Antiepileptic carbamazepine drug treatment induces alteration of membrane in red blood cells: Possible positive effects on metabolism and oxidative stress

被引:27
作者
Ficarra, Silvana [1 ]
Misiti, Francesco [2 ]
Russo, Annamaria [1 ]
Carelli-Alinovi, Cristiana [2 ]
Bellocco, Ersilia [1 ]
Barreca, Davide [1 ]
Lagana, Giuseppina [1 ]
Leuzzi, Ugo [1 ]
Toscano, Giovanni [3 ]
Giardina, Bruno [4 ,5 ]
Galtieri, Antonio [1 ]
Tellone, Ester [1 ]
机构
[1] Univ Messina, Dept Chem Sci, I-98166 Messina, Italy
[2] Univ Cassino & Southern Lazio, Dept Human Sci Soc & Hlth, I-03043 Cassino, Italy
[3] Univ Messina, Pharmacobiol Dept, I-98166 Messina, Italy
[4] Catholic Univ, Sch Med, Biochem & Clin Biochem Inst, I-00168 Rome, Italy
[5] CNR, Inst Chem Mol Recognit, I-00168 Rome, Italy
关键词
Red blood cell; Anionic transport; Carbamazepine; Nitric oxide; Acetylcholinesterase; MEDIATED CATECHOLAMINE SECRETION; HUMAN-ERYTHROCYTE; CYTOPLASMIC DOMAIN; FLIP-FLOP; BAND-3; ANION; PHOSPHORYLATION; PEROXYNITRITE; PHENYTOIN; CHANNELS;
D O I
10.1016/j.biochi.2012.11.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carbamazepine (CBZ) is an iminostilbene derivative commonly used for treatment of neuralgic pain and bipolar affective disorders. CBZ blood levels of treated patients are within the range of micromolar concentrations and therefore, significant interactions of this drug with erythrocytes are very likely. Moreover, the lipid domains of the cell membrane are believed to be one of the sites where iminostilbene derivatives exert their effects. The present study aimed to deeply characterize CBZ effects on erythrocytes, in order to identify extra and/or cytosolic cell targets. Our results indicate that erythrocyte morphological changes promoted by the drug, may be triggered by an alteration in band 3 functionality i.e. at the level of anionic flux. In addition, from a metabolic point of view this perturbation could be considered, at least in part, as a beneficial event because it could favour the CO2 elimination. Since lipid peroxidation, superoxide and free radical scavenging activities, caspase 3 activity and hemoglobin (Hb) functionality were not modified within the CBZ treated red blood cell (RBC), band 3 protein (B3) may well be a specific membrane target for CBZ and responsible for CBZ-induced toxic effects in erythrocytes. However some beneficial effects of this drug have been evidenced; among them an increased release of ATP and nitric oxide (NO) derived metabolites from erythrocytes to lumen, leading to an increased NO pool in the vasculature. In conclusion, these results indicate that CBZ, though considered responsible for toxic effects on erythrocytes, can also exhibit effects that at least in some conditions may be seen as beneficial. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:833 / 841
页数:9
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