Literature DB >> 12115902

Ammonia excretion and urea handling by fish gills: present understanding and future research challenges.

Michael Patrick Wilkie1.   

Abstract

In fresh water fishes, ammonia is excreted across the branchial epithelium via passive NH(3) diffusion. This NH(3) is subsequently trapped as NH(4)(+) in an acidic unstirred boundary layer lying next to the gill, which maintains the blood-to-gill water NH(3) partial pressure gradient. Whole animal, in situ, ultrastructural and molecular approaches suggest that boundary layer acidification results from the hydration of CO(2) in the expired gill water, and to a lesser extent H(+) excretion mediated by apical H(+)-ATPases. Boundary layer acidification is insignificant in highly buffered sea water, where ammonia excretion proceeds via NH(3) diffusion, as well as passive NH(4)(+) diffusion due to the greater ionic permeability of marine fish gills. Although Na(+)/H(+) exchangers (NHE) have been isolated in marine fish gills, possible Na(+)/NH(4)(+) exchange via these proteins awaits evaluation using modern electrophysiological and molecular techniques. Although urea excretion (J(Urea)) was thought to be via passive diffusion, it is now clear that branchial urea handling requires specialized urea transporters. Four urea transporters have been cloned in fishes, including the shark kidney urea transporter (shUT), which is a facilitated urea transporter similar to the mammalian renal UT-A2 transporter. Another urea transporter, characterized but not yet cloned, is the basolateral, Na(+) dependent urea antiporter of the dogfish gill, which is essential for urea retention in ureosmotic elasmobranchs. In ureotelic teleosts such as the Lake Magadi tilapia and the gulf toadfish, the cloned mtUT and tUT are facilitated urea transporters involved in J(Urea). A basolateral urea transporter recently cloned from the gill of the Japanese eel (eUT) may actually be important for urea retention during salt water acclimation. A multi-faceted approach, incorporating whole animal, histological, biochemical, pharmacological, and molecular techniques is required to learn more about the location, mechanism of action, and functional significance of urea transporters in fishes. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12115902     DOI: 10.1002/jez.10123

Source DB:  PubMed          Journal:  J Exp Zool        ISSN: 0022-104X


  37 in total

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3.  Physiological protective action of dissolved organic carbon on ion regulation and nitrogenous waste excretion of zebrafish (Danio rerio) exposed to low pH in ion-poor water.

Authors:  Rafael M Duarte; Chris M Wood; Adalberto L Val; D Scott Smith
Journal:  J Comp Physiol B       Date:  2018-06-11       Impact factor: 2.200

Review 4.  A broader look at ammonia production, excretion, and transport in fish: a review of impacts of feeding and the environment.

Authors:  Carol Bucking
Journal:  J Comp Physiol B       Date:  2016-08-13       Impact factor: 2.200

5.  The physiology of the Tambaqui (Colossoma macropomum) at pH 8.0.

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6.  The Gills of Reef Fish Support a Distinct Microbiome Influenced by Host-Specific Factors.

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Authors:  Dawoon Jung; J Denry Sato; Joseph R Shaw; Bruce A Stanton
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9.  Nitrogen metabolism in tambaqui (Colossoma macropomum), a neotropical model teleost: hypoxia, temperature, exercise, feeding, fasting, and high environmental ammonia.

Authors:  Chris M Wood; José Gadelha de Souza Netto; Jonathan M Wilson; Rafael M Duarte; Adalberto Luis Val
Journal:  J Comp Physiol B       Date:  2016-08-16       Impact factor: 2.200

10.  Thermal tolerance, oxygen consumption and haemato-biochemical variables of Tor putitora juveniles acclimated to five temperatures.

Authors:  M S Akhtar; A K Pal; N P Sahu; A Ciji; P C Mahanta
Journal:  Fish Physiol Biochem       Date:  2013-03-27       Impact factor: 2.794

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