Arginine vasopressin in fever: a still unsolved puzzle
(1) Administration of arginine vasopressin (AVP) in the ventral septal area (VSA) or intracerebroventricularly (i.c.v.) is thought to attenuate lipopolysaccharide (LPS) or prostaglandin (PG) E 2 fevers in rabbits and rats by acting on the V 1 receptor. (2) We found that the fever response of rabbits...
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| Veröffentlicht in: | Journal of thermal biology 2004-10, Vol.29 (7), p.407-411 |
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| container_title | Journal of thermal biology |
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| creator | Romanovsky, Andrej A. Steiner, Alexandre A. S. Branco, Luiz G. Janský, Ladislav Gourine, Valery N. |
| description | (1) Administration of arginine vasopressin (AVP) in the ventral septal area (VSA) or intracerebroventricularly (i.c.v.) is thought to attenuate lipopolysaccharide (LPS) or prostaglandin (PG) E
2 fevers in rabbits and rats by acting on the V
1 receptor. (2) We found that the fever response of rabbits to intravenous LPS (200
ng/kg) or intra-VSA PGE
2 (500
ng) was not attenuated but enhanced by intra-VSA AVP (5 μg); a pharmacological analysis showed that this fever-enhancing effect was mediated by the V
2 receptor. (3) The febrile response of rats to intraperitoneal (50
μg/kg) or i.c.v. (100
ng) LPS was unaffected by i.c.v. AVP (2.5–100
ng). (4) The role of AVP in fever should be re-examined. |
| doi_str_mv | 10.1016/j.jtherbio.2004.08.007 |
| format | Article |
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2 fevers in rabbits and rats by acting on the V
1 receptor. (2) We found that the fever response of rabbits to intravenous LPS (200
ng/kg) or intra-VSA PGE
2 (500
ng) was not attenuated but enhanced by intra-VSA AVP (5 μg); a pharmacological analysis showed that this fever-enhancing effect was mediated by the V
2 receptor. (3) The febrile response of rats to intraperitoneal (50
μg/kg) or i.c.v. (100
ng) LPS was unaffected by i.c.v. AVP (2.5–100
ng). (4) The role of AVP in fever should be re-examined.</description><identifier>ISSN: 0306-4565</identifier><identifier>EISSN: 1879-0992</identifier><identifier>DOI: 10.1016/j.jtherbio.2004.08.007</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Antipyresis ; Arginine vasopressin ; AVP ; Body temperature ; Fever ; Lipopolysaccharides ; Prostaglandins ; V 1 receptor ; V 2 receptor</subject><ispartof>Journal of thermal biology, 2004-10, Vol.29 (7), p.407-411</ispartof><rights>2004 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c321t-2c04ebaf4ad9c30b7c8ab079887eb772511cce8f7b8fda50ce2a00f185b8eb1f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jtherbio.2004.08.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Romanovsky, Andrej A.</creatorcontrib><creatorcontrib>Steiner, Alexandre A.</creatorcontrib><creatorcontrib>S. Branco, Luiz G.</creatorcontrib><creatorcontrib>Janský, Ladislav</creatorcontrib><creatorcontrib>Gourine, Valery N.</creatorcontrib><title>Arginine vasopressin in fever: a still unsolved puzzle</title><title>Journal of thermal biology</title><description>(1) Administration of arginine vasopressin (AVP) in the ventral septal area (VSA) or intracerebroventricularly (i.c.v.) is thought to attenuate lipopolysaccharide (LPS) or prostaglandin (PG) E
2 fevers in rabbits and rats by acting on the V
1 receptor. (2) We found that the fever response of rabbits to intravenous LPS (200
ng/kg) or intra-VSA PGE
2 (500
ng) was not attenuated but enhanced by intra-VSA AVP (5 μg); a pharmacological analysis showed that this fever-enhancing effect was mediated by the V
2 receptor. (3) The febrile response of rats to intraperitoneal (50
μg/kg) or i.c.v. (100
ng) LPS was unaffected by i.c.v. AVP (2.5–100
ng). (4) The role of AVP in fever should be re-examined.</description><subject>Antipyresis</subject><subject>Arginine vasopressin</subject><subject>AVP</subject><subject>Body temperature</subject><subject>Fever</subject><subject>Lipopolysaccharides</subject><subject>Prostaglandins</subject><subject>V 1 receptor</subject><subject>V 2 receptor</subject><issn>0306-4565</issn><issn>1879-0992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLxDAUhYMoOI7-BelK3LTetM2jrhwGXzDgRtchSW81pdPWpC04v94Oo1uFC3fznQPnI-SSQkKB8ps6qYcP9MZ1SQqQJyATAHFEFlSKIoaiSI_JAjLgcc44OyVnIdQAlGUMFoSv_LtrXYvRpEPXewzBtdF8FU7obyMdhcE1TTS2oWsmLKN-3O0aPCcnlW4CXvz8JXl7uH9dP8Wbl8fn9WoT2yylQ5xayNHoKtdlYTMwwkptQBRSCjRCpIxSa1FWwsiq1AwsphqgopIZiYZW2ZJcH3p7332OGAa1dcFi0-gWuzGoeSKTOaM8ndGrv1HBJQcGM8gPoPVdCB4r1Xu31f5LUVB7o6pWv0bV3qgCqWajc_DuEMR58eTQq2AdthZL59EOquzcfxXf7U2DLw</recordid><startdate>20041001</startdate><enddate>20041001</enddate><creator>Romanovsky, Andrej A.</creator><creator>Steiner, Alexandre A.</creator><creator>S. Branco, Luiz G.</creator><creator>Janský, Ladislav</creator><creator>Gourine, Valery N.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>20041001</creationdate><title>Arginine vasopressin in fever: a still unsolved puzzle</title><author>Romanovsky, Andrej A. ; Steiner, Alexandre A. ; S. Branco, Luiz G. ; Janský, Ladislav ; Gourine, Valery N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-2c04ebaf4ad9c30b7c8ab079887eb772511cce8f7b8fda50ce2a00f185b8eb1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Antipyresis</topic><topic>Arginine vasopressin</topic><topic>AVP</topic><topic>Body temperature</topic><topic>Fever</topic><topic>Lipopolysaccharides</topic><topic>Prostaglandins</topic><topic>V 1 receptor</topic><topic>V 2 receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Romanovsky, Andrej A.</creatorcontrib><creatorcontrib>Steiner, Alexandre A.</creatorcontrib><creatorcontrib>S. Branco, Luiz G.</creatorcontrib><creatorcontrib>Janský, Ladislav</creatorcontrib><creatorcontrib>Gourine, Valery N.</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of thermal biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romanovsky, Andrej A.</au><au>Steiner, Alexandre A.</au><au>S. Branco, Luiz G.</au><au>Janský, Ladislav</au><au>Gourine, Valery N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arginine vasopressin in fever: a still unsolved puzzle</atitle><jtitle>Journal of thermal biology</jtitle><date>2004-10-01</date><risdate>2004</risdate><volume>29</volume><issue>7</issue><spage>407</spage><epage>411</epage><pages>407-411</pages><issn>0306-4565</issn><eissn>1879-0992</eissn><abstract>(1) Administration of arginine vasopressin (AVP) in the ventral septal area (VSA) or intracerebroventricularly (i.c.v.) is thought to attenuate lipopolysaccharide (LPS) or prostaglandin (PG) E
2 fevers in rabbits and rats by acting on the V
1 receptor. (2) We found that the fever response of rabbits to intravenous LPS (200
ng/kg) or intra-VSA PGE
2 (500
ng) was not attenuated but enhanced by intra-VSA AVP (5 μg); a pharmacological analysis showed that this fever-enhancing effect was mediated by the V
2 receptor. (3) The febrile response of rats to intraperitoneal (50
μg/kg) or i.c.v. (100
ng) LPS was unaffected by i.c.v. AVP (2.5–100
ng). (4) The role of AVP in fever should be re-examined.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.jtherbio.2004.08.007</doi><tpages>5</tpages></addata></record> |
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| source | Elsevier ScienceDirect Journals Complete |
| subjects | Antipyresis Arginine vasopressin AVP Body temperature Fever Lipopolysaccharides Prostaglandins V 1 receptor V 2 receptor |
| title | Arginine vasopressin in fever: a still unsolved puzzle |
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