{"title":"斑马鱼的渗透呼吸损害:缺氧和急性热应激对氧气消耗、扩散水通量和钠净损失率的影响。","authors":"John O Onukwufor, Chris M Wood","doi":"10.1089/zeb.2020.1947","DOIUrl":null,"url":null,"abstract":"<p><p>The traditional thesis of the osmorespiratory compromise is that low branchial water and ion permeability would be traded off for increased O<sub>2</sub> permeability at times of elevated O<sub>2</sub> demand. However, there is growing evidence of independent regulation of these permeabilities in hypoxia-tolerant fish. Using 0.5-g zebrafish previously maintained under normoxia at 25°C, we investigated responses to acute temperature challenges (15°C or 35°C), acute hypoxia (15 min at 10% or 5% air saturation), as well as longer-term exposures to 10% hypoxia, on O<sub>2</sub> consumption (MO<sub>2</sub>), diffusive water flux, and net sodium loss rates. Exposure to 35°C increased, and 15°C decreased all three rates, with diffusive water flux showing the lowest temperature sensitivity, and Na<sup>+</sup> loss the greatest. Acute 10% and 5% hypoxia increased diffusive water flux and net Na<sup>+</sup> loss, and it reduced MO<sub>2</sub>. All these responses reflected the traditional osmorespiratory compromise. However, during prolonged 10% hypoxia, MO<sub>2</sub> recovered, diffusive water flux decreased below control levels, and Na<sup>+</sup> loss rate remained elevated, even during posthypoxia recovery. Overall, zebrafish do not fit standard patterns previously seen in either hypoxia-tolerant or -intolerant fish but are clearly able to adjust the effective permeabilities of their gills to O<sub>2</sub>, water, and ions independently during acute temperature and hypoxia exposures.</p>","PeriodicalId":23872,"journal":{"name":"Zebrafish","volume":"17 6","pages":"400-411"},"PeriodicalIF":1.4000,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/zeb.2020.1947","citationCount":"6","resultStr":"{\"title\":\"Osmorespiratory Compromise in Zebrafish (<i>Danio rerio</i>): Effects of Hypoxia and Acute Thermal Stress on Oxygen Consumption, Diffusive Water Flux, and Sodium Net Loss Rates.\",\"authors\":\"John O Onukwufor, Chris M Wood\",\"doi\":\"10.1089/zeb.2020.1947\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The traditional thesis of the osmorespiratory compromise is that low branchial water and ion permeability would be traded off for increased O<sub>2</sub> permeability at times of elevated O<sub>2</sub> demand. However, there is growing evidence of independent regulation of these permeabilities in hypoxia-tolerant fish. Using 0.5-g zebrafish previously maintained under normoxia at 25°C, we investigated responses to acute temperature challenges (15°C or 35°C), acute hypoxia (15 min at 10% or 5% air saturation), as well as longer-term exposures to 10% hypoxia, on O<sub>2</sub> consumption (MO<sub>2</sub>), diffusive water flux, and net sodium loss rates. Exposure to 35°C increased, and 15°C decreased all three rates, with diffusive water flux showing the lowest temperature sensitivity, and Na<sup>+</sup> loss the greatest. Acute 10% and 5% hypoxia increased diffusive water flux and net Na<sup>+</sup> loss, and it reduced MO<sub>2</sub>. All these responses reflected the traditional osmorespiratory compromise. However, during prolonged 10% hypoxia, MO<sub>2</sub> recovered, diffusive water flux decreased below control levels, and Na<sup>+</sup> loss rate remained elevated, even during posthypoxia recovery. Overall, zebrafish do not fit standard patterns previously seen in either hypoxia-tolerant or -intolerant fish but are clearly able to adjust the effective permeabilities of their gills to O<sub>2</sub>, water, and ions independently during acute temperature and hypoxia exposures.</p>\",\"PeriodicalId\":23872,\"journal\":{\"name\":\"Zebrafish\",\"volume\":\"17 6\",\"pages\":\"400-411\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2020-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1089/zeb.2020.1947\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zebrafish\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1089/zeb.2020.1947\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zebrafish","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1089/zeb.2020.1947","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
Osmorespiratory Compromise in Zebrafish (Danio rerio): Effects of Hypoxia and Acute Thermal Stress on Oxygen Consumption, Diffusive Water Flux, and Sodium Net Loss Rates.
The traditional thesis of the osmorespiratory compromise is that low branchial water and ion permeability would be traded off for increased O2 permeability at times of elevated O2 demand. However, there is growing evidence of independent regulation of these permeabilities in hypoxia-tolerant fish. Using 0.5-g zebrafish previously maintained under normoxia at 25°C, we investigated responses to acute temperature challenges (15°C or 35°C), acute hypoxia (15 min at 10% or 5% air saturation), as well as longer-term exposures to 10% hypoxia, on O2 consumption (MO2), diffusive water flux, and net sodium loss rates. Exposure to 35°C increased, and 15°C decreased all three rates, with diffusive water flux showing the lowest temperature sensitivity, and Na+ loss the greatest. Acute 10% and 5% hypoxia increased diffusive water flux and net Na+ loss, and it reduced MO2. All these responses reflected the traditional osmorespiratory compromise. However, during prolonged 10% hypoxia, MO2 recovered, diffusive water flux decreased below control levels, and Na+ loss rate remained elevated, even during posthypoxia recovery. Overall, zebrafish do not fit standard patterns previously seen in either hypoxia-tolerant or -intolerant fish but are clearly able to adjust the effective permeabilities of their gills to O2, water, and ions independently during acute temperature and hypoxia exposures.
期刊介绍:
Zebrafish is the only peer-reviewed journal dedicated to the central role of zebrafish and other aquarium species as models for the study of vertebrate development, evolution, toxicology, and human disease.
Due to its prolific reproduction and the external development of the transparent embryo, the zebrafish is a prime model for genetic and developmental studies. While genetically more distant from humans, the vertebrate zebrafish nevertheless has comparable organs and tissues, such as heart, kidney, pancreas, bones, and cartilage.
Zebrafish introduced the new section TechnoFish, which highlights these innovations for the general zebrafish community.
TechnoFish features two types of articles:
TechnoFish Previews: Important, generally useful technical advances or valuable transgenic lines
TechnoFish Methods: Brief descriptions of new methods, reagents, or transgenic lines that will be of widespread use in the zebrafish community
Zebrafish coverage includes:
Comparative genomics and evolution
Molecular/cellular mechanisms of cell growth
Genetic analysis of embryogenesis and disease
Toxicological and infectious disease models
Models for neurological disorders and aging
New methods, tools, and experimental approaches
Zebrafish also includes research with other aquarium species such as medaka, Fugu, and Xiphophorus.