Cerebrovascular vasodilation to extraluminal acidosis occurs via combined activation of ATP-sensitive and Ca2+-activated potassium channels

Journal of Cerebral Blood Flow and Metabolism

Volumn 23, Issue 10, 2003, Pages 1227-1238

  Lindauer, Ute ^a,b   Vogt, Johannes ^a   Schuh Hofer, Sigrid ^a   Dreier, Jens P ^a   Dirnagl, Ulrich ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

Acidosis; Isolated middle cerebral artery; Nitric oxide; Potassium channels; Vasodilation

Indexed keywords

1 (2 HYDROXY 5 TRIFLUOROMETHYLPHENYL) 5 TRIFLUOROMETHYL 2(3H) BENZIMIDAZOLONE; 4 AMINOPYRIDINE; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATE; ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; BARIUM CHLORIDE; CALCIUM ACTIVATED POTASSIUM CHANNEL; CYCLIC GMP; GLIBENCLAMIDE; INWARDLY RECTIFYING POTASSIUM CHANNEL; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; OUABAIN; PINACIDIL; POTASSIUM CHANNEL; TETRYLAMMONIUM; VOLTAGE GATED POTASSIUM CHANNEL;

ACIDOSIS; ANIMAL TISSUE; ARTICLE; BRAIN BLOOD FLOW; CELL PH; CONTROLLED STUDY; EXTRACELLULAR PH; EXTRACELLULAR SPACE; HYPERCAPNIA; MALE; MIDDLE CEREBRAL ARTERY; NONHUMAN; PRIORITY JOURNAL; RAT; VASOCONSTRICTION; VASODILATATION;

EID: 0141925685     PISSN: 0271678X     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.WCB.0000088764.02615.B7     Document Type: Article

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