<p>(<i>a</i>) Incubation with EEAC (0.01–200 µg/ml) stimulated the P-gp ATPase activity. Data were analyzed in terms of RLUs. (<i>b</i>) Verapamil (25–400 µM) showed its capacity to stimulate P-gp ATPase activity. (<i>c</i>) EEAC (1–100 µg/ml) was tested for its capacity to inhibit 200 µM verapamil-stimulated P-gp ATPase activity. Above results indicated that EEAC stimulated the P-gp ATPase activity and inhibited 200 µM verapamil-stimulated P-gp ATPase activity at concentration 5 µg/ml.</p
P-glycoprotein (Pgp) is a multidrug transporter that uses the energy from ATP binding and hydrolysis...
AbstractThe effect of EGTA on Ca2+-ATPase activity was studied in fragmented membranes and solubiliz...
PubMedID: 8828806The effects of glucose on Ca2+ATPase activity of erythrocyte membranes were investi...
<p>(<i>a</i>) Rhodamine 123 efflux assay: EEAC inhibited P-gp mediated efflux of rhodamine 123 in a ...
<p>(A) Stimulation of ATP hydrolysis by verapamil (50 µM), QZ59-<i>SSS</i> (1 µM), valinomycin (10 µ...
<p>Untreated, 100 µM Na<sub>3</sub>VO<sub>4</sub>, 100 µM verapamil and 10 µM NSC23925 -treated Pgp1...
<p>Drug efflux transporter ATPase activity was examined in P-gp (A and B) and BCRP (D and E) membran...
This research was conducted to develop a potential treatment for Alzheimer’s disease. P-glycoprotein...
AbstractWe have studied the interaction between verapamil and other modulators of the P-glycoprotein...
The effect of (A) verapamil and (B) TMR-Cl was tested on the ATPase activity of TMH1,7 and compared ...
AbstractDrug interactions with P-glycoprotein (Pgp) were quantitatively assessed using ATPase assay....
<p>(<i>a</i>) Incubation with methadone (1–40 µM) stimulated the P-gp ATPase activity. Data was anal...
International audienceConsiderable interest exists about the localization of P-gp (P-glycoprotein) i...
Background: P-glycoprotein (P-gp) is a prevalent resistance mediator and it requires considerable ce...
AbstractWe show that drugs, such as verapamil, which reverse multidrug resistance (MDR), in P-glycop...
P-glycoprotein (Pgp) is a multidrug transporter that uses the energy from ATP binding and hydrolysis...
AbstractThe effect of EGTA on Ca2+-ATPase activity was studied in fragmented membranes and solubiliz...
PubMedID: 8828806The effects of glucose on Ca2+ATPase activity of erythrocyte membranes were investi...
<p>(<i>a</i>) Rhodamine 123 efflux assay: EEAC inhibited P-gp mediated efflux of rhodamine 123 in a ...
<p>(A) Stimulation of ATP hydrolysis by verapamil (50 µM), QZ59-<i>SSS</i> (1 µM), valinomycin (10 µ...
<p>Untreated, 100 µM Na<sub>3</sub>VO<sub>4</sub>, 100 µM verapamil and 10 µM NSC23925 -treated Pgp1...
<p>Drug efflux transporter ATPase activity was examined in P-gp (A and B) and BCRP (D and E) membran...
This research was conducted to develop a potential treatment for Alzheimer’s disease. P-glycoprotein...
AbstractWe have studied the interaction between verapamil and other modulators of the P-glycoprotein...
The effect of (A) verapamil and (B) TMR-Cl was tested on the ATPase activity of TMH1,7 and compared ...
AbstractDrug interactions with P-glycoprotein (Pgp) were quantitatively assessed using ATPase assay....
<p>(<i>a</i>) Incubation with methadone (1–40 µM) stimulated the P-gp ATPase activity. Data was anal...
International audienceConsiderable interest exists about the localization of P-gp (P-glycoprotein) i...
Background: P-glycoprotein (P-gp) is a prevalent resistance mediator and it requires considerable ce...
AbstractWe show that drugs, such as verapamil, which reverse multidrug resistance (MDR), in P-glycop...
P-glycoprotein (Pgp) is a multidrug transporter that uses the energy from ATP binding and hydrolysis...
AbstractThe effect of EGTA on Ca2+-ATPase activity was studied in fragmented membranes and solubiliz...
PubMedID: 8828806The effects of glucose on Ca2+ATPase activity of erythrocyte membranes were investi...