Publication:
5-HT causes splanchnic venodilation

dc.contributor.coauthorSeitz, Bridget M.
dc.contributor.coauthorKrieger-Burke, Teresa
dc.contributor.coauthorDarios, Emma S.
dc.contributor.coauthorThompson, Janice M.
dc.contributor.coauthorFink, Gregory D.
dc.contributor.coauthorWatts, Stephanie W.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorOrer, Hakan S.
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:01:25Z
dc.date.issued2017
dc.description.abstractSerotonin [5-hydroxytryptamine (5-HT)] causes relaxation of the isolated superior mesenteric vein, a splanchnic blood vessel, through activation of the 5-HT7 receptor. As part of studies designed to identify the mechanism(s) through which chronic (>= 24 h) infusion of 5-HT lowers blood pressure, we tested the hypothesis that 5-HT causes in vitro and in vivo splanchnic venodilation that is 5-HT7 receptor dependent. In tissue baths for measurement of isometric contraction, the portal vein and abdominal inferior vena cava relaxed to 5-HT and the 5-HT1/7 receptor agonist 5-carboxamidotryptamine; relaxation was abolished by the 5-HT7 receptor antagonist SB-269970. Western blot analyses showed that the abdominal inferior vena cava and portal vein express 5-HT7 receptor protein. In contrast, the thoracic vena cava, outside the splanchnic circulation, did not relax to serotonergic agonists and exhibited minimal expression of the 5-HT7 receptor. Male SpragueDawley rats with chronically implanted radiotelemetry transmitters underwent repeated ultrasound imaging of abdominal vessels. After baseline imaging, minipumps containing vehicle (saline) or 5-HT (25 mu g.kg(-1).min(-1)) were implanted. Twenty-four hours later, venous diameters were increased in rats with 5-HT-infusion (percent increase from baseline: superior mesenteric vein, 17.5 +/- 1.9; portal vein, 17.7 +/- 1.8; and abdominal inferior vena cava, 46.9 +/- 8.0) while arterial pressure was decreased (similar to 13 mmHg). Measures returned to baseline after infusion termination. In a separate group of animals, treatment with SB-269970 (3 mg/kg iv) prevented the splanchnic venodilation and fall in blood pressure during 24 h of 5-HT infusion. Thus, 5-HT causes 5-HT7 receptor-dependent splanchnic venous dilation associated with a fall in blood pressure. NEW & NOTEWORTHY This research is noteworthy because it combines and links, through the 5-HT7 receptor, an in vitro observation (venorelaxation) with in vivo events (venodilation and fall in blood pressure). This supports the idea that splanchnic venodilation plays a role in blood pressure regulation.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipNational Heart, Lung, and Blood Institute Grant [HL-107495] This work was funded by National Heart, Lung, and Blood Institute Grant HL-107495 (to S. Watts).
dc.description.volume313
dc.identifier.doi10.1152/ajpheart.00165.2017
dc.identifier.eissn1522-1539
dc.identifier.issn0363-6135
dc.identifier.scopus2-s2.0-85029364111
dc.identifier.urihttps://doi.org/10.1152/ajpheart.00165.2017
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8235
dc.identifier.wos412064100010
dc.keywordsBlood pressure
dc.keywordsImaging
dc.keywordsPharmacology
dc.keywordsVeins
dc.keywordsSB-269970
dc.keywordsSerotonin endothelium-dependent relaxation
dc.keywordsIsolated jugular-vein
dc.keywordsBlood-pressure
dc.keywordsHypertensive-rats
dc.keywordsPharmacological evidence
dc.keywordsAnesthetized rats
dc.keywordsPulmonary vein
dc.keywordsVena-cava
dc.keywordsSerotonin
dc.keywordsReceptor
dc.language.isoeng
dc.publisherAmer Physiological Soc
dc.relation.ispartofAmerican Journal of Physiology-Heart and Circulatory Physiology
dc.subjectCardiac and cardiovascular systems
dc.subjectPhysiology
dc.subjectPeripheral vascular disease
dc.title5-HT causes splanchnic venodilation
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorOrer, Hakan S.
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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