Loading…
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants
Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful v...
Saved in:
Published in: | Frontiers in neuroscience 2018-06, Vol.12, p.382-382 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43 |
---|---|
cites | cdi_FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43 |
container_end_page | 382 |
container_issue | |
container_start_page | 382 |
container_title | Frontiers in neuroscience |
container_volume | 12 |
creator | Cai, Weigang Kim, Chan-Hee Go, Hye-Jin Egertová, Michaela Zampronio, Cleidiane G Jones, Alexandra M Park, Nam Gyu Elphick, Maurice R |
description | Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca
levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate-the starfish
(Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using
hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on
preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species,
, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in
, RT-qPCR revealed that in
the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes. |
doi_str_mv | 10.3389/fnins.2018.00382 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_699d6dbb9d1b4cda9571adf6081b7045</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_699d6dbb9d1b4cda9571adf6081b7045</doaj_id><sourcerecordid>2306236141</sourcerecordid><originalsourceid>FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43</originalsourceid><addsrcrecordid>eNpdUsuOFCEUrRiNM7buXRkSNy7sFiigChcmY_uaZHxkHBN35BYF3UyqoQVqYvstfqz0w47jisPl3HMfnKp6TPCsrlv5wnrn04xi0s4wrlt6pzolQtAp4_X3u0fM2pPqQUrXGAvaMnq_OqFS1k2D5Wn1-7ULemlWTsPwHJ15yOGAwffoyxLiCnQYwmIbRPNyB51NdL8gu-BRsGgOg3Y5lE6mV5u1QZ_MGMParLPrTULOo68ZonVp-RK9cUmHGxM32zzwpZx2xmd0GQaDIKGPY9IFXZoBfoLP6WF1z8KQzKPDOam-vXt7Nf8wvfj8_nx-djHVnIs8pW1Ta26M1i1h1HCsaUM7zsBqYSmzHSeMG20Nph0QqQmVfUMFJp02lgKrJ9X5XrcPcK3W0a0gblQAp3aBEBcKYnalNyWk7EXfdbInHdM9SN4Q6K3ALekaXPY-qV7ttdZjtzK9LvNFGG6J3n7xbqkW4UYJjCmTpAg8OwjE8GM0KatVWZsZBvAmjElRzCVmhMumUJ_-R70OY_RlVYrW5bNrQdhWEO9ZOoaUorHHZghWWxupnY3U1kZqZ6OS8uTfIY4Jf31T_wGlIcfq</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2306236141</pqid></control><display><type>article</type><title>Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants</title><source>Open Access: PubMed Central</source><source>Publicly Available Content (ProQuest)</source><creator>Cai, Weigang ; Kim, Chan-Hee ; Go, Hye-Jin ; Egertová, Michaela ; Zampronio, Cleidiane G ; Jones, Alexandra M ; Park, Nam Gyu ; Elphick, Maurice R</creator><creatorcontrib>Cai, Weigang ; Kim, Chan-Hee ; Go, Hye-Jin ; Egertová, Michaela ; Zampronio, Cleidiane G ; Jones, Alexandra M ; Park, Nam Gyu ; Elphick, Maurice R</creatorcontrib><description>Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca
levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate-the starfish
(Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using
hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on
preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species,
, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in
, RT-qPCR revealed that in
the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes.</description><identifier>ISSN: 1662-4548</identifier><identifier>ISSN: 1662-453X</identifier><identifier>EISSN: 1662-453X</identifier><identifier>DOI: 10.3389/fnins.2018.00382</identifier><identifier>PMID: 29937709</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Acetylcholine ; Adrenomedullin ; Alternative splicing ; Amylin ; Asterias rubens ; Calcitonin ; Calcitonin gene-related peptide ; Calcium (blood) ; Chemical bonds ; Contraction ; CT gene ; Diabetes ; Diuretics ; echinoderm ; Evolution ; Genes ; Genomes ; Hybridization ; Identification ; Immunohistochemistry ; Insects ; Invertebrates ; Investigations ; Ligands ; Mass spectroscopy ; Menopause ; Muscle contraction ; Muscle relaxants ; Nervous system ; neuropeptide ; Neuropeptides ; Neuroscience ; Peptides ; Physiology ; Proteins ; Smooth muscle ; starfish ; Thyroid ; Transcription</subject><ispartof>Frontiers in neuroscience, 2018-06, Vol.12, p.382-382</ispartof><rights>2018. This work is licensed 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><rights>Copyright © 2018 Cai, Kim, Go, Egertová, Zampronio, Jones, Park and Elphick. 2018 Cai, Kim, Go, Egertová, Zampronio, Jones, Park and Elphick</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43</citedby><cites>FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2306236141/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2306236141?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29937709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cai, Weigang</creatorcontrib><creatorcontrib>Kim, Chan-Hee</creatorcontrib><creatorcontrib>Go, Hye-Jin</creatorcontrib><creatorcontrib>Egertová, Michaela</creatorcontrib><creatorcontrib>Zampronio, Cleidiane G</creatorcontrib><creatorcontrib>Jones, Alexandra M</creatorcontrib><creatorcontrib>Park, Nam Gyu</creatorcontrib><creatorcontrib>Elphick, Maurice R</creatorcontrib><title>Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants</title><title>Frontiers in neuroscience</title><addtitle>Front Neurosci</addtitle><description>Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca
levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate-the starfish
(Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using
hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on
preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species,
, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in
, RT-qPCR revealed that in
the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes.</description><subject>Acetylcholine</subject><subject>Adrenomedullin</subject><subject>Alternative splicing</subject><subject>Amylin</subject><subject>Asterias rubens</subject><subject>Calcitonin</subject><subject>Calcitonin gene-related peptide</subject><subject>Calcium (blood)</subject><subject>Chemical bonds</subject><subject>Contraction</subject><subject>CT gene</subject><subject>Diabetes</subject><subject>Diuretics</subject><subject>echinoderm</subject><subject>Evolution</subject><subject>Genes</subject><subject>Genomes</subject><subject>Hybridization</subject><subject>Identification</subject><subject>Immunohistochemistry</subject><subject>Insects</subject><subject>Invertebrates</subject><subject>Investigations</subject><subject>Ligands</subject><subject>Mass spectroscopy</subject><subject>Menopause</subject><subject>Muscle contraction</subject><subject>Muscle relaxants</subject><subject>Nervous system</subject><subject>neuropeptide</subject><subject>Neuropeptides</subject><subject>Neuroscience</subject><subject>Peptides</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Smooth muscle</subject><subject>starfish</subject><subject>Thyroid</subject><subject>Transcription</subject><issn>1662-4548</issn><issn>1662-453X</issn><issn>1662-453X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUsuOFCEUrRiNM7buXRkSNy7sFiigChcmY_uaZHxkHBN35BYF3UyqoQVqYvstfqz0w47jisPl3HMfnKp6TPCsrlv5wnrn04xi0s4wrlt6pzolQtAp4_X3u0fM2pPqQUrXGAvaMnq_OqFS1k2D5Wn1-7ULemlWTsPwHJ15yOGAwffoyxLiCnQYwmIbRPNyB51NdL8gu-BRsGgOg3Y5lE6mV5u1QZ_MGMParLPrTULOo68ZonVp-RK9cUmHGxM32zzwpZx2xmd0GQaDIKGPY9IFXZoBfoLP6WF1z8KQzKPDOam-vXt7Nf8wvfj8_nx-djHVnIs8pW1Ta26M1i1h1HCsaUM7zsBqYSmzHSeMG20Nph0QqQmVfUMFJp02lgKrJ9X5XrcPcK3W0a0gblQAp3aBEBcKYnalNyWk7EXfdbInHdM9SN4Q6K3ALekaXPY-qV7ttdZjtzK9LvNFGG6J3n7xbqkW4UYJjCmTpAg8OwjE8GM0KatVWZsZBvAmjElRzCVmhMumUJ_-R70OY_RlVYrW5bNrQdhWEO9ZOoaUorHHZghWWxupnY3U1kZqZ6OS8uTfIY4Jf31T_wGlIcfq</recordid><startdate>20180608</startdate><enddate>20180608</enddate><creator>Cai, Weigang</creator><creator>Kim, Chan-Hee</creator><creator>Go, Hye-Jin</creator><creator>Egertová, Michaela</creator><creator>Zampronio, Cleidiane G</creator><creator>Jones, Alexandra M</creator><creator>Park, Nam Gyu</creator><creator>Elphick, Maurice R</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20180608</creationdate><title>Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants</title><author>Cai, Weigang ; Kim, Chan-Hee ; Go, Hye-Jin ; Egertová, Michaela ; Zampronio, Cleidiane G ; Jones, Alexandra M ; Park, Nam Gyu ; Elphick, Maurice R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetylcholine</topic><topic>Adrenomedullin</topic><topic>Alternative splicing</topic><topic>Amylin</topic><topic>Asterias rubens</topic><topic>Calcitonin</topic><topic>Calcitonin gene-related peptide</topic><topic>Calcium (blood)</topic><topic>Chemical bonds</topic><topic>Contraction</topic><topic>CT gene</topic><topic>Diabetes</topic><topic>Diuretics</topic><topic>echinoderm</topic><topic>Evolution</topic><topic>Genes</topic><topic>Genomes</topic><topic>Hybridization</topic><topic>Identification</topic><topic>Immunohistochemistry</topic><topic>Insects</topic><topic>Invertebrates</topic><topic>Investigations</topic><topic>Ligands</topic><topic>Mass spectroscopy</topic><topic>Menopause</topic><topic>Muscle contraction</topic><topic>Muscle relaxants</topic><topic>Nervous system</topic><topic>neuropeptide</topic><topic>Neuropeptides</topic><topic>Neuroscience</topic><topic>Peptides</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Smooth muscle</topic><topic>starfish</topic><topic>Thyroid</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cai, Weigang</creatorcontrib><creatorcontrib>Kim, Chan-Hee</creatorcontrib><creatorcontrib>Go, Hye-Jin</creatorcontrib><creatorcontrib>Egertová, Michaela</creatorcontrib><creatorcontrib>Zampronio, Cleidiane G</creatorcontrib><creatorcontrib>Jones, Alexandra M</creatorcontrib><creatorcontrib>Park, Nam Gyu</creatorcontrib><creatorcontrib>Elphick, Maurice R</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Science Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content (ProQuest)</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cai, Weigang</au><au>Kim, Chan-Hee</au><au>Go, Hye-Jin</au><au>Egertová, Michaela</au><au>Zampronio, Cleidiane G</au><au>Jones, Alexandra M</au><au>Park, Nam Gyu</au><au>Elphick, Maurice R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants</atitle><jtitle>Frontiers in neuroscience</jtitle><addtitle>Front Neurosci</addtitle><date>2018-06-08</date><risdate>2018</risdate><volume>12</volume><spage>382</spage><epage>382</epage><pages>382-382</pages><issn>1662-4548</issn><issn>1662-453X</issn><eissn>1662-453X</eissn><abstract>Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca
levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate-the starfish
(Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using
hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on
preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species,
, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in
, RT-qPCR revealed that in
the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes.</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>29937709</pmid><doi>10.3389/fnins.2018.00382</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1662-4548 |
ispartof | Frontiers in neuroscience, 2018-06, Vol.12, p.382-382 |
issn | 1662-4548 1662-453X 1662-453X |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_699d6dbb9d1b4cda9571adf6081b7045 |
source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Acetylcholine Adrenomedullin Alternative splicing Amylin Asterias rubens Calcitonin Calcitonin gene-related peptide Calcium (blood) Chemical bonds Contraction CT gene Diabetes Diuretics echinoderm Evolution Genes Genomes Hybridization Identification Immunohistochemistry Insects Invertebrates Investigations Ligands Mass spectroscopy Menopause Muscle contraction Muscle relaxants Nervous system neuropeptide Neuropeptides Neuroscience Peptides Physiology Proteins Smooth muscle starfish Thyroid Transcription |
title | Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A10%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biochemical,%20Anatomical,%20and%20Pharmacological%20Characterization%20of%20Calcitonin-Type%20Neuropeptides%20in%20Starfish:%20Discovery%20of%20an%20Ancient%20Role%20as%20Muscle%20Relaxants&rft.jtitle=Frontiers%20in%20neuroscience&rft.au=Cai,%20Weigang&rft.date=2018-06-08&rft.volume=12&rft.spage=382&rft.epage=382&rft.pages=382-382&rft.issn=1662-4548&rft.eissn=1662-453X&rft_id=info:doi/10.3389/fnins.2018.00382&rft_dat=%3Cproquest_doaj_%3E2306236141%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c556t-2873c5eecc8142e50c272b54afc6f24fb5145ecfe02ba19c129d72601bcef2a43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2306236141&rft_id=info:pmid/29937709&rfr_iscdi=true |