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- W2334911267 abstract "Cardiac adaptation to permanent overload induces several phenotypic changes which finally result in a system which works more economically, together with a slower Vmax. The molecular target of digitalis is the NA+, K+ ATPase, which is a polymorphic molecule. We have recently demonstrated that during cardiac hypertrophy this target is modified and that a shift occurs in the alpha 1 subunit, from the normally present alpha 2 isosubunit to alpha 3, which is a fetal isoform with a lower affinity for sodium and a higher affinity for ouabain. Such a shift explains why, in rat cardiac hypertrophy ouabain is less toxic than normal and is released from its target more slowly. It may also explain at least in part the discrepancies observed in clinical trials on the efficacy of digitalis." @default.
- W2334911267 created "2016-06-24" @default.
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- W2334911267 date "1995-05-02" @default.
- W2334911267 modified "2023-09-23" @default.
- W2334911267 title "Myocardial phenotypic changes in Na+, K+ATPase in left ventricular hypertrophy: pharmacological consequences" @default.
- W2334911267 doi "https://doi.org/10.1093/eurheartj/16.suppl_c.20" @default.
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