
- 2015
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Ingår i: Archives of Toxicology. - : Springer Science and Business Media LLC. - 0340-5761 .- 1432-0738. ; 89:12, s. 2305-2323
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Tidskriftsartikel (refereegranskat)abstract
- Amanita phalloides is responsible for more than 90 % of mushroom-related fatalities, and no effective antidote is available. alpha-Amanitin, the main toxin of A. phalloides, inhibits RNA polymerase II (RNAP II), causing hepatic and kidney failure. In silico studies included docking and molecular dynamics simulation coupled to molecular mechanics with generalized Born and surface area method energy decomposition on RNAP II. They were performed with a clinical drug that shares chemical similarities to alpha-amanitin, polymyxin B. The results show that polymyxin B potentially binds to RNAP II in the same interface of alpha-amanitin, preventing the toxin from binding to RNAP II. In vivo, the inhibition of the mRNA transcripts elicited by alpha-amanitin was efficiently reverted by polymyxin B in the kidneys. Moreover, polymyxin B significantly decreased the hepatic and renal alpha-amanitin-induced injury as seen by the histology and hepatic aminotransferases plasma data. In the survival assay, all animals exposed to alpha-amanitin died within 5 days, whereas 50 % survived up to 30 days when polymyxin B was administered 4, 8, and 12 h post-alpha-amanitin. Moreover, a single dose of polymyxin B administered concomitantly with alpha-amanitin was able to guarantee 100 % survival. Polymyxin B protects RNAP II from inactivation leading to an effective prevention of organ damage and increasing survival in alpha-amanitin-treated animals. The present use of clinically relevant concentrations of an already human-use-approved drug prompts the use of polymyxin B as an antidote for A. phalloides poisoning in humans.
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