Lithium: the pharmacodynamic actions of the amazing ion

被引:92
作者
Brown, Kayleigh M. [1 ]
Tracy, Derek K. [1 ,2 ]
机构
[1] Kings Coll London, Inst Psychiat, POB 63,Crespigny Pk,Denmark Hill, London SE5 8AF, England
[2] Oxleas NHS Fdn Trust, Dartford, England
关键词
glycogen synthase kinase 3; inositol monophosphatase; lithium; pharmacology;
D O I
10.1177/2045125312471963
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lithium has been used for the treatment of mood disorders for over 60 years, yet the exact mechanisms by which it exerts its therapeutic effects remain unclear. Two enzymatic chains or pathways emerge as targets for lithium: inositol monophosphatase within the phosphatidylinositol signalling pathway and the protein kinase glycogen synthase kinase 3. Lithium inhibits these enzymes through displacing the normal cofactor magnesium, a vital regulator of numerous signalling pathways. Here we provide an overview of evidence, supporting a role for the inhibition of glycogen synthase kinase 3 and inositol monophosphatase in the pharmacodynamic actions of lithium. We also explore how inhibition of these enzymes by lithium can lead to downstream effects of clinical relevance, both for mood disorders and neurodegenerative diseases. Establishing a better understanding of lithium's mechanisms of action may allow the development of more effective and more tolerable pharmacological agents for the treatment of a range of mental illnesses, and provide clearer insight into the pathophysiology of such disorders.
引用
收藏
页码:163 / 176
页数:14
相关论文
共 120 条
[1]   Lithium lengthens the circadian period of individual suprachiasmatic nucleus neurons [J].
Abe, M ;
Herzog, ED ;
Block, GD .
NEUROREPORT, 2000, 11 (14) :3261-3264
[2]   Myo-inositol-1-phosphate (MIP) synthase:: a possible new target for antibipolar drugs [J].
Agam, G ;
Shamir, A ;
Shaltiel, G ;
Greenberg, ML .
BIPOLAR DISORDERS, 2002, 4 :15-20
[3]   Mechanism of activation and function of protein kinase B [J].
Alessi, DR ;
Cohen, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (01) :55-62
[4]   REDUCED BRAIN INOSITOL IN LITHIUM-TREATED RATS [J].
ALLISON, JH ;
STEWART, MA .
NATURE-NEW BIOLOGY, 1971, 233 (43) :267-&
[5]   Regulation of tau phosphorylation and protection against β-amyloid-induced neurodegeneration by lithium.: Possible implications for Alzheimer's disease [J].
Alvarez, G ;
Muñoz-Montaño, JR ;
Satrústegui, J ;
Avila, J ;
Bogónez, E ;
Díaz-Nido, J .
BIPOLAR DISORDERS, 2002, 4 (03) :153-165
[6]  
Bauer M, 2003, PHARMACOPSYCHIATRY, V36, pS250
[7]   Lithium augmentation therapy in refractory depression -: Update 2002 [J].
Bauer, M ;
Forsthoff, A ;
Baethge, C ;
Adli, M ;
Berghöfer, A ;
Döpfmer, S ;
Bschor, T .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2003, 253 (03) :132-139
[8]   Greater cortical gray matter density in lithium-treated patients with bipolar disorder [J].
Bearden, Carrie E. ;
Thompson, Paul M. ;
Dalwani, Manish ;
Hayashi, Kiralee M. ;
Lee, Agatha D. ;
Nicoletti, Mark ;
Trakhtenbroit, Michael ;
Glahn, David C. ;
Brambilla, Paolo ;
Sassi, Roberto B. ;
Mallinger, Alan G. ;
Frank, Ellen ;
Kupfer, David J. ;
Soares, Jair C. .
BIOLOGICAL PSYCHIATRY, 2007, 62 (01) :7-16
[9]  
Beaulieu JM, 2008, CELL, V132, P125, DOI 10.1016/j.cell.2007.11.041
[10]   Akt/GSK3 Signaling in the Action of Psychotropic Drugs [J].
Beaulieu, Jean-Martin ;
Gainetdinov, Raul R. ;
Caron, Marc G. .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2009, 49 :327-347