Inhibition of the human intermediate conductance Ca2+-activated K+ channel, hIK1, by volatile anesthetics

European Journal of Pharmacology

Volumn 395, Issue 2, 2000, Pages 95-101

  Namba, Tsunehisa ^a   Ishii, Takahiro M ^a   Ikeda, Mitsuko ^a   Hisano, Taizo ^a   Itoh, Tatsuya ^a   Hirota, Kiichi ^a   Adelman, John P ^b   Fukuda, Kazuhiko ^a  

^a KYOTO UNIVERSITY   (Japan)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Anesthetic; Ca2+ activated; K+ channel; volatile; Xenopus oocyte

Indexed keywords

ENFLURANE; HALOTHANE; INHALATION ANESTHETIC AGENT; ISOFLURANE; POTASSIUM CHANNEL; RECEPTOR SUBTYPE; SEVOFLURANE;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CHANNEL GATING; CONDUCTANCE; CONTROLLED STUDY; IN VITRO STUDY; MOLECULAR CLONING; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; VOLTAGE CLAMP; XENOPUS;

ANESTHETICS, INHALATION; ANIMALS; CALCIUM; ENFLURANE; FEMALE; HALOTHANE; HUMANS; INTERMEDIATE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS; ISOFLURANE; METHYL ETHERS; OOCYTES; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; POTASSIUM CHANNELS, CALCIUM-ACTIVATED; SMALL-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS; XENOPUS LAEVIS;

EID: 0034724660     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-2999(00)00254-5     Document Type: Article

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