Abstract
Endothelin-1 (ET-1) is recognized as being involved in the pathophysiology of cerebrovascular diseases. Using organ culture as a model for possible pathological changes we studied changes in ET(A) and ETB receptor function using a sensitive in vitro method. We observed an up-regulation of the ET(B) receptor and an amazingly increased sensitivity to ET-1 by 3 log units in pEC50; pEC50(fresh) was 8.7 +/- 0.1, and pEC50(cultured) was 11.7 +/- 0.3. pA2 for FR139317 in the fresh vessel was 7.0 +/- 0.2 whereas it could not be obtained for the cultured vessel, indicating a possible cross-talk between the ET(A) and ET(B) receptors. The increased sensitivity to ET-1 could also take place during cerebrovascular disease such as stroke or haemorrhage rendering the vessels considerably more sensitive to ET-1.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Azepines / pharmacology
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Basilar Artery / drug effects*
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Basilar Artery / metabolism
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Basilar Artery / physiology
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Biphenyl Compounds / pharmacology
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Dipeptides / pharmacology
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Endothelin Receptor Antagonists
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Endothelin-1 / pharmacology*
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Indoles / pharmacology
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Organ Culture Techniques
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Rats
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Rats, Inbred WKY
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Receptor, Endothelin A
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Receptor, Endothelin B
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Receptors, Endothelin / agonists
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Receptors, Endothelin / metabolism
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Vasoconstriction
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Vasoconstrictor Agents / pharmacology
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Viper Venoms / pharmacology
Substances
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Azepines
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Biphenyl Compounds
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Dipeptides
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Endothelin Receptor Antagonists
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Endothelin-1
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IRL 2500
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Indoles
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Receptor, Endothelin A
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Receptor, Endothelin B
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Receptors, Endothelin
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Vasoconstrictor Agents
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Viper Venoms
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sarafotoxins s6
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FR 139317