Vascular distribution of nitric oxide synthase and vasodilation in the Australian lungfish, Neoceratodus forsteri
The presence of nitric oxide synthase (NOS) and role of nitric oxide (NO) in vascular regulation was investigated in the Australian lungfish, Neoceratodus forsteri. No evidence was found for NOS in the endothelium of large and small blood vessels following processing for NADPH-diaphorase histochemis...
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Veröffentlicht in: | Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 2008-12, Vol.151 (4), p.590-595 |
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description | The presence of nitric oxide synthase (NOS) and role of nitric oxide (NO) in vascular regulation was investigated in the Australian lungfish,
Neoceratodus forsteri. No evidence was found for NOS in the endothelium of large and small blood vessels following processing for NADPH-diaphorase histochemistry. However, both NADPH-diaphorase histochemistry and neural NOS immunohistochemistry demonstrated a sparse network of nitrergic nerves in the dorsal aorta, hepatic artery, and branchial arteries, but there were no nitrergic nerves in small blood vessels in tissues. In contrast, nitrergic nerves were found in non-vascular tissues of the lung, gut and kidney. Dual-wire myography was used to determine if NO signalling occurred in the branchial artery of
N. forsteri. Both SNP and SIN-1 had no effect on the pre-constricted branchial artery, but the particulate guanylyl cyclase (GC) activator, C-type natriuretic peptide, always caused vasodilation. Nicotine mediated a dilation that was not inhibited by the soluble GC inhibitor, ODQ, or the NOS inhibitor, L-NNA, but was blocked by the cyclooxygenase inhibitor, indomethacin. These data suggest that NO control of the branchial artery is lacking, but that prostaglandins could be endothelial relaxing factors in the vasculature of lungfish. |
doi_str_mv | 10.1016/j.cbpa.2008.07.018 |
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Neoceratodus forsteri. No evidence was found for NOS in the endothelium of large and small blood vessels following processing for NADPH-diaphorase histochemistry. However, both NADPH-diaphorase histochemistry and neural NOS immunohistochemistry demonstrated a sparse network of nitrergic nerves in the dorsal aorta, hepatic artery, and branchial arteries, but there were no nitrergic nerves in small blood vessels in tissues. In contrast, nitrergic nerves were found in non-vascular tissues of the lung, gut and kidney. Dual-wire myography was used to determine if NO signalling occurred in the branchial artery of
N. forsteri. Both SNP and SIN-1 had no effect on the pre-constricted branchial artery, but the particulate guanylyl cyclase (GC) activator, C-type natriuretic peptide, always caused vasodilation. Nicotine mediated a dilation that was not inhibited by the soluble GC inhibitor, ODQ, or the NOS inhibitor, L-NNA, but was blocked by the cyclooxygenase inhibitor, indomethacin. These data suggest that NO control of the branchial artery is lacking, but that prostaglandins could be endothelial relaxing factors in the vasculature of lungfish.</description><identifier>ISSN: 1095-6433</identifier><identifier>EISSN: 1531-4332</identifier><identifier>DOI: 10.1016/j.cbpa.2008.07.018</identifier><identifier>PMID: 18692149</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Australia ; Blood Vessels - enzymology ; Brachial Artery - drug effects ; Brachial Artery - physiology ; Endothelium, Vascular - enzymology ; Enzyme Inhibitors - pharmacology ; Female ; Fishes - physiology ; Freshwater ; Guanylate Cyclase - antagonists & inhibitors ; Guanylate Cyclase - metabolism ; Immunohistochemistry ; In Vitro Techniques ; Lungfish ; Male ; NADPH Dehydrogenase - metabolism ; Neoceratodus forsteri ; Nitric oxide ; Nitric Oxide - physiology ; Nitric Oxide Donors - pharmacology ; Nitric oxide synthase ; Nitric Oxide Synthase - antagonists & inhibitors ; Nitric Oxide Synthase - metabolism ; Nitric Oxide Synthase Type I - metabolism ; Prostaglandins ; Signal Transduction ; Tissue Distribution ; Vasodilation - drug effects ; Vasodilation - physiology</subject><ispartof>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 2008-12, Vol.151 (4), p.590-595</ispartof><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-7717350450f42d456164a27fdee6cb62681f8b93b076b9e65ecdbd2d1aeec47f3</citedby><cites>FETCH-LOGICAL-c386t-7717350450f42d456164a27fdee6cb62681f8b93b076b9e65ecdbd2d1aeec47f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1095643308010684$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18692149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jennings, Brett L.</creatorcontrib><creatorcontrib>Blake, Rachel E.</creatorcontrib><creatorcontrib>Joss, Jean M.P.</creatorcontrib><creatorcontrib>Donald, John A.</creatorcontrib><title>Vascular distribution of nitric oxide synthase and vasodilation in the Australian lungfish, Neoceratodus forsteri</title><title>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</title><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><description>The presence of nitric oxide synthase (NOS) and role of nitric oxide (NO) in vascular regulation was investigated in the Australian lungfish,
Neoceratodus forsteri. No evidence was found for NOS in the endothelium of large and small blood vessels following processing for NADPH-diaphorase histochemistry. However, both NADPH-diaphorase histochemistry and neural NOS immunohistochemistry demonstrated a sparse network of nitrergic nerves in the dorsal aorta, hepatic artery, and branchial arteries, but there were no nitrergic nerves in small blood vessels in tissues. In contrast, nitrergic nerves were found in non-vascular tissues of the lung, gut and kidney. Dual-wire myography was used to determine if NO signalling occurred in the branchial artery of
N. forsteri. Both SNP and SIN-1 had no effect on the pre-constricted branchial artery, but the particulate guanylyl cyclase (GC) activator, C-type natriuretic peptide, always caused vasodilation. Nicotine mediated a dilation that was not inhibited by the soluble GC inhibitor, ODQ, or the NOS inhibitor, L-NNA, but was blocked by the cyclooxygenase inhibitor, indomethacin. These data suggest that NO control of the branchial artery is lacking, but that prostaglandins could be endothelial relaxing factors in the vasculature of lungfish.</description><subject>Animals</subject><subject>Australia</subject><subject>Blood Vessels - enzymology</subject><subject>Brachial Artery - drug effects</subject><subject>Brachial Artery - physiology</subject><subject>Endothelium, Vascular - enzymology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Fishes - physiology</subject><subject>Freshwater</subject><subject>Guanylate Cyclase - antagonists & inhibitors</subject><subject>Guanylate Cyclase - metabolism</subject><subject>Immunohistochemistry</subject><subject>In Vitro Techniques</subject><subject>Lungfish</subject><subject>Male</subject><subject>NADPH Dehydrogenase - metabolism</subject><subject>Neoceratodus forsteri</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - physiology</subject><subject>Nitric Oxide Donors - pharmacology</subject><subject>Nitric oxide synthase</subject><subject>Nitric Oxide Synthase - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitric Oxide Synthase Type I - metabolism</subject><subject>Prostaglandins</subject><subject>Signal Transduction</subject><subject>Tissue Distribution</subject><subject>Vasodilation - drug effects</subject><subject>Vasodilation - physiology</subject><issn>1095-6433</issn><issn>1531-4332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kb1uHCEURlHkKP5JXiBFROU0njEwDMxIaSwrtiNZSZOkRQxcsqxmYQ2MZb-92exK7nwb7pXO9xUchD5T0lJCxeW6NdNWt4yQoSWyJXR4h05o39GGdx07qjsZ-0bU4xid5rwmdTjlH9AxHcTIKB9P0MNfnc0y64StzyX5aSk-BhwdDr6eBscnbwHn51BWOgPWweJHnaP1s_5P-oDLCvDVUtN69jrgeQn_nM-rC_wTooGkS7RLxi6mXCD5j-i903OGT4f3DP25-f77-q65_3X74_rqvjHdIEojJZVdT3hPHGeW94IKrpl0FkCYSTAxUDdMYzcRKaYRRA_GTpZZqgEMl647Q1_3vdsUHxbIRW18NjDPOkBcspIdp4xISSp5_iZJRz7SgbAKsj1oUsw5gVPb5Dc6PStK1E6JWqudErVToohUVUkNfTm0L9MG7Gvk4KAC3_YA1N949JBUNh6CAesTmKJs9G_1vwDnk58y</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Jennings, Brett L.</creator><creator>Blake, Rachel E.</creator><creator>Joss, Jean M.P.</creator><creator>Donald, John 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>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>Vascular distribution of nitric oxide synthase and vasodilation in the Australian lungfish, Neoceratodus forsteri</title><author>Jennings, Brett L. ; Blake, Rachel E. ; Joss, Jean M.P. ; Donald, John A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-7717350450f42d456164a27fdee6cb62681f8b93b076b9e65ecdbd2d1aeec47f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Australia</topic><topic>Blood Vessels - enzymology</topic><topic>Brachial Artery - drug effects</topic><topic>Brachial Artery - physiology</topic><topic>Endothelium, Vascular - enzymology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>Fishes - physiology</topic><topic>Freshwater</topic><topic>Guanylate Cyclase - antagonists & inhibitors</topic><topic>Guanylate Cyclase - metabolism</topic><topic>Immunohistochemistry</topic><topic>In Vitro Techniques</topic><topic>Lungfish</topic><topic>Male</topic><topic>NADPH Dehydrogenase - metabolism</topic><topic>Neoceratodus forsteri</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - physiology</topic><topic>Nitric Oxide Donors - pharmacology</topic><topic>Nitric oxide synthase</topic><topic>Nitric Oxide Synthase - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitric Oxide Synthase Type I - metabolism</topic><topic>Prostaglandins</topic><topic>Signal Transduction</topic><topic>Tissue Distribution</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jennings, Brett L.</creatorcontrib><creatorcontrib>Blake, Rachel E.</creatorcontrib><creatorcontrib>Joss, Jean M.P.</creatorcontrib><creatorcontrib>Donald, John 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>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>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jennings, Brett L.</au><au>Blake, Rachel E.</au><au>Joss, Jean M.P.</au><au>Donald, John A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular distribution of nitric oxide synthase and vasodilation in the Australian lungfish, Neoceratodus forsteri</atitle><jtitle>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>151</volume><issue>4</issue><spage>590</spage><epage>595</epage><pages>590-595</pages><issn>1095-6433</issn><eissn>1531-4332</eissn><abstract>The presence of nitric oxide synthase (NOS) and role of nitric oxide (NO) in vascular regulation was investigated in the Australian lungfish,
Neoceratodus forsteri. No evidence was found for NOS in the endothelium of large and small blood vessels following processing for NADPH-diaphorase histochemistry. However, both NADPH-diaphorase histochemistry and neural NOS immunohistochemistry demonstrated a sparse network of nitrergic nerves in the dorsal aorta, hepatic artery, and branchial arteries, but there were no nitrergic nerves in small blood vessels in tissues. In contrast, nitrergic nerves were found in non-vascular tissues of the lung, gut and kidney. Dual-wire myography was used to determine if NO signalling occurred in the branchial artery of
N. forsteri. Both SNP and SIN-1 had no effect on the pre-constricted branchial artery, but the particulate guanylyl cyclase (GC) activator, C-type natriuretic peptide, always caused vasodilation. Nicotine mediated a dilation that was not inhibited by the soluble GC inhibitor, ODQ, or the NOS inhibitor, L-NNA, but was blocked by the cyclooxygenase inhibitor, indomethacin. These data suggest that NO control of the branchial artery is lacking, but that prostaglandins could be endothelial relaxing factors in the vasculature of lungfish.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18692149</pmid><doi>10.1016/j.cbpa.2008.07.018</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Australia Blood Vessels - enzymology Brachial Artery - drug effects Brachial Artery - physiology Endothelium, Vascular - enzymology Enzyme Inhibitors - pharmacology Female Fishes - physiology Freshwater Guanylate Cyclase - antagonists & inhibitors Guanylate Cyclase - metabolism Immunohistochemistry In Vitro Techniques Lungfish Male NADPH Dehydrogenase - metabolism Neoceratodus forsteri Nitric oxide Nitric Oxide - physiology Nitric Oxide Donors - pharmacology Nitric oxide synthase Nitric Oxide Synthase - antagonists & inhibitors Nitric Oxide Synthase - metabolism Nitric Oxide Synthase Type I - metabolism Prostaglandins Signal Transduction Tissue Distribution Vasodilation - drug effects Vasodilation - physiology |
title | Vascular distribution of nitric oxide synthase and vasodilation in the Australian lungfish, Neoceratodus forsteri |
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