An Endogenous SCP-Related Peptide Modulates Ciliary Beating in the Gills of a Venerid Clam, Mercenaria mercenaria
The activities of both the lateral and frontal cilia of Mercenaria mercenaria were unaffected, either by the two endogenous SCP-related peptides AMSFYFPRMamide and YFAFPRQamide, or by FMRFamide (all at 10-6 M). Dopamine (DA) inhibited the lateral cilia; the mean EC50 was 2× 10-6 M. The peptide YFAFP...
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description | The activities of both the lateral and frontal cilia of Mercenaria mercenaria were unaffected, either by the two endogenous SCP-related peptides AMSFYFPRMamide and YFAFPRQamide, or by FMRFamide (all at 10-6 M). Dopamine (DA) inhibited the lateral cilia; the mean EC50 was 2× 10-6 M. The peptide YFAFPRQamide-but neither AMSFYFPRMamide nor FMRFamide-antagonized the inhibition induced by DA; this effect was dependent on both time and dose. At a DA concentration of 5× 10-7 M, the effect of YFAFPRQamide appeared within 20 min and became maximal within 40-60 min; the mean EC50 at these times was 4.7× 10-11 M. If the concentration of DA was increased to 10-6 M, the maximal effect of the peptide was delayed to 50 min, and the mean EC50 increased to 1.1× 10-7 M. Particle transport by the frontal cilia was inhibited by 5-hydroxytryptamine (5HT); the mean EC50 was 5.7× 10-7 M. Again, only YFAFPRQamide had an antagonistic effect on the 5HT-induced inhibition. At a 5HT concentration of 10-6 M, the effects of YFAFPRQamide did not appear until 45 min; the mean EC50 was 10-6 M. When radioimmunoassayed with an SCP antiserum, the elution profile of a gill extract overlapped those of the SCP-related peptides that had previously been identified in extracts of whole animals. These data suggest that all three SCP analogs occur in the gill. Immunohisto-chemistry of the gill, carried out with a monoclonal antibody raised to SCP B, stained many varicose neuronal fibers. Most of these were associated with the gill musculature, but a sparse innervation of the filaments underlying the cilia was also observed. Some fluorescent nerve cell bodies were also seen in the gill tissue. Our results are consistent with the hypothesis that YFAFPRQamide modulates branchial activities-muscular as well as ciliary-that are associated with feeding. |
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Dopamine (DA) inhibited the lateral cilia; the mean EC50 was 2× 10-6 M. The peptide YFAFPRQamide-but neither AMSFYFPRMamide nor FMRFamide-antagonized the inhibition induced by DA; this effect was dependent on both time and dose. At a DA concentration of 5× 10-7 M, the effect of YFAFPRQamide appeared within 20 min and became maximal within 40-60 min; the mean EC50 at these times was 4.7× 10-11 M. If the concentration of DA was increased to 10-6 M, the maximal effect of the peptide was delayed to 50 min, and the mean EC50 increased to 1.1× 10-7 M. Particle transport by the frontal cilia was inhibited by 5-hydroxytryptamine (5HT); the mean EC50 was 5.7× 10-7 M. Again, only YFAFPRQamide had an antagonistic effect on the 5HT-induced inhibition. At a 5HT concentration of 10-6 M, the effects of YFAFPRQamide did not appear until 45 min; the mean EC50 was 10-6 M. When radioimmunoassayed with an SCP antiserum, the elution profile of a gill extract overlapped those of the SCP-related peptides that had previously been identified in extracts of whole animals. These data suggest that all three SCP analogs occur in the gill. Immunohisto-chemistry of the gill, carried out with a monoclonal antibody raised to SCP B, stained many varicose neuronal fibers. Most of these were associated with the gill musculature, but a sparse innervation of the filaments underlying the cilia was also observed. Some fluorescent nerve cell bodies were also seen in the gill tissue. Our results are consistent with the hypothesis that YFAFPRQamide modulates branchial activities-muscular as well as ciliary-that are associated with feeding.</description><identifier>ISSN: 0006-3185</identifier><identifier>EISSN: 1939-8697</identifier><identifier>DOI: 10.2307/1542612</identifier><identifier>PMID: 10573837</identifier><language>eng</language><publisher>United States: Marine Biological Laboratory</publisher><subject>Amides ; Animals ; Beat frequencies ; Bivalves ; Bivalvia ; Bivalvia - physiology ; Brackish ; Cilia ; Clams ; Dopamine - metabolism ; Dose response relationship ; Epithelium ; Evaluation ; Fibers ; Filaments ; FMRFamide ; Gills ; Gills - physiology ; Immunohistochemistry ; Innervation ; Marine ; Marine biology ; Mercenaria mercenaria ; Mollusks ; Monoclonal antibodies ; Mussels ; Nerves ; Neurons ; Neuropeptides ; Neuropeptides - pharmacology ; Neuropeptides - physiology ; Peptides ; Physiology ; Sediment transport</subject><ispartof>The Biological bulletin, 1999-10, Vol.197 (2), p.159-173</ispartof><rights>Copyright 1999 The Marine Biological Laboratory</rights><rights>Copyright © 1999 by Marine Biological Laboratory</rights><rights>COPYRIGHT 1999 University of Chicago Press</rights><rights>COPYRIGHT 1999 University of Chicago Press</rights><rights>Copyright Marine Biological Laboratory Oct 1999</rights><rights>Copyright University of Chicago Press Oct 1999</rights><rights>In copyright. Digitized with the permission of the rights holder. http://creativecommons.org/licenses/by-nc-sa/3.0</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c764t-c836c371a09f9d5ff86e45e448d56586dac3949d651ece79835f692c872dd1663</citedby><cites>FETCH-LOGICAL-c764t-c836c371a09f9d5ff86e45e448d56586dac3949d651ece79835f692c872dd1663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1542612$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1542612$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,885,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10573837$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gainey, Louis F.</creatorcontrib><creatorcontrib>Vining, Kelly J.</creatorcontrib><creatorcontrib>Doble, Karen E.</creatorcontrib><creatorcontrib>Waldo, Jennifer M.</creatorcontrib><creatorcontrib>Candelario-Martinez, Aurora</creatorcontrib><creatorcontrib>Greenberg, Michael J.</creatorcontrib><title>An Endogenous SCP-Related Peptide Modulates Ciliary Beating in the Gills of a Venerid Clam, Mercenaria mercenaria</title><title>The Biological bulletin</title><addtitle>Biol Bull</addtitle><description>The activities of both the lateral and frontal cilia of Mercenaria mercenaria were unaffected, either by the two endogenous SCP-related peptides AMSFYFPRMamide and YFAFPRQamide, or by FMRFamide (all at 10-6 M). Dopamine (DA) inhibited the lateral cilia; the mean EC50 was 2× 10-6 M. The peptide YFAFPRQamide-but neither AMSFYFPRMamide nor FMRFamide-antagonized the inhibition induced by DA; this effect was dependent on both time and dose. At a DA concentration of 5× 10-7 M, the effect of YFAFPRQamide appeared within 20 min and became maximal within 40-60 min; the mean EC50 at these times was 4.7× 10-11 M. If the concentration of DA was increased to 10-6 M, the maximal effect of the peptide was delayed to 50 min, and the mean EC50 increased to 1.1× 10-7 M. Particle transport by the frontal cilia was inhibited by 5-hydroxytryptamine (5HT); the mean EC50 was 5.7× 10-7 M. Again, only YFAFPRQamide had an antagonistic effect on the 5HT-induced inhibition. At a 5HT concentration of 10-6 M, the effects of YFAFPRQamide did not appear until 45 min; the mean EC50 was 10-6 M. When radioimmunoassayed with an SCP antiserum, the elution profile of a gill extract overlapped those of the SCP-related peptides that had previously been identified in extracts of whole animals. These data suggest that all three SCP analogs occur in the gill. Immunohisto-chemistry of the gill, carried out with a monoclonal antibody raised to SCP B, stained many varicose neuronal fibers. Most of these were associated with the gill musculature, but a sparse innervation of the filaments underlying the cilia was also observed. Some fluorescent nerve cell bodies were also seen in the gill tissue. Our results are consistent with the hypothesis that YFAFPRQamide modulates branchial activities-muscular as well as ciliary-that are associated with feeding.</description><subject>Amides</subject><subject>Animals</subject><subject>Beat frequencies</subject><subject>Bivalves</subject><subject>Bivalvia</subject><subject>Bivalvia - physiology</subject><subject>Brackish</subject><subject>Cilia</subject><subject>Clams</subject><subject>Dopamine - metabolism</subject><subject>Dose response relationship</subject><subject>Epithelium</subject><subject>Evaluation</subject><subject>Fibers</subject><subject>Filaments</subject><subject>FMRFamide</subject><subject>Gills</subject><subject>Gills - physiology</subject><subject>Immunohistochemistry</subject><subject>Innervation</subject><subject>Marine</subject><subject>Marine biology</subject><subject>Mercenaria mercenaria</subject><subject>Mollusks</subject><subject>Monoclonal antibodies</subject><subject>Mussels</subject><subject>Nerves</subject><subject>Neurons</subject><subject>Neuropeptides</subject><subject>Neuropeptides - 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physiology</topic><topic>Brackish</topic><topic>Cilia</topic><topic>Clams</topic><topic>Dopamine - metabolism</topic><topic>Dose response relationship</topic><topic>Epithelium</topic><topic>Evaluation</topic><topic>Fibers</topic><topic>Filaments</topic><topic>FMRFamide</topic><topic>Gills</topic><topic>Gills - physiology</topic><topic>Immunohistochemistry</topic><topic>Innervation</topic><topic>Marine</topic><topic>Marine biology</topic><topic>Mercenaria mercenaria</topic><topic>Mollusks</topic><topic>Monoclonal antibodies</topic><topic>Mussels</topic><topic>Nerves</topic><topic>Neurons</topic><topic>Neuropeptides</topic><topic>Neuropeptides - pharmacology</topic><topic>Neuropeptides - physiology</topic><topic>Peptides</topic><topic>Physiology</topic><topic>Sediment transport</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gainey, Louis F.</creatorcontrib><creatorcontrib>Vining, Kelly J.</creatorcontrib><creatorcontrib>Doble, Karen E.</creatorcontrib><creatorcontrib>Waldo, Jennifer M.</creatorcontrib><creatorcontrib>Candelario-Martinez, Aurora</creatorcontrib><creatorcontrib>Greenberg, Michael J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>Gale In Context: Canada</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oceanic 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>Science Database (Alumni Edition)</collection><collection>STEM Database</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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</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>Research Library Prep</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biodiversity Heritage Library</collection><jtitle>The Biological bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gainey, Louis F.</au><au>Vining, Kelly J.</au><au>Doble, Karen E.</au><au>Waldo, Jennifer M.</au><au>Candelario-Martinez, Aurora</au><au>Greenberg, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Endogenous SCP-Related Peptide Modulates Ciliary Beating in the Gills of a Venerid Clam, Mercenaria mercenaria</atitle><jtitle>The Biological bulletin</jtitle><addtitle>Biol Bull</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>197</volume><issue>2</issue><spage>159</spage><epage>173</epage><pages>159-173</pages><issn>0006-3185</issn><eissn>1939-8697</eissn><abstract>The activities of both the lateral and frontal cilia of Mercenaria mercenaria were unaffected, either by the two endogenous SCP-related peptides AMSFYFPRMamide and YFAFPRQamide, or by FMRFamide (all at 10-6 M). Dopamine (DA) inhibited the lateral cilia; the mean EC50 was 2× 10-6 M. The peptide YFAFPRQamide-but neither AMSFYFPRMamide nor FMRFamide-antagonized the inhibition induced by DA; this effect was dependent on both time and dose. At a DA concentration of 5× 10-7 M, the effect of YFAFPRQamide appeared within 20 min and became maximal within 40-60 min; the mean EC50 at these times was 4.7× 10-11 M. If the concentration of DA was increased to 10-6 M, the maximal effect of the peptide was delayed to 50 min, and the mean EC50 increased to 1.1× 10-7 M. Particle transport by the frontal cilia was inhibited by 5-hydroxytryptamine (5HT); the mean EC50 was 5.7× 10-7 M. Again, only YFAFPRQamide had an antagonistic effect on the 5HT-induced inhibition. At a 5HT concentration of 10-6 M, the effects of YFAFPRQamide did not appear until 45 min; the mean EC50 was 10-6 M. When radioimmunoassayed with an SCP antiserum, the elution profile of a gill extract overlapped those of the SCP-related peptides that had previously been identified in extracts of whole animals. These data suggest that all three SCP analogs occur in the gill. Immunohisto-chemistry of the gill, carried out with a monoclonal antibody raised to SCP B, stained many varicose neuronal fibers. Most of these were associated with the gill musculature, but a sparse innervation of the filaments underlying the cilia was also observed. Some fluorescent nerve cell bodies were also seen in the gill tissue. Our results are consistent with the hypothesis that YFAFPRQamide modulates branchial activities-muscular as well as ciliary-that are associated with feeding.</abstract><cop>United States</cop><pub>Marine Biological Laboratory</pub><pmid>10573837</pmid><doi>10.2307/1542612</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amides Animals Beat frequencies Bivalves Bivalvia Bivalvia - physiology Brackish Cilia Clams Dopamine - metabolism Dose response relationship Epithelium Evaluation Fibers Filaments FMRFamide Gills Gills - physiology Immunohistochemistry Innervation Marine Marine biology Mercenaria mercenaria Mollusks Monoclonal antibodies Mussels Nerves Neurons Neuropeptides Neuropeptides - pharmacology Neuropeptides - physiology Peptides Physiology Sediment transport |
title | An Endogenous SCP-Related Peptide Modulates Ciliary Beating in the Gills of a Venerid Clam, Mercenaria mercenaria |
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