Interaction Mechanism of Anabolic Steroid Hormones with Structural Components of Erythrocyte Membranes

2011 ◽  
Vol 115 (50) ◽  
pp. 14969-14979 ◽  
Author(s):  
Lev Evgenjevich Panin ◽  
Pavel Valentinovich Mokrushnikov ◽  
Valery Georgievich Kunitsyn ◽  
Boris Nikolaevich Zaitsev
2010 ◽  
Vol 114 (29) ◽  
pp. 9462-9473 ◽  
Author(s):  
Lev Evgenjevich Panin ◽  
Pavel Valentinovich Mokrushnikov ◽  
Valery Georgievich Kunitsyn ◽  
Boris Nikolaevich Zaitsev

1985 ◽  
Vol 63 (8) ◽  
pp. 937-943 ◽  
Author(s):  
David V. Godin ◽  
Peter McGinn

The membrane perturbational actions of pentobarbital, methohexital, and phenobarbital were analyzed in terms of their effects on the incorporation of group-specific chemical probes into protein and phospholipid structural components and on the activity of various functionally distinct ATPases in erythrocyte and brain synaptosomal membranes. When compared at concentrations producing similar degrees of antihemolysis in red cells, the three analogues differed most markedly in the nature and degree of the structural and functional alterations induced in membrane proteins, with the most highly lipophilic agent, methohexital, being frequently, although not invariably, the most potent. Comparison of the effects of pentobarbital on characteristics of trinitrobenzenesulfonic acid and 5,5′-dithiobis-(2-nitrobenzoic acid) incorporation into erythrocyte membranes with results previously obtained using other anaesthetics at concentrations producing 50% antihemolysis showed that pentobarbital behaves similarly to neutral general anaesthetics but differently from cationic local anaesthetics. Our findings suggest that the membrane perturbational characteristics of barbiturates may contribute to their diverse and complex actions on excitable tissues.


1987 ◽  
Vol 15 (4) ◽  
pp. 357-361 ◽  
Author(s):  
Markku Alen ◽  
Paavo Rahkila ◽  
Matti Reinilä ◽  
Reijo Vihko

2005 ◽  
Vol 60 (7-8) ◽  
pp. 567-571 ◽  
Author(s):  
Halina Kleszczyńska ◽  
Dorota Bonarska ◽  
Hanna Pruchnik ◽  
Krzysztof Bielecki ◽  
Andrzej Piasecki ◽  
...  

Potential antioxidative activities of three series of newly synthesized N-oxides were studied. Individual components in each of the series differed in the lipophilicities and number of free radical scavenging groups. Various methods were used to determine their antioxidative efficiencies: Prevention of erythrocyte membrane lipid oxidation induced by UV irradiation and chromogen experiments in which antioxidative efficiencies of compounds were compared to that of the standard antioxidant Trolox (a water-soluble vitamin E analogue). Additionally, some hemolytic (pig erythrocytes) and differential scanning calorimetry (DSC) measurements were performed to determine a mechanism of the interaction between membranes and N-oxides. It was found that N-oxides, especially those of long alkyl chains (> C12H25), readily interacted with both, erythrocyte and liposomal membranes. No marked differences were found in their protection of erythrocytes against oxidation. In most cases inhibition of oxidation changed between 15% and 25%. Still, it was far better than in chromogen experiments where suppression of free radicals reached 20% in the best case. It may be concluded that antioxidative capabilities of N-oxides are moderate. Studies on the interaction mechanism showed that incorporation of particular compounds into model membranes varied. Hemolysing activities of compounds increased with the elongation of the alkyl chain but differed for corresponding compounds of particular series indicating that lipophilicity of compounds is not the only factor determing their interaction with erythrocyte membranes. DSC experiments showed that N-oxides, upon incorporation into 1,2-dipalmitoyl-3-snphosphatidylcholine liposomes, shifted the subtransition (Tp) and the main transition (Tm). The shifts observed depended on the alkyl chain length. The effects differed for each series. It seems that in the case of long alkyl chain compounds the domain formation may take place. Generally, the decrease of Tm was greatest for the same compounds that exhibited the best hemolytic efficacy. The same conclusion concerns the decrease of cooperativity of the main transition and the observed changes suggest an increase in membrane fluidity. Both, erythrocyte and DSC experiments seem to indicate that compounds of particular series incorporate in a somewhat different way into membranes.


2009 ◽  
Vol 26 (5) ◽  
pp. 640-671 ◽  
Author(s):  
J. Scarth ◽  
C. Akre ◽  
L. van Ginkel ◽  
B. Le Bizec ◽  
H. De Brabander ◽  
...  

2011 ◽  
Vol 3 (10) ◽  
pp. 676-681 ◽  
Author(s):  
Irmgard Riedmaier ◽  
Michael W. Pfaffl ◽  
Heinrich H. D. Meyer

1985 ◽  
Vol 66 (1) ◽  
pp. 48-50
Author(s):  
V. V. Semenov ◽  
V. A. Glumova ◽  
V. V. Trusov

Drugs that affect metabolic processes in the body include anabolic steroid hormones, synthetic analogs of male sex hormones, devoid of sexual activity, but retaining a positive effect on growth, body weight, myotropic activity and nitrogen balance.


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