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http://hdl.handle.net/11452/32309
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DC Field | Value | Language |
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dc.contributor.author | Millington, William R. | - |
dc.contributor.author | Feleder, Carlos | - |
dc.date.accessioned | 2023-04-11T08:02:49Z | - |
dc.date.available | 2023-04-11T08:02:49Z | - |
dc.date.issued | 2016-03-21 | - |
dc.identifier.citation | Millington, W. R. vd. (2016). "The initial fall in arterial pressure evoked by endotoxin is mediated by the ventrolateral periaqueductal gray". Clinical and Experimental Pharmacology and Physiology, 43(6), 612-615. | en_US |
dc.identifier.issn | 1440-1681 | - |
dc.identifier.uri | https://doi.org/10.1111/1440-1681.12573 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/1440-1681.12573 | - |
dc.identifier.uri | http://hdl.handle.net/11452/32309 | - |
dc.description.abstract | This study tested the hypothesis that the initial fall in arterial pressure evoked by lipopolysaccharide (LPS) is mediated by the ventrolateral column of the midbrain periaqueductal gray region (vlPAG). To test this hypothesis, the local anaesthetic lidocaine (2%; 0.1L, 0.2L or 1.0L), the delta opioid receptor antagonist naltrindole (2nmol) or saline was microinjected into the vlPAG of isoflurane-anaesthetized rats bilaterally and LPS (1mg/kg) or saline was administered intravenously 2min later. Both lidocaine and naltrindole inhibited LPS-evoked hypotension significantly but did not affect arterial pressure in saline-treated control animals. Neither lidocaine nor naltrindole altered heart rate significantly in either LPS-treated or control animals. Microinjection of lidocaine or naltrindole into the dorsolateral PAG was ineffective. These data indicate that the vlPAG plays an important role in the initiation of endotoxic hypotension and further show that delta opioid receptors in the vlPAG participate in the response. | en_US |
dc.description.sponsorship | United States Department of Health & Human Services | en_US |
dc.description.sponsorship | National Institutes of Health (NIH) - USA | en_US |
dc.description.sponsorship | NIH National Institute of Allergy & Infectious Diseases (NIAID) - R15AI072744 | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Pharmacology & pharmacy | en_US |
dc.subject | Physiology | en_US |
dc.subject | Delta receptor | en_US |
dc.subject | Endotoxin | en_US |
dc.subject | Endotoxin shock | en_US |
dc.subject | Lipopolysaccharide | en_US |
dc.subject | Opioid receptor | en_US |
dc.subject | Periaqueductal gray | en_US |
dc.subject | Preoptic area | en_US |
dc.subject | Anterior hypothalamic area | en_US |
dc.subject | Sympathetic-nerve activity | en_US |
dc.subject | Delta-opioid receptors | en_US |
dc.subject | Cardiovascular-responses | en_US |
dc.subject | Induced hypotension | en_US |
dc.subject | Projection pathway | en_US |
dc.subject | Preoptic area | en_US |
dc.subject | Rats | en_US |
dc.subject | Shock | en_US |
dc.subject | Nucleus | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Arterial pressure | en_US |
dc.subject.mesh | Endotoxins | en_US |
dc.subject.mesh | Injections, intraventricular | en_US |
dc.subject.mesh | Lipopolysaccharides | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Periaqueductal gray | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, sprague-dawley | en_US |
dc.title | The initial fall in arterial pressure evoked by endotoxin is mediated by the ventrolateral periaqueductal gray | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000375936600004 | tr_TR |
dc.identifier.scopus | 2-s2.0-84964902052 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Farmakoloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-9496-1475 | tr_TR |
dc.identifier.startpage | 612 | tr_TR |
dc.identifier.endpage | 615 | tr_TR |
dc.identifier.volume | 43 | tr_TR |
dc.identifier.issue | 6 | tr_TR |
dc.relation.journal | Clinical and Experimental Pharmacology and Physiology | en_US |
dc.contributor.buuauthor | Yılmaz, Mustafa Sertaç | - |
dc.contributor.researcherid | AAH-1571-2021 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.identifier.pubmed | 27009880 | tr_TR |
dc.subject.wos | Pharmacology & pharmacy | en_US |
dc.subject.wos | Physiology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.contributor.scopusid | 8895544100 | tr_TR |
dc.subject.scopus | Periaqueductal Gray; Animals; Escape Reaction | en_US |
dc.subject.emtree | Delta opiate receptor | en_US |
dc.subject.emtree | Endotoxin | en_US |
dc.subject.emtree | Isoflurane | en_US |
dc.subject.emtree | Lidocaine | en_US |
dc.subject.emtree | Lipopolysaccharide | en_US |
dc.subject.emtree | Naltrindole | en_US |
dc.subject.emtree | Sodium chloride | en_US |
dc.subject.emtree | Endotoxin | en_US |
dc.subject.emtree | Animal experiment | en_US |
dc.subject.emtree | Arterial pressure | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Heart rate | en_US |
dc.subject.emtree | Hypotension | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Periaqueductal gray matter | en_US |
dc.subject.emtree | Rat | en_US |
dc.subject.emtree | Treatment response | en_US |
dc.subject.emtree | Animal | en_US |
dc.subject.emtree | Arterial pressure | en_US |
dc.subject.emtree | Drug effects | en_US |
dc.subject.emtree | Intracerebroventricular drug administration | en_US |
dc.subject.emtree | Periaqueductal gray matter | en_US |
dc.subject.emtree | Physiology | en_US |
dc.subject.emtree | Sprague dawley rat | en_US |
Appears in Collections: | Scopus Web of Science |
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