ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation
The work was performed to establish which of the major ATP-consuming processes is the most important for surviving of hepatocytes of female lampreys on the course of prespawning starvation. The requirements of protein synthesis and Na+-K+-ATPase for ATP in the cells were monitored by the changes in...
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Veröffentlicht in: | Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 2016-11, Vol.201, p.95-100 |
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description | The work was performed to establish which of the major ATP-consuming processes is the most important for surviving of hepatocytes of female lampreys on the course of prespawning starvation. The requirements of protein synthesis and Na+-K+-ATPase for ATP in the cells were monitored by the changes in mitochondrial membrane potential (MMP) in the presence of corresponding inhibitors from the peak of metabolic depression (January–February) to the time of recovery from it (March–April) and spawning (May). Integrity of lamprey liver cells was estimated by catalytic activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in blood plasma. In January–February, the share of ATP necessary for protein synthesis was 20–22%, whereas before spawning it decreased to 8–11%. Functioning of Na+-K+-pump required 22% of cellular ATP at the peak of metabolic depression, but 38% and 62% of ATP in March–April and May, respectively. Progression of prespawning period was accompanied by 3.75- and 1.6-fold rise of ALT and AST activities in blood plasma, respectively, whereas de Ritis coefficient decreased from 2.51±0.34 to 0.81±0.08, what indicates severe damage of hepatocyte membranes. Thus, the adaptive strategy of lamprey hepatocytes to develop metabolic depression under conditions of energy limitation is the selective production of proteins necessary for spawning, most probably vitellogenins. As spawning approaches, the maintenance of transmembrane ion gradients, membrane potential and cell volume to prevent premature cell death becomes the priority cell function. |
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The requirements of protein synthesis and Na+-K+-ATPase for ATP in the cells were monitored by the changes in mitochondrial membrane potential (MMP) in the presence of corresponding inhibitors from the peak of metabolic depression (January–February) to the time of recovery from it (March–April) and spawning (May). Integrity of lamprey liver cells was estimated by catalytic activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in blood plasma. In January–February, the share of ATP necessary for protein synthesis was 20–22%, whereas before spawning it decreased to 8–11%. Functioning of Na+-K+-pump required 22% of cellular ATP at the peak of metabolic depression, but 38% and 62% of ATP in March–April and May, respectively. Progression of prespawning period was accompanied by 3.75- and 1.6-fold rise of ALT and AST activities in blood plasma, respectively, whereas de Ritis coefficient decreased from 2.51±0.34 to 0.81±0.08, what indicates severe damage of hepatocyte membranes. Thus, the adaptive strategy of lamprey hepatocytes to develop metabolic depression under conditions of energy limitation is the selective production of proteins necessary for spawning, most probably vitellogenins. As spawning approaches, the maintenance of transmembrane ion gradients, membrane potential and cell volume to prevent premature cell death becomes the priority cell function.</description><identifier>ISSN: 1095-6433</identifier><identifier>EISSN: 1531-4332</identifier><identifier>DOI: 10.1016/j.cbpa.2016.07.002</identifier><identifier>PMID: 27399971</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenosine Triphosphate - metabolism ; Alanine Transaminase - blood ; Aminotransferases ; Animals ; Aspartate Aminotransferases - blood ; Coumaric Acids - pharmacology ; Cycloheximide - pharmacology ; Female ; Gluconeogenesis - drug effects ; Hepatocytes ; Hepatocytes - drug effects ; Hepatocytes - metabolism ; Lamprey ; Lampreys - metabolism ; Lampreys - physiology ; Membrane Potential, Mitochondrial - drug effects ; Metabolic depression ; Mitochondria, Liver - metabolism ; Mitochondrial membrane potential ; Na+-K+-pump ; Oviposition - physiology ; Phenylpyruvic Acids - pharmacology ; Prespawning starvation ; Protein synthesis ; Protein Synthesis Inhibitors - pharmacology ; Rivers ; Seasons ; Sodium-Potassium-Exchanging ATPase - metabolism ; Starvation - metabolism</subject><ispartof>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 2016-11, Vol.201, p.95-100</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-f58538949d0db2803b2416b07e1bf75da4710b9e2dff6dd1b06328055045283c3</citedby><cites>FETCH-LOGICAL-c356t-f58538949d0db2803b2416b07e1bf75da4710b9e2dff6dd1b06328055045283c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cbpa.2016.07.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27399971$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Agalakova, Natalia I.</creatorcontrib><creatorcontrib>Brailovskaya, Irina V.</creatorcontrib><creatorcontrib>Konovalova, Svetlana A.</creatorcontrib><creatorcontrib>Korotkov, Sergei M.</creatorcontrib><creatorcontrib>Lavrova, Elena A.</creatorcontrib><creatorcontrib>Nikiforov, Anatolii A.</creatorcontrib><title>ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation</title><title>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</title><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><description>The work was performed to establish which of the major ATP-consuming processes is the most important for surviving of hepatocytes of female lampreys on the course of prespawning starvation. The requirements of protein synthesis and Na+-K+-ATPase for ATP in the cells were monitored by the changes in mitochondrial membrane potential (MMP) in the presence of corresponding inhibitors from the peak of metabolic depression (January–February) to the time of recovery from it (March–April) and spawning (May). Integrity of lamprey liver cells was estimated by catalytic activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in blood plasma. In January–February, the share of ATP necessary for protein synthesis was 20–22%, whereas before spawning it decreased to 8–11%. Functioning of Na+-K+-pump required 22% of cellular ATP at the peak of metabolic depression, but 38% and 62% of ATP in March–April and May, respectively. Progression of prespawning period was accompanied by 3.75- and 1.6-fold rise of ALT and AST activities in blood plasma, respectively, whereas de Ritis coefficient decreased from 2.51±0.34 to 0.81±0.08, what indicates severe damage of hepatocyte membranes. Thus, the adaptive strategy of lamprey hepatocytes to develop metabolic depression under conditions of energy limitation is the selective production of proteins necessary for spawning, most probably vitellogenins. As spawning approaches, the maintenance of transmembrane ion gradients, membrane potential and cell volume to prevent premature cell death becomes the priority cell function.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Alanine Transaminase - blood</subject><subject>Aminotransferases</subject><subject>Animals</subject><subject>Aspartate Aminotransferases - blood</subject><subject>Coumaric Acids - pharmacology</subject><subject>Cycloheximide - pharmacology</subject><subject>Female</subject><subject>Gluconeogenesis - drug effects</subject><subject>Hepatocytes</subject><subject>Hepatocytes - drug effects</subject><subject>Hepatocytes - metabolism</subject><subject>Lamprey</subject><subject>Lampreys - metabolism</subject><subject>Lampreys - physiology</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Metabolic depression</subject><subject>Mitochondria, Liver - metabolism</subject><subject>Mitochondrial membrane potential</subject><subject>Na+-K+-pump</subject><subject>Oviposition - physiology</subject><subject>Phenylpyruvic Acids - pharmacology</subject><subject>Prespawning starvation</subject><subject>Protein synthesis</subject><subject>Protein Synthesis Inhibitors - pharmacology</subject><subject>Rivers</subject><subject>Seasons</subject><subject>Sodium-Potassium-Exchanging ATPase - metabolism</subject><subject>Starvation - metabolism</subject><issn>1095-6433</issn><issn>1531-4332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEuP1DAQhC0EYpeFP8AB-cglwc88JC6r1fKQRoLDcrYcu8N6lMTBdgbNv6ejWTjSl-6WviqpipC3nNWc8ebDsXbDamuBd83amjHxjFxzLXmlpBTP8Wa9rhp8rsirnI8MR3H1klyJVvZ93_JrUm4fvlcuLnmbw_KTrik6yBkyDQt9hNWW6M4F3zjSFE6Q6GTnNcGZHnBDSZaO03YKtoQpILXQ8gjUxS1l2DWI5tX-XnbvXGw6IRiX1-TFaKcMb572Dfnx6f7h7kt1-Pb5693toXJSN6Uadadl16veMz-IjslBKN4MrAU-jK32VrWcDT0IP46N93xgjURMa6a06KSTN-T9xRdj_dogFzOH7GCa7AJxy4Z3QmmlUYGouKAuxZwTjGZNYbbpbDgze9vmaPa2zd62Ya3BtlH07sl_G2bw_yR_60Xg4wUATHkKkEx2ARYHPiRwxfgY_uf_B8bHkiU</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Agalakova, Natalia I.</creator><creator>Brailovskaya, Irina V.</creator><creator>Konovalova, Svetlana A.</creator><creator>Korotkov, Sergei M.</creator><creator>Lavrova, Elena A.</creator><creator>Nikiforov, Anatolii A.</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>201611</creationdate><title>ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation</title><author>Agalakova, Natalia I. ; Brailovskaya, Irina V. ; Konovalova, Svetlana A. ; Korotkov, Sergei M. ; Lavrova, Elena A. ; Nikiforov, Anatolii A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-f58538949d0db2803b2416b07e1bf75da4710b9e2dff6dd1b06328055045283c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Alanine Transaminase - blood</topic><topic>Aminotransferases</topic><topic>Animals</topic><topic>Aspartate Aminotransferases - blood</topic><topic>Coumaric Acids - pharmacology</topic><topic>Cycloheximide - pharmacology</topic><topic>Female</topic><topic>Gluconeogenesis - drug effects</topic><topic>Hepatocytes</topic><topic>Hepatocytes - drug effects</topic><topic>Hepatocytes - metabolism</topic><topic>Lamprey</topic><topic>Lampreys - metabolism</topic><topic>Lampreys - physiology</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Metabolic depression</topic><topic>Mitochondria, Liver - metabolism</topic><topic>Mitochondrial membrane potential</topic><topic>Na+-K+-pump</topic><topic>Oviposition - physiology</topic><topic>Phenylpyruvic Acids - pharmacology</topic><topic>Prespawning starvation</topic><topic>Protein synthesis</topic><topic>Protein Synthesis Inhibitors - pharmacology</topic><topic>Rivers</topic><topic>Seasons</topic><topic>Sodium-Potassium-Exchanging ATPase - metabolism</topic><topic>Starvation - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agalakova, Natalia I.</creatorcontrib><creatorcontrib>Brailovskaya, Irina V.</creatorcontrib><creatorcontrib>Konovalova, Svetlana A.</creatorcontrib><creatorcontrib>Korotkov, Sergei M.</creatorcontrib><creatorcontrib>Lavrova, Elena A.</creatorcontrib><creatorcontrib>Nikiforov, Anatolii A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agalakova, Natalia I.</au><au>Brailovskaya, Irina V.</au><au>Konovalova, Svetlana A.</au><au>Korotkov, Sergei M.</au><au>Lavrova, Elena A.</au><au>Nikiforov, Anatolii A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation</atitle><jtitle>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><date>2016-11</date><risdate>2016</risdate><volume>201</volume><spage>95</spage><epage>100</epage><pages>95-100</pages><issn>1095-6433</issn><eissn>1531-4332</eissn><abstract>The work was performed to establish which of the major ATP-consuming processes is the most important for surviving of hepatocytes of female lampreys on the course of prespawning starvation. The requirements of protein synthesis and Na+-K+-ATPase for ATP in the cells were monitored by the changes in mitochondrial membrane potential (MMP) in the presence of corresponding inhibitors from the peak of metabolic depression (January–February) to the time of recovery from it (March–April) and spawning (May). Integrity of lamprey liver cells was estimated by catalytic activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in blood plasma. In January–February, the share of ATP necessary for protein synthesis was 20–22%, whereas before spawning it decreased to 8–11%. Functioning of Na+-K+-pump required 22% of cellular ATP at the peak of metabolic depression, but 38% and 62% of ATP in March–April and May, respectively. Progression of prespawning period was accompanied by 3.75- and 1.6-fold rise of ALT and AST activities in blood plasma, respectively, whereas de Ritis coefficient decreased from 2.51±0.34 to 0.81±0.08, what indicates severe damage of hepatocyte membranes. Thus, the adaptive strategy of lamprey hepatocytes to develop metabolic depression under conditions of energy limitation is the selective production of proteins necessary for spawning, most probably vitellogenins. As spawning approaches, the maintenance of transmembrane ion gradients, membrane potential and cell volume to prevent premature cell death becomes the priority cell function.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27399971</pmid><doi>10.1016/j.cbpa.2016.07.002</doi><tpages>6</tpages></addata></record> |
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subjects | Adenosine Triphosphate - metabolism Alanine Transaminase - blood Aminotransferases Animals Aspartate Aminotransferases - blood Coumaric Acids - pharmacology Cycloheximide - pharmacology Female Gluconeogenesis - drug effects Hepatocytes Hepatocytes - drug effects Hepatocytes - metabolism Lamprey Lampreys - metabolism Lampreys - physiology Membrane Potential, Mitochondrial - drug effects Metabolic depression Mitochondria, Liver - metabolism Mitochondrial membrane potential Na+-K+-pump Oviposition - physiology Phenylpyruvic Acids - pharmacology Prespawning starvation Protein synthesis Protein Synthesis Inhibitors - pharmacology Rivers Seasons Sodium-Potassium-Exchanging ATPase - metabolism Starvation - metabolism |
title | ATP-consuming processes in hepatocytes of river lamprey Lampetra fluviatilis on the course of prespawning starvation |
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