The crab-eating frog, Rana cancrivora, up-regulates hepatic carbamoyl phosphate synthetase I activity and tissue osmolyte levels in response to increased salinity
The crab‐eating frog Rana cancrivora is one of only a handful of amphibians worldwide that tolerate saline waters. They typically inhabit brackish water of mangrove forests of Southeast Asia, but live happily in freshwater and can be acclimated to 75% seawater (25 ppt) or higher. We report here that...
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Veröffentlicht in: | Journal of experimental zoology. Part A, Comparative experimental biology Comparative experimental biology, 2004-07, Vol.301A (7), p.559-568 |
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description | The crab‐eating frog Rana cancrivora is one of only a handful of amphibians worldwide that tolerate saline waters. They typically inhabit brackish water of mangrove forests of Southeast Asia, but live happily in freshwater and can be acclimated to 75% seawater (25 ppt) or higher. We report here that after transfer of juvenile R. cancrivora from freshwater (1 ppt) to brackish water (10 →20 or 20 →25 ppt; 4–8 d) there was a significant increase in the specific activity of the key hepatic ornithine urea cycle enzyme (OUC), carbamoyl phosphate synthetase I (CPSase I). At 20 ppt, plasma, liver and muscle urea levels increased by 22‐, 21‐, and 11‐fold, respectively. As well, muscle total amino acid levels were significantly elevated by 6‐fold, with the largest changes occurring in glycine and β‐alanine levels. In liver, taurine levels were 5‐fold higher in frogs acclimated to 20 ppt. There were no significant changes in urea or ammonia excretion rates to the environment. As well, the rate of urea influx (Jinurea) and efflux (Jouturea) across the ventral pelvic skin did not differ between frogs acclimated to 1 versus 20 ppt. Taken together, these findings suggest that acclimation to saline water involves the up‐regulation of hepatic urea synthesis, which in turn contributes to the dramatic rise in tissue urea levels. The lack of change in urea excretion rates, despite the large increase in tissue‐to‐water gradients further indicates that mechanisms must be in place to prevent excessive loss of urea in saline waters, but these mechanisms do not include cutaneous urea uptake. Also, amino acid accumulation may contribute to an overall rise in the osmolarity of the muscle tissue, but relative to urea, the contribution is small. J. Exp. Zool. 301A:559–568, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jez.a.54 |
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They typically inhabit brackish water of mangrove forests of Southeast Asia, but live happily in freshwater and can be acclimated to 75% seawater (25 ppt) or higher. We report here that after transfer of juvenile R. cancrivora from freshwater (1 ppt) to brackish water (10 →20 or 20 →25 ppt; 4–8 d) there was a significant increase in the specific activity of the key hepatic ornithine urea cycle enzyme (OUC), carbamoyl phosphate synthetase I (CPSase I). At 20 ppt, plasma, liver and muscle urea levels increased by 22‐, 21‐, and 11‐fold, respectively. As well, muscle total amino acid levels were significantly elevated by 6‐fold, with the largest changes occurring in glycine and β‐alanine levels. In liver, taurine levels were 5‐fold higher in frogs acclimated to 20 ppt. There were no significant changes in urea or ammonia excretion rates to the environment. As well, the rate of urea influx (Jinurea) and efflux (Jouturea) across the ventral pelvic skin did not differ between frogs acclimated to 1 versus 20 ppt. Taken together, these findings suggest that acclimation to saline water involves the up‐regulation of hepatic urea synthesis, which in turn contributes to the dramatic rise in tissue urea levels. The lack of change in urea excretion rates, despite the large increase in tissue‐to‐water gradients further indicates that mechanisms must be in place to prevent excessive loss of urea in saline waters, but these mechanisms do not include cutaneous urea uptake. Also, amino acid accumulation may contribute to an overall rise in the osmolarity of the muscle tissue, but relative to urea, the contribution is small. J. Exp. 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Part A, Comparative experimental biology</title><addtitle>J. Exp. Zool</addtitle><description>The crab‐eating frog Rana cancrivora is one of only a handful of amphibians worldwide that tolerate saline waters. They typically inhabit brackish water of mangrove forests of Southeast Asia, but live happily in freshwater and can be acclimated to 75% seawater (25 ppt) or higher. We report here that after transfer of juvenile R. cancrivora from freshwater (1 ppt) to brackish water (10 →20 or 20 →25 ppt; 4–8 d) there was a significant increase in the specific activity of the key hepatic ornithine urea cycle enzyme (OUC), carbamoyl phosphate synthetase I (CPSase I). At 20 ppt, plasma, liver and muscle urea levels increased by 22‐, 21‐, and 11‐fold, respectively. As well, muscle total amino acid levels were significantly elevated by 6‐fold, with the largest changes occurring in glycine and β‐alanine levels. In liver, taurine levels were 5‐fold higher in frogs acclimated to 20 ppt. There were no significant changes in urea or ammonia excretion rates to the environment. As well, the rate of urea influx (Jinurea) and efflux (Jouturea) across the ventral pelvic skin did not differ between frogs acclimated to 1 versus 20 ppt. Taken together, these findings suggest that acclimation to saline water involves the up‐regulation of hepatic urea synthesis, which in turn contributes to the dramatic rise in tissue urea levels. The lack of change in urea excretion rates, despite the large increase in tissue‐to‐water gradients further indicates that mechanisms must be in place to prevent excessive loss of urea in saline waters, but these mechanisms do not include cutaneous urea uptake. Also, amino acid accumulation may contribute to an overall rise in the osmolarity of the muscle tissue, but relative to urea, the contribution is small. J. Exp. Zool. 301A:559–568, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Amino Acids - metabolism</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological Transport</subject><subject>Brackish</subject><subject>Carbamoyl-Phosphate Synthase (Ammonia) - biosynthesis</subject><subject>Enzyme Induction</subject><subject>Fresh Water</subject><subject>Freshwater</subject><subject>Liver - enzymology</subject><subject>Liver - metabolism</subject><subject>Marine</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Rana cancrivora</subject><subject>Ranidae - metabolism</subject><subject>Ranidae - physiology</subject><subject>Seawater</subject><subject>Sodium Chloride - metabolism</subject><subject>Taurine - metabolism</subject><subject>Urea - metabolism</subject><subject>Water-Electrolyte Balance - physiology</subject><issn>1548-8969</issn><issn>0022-104X</issn><issn>1552-499X</issn><issn>1097-010X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ctu1DAUBuAIgegFJJ4AeYWQaAZfYidZVlUpRaVI1SAQG8txTiYuThxsZ0p4HJ4UlxnBCuGNbfn7_4VPlj0jeEUwpq9v4cdKrXjxIDsknNO8qOvPD-_PRZVXtagPsqMQbpMUmBePswPCKa0rIQ6zn-sekPaqyUFFM25Q593mBN2oUSGtRu3N1nl1guYp97CZrYoQUA9TwjoB36jBLRZNvQtTnx5RWMbYQ1QB0CVSOpqtiQtSY4uiCWEG5MLg7JKkhS3YgMyIPITJjSkRXbpqDyndoqCsGVP4SfaoUzbA0_1-nH18c74-e5tffbi4PDu9ynXBcZEzphltMa9LXlaiZEXdMsZKrXHHMG10UTY17hQIXJGuwxgUEZw2QlQMcEtrdpy92PVO3n2bIUQ5mKDBWjWCm4MUaXFa0f9CUla0LHmV4Msd1N6F4KGTkzeD8oskWN4PTqbBSSV5kejzfefcDND-hftJJfBqB-6MheWfRfLd-ZffdflOmxDh-x-t_FeZvqbk8tP1hVxf31BM1u8lYb8APky0KQ</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Wright, Patricia</creator><creator>Anderson, Paul</creator><creator>Weng, Lei</creator><creator>Frick, Natasha</creator><creator>Wong, Wei Peng</creator><creator>IP, Yuen Kwong</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>20040701</creationdate><title>The crab-eating frog, Rana cancrivora, up-regulates hepatic carbamoyl phosphate synthetase I activity and tissue osmolyte levels in response to increased salinity</title><author>Wright, Patricia ; Anderson, Paul ; Weng, Lei ; Frick, Natasha ; Wong, Wei Peng ; IP, Yuen Kwong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4504-33c32d059757867349d3337cc0f302bc47b90fae6081ff00ea1652b6683e0d293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acids - metabolism</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biological Transport</topic><topic>Brackish</topic><topic>Carbamoyl-Phosphate Synthase (Ammonia) - biosynthesis</topic><topic>Enzyme Induction</topic><topic>Fresh Water</topic><topic>Freshwater</topic><topic>Liver - enzymology</topic><topic>Liver - metabolism</topic><topic>Marine</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Rana cancrivora</topic><topic>Ranidae - metabolism</topic><topic>Ranidae - physiology</topic><topic>Seawater</topic><topic>Sodium Chloride - metabolism</topic><topic>Taurine - metabolism</topic><topic>Urea - metabolism</topic><topic>Water-Electrolyte Balance - physiology</topic><toplevel>online_resources</toplevel><creatorcontrib>Wright, Patricia</creatorcontrib><creatorcontrib>Anderson, Paul</creatorcontrib><creatorcontrib>Weng, Lei</creatorcontrib><creatorcontrib>Frick, Natasha</creatorcontrib><creatorcontrib>Wong, Wei Peng</creatorcontrib><creatorcontrib>IP, Yuen Kwong</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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><collection>MEDLINE - Academic</collection><jtitle>Journal of experimental zoology. Part A, Comparative experimental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wright, Patricia</au><au>Anderson, Paul</au><au>Weng, Lei</au><au>Frick, Natasha</au><au>Wong, Wei Peng</au><au>IP, Yuen Kwong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The crab-eating frog, Rana cancrivora, up-regulates hepatic carbamoyl phosphate synthetase I activity and tissue osmolyte levels in response to increased salinity</atitle><jtitle>Journal of experimental zoology. Part A, Comparative experimental biology</jtitle><addtitle>J. Exp. Zool</addtitle><date>2004-07-01</date><risdate>2004</risdate><volume>301A</volume><issue>7</issue><spage>559</spage><epage>568</epage><pages>559-568</pages><issn>1548-8969</issn><issn>0022-104X</issn><eissn>1552-499X</eissn><eissn>1097-010X</eissn><abstract>The crab‐eating frog Rana cancrivora is one of only a handful of amphibians worldwide that tolerate saline waters. They typically inhabit brackish water of mangrove forests of Southeast Asia, but live happily in freshwater and can be acclimated to 75% seawater (25 ppt) or higher. We report here that after transfer of juvenile R. cancrivora from freshwater (1 ppt) to brackish water (10 →20 or 20 →25 ppt; 4–8 d) there was a significant increase in the specific activity of the key hepatic ornithine urea cycle enzyme (OUC), carbamoyl phosphate synthetase I (CPSase I). At 20 ppt, plasma, liver and muscle urea levels increased by 22‐, 21‐, and 11‐fold, respectively. As well, muscle total amino acid levels were significantly elevated by 6‐fold, with the largest changes occurring in glycine and β‐alanine levels. In liver, taurine levels were 5‐fold higher in frogs acclimated to 20 ppt. There were no significant changes in urea or ammonia excretion rates to the environment. As well, the rate of urea influx (Jinurea) and efflux (Jouturea) across the ventral pelvic skin did not differ between frogs acclimated to 1 versus 20 ppt. Taken together, these findings suggest that acclimation to saline water involves the up‐regulation of hepatic urea synthesis, which in turn contributes to the dramatic rise in tissue urea levels. The lack of change in urea excretion rates, despite the large increase in tissue‐to‐water gradients further indicates that mechanisms must be in place to prevent excessive loss of urea in saline waters, but these mechanisms do not include cutaneous urea uptake. Also, amino acid accumulation may contribute to an overall rise in the osmolarity of the muscle tissue, but relative to urea, the contribution is small. J. Exp. Zool. 301A:559–568, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15229866</pmid><doi>10.1002/jez.a.54</doi><tpages>10</tpages></addata></record> |
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subjects | Amino Acids - metabolism Analysis of Variance Animals Biological Transport Brackish Carbamoyl-Phosphate Synthase (Ammonia) - biosynthesis Enzyme Induction Fresh Water Freshwater Liver - enzymology Liver - metabolism Marine Muscle, Skeletal - metabolism Rana cancrivora Ranidae - metabolism Ranidae - physiology Seawater Sodium Chloride - metabolism Taurine - metabolism Urea - metabolism Water-Electrolyte Balance - physiology |
title | The crab-eating frog, Rana cancrivora, up-regulates hepatic carbamoyl phosphate synthetase I activity and tissue osmolyte levels in response to increased salinity |
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