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Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)

Developmental plasticity of cardiorespiratory physiology in response to chronic hypoxia is poorly understood in larval fishes, especially larval air‐breathing fishes, which eventually in their development can at least partially “escape” hypoxia through air breathing. Whether the development air brea...

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Detalles Bibliográficos
Autores principales: Mendez‐Sanchez, Jose F., Burggren, Warren W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555888/
https://www.ncbi.nlm.nih.gov/pubmed/28778991
http://dx.doi.org/10.14814/phy2.13359
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author Mendez‐Sanchez, Jose F.
Burggren, Warren W.
author_facet Mendez‐Sanchez, Jose F.
Burggren, Warren W.
author_sort Mendez‐Sanchez, Jose F.
collection PubMed
description Developmental plasticity of cardiorespiratory physiology in response to chronic hypoxia is poorly understood in larval fishes, especially larval air‐breathing fishes, which eventually in their development can at least partially “escape” hypoxia through air breathing. Whether the development air breathing makes these larval fishes less or more developmentally plastic than strictly water breathing larval fishes remains unknown. Consequently, developmental plasticity of cardiorespiratory physiology was determined in two air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus). Larvae of both species experienced an hypoxic exposure that mimicked their natural environmental conditions, namely chronic nocturnal hypoxia (12 h at 17 kPa or 14 kPa), with a daily return to diurnal normoxia. Chronic hypoxic exposures were made from hatching through 35 days postfertilization, and opercular and heart rates measured as development progressed. Opercular and heart rates in normoxia were not affected by chronic nocturnal hypoxic. However, routine oxygen consumption [Formula: see text] (~4 μmol·O(2)/g per hour in normoxia in larval Betta) was significantly elevated by chronic nocturnal hypoxia at 17 kPa but not by more severe (14 kPa) nocturnal hypoxia. Routine [Formula: see text] in Trichopodus (6–7 μmol·O(2)/g per hour), significantly higher than in Betta, was unaffected by either level of chronic hypoxia. P (Crit), the PO(2) at which [Formula: see text] decreases as ambient PO(2) falls, was measured at 35 dpf, and decreased with increasing chronic hypoxia in Betta, indicating a large, relatively plastic hypoxic tolerance. However, in contrast, P (Crit) in Trichopodus increased as rearing conditions grew more hypoxic, suggesting that hypoxic acclimation led to lowered hypoxic resistance. Species‐specific differences in larval physiological developmental plasticity thus emerge between the relatively closely related Betta and Trichopodus. Hypoxic rearing increased hypoxic tolerance in Betta, which inhabits temporary ponds with nocturnal hypoxia. Trichopodus, inhabiting more permanent oxygenated bodies of water, showed few responses to hypoxia, reflecting a lower degree of developmental phenotypic plasticity.
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spelling pubmed-55558882017-08-16 Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus) Mendez‐Sanchez, Jose F. Burggren, Warren W. Physiol Rep Original Research Developmental plasticity of cardiorespiratory physiology in response to chronic hypoxia is poorly understood in larval fishes, especially larval air‐breathing fishes, which eventually in their development can at least partially “escape” hypoxia through air breathing. Whether the development air breathing makes these larval fishes less or more developmentally plastic than strictly water breathing larval fishes remains unknown. Consequently, developmental plasticity of cardiorespiratory physiology was determined in two air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus). Larvae of both species experienced an hypoxic exposure that mimicked their natural environmental conditions, namely chronic nocturnal hypoxia (12 h at 17 kPa or 14 kPa), with a daily return to diurnal normoxia. Chronic hypoxic exposures were made from hatching through 35 days postfertilization, and opercular and heart rates measured as development progressed. Opercular and heart rates in normoxia were not affected by chronic nocturnal hypoxic. However, routine oxygen consumption [Formula: see text] (~4 μmol·O(2)/g per hour in normoxia in larval Betta) was significantly elevated by chronic nocturnal hypoxia at 17 kPa but not by more severe (14 kPa) nocturnal hypoxia. Routine [Formula: see text] in Trichopodus (6–7 μmol·O(2)/g per hour), significantly higher than in Betta, was unaffected by either level of chronic hypoxia. P (Crit), the PO(2) at which [Formula: see text] decreases as ambient PO(2) falls, was measured at 35 dpf, and decreased with increasing chronic hypoxia in Betta, indicating a large, relatively plastic hypoxic tolerance. However, in contrast, P (Crit) in Trichopodus increased as rearing conditions grew more hypoxic, suggesting that hypoxic acclimation led to lowered hypoxic resistance. Species‐specific differences in larval physiological developmental plasticity thus emerge between the relatively closely related Betta and Trichopodus. Hypoxic rearing increased hypoxic tolerance in Betta, which inhabits temporary ponds with nocturnal hypoxia. Trichopodus, inhabiting more permanent oxygenated bodies of water, showed few responses to hypoxia, reflecting a lower degree of developmental phenotypic plasticity. John Wiley and Sons Inc. 2017-08-04 /pmc/articles/PMC5555888/ /pubmed/28778991 http://dx.doi.org/10.14814/phy2.13359 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Mendez‐Sanchez, Jose F.
Burggren, Warren W.
Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title_full Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title_fullStr Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title_full_unstemmed Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title_short Cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (Betta splendens and Trichopodus trichopterus)
title_sort cardiorespiratory physiological phenotypic plasticity in developing air‐breathing anabantid fishes (betta splendens and trichopodus trichopterus)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555888/
https://www.ncbi.nlm.nih.gov/pubmed/28778991
http://dx.doi.org/10.14814/phy2.13359
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