Therapeutic potential of fluoxetine in neurological disorders

被引:73
作者
Mostert, Jop P. [1 ]
Koch, Marcus W. [1 ]
Heerings, Marco [1 ]
Heersema, Dorothea J. [1 ]
De Keyser, Jacques [1 ]
机构
[1] Univ Groningen, Dept Neurol, Univ Med Ctr Groningen, NL-9713 GZ Groningen, Netherlands
关键词
fluoxetine; neurodegeneration; neurological disorders; neuroprotection;
D O I
10.1111/j.1527-3458.2008.00040.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The selective serotonin reuptake inhibitor (SSRI) fluoxetine, which is registered for a variety of psychiatric disorders, has been found to stimulate the cAMP-responsive element binding protein (CREB), increase the production of brain-derived neurotrophic factor (BNDF) and the neurotrophic peptide S100 beta, enhance glycogenolysis in astrocytes, block voltage-gated calcium and sodium channels, and decrease the conductance of mitochondrial voltage-dependent anion channels (VDACs). These mechanisms of actions suggest that fluoxetine may also have potential for the treatment of a number of neurological disorders. We performed a Pubmed search to review what is known about possible therapeutic effects of fluoxetine in animal models and patients with neurological disorders. Beneficial effects of fluoxetine have been noted in animal models of stroke, multiple sclerosis, and epilepsy. Fluoxetine was reported to improve neurological manifestations in patients with Alzheimer's disease, stroke, Huntington's disease, multiple sclerosis, traumatic brain injury, and epilepsy. Clinical studies so far were small and often poorly designed. Results were inconclusive and contradictory. However, the available preclinical data justify further clinical trials to determine the therapeutic potential of fluoxetine in neurological disorders.
引用
收藏
页码:153 / 164
页数:12
相关论文
共 83 条
[21]   MINI-MENTAL STATE - PRACTICAL METHOD FOR GRADING COGNITIVE STATE OF PATIENTS FOR CLINICIAN [J].
FOLSTEIN, MF ;
FOLSTEIN, SE ;
MCHUGH, PR .
JOURNAL OF PSYCHIATRIC RESEARCH, 1975, 12 (03) :189-198
[22]   Effects of antidepressant treatment with rTMS and fluoxetine on brain perfusion in PD [J].
Fregni, F. ;
Ono, C. R. ;
Santos, C. M. ;
Bermpohl, F. ;
Buchpiguel, C. ;
Barbosa, E. R. ;
Marcolin, M. A. ;
Pascual-Leone, A. ;
Valente, K. D. .
NEUROLOGY, 2006, 66 (11) :1629-1637
[23]   Repetitive transcranial magnetic stimulation is as effective as fluoxetine in the treatment of depression in patients with Parkinson's disease [J].
Fregni, F ;
Santos, CM ;
Myczkowski, ML ;
Rigolino, R ;
Gallucci-Neto, J ;
Barbosa, ER ;
Valente, KD ;
Pascual-Leone, A ;
Marcolin, MA .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2004, 75 (08) :1171-1174
[24]   HIPPOCAMPAL SEROTONIN LEVELS INFLUENCE THE EXPRESSION OF S100-BETA DETECTED BY IMMUNOCYTOCHEMISTRY [J].
HARING, JH ;
HAGAN, A ;
OLSON, J ;
RODGERS, B .
BRAIN RESEARCH, 1993, 631 (01) :119-123
[25]   FLUVOXAMINE - AN ANTIDEPRESSANT WITH LOW (OR NO) EPILEPTOGENIC EFFECT [J].
HARMANT, J ;
VANRIJCKEVORSELHARMANT, K ;
DEBARSY, T .
LANCET, 1990, 336 (8711) :386-386
[26]   Fluoxetine's effects on cognitive performance in patients with traumatic brain injury [J].
Horsfield, SA ;
Rosse, RB ;
Tomasino, V ;
Schwartz, BL ;
Mastropaolo, J ;
Deutsch, SI .
INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE, 2002, 32 (04) :337-344
[27]   Molecular, pharmacological and functional diversity of 5-HT receptors [J].
Hoyer, D ;
Hannon, JP ;
Martin, GR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 71 (04) :533-554
[28]   The serotonergic and noradrenergic effects of antidepressant drugs are anticonvulsant, not proconvulsant [J].
Jobe, PC ;
Browning, RA .
EPILEPSY & BEHAVIOR, 2005, 7 (04) :602-619
[29]  
KARSON CN, 1993, J NEUROPSYCH CLIN N, V5, P322
[30]   Norfluoxetine and fluoxetine have similar anticonvulsant and Ca2+ channel blocking potencies [J].
Kecskeméti, V ;
Rusznák, Z ;
Riba, P ;
Pál, B ;
Wagner, R ;
Harasztosi, C ;
Nánási, MP ;
Szûcs, G .
BRAIN RESEARCH BULLETIN, 2005, 67 (1-2) :126-132