Molecular Organization of Polyene Antibiotic Amphotericin B Studied by Means of Fluorescence Technique

Author(s):  
Wieslaw I. Gruszecki ◽  
Rafal Luchowski ◽  
Piotr Wasko ◽  
Zygmunt Gryczynski ◽  
Ignacy Gryczynski
1989 ◽  
Vol 981 (2) ◽  
pp. 207-212 ◽  
Author(s):  
Maria Teresa Lamy-Freund ◽  
Vergínia F.N. Ferreira ◽  
Shirley Schreier

2011 ◽  
Vol 48 (2) ◽  
pp. 225-241 ◽  
Author(s):  
Agnieszka Knopik-Skrocka ◽  
Józef Bielawski ◽  
Szymon Chowański ◽  
Paulina Walkowiak

Changes in erythrocyte membrane permeability induced by verapamil, chlorpromazine, and their combinations with amphotericin BHemolysis induced by 2 amphipathic agents, verapamil and chlorpromazine, was investigated in various incubation conditions. Changes in absorbance of erythrocyte suspension were monitored by absorption spectrophotometry at a wavelength of 590 nm. The hemolysis induced by verapamil or chlorpromazine is of the permeability type. The resistance of erythrocytes to verapamil is much higher than their resistance to chlorpromazine. No evident difference is found between human and pig erythrocytes in their resistance to verapamil. Only a small decrease in the rate of hemolysis induced by verapamil is observed in isotonic CaCl2, MgCl2or K2SO4solutions, compared to 160 mM KCl (the standard incubation medium). The changes in hemolytic activity of chlorpromazine in the presence of the divalent cations and anions are less evident. No decrease in hemolytic activity of chlorpromazine and verapamil is observed in the sucrose medium. The hemolytic activity of both the agents increases when they act in combination with polyene antibiotic amphotericin B. The results indicate a strong synergy between amphotericin B and verapamil or chlorpromazine. By contrast, a combined effect of verapamil and chlorpromazine on erythrocytes leads to a decrease in their hemolytic activity. This indicates antagonism between verapamil and chlorpromazine.


2000 ◽  
Vol 1464 (2) ◽  
pp. 299-308 ◽  
Author(s):  
Isabelle Blanc ◽  
Maria-Helena Bueno Da Costa ◽  
Jacques Bolard ◽  
Michèle Saint-Pierre Chazalet

2012 ◽  
Vol 9 (5) ◽  
pp. 1511-1520 ◽  
Author(s):  
Piotr Wasko ◽  
Rafal Luchowski ◽  
Krzysztof Tutaj ◽  
Wojciech Grudzinski ◽  
Przemyslaw Adamkiewicz ◽  
...  

1991 ◽  
Vol 69 (9) ◽  
pp. 618-623 ◽  
Author(s):  
D. A. O'Keefe ◽  
D. R. James ◽  
W. R. Ware ◽  
N. O. Petersen

Addition of the polyene antibiotic amphotericin B or tissue culture medium to nondifferentiated HL-60 cells in the presence of luminol induces a chemiluminescence signal that reaches a peak value within a few seconds and decays exponentially in less than a minute. The kinetics of the signal and its modulation by superoxide dismutase, catalase, and horseradish peroxidase are consistent with a series of solution biochemical processes with a rate-determining step corresponding to the disproportionation of a luminal–superoxide complex. The effects of the enzymes demonstrate that superoxide is a precursor to the rate-determining intermediate and that both catalase and peroxide enhance a reaction that competes with the rate-limiting process.Key words: chemiluminescence, luminol, amphotericin B, superoxide, HL-60 cells.


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