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Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism

Transport processes between aquaculture facilities activate the stress response in fish. To deal with these situations, the hypothalamic-pituitary-interrenal (HPI) axis releases cortisol, leading to an increase in circulating energy resources to restore homeostasis. However, if the allostatic load g...

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Autores principales: Jerez-Cepa, Ismael, Fernández-Castro, Miriam, Del Santo O'Neill, Thomas Julian, Martos-Sitcha, Juan Antonio, Martínez-Rodríguez, Gonzalo, Mancera, Juan Miguel, Ruiz-Jarabo, Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555194/
https://www.ncbi.nlm.nih.gov/pubmed/31214040
http://dx.doi.org/10.3389/fphys.2019.00612
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author Jerez-Cepa, Ismael
Fernández-Castro, Miriam
Del Santo O'Neill, Thomas Julian
Martos-Sitcha, Juan Antonio
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Ruiz-Jarabo, Ignacio
author_facet Jerez-Cepa, Ismael
Fernández-Castro, Miriam
Del Santo O'Neill, Thomas Julian
Martos-Sitcha, Juan Antonio
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Ruiz-Jarabo, Ignacio
author_sort Jerez-Cepa, Ismael
collection PubMed
description Transport processes between aquaculture facilities activate the stress response in fish. To deal with these situations, the hypothalamic-pituitary-interrenal (HPI) axis releases cortisol, leading to an increase in circulating energy resources to restore homeostasis. However, if the allostatic load generated exceeds fish tolerance limits, stress-related responses will compromise health and welfare of the animals. In this context, anesthetics have arisen as potential agents aiming to reduce negative effects of stress response. Here we assessed the effects of a sedative dose of clove oil (CO) and MS-222 on hallmarks involved in HPI axis regulation and energy management after simulated transport, and further recovery, in gilthead seabream (Sparus aurata L.) juveniles. Fish were placed in a mobile setup of water tanks where transport conditions were simulated for 6 h. Sedation doses of either CO (2.5 mg L(−1)) or MS-222 (5 mg L(−1)) were added in the water tanks. A control group without anesthetics was also included in the setup. Half of the animals (n = 12 per group) were sampled immediately after transport, while remaining animals were allowed to recover for 18 h in clean water tanks and then sampled. Our results showed that the HPI axis response was modified at peripheral level, with differences depending on the anesthetic employed. Head kidney gene-expressions related to cortisol production (star and cyp11b1) matched concomitantly with increased plasma cortisol levels immediately after transport in CO-sedated fish, but these levels remained constant in MS-222-sedated fish. Differential changes in the energy management of carbohydrates, lipids and amino acids, depending on the anesthetic employed, were also observed. The use of CO stimulated amino acids catabolism, while MS-222-sedated fish tended to consume liver glycogen and mobilize triglycerides. Further studies, including alternative doses of both anestethics, as well as the assessment of time-course HPI activation and longer recovery periods, are necessary to better understand if the use of clove oil and MS-222 is beneficial for S. aurata under these circumstances.
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spelling pubmed-65551942019-06-18 Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism Jerez-Cepa, Ismael Fernández-Castro, Miriam Del Santo O'Neill, Thomas Julian Martos-Sitcha, Juan Antonio Martínez-Rodríguez, Gonzalo Mancera, Juan Miguel Ruiz-Jarabo, Ignacio Front Physiol Physiology Transport processes between aquaculture facilities activate the stress response in fish. To deal with these situations, the hypothalamic-pituitary-interrenal (HPI) axis releases cortisol, leading to an increase in circulating energy resources to restore homeostasis. However, if the allostatic load generated exceeds fish tolerance limits, stress-related responses will compromise health and welfare of the animals. In this context, anesthetics have arisen as potential agents aiming to reduce negative effects of stress response. Here we assessed the effects of a sedative dose of clove oil (CO) and MS-222 on hallmarks involved in HPI axis regulation and energy management after simulated transport, and further recovery, in gilthead seabream (Sparus aurata L.) juveniles. Fish were placed in a mobile setup of water tanks where transport conditions were simulated for 6 h. Sedation doses of either CO (2.5 mg L(−1)) or MS-222 (5 mg L(−1)) were added in the water tanks. A control group without anesthetics was also included in the setup. Half of the animals (n = 12 per group) were sampled immediately after transport, while remaining animals were allowed to recover for 18 h in clean water tanks and then sampled. Our results showed that the HPI axis response was modified at peripheral level, with differences depending on the anesthetic employed. Head kidney gene-expressions related to cortisol production (star and cyp11b1) matched concomitantly with increased plasma cortisol levels immediately after transport in CO-sedated fish, but these levels remained constant in MS-222-sedated fish. Differential changes in the energy management of carbohydrates, lipids and amino acids, depending on the anesthetic employed, were also observed. The use of CO stimulated amino acids catabolism, while MS-222-sedated fish tended to consume liver glycogen and mobilize triglycerides. Further studies, including alternative doses of both anestethics, as well as the assessment of time-course HPI activation and longer recovery periods, are necessary to better understand if the use of clove oil and MS-222 is beneficial for S. aurata under these circumstances. Frontiers Media S.A. 2019-05-31 /pmc/articles/PMC6555194/ /pubmed/31214040 http://dx.doi.org/10.3389/fphys.2019.00612 Text en Copyright © 2019 Jerez-Cepa, Fernández-Castro, Del Santo O'Neill, Martos-Sitcha, Martínez-Rodríguez, Mancera and Ruiz-Jarabo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Jerez-Cepa, Ismael
Fernández-Castro, Miriam
Del Santo O'Neill, Thomas Julian
Martos-Sitcha, Juan Antonio
Martínez-Rodríguez, Gonzalo
Mancera, Juan Miguel
Ruiz-Jarabo, Ignacio
Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title_full Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title_fullStr Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title_full_unstemmed Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title_short Transport and Recovery of Gilthead Seabream (Sparus aurata L.) Sedated With Clove Oil and MS-222: Effects on Stress Axis Regulation and Intermediary Metabolism
title_sort transport and recovery of gilthead seabream (sparus aurata l.) sedated with clove oil and ms-222: effects on stress axis regulation and intermediary metabolism
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555194/
https://www.ncbi.nlm.nih.gov/pubmed/31214040
http://dx.doi.org/10.3389/fphys.2019.00612
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