Identification of the NA+/K+-ATPase α-Isoforms in Six Species of Poison Dart Frogs and their Sensitivity to Cardiotonic Steroids
Cardiotonic steroids (CTS) are a group of compounds known to be toxic due to their ability to inhibit the Na + /K + -ATPase (NKA), which is essential to maintain the balance of ions in animal cells. An evolutionary strategy of molecular adaptation to avoid self-intoxication acquired by CTS defended...
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creator | Medina-Ortiz, Katherine Navia, Felipe Mosquera-Gil, Claudia Sánchez, Adalberto Sterling, Gonzalo Fierro, Leonardo Castaño, Santiago |
description | Cardiotonic steroids (CTS) are a group of compounds known to be toxic due to their ability to inhibit the Na
+
/K
+
-ATPase (NKA), which is essential to maintain the balance of ions in animal cells. An evolutionary strategy of molecular adaptation to avoid self-intoxication acquired by CTS defended organisms and their predators is the structural modification of their NKA where specific amino acid substitutions confer resistant phenotypes. Several lineages of poison dart frogs (Dendrobatidae) are well known to sequester a wide variety of lipophilic alkaloids from their arthropod diet, however there is no evidence of CTS-sequestration or dietary exposure. Interestingly this study identified the presence of α-NKA isoforms (α
1
and α
2
) with amino acid substitutions indicative of CTS-resistant phenotypes in skeletal muscle transcriptomes obtained from six species of dendrobatids:
Phyllobates aurotaenia
,
Oophaga anchicayensis
,
Epipedobates boulengeri
,
Andinobates bombetes
,
Andinobates minutus,
and
Leucostethus brachistriatus,
collected in the Valle del Cauca (Colombia).
P. aurotaenia
,
A. minutus
, and
E. boulengeri
presented two variants for α
1
-NKA, with one of them having these substitutions. In contrast,
O. anchicayensis
and
A. bombetes
have only one α
1
-NKA isoform with an amino acid sequence indicative of CTS susceptibility and an α
2
-NKA with one substitution that could confer a reduced affinity for CTS. The α
1
and α
2
isoforms of
L. brachistriatus
do not contain substitutions imparting CTS resistance. Our findings indicate that poison dart frogs express α-NKA isoforms with different affinities for CTS and the pattern of this expression might be influenced by factors related to evolutionary, physiological, ecological, and geographical burdens. |
doi_str_mv | 10.1007/s10886-023-01404-7 |
format | Article |
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+
/K
+
-ATPase (NKA), which is essential to maintain the balance of ions in animal cells. An evolutionary strategy of molecular adaptation to avoid self-intoxication acquired by CTS defended organisms and their predators is the structural modification of their NKA where specific amino acid substitutions confer resistant phenotypes. Several lineages of poison dart frogs (Dendrobatidae) are well known to sequester a wide variety of lipophilic alkaloids from their arthropod diet, however there is no evidence of CTS-sequestration or dietary exposure. Interestingly this study identified the presence of α-NKA isoforms (α
1
and α
2
) with amino acid substitutions indicative of CTS-resistant phenotypes in skeletal muscle transcriptomes obtained from six species of dendrobatids:
Phyllobates aurotaenia
,
Oophaga anchicayensis
,
Epipedobates boulengeri
,
Andinobates bombetes
,
Andinobates minutus,
and
Leucostethus brachistriatus,
collected in the Valle del Cauca (Colombia).
P. aurotaenia
,
A. minutus
, and
E. boulengeri
presented two variants for α
1
-NKA, with one of them having these substitutions. In contrast,
O. anchicayensis
and
A. bombetes
have only one α
1
-NKA isoform with an amino acid sequence indicative of CTS susceptibility and an α
2
-NKA with one substitution that could confer a reduced affinity for CTS. The α
1
and α
2
isoforms of
L. brachistriatus
do not contain substitutions imparting CTS resistance. Our findings indicate that poison dart frogs express α-NKA isoforms with different affinities for CTS and the pattern of this expression might be influenced by factors related to evolutionary, physiological, ecological, and geographical burdens.</description><identifier>ISSN: 0098-0331</identifier><identifier>EISSN: 1573-1561</identifier><identifier>DOI: 10.1007/s10886-023-01404-7</identifier><identifier>PMID: 36877397</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Acid resistance ; Affinity ; Agriculture ; amino acid sequences ; Amino acid substitution ; Amino acids ; Amphibians ; Andinobates ; Animals ; arthropods ; Biochemistry ; Biological Microscopy ; Biomedical and Life Sciences ; Cardiac Glycosides ; Colombia ; diet ; dietary exposure ; Ecological effects ; Ecology ; Entomology ; Enzyme inhibitors ; Epipedobates ; Frogs ; Gene expression ; Intoxication ; Ions - metabolism ; Isoenzymes - genetics ; Isoenzymes - metabolism ; Isoforms ; Life Sciences ; Lipophilic ; lipophilicity ; Na+/K+-exchanging ATPase ; Oophaga ; Phenotypes ; Phyllobates ; Phyllobates aurotaenia ; Physiological effects ; Poisons ; Predators ; Reptiles & amphibians ; Skeletal muscle ; Sodium - metabolism ; sodium-potassium-exchanging ATPase ; Sodium-Potassium-Exchanging ATPase - genetics ; Sodium-Potassium-Exchanging ATPase - metabolism ; Steroid hormones ; Steroids ; toxicity ; Toxins ; transcriptome ; Transcriptomes</subject><ispartof>Journal of chemical ecology, 2023-04, Vol.49 (3-4), p.116-132</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-aedd587dc7d6cb3c3eb46a91b6aeb9363a98f6880393f12b1cf618b47fd857fc3</citedby><cites>FETCH-LOGICAL-c508t-aedd587dc7d6cb3c3eb46a91b6aeb9363a98f6880393f12b1cf618b47fd857fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10886-023-01404-7$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10886-023-01404-7$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27902,27903,41466,42535,51296</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36877397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Medina-Ortiz, Katherine</creatorcontrib><creatorcontrib>Navia, Felipe</creatorcontrib><creatorcontrib>Mosquera-Gil, Claudia</creatorcontrib><creatorcontrib>Sánchez, Adalberto</creatorcontrib><creatorcontrib>Sterling, Gonzalo</creatorcontrib><creatorcontrib>Fierro, Leonardo</creatorcontrib><creatorcontrib>Castaño, Santiago</creatorcontrib><title>Identification of the NA+/K+-ATPase α-Isoforms in Six Species of Poison Dart Frogs and their Sensitivity to Cardiotonic Steroids</title><title>Journal of chemical ecology</title><addtitle>J Chem Ecol</addtitle><addtitle>J Chem Ecol</addtitle><description>Cardiotonic steroids (CTS) are a group of compounds known to be toxic due to their ability to inhibit the Na
+
/K
+
-ATPase (NKA), which is essential to maintain the balance of ions in animal cells. An evolutionary strategy of molecular adaptation to avoid self-intoxication acquired by CTS defended organisms and their predators is the structural modification of their NKA where specific amino acid substitutions confer resistant phenotypes. Several lineages of poison dart frogs (Dendrobatidae) are well known to sequester a wide variety of lipophilic alkaloids from their arthropod diet, however there is no evidence of CTS-sequestration or dietary exposure. Interestingly this study identified the presence of α-NKA isoforms (α
1
and α
2
) with amino acid substitutions indicative of CTS-resistant phenotypes in skeletal muscle transcriptomes obtained from six species of dendrobatids:
Phyllobates aurotaenia
,
Oophaga anchicayensis
,
Epipedobates boulengeri
,
Andinobates bombetes
,
Andinobates minutus,
and
Leucostethus brachistriatus,
collected in the Valle del Cauca (Colombia).
P. aurotaenia
,
A. minutus
, and
E. boulengeri
presented two variants for α
1
-NKA, with one of them having these substitutions. In contrast,
O. anchicayensis
and
A. bombetes
have only one α
1
-NKA isoform with an amino acid sequence indicative of CTS susceptibility and an α
2
-NKA with one substitution that could confer a reduced affinity for CTS. The α
1
and α
2
isoforms of
L. brachistriatus
do not contain substitutions imparting CTS resistance. Our findings indicate that poison dart frogs express α-NKA isoforms with different affinities for CTS and the pattern of this expression might be influenced by factors related to evolutionary, physiological, ecological, and geographical burdens.</description><subject>Acid resistance</subject><subject>Affinity</subject><subject>Agriculture</subject><subject>amino acid sequences</subject><subject>Amino acid substitution</subject><subject>Amino acids</subject><subject>Amphibians</subject><subject>Andinobates</subject><subject>Animals</subject><subject>arthropods</subject><subject>Biochemistry</subject><subject>Biological Microscopy</subject><subject>Biomedical and Life Sciences</subject><subject>Cardiac Glycosides</subject><subject>Colombia</subject><subject>diet</subject><subject>dietary exposure</subject><subject>Ecological effects</subject><subject>Ecology</subject><subject>Entomology</subject><subject>Enzyme inhibitors</subject><subject>Epipedobates</subject><subject>Frogs</subject><subject>Gene expression</subject><subject>Intoxication</subject><subject>Ions - metabolism</subject><subject>Isoenzymes - genetics</subject><subject>Isoenzymes - metabolism</subject><subject>Isoforms</subject><subject>Life Sciences</subject><subject>Lipophilic</subject><subject>lipophilicity</subject><subject>Na+/K+-exchanging ATPase</subject><subject>Oophaga</subject><subject>Phenotypes</subject><subject>Phyllobates</subject><subject>Phyllobates aurotaenia</subject><subject>Physiological effects</subject><subject>Poisons</subject><subject>Predators</subject><subject>Reptiles & amphibians</subject><subject>Skeletal muscle</subject><subject>Sodium - metabolism</subject><subject>sodium-potassium-exchanging ATPase</subject><subject>Sodium-Potassium-Exchanging ATPase - genetics</subject><subject>Sodium-Potassium-Exchanging ATPase - metabolism</subject><subject>Steroid hormones</subject><subject>Steroids</subject><subject>toxicity</subject><subject>Toxins</subject><subject>transcriptome</subject><subject>Transcriptomes</subject><issn>0098-0331</issn><issn>1573-1561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFks1uUzEQhS0EoqHwAiyQJTZI1aXj63v9s0JRoBBRQaWUteXra6euEju1nYoueSRehGfCIaX8LGDlxXznjGfmIPSUwEsCwI8zASFYAy1tgHTQNfwempCe04b0jNxHEwApGqCUHKBHOV8CQMtE_xAdUCY4p5JP0Jf5aEPxzhtdfAw4OlwuLP4wPTp-f9RMz890tvjb12aeo4tpnbEPeOE_48XGGm_zjj-LPlfla50KPklxmbEO487FJ7ywIfvir325wSXimU6jjyUGb_Ci2BT9mB-jB06vsn1y-x6iTydvzmfvmtOPb-ez6WljehCl0XYce8FHw0dmBmqoHTqmJRmYtoOkjGopHBMCqKSOtAMxjhExdNyNoufO0EP0au-72Q5rO5o6dtIrtUl-rdONitqrPyvBX6hlvFYECLTAWHV4ceuQ4tXW5qLWPhu7Wulg4zYrSnpKhJSy_y_ackG5bAlrK_r8L_QyblOoq1CtAOhA9B2pVLunTIo5J-vuPk5A7dKg9mlQNQ3qRxoUr6Jnv498J_l5_grQPZBrKSxt-tX7H7bfAb-SwVQ</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Medina-Ortiz, Katherine</creator><creator>Navia, Felipe</creator><creator>Mosquera-Gil, Claudia</creator><creator>Sánchez, Adalberto</creator><creator>Sterling, Gonzalo</creator><creator>Fierro, Leonardo</creator><creator>Castaño, Santiago</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20230401</creationdate><title>Identification of the NA+/K+-ATPase α-Isoforms in Six Species of Poison Dart Frogs and their Sensitivity to Cardiotonic Steroids</title><author>Medina-Ortiz, Katherine ; Navia, Felipe ; Mosquera-Gil, Claudia ; Sánchez, Adalberto ; Sterling, Gonzalo ; Fierro, Leonardo ; Castaño, Santiago</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-aedd587dc7d6cb3c3eb46a91b6aeb9363a98f6880393f12b1cf618b47fd857fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acid resistance</topic><topic>Affinity</topic><topic>Agriculture</topic><topic>amino acid sequences</topic><topic>Amino acid substitution</topic><topic>Amino acids</topic><topic>Amphibians</topic><topic>Andinobates</topic><topic>Animals</topic><topic>arthropods</topic><topic>Biochemistry</topic><topic>Biological Microscopy</topic><topic>Biomedical and Life Sciences</topic><topic>Cardiac Glycosides</topic><topic>Colombia</topic><topic>diet</topic><topic>dietary exposure</topic><topic>Ecological effects</topic><topic>Ecology</topic><topic>Entomology</topic><topic>Enzyme inhibitors</topic><topic>Epipedobates</topic><topic>Frogs</topic><topic>Gene expression</topic><topic>Intoxication</topic><topic>Ions - metabolism</topic><topic>Isoenzymes - genetics</topic><topic>Isoenzymes - metabolism</topic><topic>Isoforms</topic><topic>Life Sciences</topic><topic>Lipophilic</topic><topic>lipophilicity</topic><topic>Na+/K+-exchanging ATPase</topic><topic>Oophaga</topic><topic>Phenotypes</topic><topic>Phyllobates</topic><topic>Phyllobates aurotaenia</topic><topic>Physiological effects</topic><topic>Poisons</topic><topic>Predators</topic><topic>Reptiles & amphibians</topic><topic>Skeletal muscle</topic><topic>Sodium - metabolism</topic><topic>sodium-potassium-exchanging ATPase</topic><topic>Sodium-Potassium-Exchanging ATPase - genetics</topic><topic>Sodium-Potassium-Exchanging ATPase - metabolism</topic><topic>Steroid hormones</topic><topic>Steroids</topic><topic>toxicity</topic><topic>Toxins</topic><topic>transcriptome</topic><topic>Transcriptomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Medina-Ortiz, Katherine</creatorcontrib><creatorcontrib>Navia, Felipe</creatorcontrib><creatorcontrib>Mosquera-Gil, Claudia</creatorcontrib><creatorcontrib>Sánchez, Adalberto</creatorcontrib><creatorcontrib>Sterling, Gonzalo</creatorcontrib><creatorcontrib>Fierro, Leonardo</creatorcontrib><creatorcontrib>Castaño, Santiago</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of chemical ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Medina-Ortiz, Katherine</au><au>Navia, Felipe</au><au>Mosquera-Gil, Claudia</au><au>Sánchez, Adalberto</au><au>Sterling, Gonzalo</au><au>Fierro, Leonardo</au><au>Castaño, Santiago</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of the NA+/K+-ATPase α-Isoforms in Six Species of Poison Dart Frogs and their Sensitivity to Cardiotonic Steroids</atitle><jtitle>Journal of chemical ecology</jtitle><stitle>J Chem Ecol</stitle><addtitle>J Chem Ecol</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>49</volume><issue>3-4</issue><spage>116</spage><epage>132</epage><pages>116-132</pages><issn>0098-0331</issn><eissn>1573-1561</eissn><abstract>Cardiotonic steroids (CTS) are a group of compounds known to be toxic due to their ability to inhibit the Na
+
/K
+
-ATPase (NKA), which is essential to maintain the balance of ions in animal cells. An evolutionary strategy of molecular adaptation to avoid self-intoxication acquired by CTS defended organisms and their predators is the structural modification of their NKA where specific amino acid substitutions confer resistant phenotypes. Several lineages of poison dart frogs (Dendrobatidae) are well known to sequester a wide variety of lipophilic alkaloids from their arthropod diet, however there is no evidence of CTS-sequestration or dietary exposure. Interestingly this study identified the presence of α-NKA isoforms (α
1
and α
2
) with amino acid substitutions indicative of CTS-resistant phenotypes in skeletal muscle transcriptomes obtained from six species of dendrobatids:
Phyllobates aurotaenia
,
Oophaga anchicayensis
,
Epipedobates boulengeri
,
Andinobates bombetes
,
Andinobates minutus,
and
Leucostethus brachistriatus,
collected in the Valle del Cauca (Colombia).
P. aurotaenia
,
A. minutus
, and
E. boulengeri
presented two variants for α
1
-NKA, with one of them having these substitutions. In contrast,
O. anchicayensis
and
A. bombetes
have only one α
1
-NKA isoform with an amino acid sequence indicative of CTS susceptibility and an α
2
-NKA with one substitution that could confer a reduced affinity for CTS. The α
1
and α
2
isoforms of
L. brachistriatus
do not contain substitutions imparting CTS resistance. Our findings indicate that poison dart frogs express α-NKA isoforms with different affinities for CTS and the pattern of this expression might be influenced by factors related to evolutionary, physiological, ecological, and geographical burdens.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36877397</pmid><doi>10.1007/s10886-023-01404-7</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0098-0331 |
ispartof | Journal of chemical ecology, 2023-04, Vol.49 (3-4), p.116-132 |
issn | 0098-0331 1573-1561 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10102066 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Acid resistance Affinity Agriculture amino acid sequences Amino acid substitution Amino acids Amphibians Andinobates Animals arthropods Biochemistry Biological Microscopy Biomedical and Life Sciences Cardiac Glycosides Colombia diet dietary exposure Ecological effects Ecology Entomology Enzyme inhibitors Epipedobates Frogs Gene expression Intoxication Ions - metabolism Isoenzymes - genetics Isoenzymes - metabolism Isoforms Life Sciences Lipophilic lipophilicity Na+/K+-exchanging ATPase Oophaga Phenotypes Phyllobates Phyllobates aurotaenia Physiological effects Poisons Predators Reptiles & amphibians Skeletal muscle Sodium - metabolism sodium-potassium-exchanging ATPase Sodium-Potassium-Exchanging ATPase - genetics Sodium-Potassium-Exchanging ATPase - metabolism Steroid hormones Steroids toxicity Toxins transcriptome Transcriptomes |
title | Identification of the NA+/K+-ATPase α-Isoforms in Six Species of Poison Dart Frogs and their Sensitivity to Cardiotonic Steroids |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T08%3A56%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20of%20the%20NA+/K+-ATPase%20%CE%B1-Isoforms%20in%20Six%20Species%20of%20Poison%20Dart%20Frogs%20and%20their%20Sensitivity%20to%20Cardiotonic%20Steroids&rft.jtitle=Journal%20of%20chemical%20ecology&rft.au=Medina-Ortiz,%20Katherine&rft.date=2023-04-01&rft.volume=49&rft.issue=3-4&rft.spage=116&rft.epage=132&rft.pages=116-132&rft.issn=0098-0331&rft.eissn=1573-1561&rft_id=info:doi/10.1007/s10886-023-01404-7&rft_dat=%3Cproquest_pubme%3E2783792162%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2800408541&rft_id=info:pmid/36877397&rfr_iscdi=true |