Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2-3
pubmed:dateCreated
1997-7-14
pubmed:abstractText
M7 (5,6-dihydroxy-2-dimethylaminotetralin) produces in anesthetized rats a hypotensive response previously attributed to peripheral dopaminergic mechanisms. We re-examined the effects of this drug on arterial blood pressure, heart rate and sympathetic nerve activity in anesthetized rats and dogs. M7 (1-100 micrograms/kg i.v.) produced in the rats transient dose-dependent pressor effects, with bradycardia and sympatho-inhibition, followed by long-lasting dose-dependent hypotension, bradycardia and sympatho-inhibition. The sympatho-inhibitory and hypotensive effects were comparable in baroreceptor-denervated rats and were reversed by idazoxan (0.1 mg/kg i.v.). The sympatho-inhibitory response induced by M7 (1-100 micrograms/kg) was prevented by treatment with the specific alpha 2-adrenoceptor antagonist, 2-methoxy-idazoxan (0.03 mg/kg i.v.). This central effect of M7 was not altered by treatment with the alpha 1-adrenoceptor antagonist, prazosin (0.1 mg/kg i.v.), and was reduced by treatment with the alpha 2-adrenoceptor antagonists, yohimbine (1 mg/kg i.v.) or idazoxan (0.3 mg/kg i.v.), and the dopaminergic antagonists, haloperidol (0.5 mg/kg i.v.) or sulpiride (3 mg/kg i.v.). Bilateral microinjections of M7 (0.3-3 nmol) into the rostroventral medulla in the rat produced dose-dependent hypotension, bradycardia and sympathetic nerve inhibition which were reversed and prevented by bilateral microinjection of 2-methoxy-idazoxan (1 nmol) into the same sites. Microinjections of 2-methoxy-idazoxan into the rostroventral medulla also inhibited the central effects of M7 at 0.03 mg/kg i.v. In anesthetized dogs, M7 administered into the cisterna magna (1-10 micrograms/kg) reduced arterial blood pressure, heart rate and sympathetic nerve activity; these effects were reversed by administration of 2-methoxy-idazoxan (0.03 mg/kg i.v.). In conclusion, M7, a rigid catecholamine, produces a potent central sympatho-inhibitory and hypotensive effect by activation of alpha 2-adrenoceptors.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0014-2999
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
320
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
151-9
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed-meshheading:9059848-Adrenergic alpha-Antagonists, pubmed-meshheading:9059848-Anesthesia, pubmed-meshheading:9059848-Animals, pubmed-meshheading:9059848-Blood Pressure, pubmed-meshheading:9059848-Central Nervous System, pubmed-meshheading:9059848-Cisterna Magna, pubmed-meshheading:9059848-Dogs, pubmed-meshheading:9059848-Dopamine Antagonists, pubmed-meshheading:9059848-Dose-Response Relationship, Drug, pubmed-meshheading:9059848-Emetics, pubmed-meshheading:9059848-Female, pubmed-meshheading:9059848-Heart Rate, pubmed-meshheading:9059848-Idazoxan, pubmed-meshheading:9059848-Male, pubmed-meshheading:9059848-Microinjections, pubmed-meshheading:9059848-Naphthols, pubmed-meshheading:9059848-Pressoreceptors, pubmed-meshheading:9059848-Rats, pubmed-meshheading:9059848-Rats, Sprague-Dawley, pubmed-meshheading:9059848-Receptors, Adrenergic, alpha-2, pubmed-meshheading:9059848-Splanchnic Nerves, pubmed-meshheading:9059848-Sympathetic Nervous System, pubmed-meshheading:9059848-Vagotomy
pubmed:year
1997
pubmed:articleTitle
The central sympatho-inhibitory effect of 5,6-dihydroxy-2-dimethylaminotetralin (M7) is mediated by alpha 2-adrenoceptors.
pubmed:affiliation
Division of Angiology, Servier Research Institute, Suresnes, France.
pubmed:publicationType
Journal Article