Title : hERG K+ channel-associated cardiac effects of the antidepressant drug desipramine.

Pub. Date : 2011 Feb

PMID : 21120454






6 Functional Relationships(s)
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1 hERG K+ channel-associated cardiac effects of the antidepressant drug desipramine. Desipramine ETS transcription factor ERG Homo sapiens
2 We found that desipramine reduced hERG currents by binding to a receptor site inside the channel pore. Desipramine ETS transcription factor ERG Homo sapiens
3 Finally, desipramine triggered apoptosis in cells expressing hERG channels. Desipramine ETS transcription factor ERG Homo sapiens
4 Desipramine exerts at least four different cellular effects: (1) direct hERG channel block, (2) acute reduction of hERG surface expression, (3) chronic disruption of hERG trafficking, and (4) induction of apoptosis. Desipramine ETS transcription factor ERG Homo sapiens
5 Desipramine exerts at least four different cellular effects: (1) direct hERG channel block, (2) acute reduction of hERG surface expression, (3) chronic disruption of hERG trafficking, and (4) induction of apoptosis. Desipramine ETS transcription factor ERG Homo sapiens
6 Desipramine exerts at least four different cellular effects: (1) direct hERG channel block, (2) acute reduction of hERG surface expression, (3) chronic disruption of hERG trafficking, and (4) induction of apoptosis. Desipramine ETS transcription factor ERG Homo sapiens