adenosine-5--o-(3-thiotriphosphate) and herbimycin

adenosine-5--o-(3-thiotriphosphate) has been researched along with herbimycin* in 1 studies

Other Studies

1 other study(ies) available for adenosine-5--o-(3-thiotriphosphate) and herbimycin

ArticleYear
Tyrosine protein kinase inhibitors prevent activation of cardiac swelling-induced chloride current.
    Pflugers Archiv : European journal of physiology, 1995, Volume: 431, Issue:2

    The effect of tyrosine protein kinase inhibitors on the swelling-induced chloride current (ICl-swelling) of dog atrial myocytes was studied using the whole-cell patch-clamp recording technique. Currents were measured during hyperpolarizing voltage ramps with potassium currents blocked by cesium. Osmolarity was varied using mannitol. Exposure to hypotonic solution (approximately 249 mosmol/kg) activated ICl-swelling. Hypertonic solution (approximately 363 mosmol/kg) was used to shrink swollen cells and turn off ICl-swelling. In studies on the acute effect of tyrosine protein kinase inhibitors each cell was swollen three separate times. Control, treatment, and washout ICl-swelling were compared. Genistein (50-80 microM) prevented reactivation of ICl-swelling without affecting cell size. The effect of genistein partially subsided upon washout. The effect of genistein on ICl-swelling was not mimicked by 80 microM daidzein, a related compound that does not inhibit tyrosine protein kinases. When intracellular adenosine 5'-O-(3-thiotriphosphate (ATP[gamma S]) was used, genistein did not prevent the reactivation of ICl-swelling. Intracellular ATP[gamma S] did not result in a persistent activation of ICl-swelling when cell size was returned to control. Acute exposure to 1 microM herbimycin A or 100 microM tyrphostin 51 did not prohibit the activation of ICl-swelling. A 24-h exposure to 1 microM herbimycin A did inhibit ICl-swelling. The results provide important clues regarding the activation mechanism for ICl-swelling and suggest that a tyrosine protein phosphorylation may be necessary, but not sufficient, for activation of ICl-swelling.

    Topics: Adenosine Triphosphate; Animals; Benzoquinones; Cell Size; Chloride Channels; Dogs; Electrophysiology; Enzyme Inhibitors; Genistein; Heart; Hypotonic Solutions; In Vitro Techniques; Isoflavones; Lactams, Macrocyclic; Membrane Potentials; Myocardium; Patch-Clamp Techniques; Phosphorylation; Protein-Tyrosine Kinases; Quinones; Rifabutin

1995