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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 |
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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. |
doi_str_mv | 10.1007/s00360-015-0898-4 |
format | article |
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−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.</description><identifier>ISSN: 0174-1578</identifier><identifier>EISSN: 1432-136X</identifier><identifier>DOI: 10.1007/s00360-015-0898-4</identifier><identifier>PMID: 25794843</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>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</subject><ispartof>Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 2015-07, Vol.185 (5), p.511-525</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-fc1987b0cc99b22395347241a442f9dec7f903f3c6e603f4decac02faccb34bb3</citedby><cites>FETCH-LOGICAL-c475t-fc1987b0cc99b22395347241a442f9dec7f903f3c6e603f4decac02faccb34bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25794843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nawata, C. Michele</creatorcontrib><creatorcontrib>Walsh, Patrick J.</creatorcontrib><creatorcontrib>Wood, Chris M.</creatorcontrib><title>Nitrogen metabolism, acid–base regulation, and molecular responses to ammonia and acid infusions in the spiny dogfish shark (Squalus acanthias)</title><title>Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology</title><addtitle>J Comp Physiol B</addtitle><addtitle>J Comp Physiol B</addtitle><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.</description><subject>Acid-Base Equilibrium - drug effects</subject><subject>Acid-Base Equilibrium - physiology</subject><subject>Acidosis</subject><subject>Ammonia</subject><subject>Ammonia - blood</subject><subject>Ammonium Chloride - administration & dosage</subject><subject>Ammonium Chloride - adverse effects</subject><subject>Analysis of Variance</subject><subject>Animal Physiology</subject><subject>Animals</subject><subject>Bicarbonates - administration & dosage</subject><subject>Bicarbonates - adverse effects</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>DNA Primers - genetics</subject><subject>Elasmobranchii</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glycoproteins</subject><subject>Human Physiology</subject><subject>Hydrochloric Acid</subject><subject>Life Sciences</subject><subject>Marine</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Metabolism</subject><subject>Nitrogen</subject><subject>Nitrogen - metabolism</subject><subject>Original Paper</subject><subject>Plasma</subject><subject>Polymerase Chain Reaction</subject><subject>Sodium Chloride</subject><subject>Spectrophotometry, Atomic</subject><subject>Squalus acanthias</subject><subject>Squalus acanthias - metabolism</subject><subject>Squalus acanthias - physiology</subject><subject>Urea</subject><subject>Urea - metabolism</subject><subject>Zoology</subject><issn>0174-1578</issn><issn>1432-136X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkc9qFTEUxoNY7LX6AG4k4KaCoyd_ZjJZlqKtUHShgruQyWTuTZ1JbnNmFt35CuIb9kma621FBHF1wnd-3xeSj5BnDF4zAPUGAUQDFbC6gla3lXxAVkwKXjHRfH1IVsCUrFit2kPyGPESACRr5SNyyGulZSvFivz4EOac1j7Syc-2S2PA6RW1LvQ33392Fj3Nfr2Mdg4pFj32dEqjd0XJZYPbFNEjnRO105RisL-QnZ2GOCxYXFhOdN54itsQr2mf1kPADcWNzd_o8aerxY4LFouN8yZYfPmEHAx2RP_0bh6RL-_efj49ry4-nr0_PbmonFT1XA2O6VZ14JzWHedC10IqLpmVkg-6904NGsQgXOObMmVRrAM-WOc6IbtOHJHjfe42p6vF42ymgM6Po40-LWiYAiaVKrn_R5tWNxykbgr64i_0Mi05lofsqPLlTaugUGxPuZwQsx_MNofJ5mvDwOyqNftqTanW7Ko1snie3yUv3eT73477LgvA9wCWVVz7_MfV_0y9BVSdsWs</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Nawata, C. 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Michele ; Walsh, Patrick J. ; Wood, Chris M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-fc1987b0cc99b22395347241a442f9dec7f903f3c6e603f4decac02faccb34bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acid-Base Equilibrium - drug effects</topic><topic>Acid-Base Equilibrium - physiology</topic><topic>Acidosis</topic><topic>Ammonia</topic><topic>Ammonia - blood</topic><topic>Ammonium Chloride - administration & dosage</topic><topic>Ammonium Chloride - adverse effects</topic><topic>Analysis of Variance</topic><topic>Animal Physiology</topic><topic>Animals</topic><topic>Bicarbonates - administration & dosage</topic><topic>Bicarbonates - adverse effects</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>DNA Primers - genetics</topic><topic>Elasmobranchii</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Glycoproteins</topic><topic>Human Physiology</topic><topic>Hydrochloric Acid</topic><topic>Life Sciences</topic><topic>Marine</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Metabolism</topic><topic>Nitrogen</topic><topic>Nitrogen - metabolism</topic><topic>Original Paper</topic><topic>Plasma</topic><topic>Polymerase Chain Reaction</topic><topic>Sodium Chloride</topic><topic>Spectrophotometry, Atomic</topic><topic>Squalus acanthias</topic><topic>Squalus acanthias - metabolism</topic><topic>Squalus acanthias - physiology</topic><topic>Urea</topic><topic>Urea - metabolism</topic><topic>Zoology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nawata, C. Michele</creatorcontrib><creatorcontrib>Walsh, Patrick J.</creatorcontrib><creatorcontrib>Wood, Chris M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nawata, C. Michele</au><au>Walsh, Patrick J.</au><au>Wood, Chris M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitrogen metabolism, acid–base regulation, and molecular responses to ammonia and acid infusions in the spiny dogfish shark (Squalus acanthias)</atitle><jtitle>Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology</jtitle><stitle>J Comp Physiol B</stitle><addtitle>J Comp Physiol B</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>185</volume><issue>5</issue><spage>511</spage><epage>525</epage><pages>511-525</pages><issn>0174-1578</issn><eissn>1432-136X</eissn><abstract>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.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25794843</pmid><doi>10.1007/s00360-015-0898-4</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0174-1578 |
ispartof | Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 2015-07, Vol.185 (5), p.511-525 |
issn | 0174-1578 1432-136X |
language | eng |
recordid | cdi_proquest_miscellaneous_1701477953 |
source | Springer Nature |
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) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T14%3A20%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nitrogen%20metabolism,%20acid%E2%80%93base%20regulation,%20and%20molecular%20responses%20to%20ammonia%20and%20acid%20infusions%20in%20the%20spiny%20dogfish%20shark%20(Squalus%20acanthias)&rft.jtitle=Journal%20of%20comparative%20physiology.%20B,%20Biochemical,%20systemic,%20and%20environmental%20physiology&rft.au=Nawata,%20C.%20Michele&rft.date=2015-07-01&rft.volume=185&rft.issue=5&rft.spage=511&rft.epage=525&rft.pages=511-525&rft.issn=0174-1578&rft.eissn=1432-136X&rft_id=info:doi/10.1007/s00360-015-0898-4&rft_dat=%3Cproquest_cross%3E1689620496%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-fc1987b0cc99b22395347241a442f9dec7f903f3c6e603f4decac02faccb34bb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1688436870&rft_id=info:pmid/25794843&rfr_iscdi=true |