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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1984-4-26
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pubmed:abstractText |
Studies in clinical and experimental hypertension have identified alterations both in intracellular [Na+] and in response to hormones and neurotransmitters. We propose a hypothesis that links these two alterations. Based on recent data showing that changes in intracellular [Na+] can alter the affinity and function of platelet alpha2-adrenergic receptors, we hypothesize that elevated intracellular [Na+] in hypertension leads to enhanced response at membrane receptors. This enhancement in response to hormones and/or neurotransmitters could then contribute to the development and maintenance of the hypertensive state. Because a variety of membrane receptors are Na+-sensitive (e.g., adrenergic, muscarinic cholinergic, opiate, angiotensin, dopamine, histamine H1), this mechanism may be operative at one or more receptor types located in tissues critical to the pathophysiology of hypertension.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0024-3205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
12
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1009-13
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6321865-Animals,
pubmed-meshheading:6321865-Blood Pressure,
pubmed-meshheading:6321865-Cell Membrane,
pubmed-meshheading:6321865-Humans,
pubmed-meshheading:6321865-Hypertension,
pubmed-meshheading:6321865-Kidney,
pubmed-meshheading:6321865-Receptors, Adrenergic,
pubmed-meshheading:6321865-Receptors, Cell Surface,
pubmed-meshheading:6321865-Receptors, Neurotransmitter,
pubmed-meshheading:6321865-Sodium
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pubmed:year |
1984
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pubmed:articleTitle |
A hypothesis linking intracellular sodium, membrane receptors, and hypertension.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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