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Nitrogen metabolism, acid–base regulation, and molecular responses to ammonia and acid infusions in the spiny dogfish shark (Squalus acanthias)

Although they are ureotelic, marine elasmobranchs express Rh glycoproteins, putative ammonia channels. To address questions raised by a recent study on high environmental ammonia (HEA) exposure, dogfish were intravascularly infused for 24 h at 3 ml kg −1 h −1 with isosmotic NaCl (500 mmol l −1 , con...

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Published in:Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology Biochemical, systemic, and environmental physiology, 2015-07, Vol.185 (5), p.511-525
Main Authors: Nawata, C. Michele, Walsh, Patrick J., Wood, Chris M.
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container_title Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology
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description Although they are ureotelic, marine elasmobranchs express Rh glycoproteins, putative ammonia channels. To address questions raised by a recent study on high environmental ammonia (HEA) exposure, dogfish were intravascularly infused for 24 h at 3 ml kg −1 h −1 with isosmotic NaCl (500 mmol l −1 , control), NH 4 HCO 3 (500 mmol l −1 ), NH 4 Cl (500 mmol l −1 ), or HCl (as 125 mmol l −1 HCl + 375 mmol l −1 NaCl). While NaCl had no effect on arterial acid–base status, NH 4 HCO 3 caused mild alkalosis, NH 4 Cl caused strong acidosis, and HCl caused lesser acidosis, all predominantly metabolic in nature. Total plasma ammonia (T Amm ) and excretion rates of ammonia ( J Amm ) and urea-N ( J Urea-N ) were unaffected by NaCl or HCl. However, despite equal loading rates, plasma T Amm increased to a greater extent with NH 4 Cl, while J Amm increased to a greater extent with NH 4 HCO 3 due to much greater increases in blood-to-water PNH 3 gradients. As with HEA, both treatments caused large (90 %) elevations of J Urea-N , indicating that urea-N synthesis by the ornithine-urea cycle (OUC) is driven primarily by ammonia rather than HCO 3 − . Branchial mRNA expressions of Rhbg and Rhp2 were unaffected by NH 4 HCO 3 or NH 4 Cl, but v - type H + - ATPase was down-regulated by both treatments, and Rhbg and Na + /H + exchanger NHE2 were up-regulated by HCl. In the kidney, Rhbg was unresponsive to all treatments, but Rhp2 was up-regulated by HCl, and the urea transporter UT was up-regulated by HCl and NH 4 Cl. These responses are discussed in the context of current ideas about branchial, renal, and OUC function in this nitrogen-limited predator.
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subjects Acid-Base Equilibrium - drug effects
Acid-Base Equilibrium - physiology
Acidosis
Ammonia
Ammonia - blood
Ammonium Chloride - administration & dosage
Ammonium Chloride - adverse effects
Analysis of Variance
Animal Physiology
Animals
Bicarbonates - administration & dosage
Bicarbonates - adverse effects
Biochemistry
Biomedical and Life Sciences
Biomedicine
DNA Primers - genetics
Elasmobranchii
Gene Expression Regulation - drug effects
Glycoproteins
Human Physiology
Hydrochloric Acid
Life Sciences
Marine
Membrane Glycoproteins - metabolism
Metabolism
Nitrogen
Nitrogen - metabolism
Original Paper
Plasma
Polymerase Chain Reaction
Sodium Chloride
Spectrophotometry, Atomic
Squalus acanthias
Squalus acanthias - metabolism
Squalus acanthias - physiology
Urea
Urea - metabolism
Zoology
title Nitrogen metabolism, acid–base regulation, and molecular responses to ammonia and acid infusions in the spiny dogfish shark (Squalus acanthias)
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