scholarly journals Short-term exposure to repeated chasing stress does not induce habituation in Senegalese sole, Solea senegalensis

Aquaculture ◽  
2018 ◽  
Vol 487 ◽  
pp. 32-40 ◽  
Author(s):  
Marta Conde-Sieira ◽  
Luisa M.P. Valente ◽  
Juan Hernández-Pérez ◽  
José L. Soengas ◽  
Jesús M. Míguez ◽  
...  
Aquaculture ◽  
2020 ◽  
Vol 516 ◽  
pp. 734649 ◽  
Author(s):  
Wendy Ángela González-López ◽  
Sandra Ramos-Júdez ◽  
Ignacio Giménez ◽  
Neil J. Duncan

2021 ◽  
Author(s):  
Mário Araújo ◽  
Amadeu Soares ◽  
Marta Monteiro

Abstract Many personal care products integrate UV-filters, such as 4-methylbenzylidene camphor (4-MBC) which has been detected in aquatic habitats. Possible effects of 4-MBC to aquatic organisms have been poorly studied. Therefore, the main objective of this work is to study the effects of 4-MBC exposure to Solea senegalensis during metamorphosis, a sensitive life stage of this flatfish. To achieve this, at the beginning of metamorphosis (13 days after hatching, dah) fish were exposed to 4-MBC (0.2–2.0 mg L− 1) for 48 h. After this period, fish were transferred to clean medium and were fed and maintained until more than 80% of fish in control group completed the metamorphosis (24 dah). Mortality, malformations and metamorphosis progression were studied on a daily basis. In addition, growth, behavior and biochemical markers of neurotransmission (acetylcholinesterase, AChE), oxidative stress (catalase, CAT; glutathione S-transferase, GST, and lipid peroxidation, LPO) and anaerobic metabolism (lactate dehydrogenase, LDH) were determined at the end of the experiment. An acceleration of metamorphosis progression was observed during and 2 days after the 4-MBC exposure in all concentrations tested. In addition, decreased length, inhibition of CAT activity and induction of oxidative damage (LOEC = 0.928 mg L− 1 4-MBC for length, CAT and LPO) were observed. A short-term exposure to 4-MBC at the onset of metamorphosis, a critical period of development, affected S. senegalensis at several levels of organization, even after nine days in clean medium, including growth and metamorphosis progression, suggesting possible long-term adverse effects to this species.


2012 ◽  
Vol 38 (6) ◽  
pp. 1741-1751 ◽  
Author(s):  
Marcelino Herrera ◽  
Cláudia Aragão ◽  
Ismael Hachero ◽  
Ignacio Ruiz-Jarabo ◽  
Luis Vargas-Chacoff ◽  
...  

1976 ◽  
Vol 36 (01) ◽  
pp. 221-229 ◽  
Author(s):  
Charles A. Schiffer ◽  
Caroline L. Whitaker ◽  
Morton Schmukler ◽  
Joseph Aisner ◽  
Steven L. Hilbert

SummaryAlthough dimethyl sulfoxide (DMSO) has been used extensively as a cryopreservative for platelets there are few studies dealing with the effect of DMSO on platelet function. Using techniques similar to those employed in platelet cryopreservation platelets were incubated with final concentrations of 2-10% DMSO at 25° C. After exposure to 5 and 10% DMSO platelets remained discoid and electron micrographs revealed no structural abnormalities. There was no significant change in platelet count. In terms of injury to platelet membranes, there was no increased availability of platelet factor-3 or leakage of nucleotides, 5 hydroxytryptamine (5HT) or glycosidases with final DMSO concentrations of 2.5, 5 and 10% DMSO. Thrombin stimulated nucleotide and 5HT release was reduced by 10% DMSO. Impairment of thrombin induced glycosidase release was noted at lower DMSO concentrations and was dose related. Similarly, aggregation to ADP was progressively impaired at DMSO concentrations from 1-5% and was dose related. After the platelets exposed to DMSO were washed, however, aggregation and release returned to control values. Platelet aggregation by epinephrine was also inhibited by DMSO and this could not be corrected by washing the platelets. DMSO-plasma solutions are hypertonic but only minimal increases in platelet volume (at 10% DMSO) could be detected. Shrinkage of platelets was seen with hypertonic solutions of sodium chloride or sucrose suggesting that the rapid transmembrane passage of DMSO prevented significant shifts of water. These studies demonstrate that there are minimal irreversible alterations in in vitro platelet function after short-term exposure to DMSO.


2016 ◽  
Vol 307 ◽  
pp. 137-144 ◽  
Author(s):  
Gaëtan Philippot ◽  
Fred Nyberg ◽  
Torsten Gordh ◽  
Anders Fredriksson ◽  
Henrik Viberg

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