Role of endothelium in hypoxic contraction of canine basilar artery
1 Reversible contraction of canine basilar artery, produced by hypoxia, persisted after mechanical and chemical removal of the endothelium. The removal of endothelium was confirmed by scanning electron microscopy as well as by the abolition or reversal of the relaxant response to acetylcholine or ar...
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Veröffentlicht in: | British journal of pharmacology 1989-04, Vol.96 (4), p.949-955 |
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description | 1
Reversible contraction of canine basilar artery, produced by hypoxia, persisted after mechanical and chemical removal of the endothelium. The removal of endothelium was confirmed by scanning electron microscopy as well as by the abolition or reversal of the relaxant response to acetylcholine or arginine8‐vasopressin.
2
Hydroquinone, believed to block selectively endothelium‐mediated relaxation, also preferentially attenuated hypoxic contractions even in the absence of endothelium but did not reduce responses to 5‐hydroxytryptamine (5‐HT) or high external potassium.
3
Contractions induced by red blood cell haemolysate, which occur independently of the endothelium, were also selectively attenuated by hydroquinone.
4
Contractions caused by hypoxia were inhibited by pretreatment with adenosine or by its application after contraction had developed.
5
Hypoxic contraction in canine basilar artery may result partly from a direct effect on smooth muscle as well as through the endothelium.
6
Hydroquinone may have an additional locus of action in smooth muscle cells besides its well known effect on the endothelium. |
doi_str_mv | 10.1111/j.1476-5381.1989.tb11906.x |
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Reversible contraction of canine basilar artery, produced by hypoxia, persisted after mechanical and chemical removal of the endothelium. The removal of endothelium was confirmed by scanning electron microscopy as well as by the abolition or reversal of the relaxant response to acetylcholine or arginine8‐vasopressin.
2
Hydroquinone, believed to block selectively endothelium‐mediated relaxation, also preferentially attenuated hypoxic contractions even in the absence of endothelium but did not reduce responses to 5‐hydroxytryptamine (5‐HT) or high external potassium.
3
Contractions induced by red blood cell haemolysate, which occur independently of the endothelium, were also selectively attenuated by hydroquinone.
4
Contractions caused by hypoxia were inhibited by pretreatment with adenosine or by its application after contraction had developed.
5
Hypoxic contraction in canine basilar artery may result partly from a direct effect on smooth muscle as well as through the endothelium.
6
Hydroquinone may have an additional locus of action in smooth muscle cells besides its well known effect on the endothelium.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/j.1476-5381.1989.tb11906.x</identifier><identifier>PMID: 2743085</identifier><identifier>CODEN: BJPCBM</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine - pharmacology ; Animals ; Arginine Vasopressin - pharmacology ; Basilar Artery - physiology ; Biological and medical sciences ; Blood vessels and receptors ; Dogs ; endothelium ; Endothelium, Vascular - physiology ; Female ; Fundamental and applied biological sciences. Psychology ; Hemoglobins - pharmacology ; Hydroquinones - pharmacology ; hypoxia ; Hypoxia - physiopathology ; In Vitro Techniques ; Isometric Contraction - drug effects ; Male ; Microscopy, Electron, Scanning ; Muscle Contraction - drug effects ; Muscle Relaxation - drug effects ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - physiology ; Potassium Chloride - pharmacology ; smooth muscle ; Vertebrates: cardiovascular system</subject><ispartof>British journal of pharmacology, 1989-04, Vol.96 (4), p.949-955</ispartof><rights>1989 British Pharmacological Society</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6046-9ed7ddbd16fb95982d4db1ac2b61e3a4a1d3f52bc135258f43234bf6c87d91be3</citedby><cites>FETCH-LOGICAL-c6046-9ed7ddbd16fb95982d4db1ac2b61e3a4a1d3f52bc135258f43234bf6c87d91be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1854431/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1854431/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6771416$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2743085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elliott, D.A.</creatorcontrib><creatorcontrib>Ong, B.Y.</creatorcontrib><creatorcontrib>Bruni, J.E.</creatorcontrib><creatorcontrib>Bose, D.</creatorcontrib><title>Role of endothelium in hypoxic contraction of canine basilar artery</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>1
Reversible contraction of canine basilar artery, produced by hypoxia, persisted after mechanical and chemical removal of the endothelium. The removal of endothelium was confirmed by scanning electron microscopy as well as by the abolition or reversal of the relaxant response to acetylcholine or arginine8‐vasopressin.
2
Hydroquinone, believed to block selectively endothelium‐mediated relaxation, also preferentially attenuated hypoxic contractions even in the absence of endothelium but did not reduce responses to 5‐hydroxytryptamine (5‐HT) or high external potassium.
3
Contractions induced by red blood cell haemolysate, which occur independently of the endothelium, were also selectively attenuated by hydroquinone.
4
Contractions caused by hypoxia were inhibited by pretreatment with adenosine or by its application after contraction had developed.
5
Hypoxic contraction in canine basilar artery may result partly from a direct effect on smooth muscle as well as through the endothelium.
6
Hydroquinone may have an additional locus of action in smooth muscle cells besides its well known effect on the endothelium.</description><subject>Adenosine - pharmacology</subject><subject>Animals</subject><subject>Arginine Vasopressin - pharmacology</subject><subject>Basilar Artery - physiology</subject><subject>Biological and medical sciences</subject><subject>Blood vessels and receptors</subject><subject>Dogs</subject><subject>endothelium</subject><subject>Endothelium, Vascular - physiology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hemoglobins - pharmacology</subject><subject>Hydroquinones - pharmacology</subject><subject>hypoxia</subject><subject>Hypoxia - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Isometric Contraction - drug effects</subject><subject>Male</subject><subject>Microscopy, Electron, Scanning</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Relaxation - drug effects</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Potassium Chloride - pharmacology</subject><subject>smooth muscle</subject><subject>Vertebrates: cardiovascular system</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU-r1DAUxYMoz_HpRxCKiLvW3CZpEheiDuoTHiii65B_dTJkmjHp6My3t3XKoCsxWeTC-d3DCQehJ4AbmM7zbQOUdzUjAhqQQjajAZC4a4530Ooi3UUrjDGvAYS4jx6UssV4Ejm7QlctpwQLtkLrzyn6KvWVH1waNz6Gw64KQ7U57dMx2MqmYczajiENM2X1EAZfGV1C1LnSefT59BDd63Us_tHyXqOv795-Wd_Utx_ff1i_vq1th2lXS--4c8ZB1xvJpGgddQa0bU0HnmiqwZGetcYCYS0TPSUtoabvrOBOgvHkGr08--4PZued9XO0qPY57HQ-qaSD-lsZwkZ9Sz8UCEYpgcng2WKQ0_eDL6PahWJ9jHrw6VAUl3i6gv8TBNbSVgg5gS_OoM2plOz7SxrAau5KbdVciJoLUXNXaulKHaflx3_-57K6lDPpTxddF6tjn_VgQ7lgHedAoZuwV2fsZ4j-9B8B1JtPN79H8gv-sLMK</recordid><startdate>198904</startdate><enddate>198904</enddate><creator>Elliott, D.A.</creator><creator>Ong, B.Y.</creator><creator>Bruni, J.E.</creator><creator>Bose, D.</creator><general>Blackwell Publishing Ltd</general><general>Nature Publishing</general><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>198904</creationdate><title>Role of endothelium in hypoxic contraction of canine basilar artery</title><author>Elliott, D.A. ; Ong, B.Y. ; Bruni, J.E. ; Bose, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6046-9ed7ddbd16fb95982d4db1ac2b61e3a4a1d3f52bc135258f43234bf6c87d91be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adenosine - pharmacology</topic><topic>Animals</topic><topic>Arginine Vasopressin - pharmacology</topic><topic>Basilar Artery - physiology</topic><topic>Biological and medical sciences</topic><topic>Blood vessels and receptors</topic><topic>Dogs</topic><topic>endothelium</topic><topic>Endothelium, Vascular - physiology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hemoglobins - pharmacology</topic><topic>Hydroquinones - pharmacology</topic><topic>hypoxia</topic><topic>Hypoxia - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Isometric Contraction - drug effects</topic><topic>Male</topic><topic>Microscopy, Electron, Scanning</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Relaxation - drug effects</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Potassium Chloride - pharmacology</topic><topic>smooth muscle</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elliott, D.A.</creatorcontrib><creatorcontrib>Ong, B.Y.</creatorcontrib><creatorcontrib>Bruni, J.E.</creatorcontrib><creatorcontrib>Bose, D.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elliott, D.A.</au><au>Ong, B.Y.</au><au>Bruni, J.E.</au><au>Bose, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of endothelium in hypoxic contraction of canine basilar artery</atitle><jtitle>British journal of pharmacology</jtitle><addtitle>Br J Pharmacol</addtitle><date>1989-04</date><risdate>1989</risdate><volume>96</volume><issue>4</issue><spage>949</spage><epage>955</epage><pages>949-955</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><coden>BJPCBM</coden><abstract>1
Reversible contraction of canine basilar artery, produced by hypoxia, persisted after mechanical and chemical removal of the endothelium. The removal of endothelium was confirmed by scanning electron microscopy as well as by the abolition or reversal of the relaxant response to acetylcholine or arginine8‐vasopressin.
2
Hydroquinone, believed to block selectively endothelium‐mediated relaxation, also preferentially attenuated hypoxic contractions even in the absence of endothelium but did not reduce responses to 5‐hydroxytryptamine (5‐HT) or high external potassium.
3
Contractions induced by red blood cell haemolysate, which occur independently of the endothelium, were also selectively attenuated by hydroquinone.
4
Contractions caused by hypoxia were inhibited by pretreatment with adenosine or by its application after contraction had developed.
5
Hypoxic contraction in canine basilar artery may result partly from a direct effect on smooth muscle as well as through the endothelium.
6
Hydroquinone may have an additional locus of action in smooth muscle cells besides its well known effect on the endothelium.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>2743085</pmid><doi>10.1111/j.1476-5381.1989.tb11906.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine - pharmacology Animals Arginine Vasopressin - pharmacology Basilar Artery - physiology Biological and medical sciences Blood vessels and receptors Dogs endothelium Endothelium, Vascular - physiology Female Fundamental and applied biological sciences. Psychology Hemoglobins - pharmacology Hydroquinones - pharmacology hypoxia Hypoxia - physiopathology In Vitro Techniques Isometric Contraction - drug effects Male Microscopy, Electron, Scanning Muscle Contraction - drug effects Muscle Relaxation - drug effects Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - physiology Potassium Chloride - pharmacology smooth muscle Vertebrates: cardiovascular system |
title | Role of endothelium in hypoxic contraction of canine basilar artery |
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