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      Ethanol metabolism varies with hypoxia tolerance in ten cyprinid species.

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          Abstract

          During periods of severe hypoxia or anoxia, Carassius spp. are known for their ability to produce ethanol as their anaerobic end product, which diffuses into the environment thereby reducing the osmotic and acidotic load associated with "anaerobic" glycolysis. However, the relationship between alcohol dehydrogenase (ADH) and acetaldehyde dehydrogenase (ALDH) activities, key ethanol metabolizing enzymes, and hypoxia tolerance among Carassius spp. and their closely related non-ethanol-producing cyprinids remains unclear. To address this, we quantified the activity levels of key anaerobic enzymes in liver and muscle in species of cyprinids over 48 h of severe hypoxia exposure (0.7 kPa). As predicted, muscle ADH activity was highest in the two most hypoxia-tolerant species (Carassius spp.), with very low levels present in the other species examined. However, liver ADH activities showed an inverse relationship with hypoxia tolerance, with the most hypoxia-tolerant fish having the lowest ADH activity. There was no correlation between hypoxia tolerance and ALDH and LDH activities in muscle or liver. All species produced lactate, reaching their highest levels after 8 h, but returning to near-baseline levels by 48 h of sustained exposure to hypoxia, suggesting lactate oxidation or depressed ATP demand. Liver glycogen content was not affected by 48 h hypoxia exposure in the most hypoxia-tolerant species, whereas the least tolerant species consumed the majority of the liver glycogen stores, which is probably due to the greater relative hypoxia exposure experienced by these species. Our findings that liver ADH activities were inversely related to hypoxia tolerance suggests that in all but Carassius spp., the ethanol metabolizing pathways in cyprinids is largely similar to that observed in other vertebrates and plays a role in the detoxification of ethanol. Furthermore, conservation of glycogen stores may be the result of metabolic-depressing pathways in the more tolerant species, regardless of the ability to produce ethanol, or adaptations that improve oxygen uptake to reduce metabolic demands due to hypoxia.

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          Author and article information

          Journal
          J Comp Physiol B
          Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology
          Springer Science and Business Media LLC
          1432-136X
          0174-1578
          March 2018
          : 188
          : 2
          Affiliations
          [1 ] Department of Biomolecular Chemistry, University of Wisconsin, 330 North Orchard Street, Madison, WI, 53715, USA. rdhillon2@wisc.edu.
          [2 ] Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, BC, V6T 1Z4, Canada. rdhillon2@wisc.edu.
          [3 ] Department of Biology, University of Ottawa, 30 Marie Curie Private, Ottawa, ON, K1N 6N5, Canada.
          [4 ] Department of Biomolecular Chemistry, University of Wisconsin, 330 North Orchard Street, Madison, WI, 53715, USA.
          [5 ] Laboratory of Evolutionary Physiology and Behaviour, Chongqing Key Laboratory of Animal Biology, Chongqing Normal University, Chongqing, China.
          [6 ] Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, BC, V6T 1Z4, Canada.
          [7 ] Department of Biology, Queen's University, 116 Barrie Street, Kingston, ON, K7L 3N6, Canada.
          Article
          10.1007/s00360-017-1131-4
          10.1007/s00360-017-1131-4
          29032388
          0fcfab1c-aa24-44a3-a17f-efe1a778f7e2
          History

          Acetaldehyde dehydrogenase,Aerobic,Alcohol dehydrogenase,Anaerobic metabolism,Cyprinids,Ethanol,Hypoxia

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