Increased oxidative stress and DNA damage in bipolar disorder:: A twin-case report

被引:95
作者
Frey, Benicio N.
Andreazza, Ana C.
Kunz, Mauricio
Gomes, Fabiano A.
Quevedo, Joao
Salvador, Mirian
Goncalves, Carlos Alberto
Kapczinski, Flavio
机构
[1] Hosp Clin Porto Alegre, Bipolar Disorders Program, Ctr Pesquisas, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Dept Bioquim, Inst Ciencias Basicas Saude, BR-90035003 Porto Alegre, RS, Brazil
[3] Univ Extremo Sul Catarinense, Lab Neurociencias, BR-88806000 Criciuma, SC, Brazil
[4] Univ Caxias Do Sul, Inst Biotecnol, BR-95070560 Caxias Do Sul, RS, Brazil
关键词
bipolar disorder; DNA damage; oxidative stress; pathophysiology;
D O I
10.1016/j.pnpbp.2006.06.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: There is an emerging body of data suggesting that oxidative stress may be associated with the pathophysiology of bipolar disorder (1313). In the present study we investigated the oxidative stress profile in two monozygotic twins during a manic episode. Methods: Two monozygotic twins diagnosed as currently manic by the Structured Clinical Interview for DSM-IV were studied. Serum thiobarbituric acid reactive substances (TBARS), superoxide dismutase (SOD) and catalase (CAT) were measured as parameters of oxidative stress. DNA damage was assessed using the single cell gel electrophoresis technique (Comet Assay). All biochemical measures were conducted at baseline and after a 6-week treatment. Results: Bipolar twins had higher TBARS, SOD and DNA damage, and lower CAT than the healthy control. TBARS and SOD were normalized after mood stabilization, whereas CAT and DNA damage remained altered at week 6. Conclusions: These findings support that oxidative stress may play a role in the pathophysiology of BD and that pharmacological treatment may exert antioxidant effects. Studies with larger samples are warranted to further clarify this issue. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:283 / 285
页数:3
相关论文
共 15 条
[1]  
ANDREAZZA AC, IN PRESS PSYCHIAT RE
[2]   The expression of proapoptosis genes is increased in bipolar disorder, but not in schizophrenia [J].
Benes, FM ;
Matzilevich, D ;
Burke, RE ;
Walsh, J .
MOLECULAR PSYCHIATRY, 2006, 11 (03) :241-251
[3]   DNA fragmentation decreased in schizophrenia but not bipolar disorder [J].
Benes, FM ;
Walsh, J ;
Bhattacharyya, S ;
Sheth, A ;
Berretta, S .
ARCHIVES OF GENERAL PSYCHIATRY, 2003, 60 (04) :359-364
[4]  
First M, 2016, Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition (SCID-I/P)
[5]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[6]   Lipid peroxidation and antioxidant enzyme levels in patients with schizophrenia and bipolar disorder [J].
Kuloglu, M ;
Ustundag, B ;
Atmaca, M ;
Canatan, H ;
Tezcan, AE ;
Cinkilinc, N .
CELL BIOCHEMISTRY AND FUNCTION, 2002, 20 (02) :171-175
[7]   Free radical pathology and antioxidant defense in schizophrenia: A review [J].
Mahadik, SP ;
Mukherjee, S .
SCHIZOPHRENIA RESEARCH, 1996, 19 (01) :1-17
[8]   Antioxidant enzyme activities and oxidative stress in affective disorders [J].
Ozcan, ME ;
Gulec, M ;
Ozerol, E ;
Polat, R ;
Akyol, O .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2004, 19 (02) :89-95
[9]  
PILLAI A, IN PRESS J PSYCHIAT
[10]   Decreased antioxidant enzymes and membrane essential polyunsaturated fatty acids in schizophrenic and bipolar mood disorder patients [J].
Ranjekar, PK ;
Hinge, A ;
Hegde, MV ;
Ghate, M ;
Kale, A ;
Sitasawad, S ;
Wagh, UV ;
Debsikdar, VB ;
Mahadik, SP .
PSYCHIATRY RESEARCH, 2003, 121 (02) :109-122