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Silver catfish Rhamdia quelen immersion anaesthesia with essential oil of Aloysia triphylla (L'Hérit) Britton or tricaine methanesulfonate: effect on stress response and antioxidant status
Author(s) -
Gressler Luciane Tourem,
Riffel Ana Paula Konzen,
Parodi Thaylise Vey,
Saccol Etiane Medianeira Hundertmarck,
Koakoski Gessi,
Costa Sílvio Teixeira,
Pavanato Maria Amália,
Heinzmann Berta Maria,
Caron Bráulio,
Schmidt Denise,
Llesuy Susana Francisca,
Barcellos Leonardo José Gil,
Baldisserotto Bernardo
Publication year - 2014
Publication title -
aquaculture research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 89
eISSN - 1365-2109
pISSN - 1355-557X
DOI - 10.1111/are.12043
Subject(s) - catfish , catalase , essential oil , oxidative stress , antioxidant , lipid peroxidation , biology , glutathione , hematocrit , anesthesia , zoology , pharmacology , biochemistry , medicine , endocrinology , food science , fishery , fish <actinopterygii> , enzyme
Responses to anaesthesia with essential oil ( EO ) of Aloysia triphylla (135 and 180 mg L −1 ) and tricaine methanesulfonate ( MS 222) (150 and 300 mg L −1 ) were assessed in silver catfish. Exposure to the anaesthetics elicited a stress response in the species. In the case of MS 222, it was displayed as a release of cortisol into bloodstream, elevation in hematocrit and plasma ion loss. The EO presented cortisol‐blocking properties, but increased haematocrit and disturbances of hydromineral balance were observed. Liver antioxidant/oxidant status of EO and MS 222‐anaesthetized silver catfish was also estimated. The synthetic anaesthetic induced lipoperoxidation, notwithstanding increased catalase contents, whereas the naturally occurring product was capable of preventing the formation of lipid peroxides, possibly due to combined actions of catalase and glutathione‐S‐transferase. Anaesthetic efficacy was also tested via induction and recovery times. Overall, the promising results obtained for the physiological parameters of the EO ‐treated fish counterbalanced the slight prolonged induction time observed for 180 mg L −1 . As for 135 mg L −1 , both induction and recovery times were lengthy; despite that, the EO was able to promote oxidative protection and mitigate stress. None of the MS 222 concentrations prompted such responses concomitantly.