Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1990-12-7
|
pubmed:abstractText |
In vitro studies were undertaken to investigate the effects of external potassium [K+]o, 0-7.1 mM, and magnesium [Mg2+]o, 0-4.8 mM, concentration on canine middle cerebral and basilar arterial basal tone and on 5-hydroxytryptamine (5-HT)-induced contractions. The lower the [K+]o, the greater the degree of spontaneous contraction upon acute withdrawal of [Mg2+]o. An inverse linear relationship between the concentration of [K+]o and the degree of cerebrovasospasm upon acute withdrawal of [Mg2+]o was observed over the range of 1-6 mM [K+]o. As [K+]o was increased, stepwise, the slow phase of the contractions became attenuated, while the magnitude of the fast phase became progressively smaller. Acute withdrawal of [K+]o produced contraction of middle cerebral and basilar arteries which could be modulated by the concentration of [Mg2+]o. The higher the [Mg2+]o, the less the tension developed upon acute withdrawal of [K+]o. Contractility to 5-HT was depressed when [K+]o was lowered. This attenuation was reversed completely when [Mg2+]o was acutely withdrawn. Sensitivity (EC50) of canine middle cerebral and basilar arteries to 5-HT was inversely related to the [K+]o/[Mg2+]o ratio. These actions took place over pathophysiological ranges of [K+]o and [Mg2+]o. Maintenance of a constant [K+]o/[Mg2+]o ratio, irrespective of the exact [K+]o and [Mg2+]o, produced similar degrees of maximum tension and sensitivity (EC50) to 5-HT. Use of intact ring preparations and helically cut vascular strips produced similar results with varying [K+]o/[Mg2+]o. A variety of pharmacological receptor antagonists (phentolamine, propranolol, atropine, diphenhydramine, cimetidine), as well as a prostaglandin cyclo-oxygenase inhibitor, did not modify the altered contractile responses or basal tone evoked by varying the [K+]o/[Mg2+]o ratios. These experiments suggest: (1) that basal tone and contractility of canine cerebral vascular smooth muscle cells appear to be exquisitely sensitive to alterations in extracellular K+ and Mg2+ and (2) that 5-HT receptor-operated Ca2+ channels, as well as those Ca2+ channels involved in the generation of cerebral arterial basal tone, are modulated and controlled by the precise concentrations of [K+]o and [Mg2+]o.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
1015-3845
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
9
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
79-93
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:2222803-Animals,
pubmed-meshheading:2222803-Cerebral Arteries,
pubmed-meshheading:2222803-Dogs,
pubmed-meshheading:2222803-Dose-Response Relationship, Drug,
pubmed-meshheading:2222803-Female,
pubmed-meshheading:2222803-Magnesium,
pubmed-meshheading:2222803-Male,
pubmed-meshheading:2222803-Muscle, Smooth, Vascular,
pubmed-meshheading:2222803-Muscle Contraction,
pubmed-meshheading:2222803-Muscle Tonus,
pubmed-meshheading:2222803-Potassium,
pubmed-meshheading:2222803-Serotonin
|
pubmed:year |
1990
|
pubmed:articleTitle |
Extracellular magnesium and potassium concentrations interact to modulate tone and reactivity of isolated canine cerebral vascular muscle.
|
pubmed:affiliation |
Department of Physiology, State University of New York, Brooklyn.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|