Influence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the rat
In this study we investigated the influence of d(CH 2) 5-Tyr(Me)-[Arg 8]vasopressin (AAVP) and [adamanteanacetyl 1,0-ET- d-Tyr 2,Val 4,aminobutyryl 6,Arg 8,9]-[Arg 8]vasopressin (ATAVP), which are antagonists of vasopressin V 1 and V 2 receptors, and the effects of losartan, a selective angiotensin...
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| Veröffentlicht in: | Autonomic neuroscience 2004-03, Vol.111 (1), p.66-70 |
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| creator | Abrão Saad, Wilson Antonio de Arruda Camargo, Luiz Sérgio Cerri, Paulo Simões, Silvio Abrão Saad, William Garcia, Gustavo Izabel Gutierrez, Laura Guarda, Ismael Saad Guarda, Renata |
| description | In this study we investigated the influence of d(CH
2)
5-Tyr(Me)-[Arg
8]vasopressin (AAVP) and [adamanteanacetyl
1,0-ET-
d-Tyr
2,Val
4,aminobutyryl
6,Arg
8,9]-[Arg
8]vasopressin (ATAVP), which are antagonists of vasopressin V
1 and V
2 receptors, and the effects of losartan, a selective angiotensin AT
1 receptor antagonist, and CGP42112A, a selective AT
2 receptor antagonist, injected into the lateral septal area (LSA) on thirst and hypertension induced by [Arg
8]vasopressin (AVP). AAVP and ATAVP injected into the LSA reduced the drinking responses elicited by injecting AVP into the LSA. Both the AT
1 and AT
2 ligands administered into the LSA elicited a concentration-dependent decrease in the water intake induced by AVP injected into the LSA, but losartan was more effective than CGP42112A. The increase in MAP, due to injection of AVP into the LSA, was reduced by prior injection of AAVP from 18±1 to 6±1 mm Hg. Losartan injected into the LSA prior to AVP reduced the increase in MAP to 7±0.8 mm Hg. ATAVP and CGP42112A produced no changes in the pressor effect of AVP. These results suggest that the dipsogenic effects induced by injecting AVP into the LSA were mediated primarily by AT
1 receptors. However, doses of losartan were more effective when combined with CGP42112A than when given alone, suggesting that the thirst induced by AVP injections into LSA may involve activation of multiple AVP and angiotensin II receptor subtypes. The pressor response of AVP was reduced by losartan and by AAVP. CGP42112A and ATAVP did not change the AVP pressor response. These results suggest that facilitator effects of AVP on water intake are mediated through the activation of V
1 receptors and that the inhibitory effect requires V
2 receptors. The involvement of AT
1 and AT
2 receptors can be postulated. Based on the present findings, we suggest that the AVP in the LSA may play a role in the control of water and arterial blood pressure balance. |
| doi_str_mv | 10.1016/j.autneu.2003.08.013 |
| format | Article |
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2)
5-Tyr(Me)-[Arg
8]vasopressin (AAVP) and [adamanteanacetyl
1,0-ET-
d-Tyr
2,Val
4,aminobutyryl
6,Arg
8,9]-[Arg
8]vasopressin (ATAVP), which are antagonists of vasopressin V
1 and V
2 receptors, and the effects of losartan, a selective angiotensin AT
1 receptor antagonist, and CGP42112A, a selective AT
2 receptor antagonist, injected into the lateral septal area (LSA) on thirst and hypertension induced by [Arg
8]vasopressin (AVP). AAVP and ATAVP injected into the LSA reduced the drinking responses elicited by injecting AVP into the LSA. Both the AT
1 and AT
2 ligands administered into the LSA elicited a concentration-dependent decrease in the water intake induced by AVP injected into the LSA, but losartan was more effective than CGP42112A. The increase in MAP, due to injection of AVP into the LSA, was reduced by prior injection of AAVP from 18±1 to 6±1 mm Hg. Losartan injected into the LSA prior to AVP reduced the increase in MAP to 7±0.8 mm Hg. ATAVP and CGP42112A produced no changes in the pressor effect of AVP. These results suggest that the dipsogenic effects induced by injecting AVP into the LSA were mediated primarily by AT
1 receptors. However, doses of losartan were more effective when combined with CGP42112A than when given alone, suggesting that the thirst induced by AVP injections into LSA may involve activation of multiple AVP and angiotensin II receptor subtypes. The pressor response of AVP was reduced by losartan and by AAVP. CGP42112A and ATAVP did not change the AVP pressor response. These results suggest that facilitator effects of AVP on water intake are mediated through the activation of V
1 receptors and that the inhibitory effect requires V
2 receptors. The involvement of AT
1 and AT
2 receptors can be postulated. Based on the present findings, we suggest that the AVP in the LSA may play a role in the control of water and arterial blood pressure balance.</description><identifier>ISSN: 1566-0702</identifier><identifier>EISSN: 1872-7484</identifier><identifier>DOI: 10.1016/j.autneu.2003.08.013</identifier><identifier>PMID: 15109940</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Angiotensin receptor subtypes ; Animals ; Antagonist V 1 ; Antagonist V 2 ; Antidiuretic Hormone Receptor Antagonists ; Antihypertensive Agents - administration & dosage ; Arterial pressure ; Biological and medical sciences ; Blood Pressure - drug effects ; Blood Pressure - physiology ; Dose-Response Relationship, Drug ; Drinking - drug effects ; Drinking - physiology ; Fundamental and applied biological sciences. Psychology ; Injections, Intraventricular ; Lateral septal area ; Losartan - administration & dosage ; Male ; Oligopeptides - pharmacology ; Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ ; Rats ; Receptors, Angiotensin ; Septum of Brain - drug effects ; Vasoconstrictor Agents - administration & dosage ; Vasopressin ; Vasopressins - administration & dosage ; Vertebrates: nervous system and sense organs ; Water intake</subject><ispartof>Autonomic neuroscience, 2004-03, Vol.111 (1), p.66-70</ispartof><rights>2004 Elsevier B.V.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2004 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-14a4529f123e80c2ab84ec76b0f715ff16bfbb013280eebd8dc6ca43776ec51e3</citedby><cites>FETCH-LOGICAL-c388t-14a4529f123e80c2ab84ec76b0f715ff16bfbb013280eebd8dc6ca43776ec51e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.autneu.2003.08.013$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15688992$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15109940$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abrão Saad, Wilson</creatorcontrib><creatorcontrib>Antonio de Arruda Camargo, Luiz</creatorcontrib><creatorcontrib>Sérgio Cerri, Paulo</creatorcontrib><creatorcontrib>Simões, Silvio</creatorcontrib><creatorcontrib>Abrão Saad, William</creatorcontrib><creatorcontrib>Garcia, Gustavo</creatorcontrib><creatorcontrib>Izabel Gutierrez, Laura</creatorcontrib><creatorcontrib>Guarda, Ismael</creatorcontrib><creatorcontrib>Saad Guarda, Renata</creatorcontrib><title>Influence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the rat</title><title>Autonomic neuroscience</title><addtitle>Auton Neurosci</addtitle><description>In this study we investigated the influence of d(CH
2)
5-Tyr(Me)-[Arg
8]vasopressin (AAVP) and [adamanteanacetyl
1,0-ET-
d-Tyr
2,Val
4,aminobutyryl
6,Arg
8,9]-[Arg
8]vasopressin (ATAVP), which are antagonists of vasopressin V
1 and V
2 receptors, and the effects of losartan, a selective angiotensin AT
1 receptor antagonist, and CGP42112A, a selective AT
2 receptor antagonist, injected into the lateral septal area (LSA) on thirst and hypertension induced by [Arg
8]vasopressin (AVP). AAVP and ATAVP injected into the LSA reduced the drinking responses elicited by injecting AVP into the LSA. Both the AT
1 and AT
2 ligands administered into the LSA elicited a concentration-dependent decrease in the water intake induced by AVP injected into the LSA, but losartan was more effective than CGP42112A. The increase in MAP, due to injection of AVP into the LSA, was reduced by prior injection of AAVP from 18±1 to 6±1 mm Hg. Losartan injected into the LSA prior to AVP reduced the increase in MAP to 7±0.8 mm Hg. ATAVP and CGP42112A produced no changes in the pressor effect of AVP. These results suggest that the dipsogenic effects induced by injecting AVP into the LSA were mediated primarily by AT
1 receptors. However, doses of losartan were more effective when combined with CGP42112A than when given alone, suggesting that the thirst induced by AVP injections into LSA may involve activation of multiple AVP and angiotensin II receptor subtypes. The pressor response of AVP was reduced by losartan and by AAVP. CGP42112A and ATAVP did not change the AVP pressor response. These results suggest that facilitator effects of AVP on water intake are mediated through the activation of V
1 receptors and that the inhibitory effect requires V
2 receptors. The involvement of AT
1 and AT
2 receptors can be postulated. Based on the present findings, we suggest that the AVP in the LSA may play a role in the control of water and arterial blood pressure balance.</description><subject>Angiotensin receptor subtypes</subject><subject>Animals</subject><subject>Antagonist V 1</subject><subject>Antagonist V 2</subject><subject>Antidiuretic Hormone Receptor Antagonists</subject><subject>Antihypertensive Agents - administration & dosage</subject><subject>Arterial pressure</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Blood Pressure - physiology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drinking - drug effects</subject><subject>Drinking - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Injections, Intraventricular</subject><subject>Lateral septal area</subject><subject>Losartan - administration & dosage</subject><subject>Male</subject><subject>Oligopeptides - pharmacology</subject><subject>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</subject><subject>Rats</subject><subject>Receptors, Angiotensin</subject><subject>Septum of Brain - drug effects</subject><subject>Vasoconstrictor Agents - administration & dosage</subject><subject>Vasopressin</subject><subject>Vasopressins - administration & dosage</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Water intake</subject><issn>1566-0702</issn><issn>1872-7484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1TAQhSMEoqXwBgh5A7uEcX4cZ4OEKqCVKnXTri3bGRdfcu1gO0X3AXmvOs2VWjYsrLFmvjkzmlMU7ylUFCj7vKvkkhwuVQ3QVMAroM2L4pTyvi77lrcv879jrIQe6pPiTYw7AOAwsNfFCe0oDEMLp8XfS2emBZ1G4g2R4c4665Dcy-jngDFaRwJqnJMPkUg35ndnfUL3vELiotJhxki8I-knkj8yYSDWJfkLt66QE1ZORE3ej-RRegmYkXHROBJ1-GekdTvUKeezhH9UnFbF3B_zwBxkQLkuvJaCTG-LV0ZOEd8d41lx-_3bzflFeXX94_L861WpG85TSVvZdvVgaN0gB11LxVvUPVNgetoZQ5kySuU71hwQ1chHzbRsm75nqDuKzVnxadOdg_-9YExib6PGaZIO_RJFTzmrew4ZbDdQBx9jQCPmYPcyHAQFsdondmKzT6z2CeAij81tH476i9rj-NR09CsDH4-AjFpOJkinbXzGMc6Hoc7cl43DfI17i0FEbVeXR5tNS2L09v-bPAAaVcEw</recordid><startdate>20040331</startdate><enddate>20040331</enddate><creator>Abrão Saad, Wilson</creator><creator>Antonio de Arruda Camargo, Luiz</creator><creator>Sérgio Cerri, Paulo</creator><creator>Simões, Silvio</creator><creator>Abrão Saad, William</creator><creator>Garcia, Gustavo</creator><creator>Izabel Gutierrez, Laura</creator><creator>Guarda, Ismael</creator><creator>Saad Guarda, Renata</creator><general>Elsevier B.V</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>20040331</creationdate><title>Influence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the rat</title><author>Abrão Saad, Wilson ; Antonio de Arruda Camargo, Luiz ; Sérgio Cerri, Paulo ; Simões, Silvio ; Abrão Saad, William ; Garcia, Gustavo ; Izabel Gutierrez, Laura ; Guarda, Ismael ; Saad Guarda, Renata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-14a4529f123e80c2ab84ec76b0f715ff16bfbb013280eebd8dc6ca43776ec51e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Angiotensin receptor subtypes</topic><topic>Animals</topic><topic>Antagonist V 1</topic><topic>Antagonist V 2</topic><topic>Antidiuretic Hormone Receptor Antagonists</topic><topic>Antihypertensive Agents - administration & dosage</topic><topic>Arterial pressure</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Blood Pressure - physiology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drinking - drug effects</topic><topic>Drinking - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Injections, Intraventricular</topic><topic>Lateral septal area</topic><topic>Losartan - administration & dosage</topic><topic>Male</topic><topic>Oligopeptides - pharmacology</topic><topic>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</topic><topic>Rats</topic><topic>Receptors, Angiotensin</topic><topic>Septum of Brain - drug effects</topic><topic>Vasoconstrictor Agents - administration & dosage</topic><topic>Vasopressin</topic><topic>Vasopressins - administration & dosage</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Water intake</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abrão Saad, Wilson</creatorcontrib><creatorcontrib>Antonio de Arruda Camargo, Luiz</creatorcontrib><creatorcontrib>Sérgio Cerri, Paulo</creatorcontrib><creatorcontrib>Simões, Silvio</creatorcontrib><creatorcontrib>Abrão Saad, William</creatorcontrib><creatorcontrib>Garcia, Gustavo</creatorcontrib><creatorcontrib>Izabel Gutierrez, Laura</creatorcontrib><creatorcontrib>Guarda, Ismael</creatorcontrib><creatorcontrib>Saad Guarda, Renata</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>MEDLINE - Academic</collection><jtitle>Autonomic neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abrão Saad, Wilson</au><au>Antonio de Arruda Camargo, Luiz</au><au>Sérgio Cerri, Paulo</au><au>Simões, Silvio</au><au>Abrão Saad, William</au><au>Garcia, Gustavo</au><au>Izabel Gutierrez, Laura</au><au>Guarda, Ismael</au><au>Saad Guarda, Renata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the rat</atitle><jtitle>Autonomic neuroscience</jtitle><addtitle>Auton Neurosci</addtitle><date>2004-03-31</date><risdate>2004</risdate><volume>111</volume><issue>1</issue><spage>66</spage><epage>70</epage><pages>66-70</pages><issn>1566-0702</issn><eissn>1872-7484</eissn><abstract>In this study we investigated the influence of d(CH
2)
5-Tyr(Me)-[Arg
8]vasopressin (AAVP) and [adamanteanacetyl
1,0-ET-
d-Tyr
2,Val
4,aminobutyryl
6,Arg
8,9]-[Arg
8]vasopressin (ATAVP), which are antagonists of vasopressin V
1 and V
2 receptors, and the effects of losartan, a selective angiotensin AT
1 receptor antagonist, and CGP42112A, a selective AT
2 receptor antagonist, injected into the lateral septal area (LSA) on thirst and hypertension induced by [Arg
8]vasopressin (AVP). AAVP and ATAVP injected into the LSA reduced the drinking responses elicited by injecting AVP into the LSA. Both the AT
1 and AT
2 ligands administered into the LSA elicited a concentration-dependent decrease in the water intake induced by AVP injected into the LSA, but losartan was more effective than CGP42112A. The increase in MAP, due to injection of AVP into the LSA, was reduced by prior injection of AAVP from 18±1 to 6±1 mm Hg. Losartan injected into the LSA prior to AVP reduced the increase in MAP to 7±0.8 mm Hg. ATAVP and CGP42112A produced no changes in the pressor effect of AVP. These results suggest that the dipsogenic effects induced by injecting AVP into the LSA were mediated primarily by AT
1 receptors. However, doses of losartan were more effective when combined with CGP42112A than when given alone, suggesting that the thirst induced by AVP injections into LSA may involve activation of multiple AVP and angiotensin II receptor subtypes. The pressor response of AVP was reduced by losartan and by AAVP. CGP42112A and ATAVP did not change the AVP pressor response. These results suggest that facilitator effects of AVP on water intake are mediated through the activation of V
1 receptors and that the inhibitory effect requires V
2 receptors. The involvement of AT
1 and AT
2 receptors can be postulated. Based on the present findings, we suggest that the AVP in the LSA may play a role in the control of water and arterial blood pressure balance.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15109940</pmid><doi>10.1016/j.autneu.2003.08.013</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1566-0702 |
| ispartof | Autonomic neuroscience, 2004-03, Vol.111 (1), p.66-70 |
| issn | 1566-0702 1872-7484 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_71862780 |
| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | Angiotensin receptor subtypes Animals Antagonist V 1 Antagonist V 2 Antidiuretic Hormone Receptor Antagonists Antihypertensive Agents - administration & dosage Arterial pressure Biological and medical sciences Blood Pressure - drug effects Blood Pressure - physiology Dose-Response Relationship, Drug Drinking - drug effects Drinking - physiology Fundamental and applied biological sciences. Psychology Injections, Intraventricular Lateral septal area Losartan - administration & dosage Male Oligopeptides - pharmacology Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ Rats Receptors, Angiotensin Septum of Brain - drug effects Vasoconstrictor Agents - administration & dosage Vasopressin Vasopressins - administration & dosage Vertebrates: nervous system and sense organs Water intake |
| title | Influence of arginine vasopressin receptors and angiotensin receptor subtypes on the water intake and arterial blood pressure induced by vasopressin injected into the lateral septal area of the rat |
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