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Molecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disorders.
Pharmacol Ther. 2010 Nov; 128(2):281-304.P&T

Abstract

Lithium has been used clinically to treat bipolar disorder for over half a century, and remains a fundamental pharmacological therapy for patients with this illness. Although lithium's therapeutic mechanisms are not fully understood, substantial in vitro and in vivo evidence suggests that it has neuroprotective/neurotrophic properties against various insults, and considerable clinical potential for the treatment of several neurodegenerative conditions. Evidence from pharmacological and gene manipulation studies support the notion that glycogen synthase kinase-3 inhibition and induction of brain-derived neurotrophic factor-mediated signaling are lithium's main mechanisms of action, leading to enhanced cell survival pathways and alteration of a wide variety of downstream effectors. By inhibiting N-methyl-D-aspartate receptor-mediated calcium influx, lithium also contributes to calcium homeostasis and suppresses calcium-dependent activation of pro-apoptotic signaling pathways. In addition, lithium decreases inositol 1,4,5-trisphosphate by inhibiting phosphoinositol phosphatases, a process recently identified as a novel mechanism for inducing autophagy. Through these mechanisms, therapeutic doses of lithium have been demonstrated to defend neuronal cells against diverse forms of death insults and to improve behavioral as well as cognitive deficits in various animal models of neurodegenerative diseases, including stroke, amyotrophic lateral sclerosis, fragile X syndrome, as well as Huntington's, Alzheimer's, and Parkinson's diseases, among others. Several clinical trials are also underway to assess the therapeutic effects of lithium for treating these disorders. This article reviews the most recent findings regarding the potential targets involved in lithium's neuroprotective effects, and the implication of these findings for the treatment of a variety of diseases.

Authors+Show Affiliations

Molecular Neurobiology Section, Mood and Anxiety Disorders Program, National Institute of Mental Health, National Institutes of Health, 10 Center Drive MSC 1363, Bethesda, MD 20892-1363, USA.No affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Intramural
Review

Language

eng

PubMed ID

20705090

Citation

Chiu, Chi-Tso, and De-Maw Chuang. "Molecular Actions and Therapeutic Potential of Lithium in Preclinical and Clinical Studies of CNS Disorders." Pharmacology & Therapeutics, vol. 128, no. 2, 2010, pp. 281-304.
Chiu CT, Chuang DM. Molecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disorders. Pharmacol Ther. 2010;128(2):281-304.
Chiu, C. T., & Chuang, D. M. (2010). Molecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disorders. Pharmacology & Therapeutics, 128(2), 281-304. https://doi.org/10.1016/j.pharmthera.2010.07.006
Chiu CT, Chuang DM. Molecular Actions and Therapeutic Potential of Lithium in Preclinical and Clinical Studies of CNS Disorders. Pharmacol Ther. 2010;128(2):281-304. PubMed PMID: 20705090.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Molecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disorders. AU - Chiu,Chi-Tso, AU - Chuang,De-Maw, Y1 - 2010/08/10/ PY - 2010/07/02/received PY - 2010/07/08/accepted PY - 2010/8/14/entrez PY - 2010/8/14/pubmed PY - 2011/8/25/medline SP - 281 EP - 304 JF - Pharmacology & therapeutics JO - Pharmacol Ther VL - 128 IS - 2 N2 - Lithium has been used clinically to treat bipolar disorder for over half a century, and remains a fundamental pharmacological therapy for patients with this illness. Although lithium's therapeutic mechanisms are not fully understood, substantial in vitro and in vivo evidence suggests that it has neuroprotective/neurotrophic properties against various insults, and considerable clinical potential for the treatment of several neurodegenerative conditions. Evidence from pharmacological and gene manipulation studies support the notion that glycogen synthase kinase-3 inhibition and induction of brain-derived neurotrophic factor-mediated signaling are lithium's main mechanisms of action, leading to enhanced cell survival pathways and alteration of a wide variety of downstream effectors. By inhibiting N-methyl-D-aspartate receptor-mediated calcium influx, lithium also contributes to calcium homeostasis and suppresses calcium-dependent activation of pro-apoptotic signaling pathways. In addition, lithium decreases inositol 1,4,5-trisphosphate by inhibiting phosphoinositol phosphatases, a process recently identified as a novel mechanism for inducing autophagy. Through these mechanisms, therapeutic doses of lithium have been demonstrated to defend neuronal cells against diverse forms of death insults and to improve behavioral as well as cognitive deficits in various animal models of neurodegenerative diseases, including stroke, amyotrophic lateral sclerosis, fragile X syndrome, as well as Huntington's, Alzheimer's, and Parkinson's diseases, among others. Several clinical trials are also underway to assess the therapeutic effects of lithium for treating these disorders. This article reviews the most recent findings regarding the potential targets involved in lithium's neuroprotective effects, and the implication of these findings for the treatment of a variety of diseases. SN - 1879-016X UR - https://www.unboundmedicine.com/medline/citation/20705090/Molecular_actions_and_therapeutic_potential_of_lithium_in_preclinical_and_clinical_studies_of_CNS_disorders_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0163-7258(10)00149-X DB - PRIME DP - Unbound Medicine ER -