4.2 Article

(Uncommon) Mechanisms of Branchial Ammonia Excretion in the Common Carp (Cyprinus carpio) in Response to Environmentally Induced Metabolic Acidosis

Journal

PHYSIOLOGICAL AND BIOCHEMICAL ZOOLOGY
Volume 89, Issue 1, Pages 26-40

Publisher

UNIV CHICAGO PRESS
DOI: 10.1086/683990

Keywords

Rhesus glycoproteins; H+-ATPase; Na+/H+ exchanger 3 (NHE3); Rhcg-b; metabolic acidosis

Funding

  1. Natural Sciences and Engineering Research Council Discovery Grants Program
  2. Portuguese Foundation for Science and Technology (FCT) grant [PTDC/MAR/98035]
  3. European Regional Development Fund (COMPETE-Operational Competitiveness Program)
  4. FCT [Pest- C/MAR/LA0015/2011]
  5. Canada Research Chair program

Ask authors/readers for more resources

Freshwater fishes generally increase ammonia excretion in acidic waters. The new model of ammonia transport in freshwater fish involves an association between the Rhesus (Rh) protein Rhcg-b, the Na+/H+ exchanger (NHE), and a suite of other membrane transporters. We tested the hypothesis that Rhcg-b and NHE3 together play a critical role in branchial ammonia excretion in common carp (Cyprinus carpio) chronically exposed to a low-pH environment. Carp were exposed to three sequential environmental treatments-control pH 7.6 water (24 h), pH 4.0 water (72 h), and recovery pH 7.6 water (24 h)-or in a separate series were simply exposed to either control (72 h) or pH 4.0 (72 h) water. Branchial ammonia excretion was increased by similar to 2.5-fold in the acid compared with the control period, despite the absence of an increase in the plasmato- water partial pressure NH3 gradient. Alanine aminotransferase activity was higher in the gills of fish exposed to pH 4 versus control water, suggesting that ammonia may be generated in gill tissue. Gill Rhcg-b and NHE3b messenger RNA levels were significantly elevated in acid-treated relative to control fish, but at the protein level Rhcg-b decreased (30%) and NHE3b increased (2-fold) in response to water of pH 4.0. Using immunofluorescence microscopy, NHE3b and Rhcg-b were found to be colocalized to ionocytes along the interlamellar space of the filament of control fish. After 72 h of acid exposure, Rhcg-b staining almost disappeared from this region, and NHE3b was more prominent along the lamellae. We propose that ammoniagenesis within the gill tissue itself is responsible for the higher rates of branchial ammonia excretion during chronic metabolic acidosis. Unexpectedly, gill Rhcg-b does not appear to be important in gill ammonia transport in low-pH water, but the strong induction of NHE3b suggests that some NH4(+) may be eliminated directly in exchange for Na+. These findings contrast with previous studies in larval zebrafish (Danio rerio) and medaka (Oryzias latipes), underlining the importance of species comparisons.

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