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Translating neurotrophic and cellular plasticity: from pathophysiology to improved therapeutics for bipolar disorder.
Acta Psychiatr Scand. 2012 Nov; 126(5):332-41.AP

Abstract

OBJECTIVE

Bipolar disorder (BD) likely involves, at a molecular and cellular level, dysfunctions of critical neurotrophic, cellular plasticity and resilience pathways and neuroprotective processes. Therapeutic properties of mood stabilizers are presumed to result from a restoration of the function of these altered pathways and processes through a wide range of biochemical and molecular effects. We aimed to review the altered pathways and processes implicated in BD, such as neurotrophic factors, mitogen-activated protein kinases, Bcl-2, phosphoinositol signaling, intracellular calcium and glycogen synthase kinase-3.

METHODS

We undertook a literature search of recent relevant journal articles, book chapter and reviews on neurodegeneration and neuroprotection in BD. Search words entered were 'brain-derived neurotrophic factor,''Bcl-2,''mitogen-activated protein kinases,''neuroprotection,''calcium,''bipolar disorder,''mania,' and 'depression.'

RESULTS

The most consistent and replicated findings in the pathophysiology of BD may be classified as follows: i) calcium dysregulation, ii) mitochondrial/endoplasmic reticulum dysfunction, iii) glial and neuronal death/atrophy and iv) loss of neurotrophic/plasticity effects in brain areas critically involved in mood regulation. In addition, the evidence supports that treatment with mood stabilizers; in particular, lithium restores these pathophysiological changes.

CONCLUSION

Bipolar disorder is associated with impairments in neurotrophic, cellular plasticity and resilience pathways as well as in neuroprotective processes. The evidence supports that treatment with mood stabilizers, in particular lithium, restores these pathophysiological changes. Studies that attempt to prevent (intervene before the onset of the molecular and cellular changes), treat (minimize severity of these deficits over time), and rectify (reverse molecular and cellular deficits) are promising therapeutic strategies for developing improved treatments for bipolar disorder.

Authors+Show Affiliations

Mood Disorders Unit (GRUDA), Department and Institute of Psychiatry, School of Medicine, University of Sao Paulo (HC-FMUSP), São Paulo, Brazil.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Review

Language

eng

PubMed ID

22676371

Citation

Soeiro-de-Souza, M G., et al. "Translating Neurotrophic and Cellular Plasticity: From Pathophysiology to Improved Therapeutics for Bipolar Disorder." Acta Psychiatrica Scandinavica, vol. 126, no. 5, 2012, pp. 332-41.
Soeiro-de-Souza MG, Dias VV, Figueira ML, et al. Translating neurotrophic and cellular plasticity: from pathophysiology to improved therapeutics for bipolar disorder. Acta Psychiatr Scand. 2012;126(5):332-41.
Soeiro-de-Souza, M. G., Dias, V. V., Figueira, M. L., Forlenza, O. V., Gattaz, W. F., Zarate, C. A., & Machado-Vieira, R. (2012). Translating neurotrophic and cellular plasticity: from pathophysiology to improved therapeutics for bipolar disorder. Acta Psychiatrica Scandinavica, 126(5), 332-41. https://doi.org/10.1111/j.1600-0447.2012.01889.x
Soeiro-de-Souza MG, et al. Translating Neurotrophic and Cellular Plasticity: From Pathophysiology to Improved Therapeutics for Bipolar Disorder. Acta Psychiatr Scand. 2012;126(5):332-41. PubMed PMID: 22676371.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Translating neurotrophic and cellular plasticity: from pathophysiology to improved therapeutics for bipolar disorder. AU - Soeiro-de-Souza,M G, AU - Dias,V V, AU - Figueira,M L, AU - Forlenza,O V, AU - Gattaz,W F, AU - Zarate,C A,Jr AU - Machado-Vieira,R, Y1 - 2012/06/08/ PY - 2012/6/9/entrez PY - 2012/6/9/pubmed PY - 2013/3/22/medline SP - 332 EP - 41 JF - Acta psychiatrica Scandinavica JO - Acta Psychiatr Scand VL - 126 IS - 5 N2 - OBJECTIVE: Bipolar disorder (BD) likely involves, at a molecular and cellular level, dysfunctions of critical neurotrophic, cellular plasticity and resilience pathways and neuroprotective processes. Therapeutic properties of mood stabilizers are presumed to result from a restoration of the function of these altered pathways and processes through a wide range of biochemical and molecular effects. We aimed to review the altered pathways and processes implicated in BD, such as neurotrophic factors, mitogen-activated protein kinases, Bcl-2, phosphoinositol signaling, intracellular calcium and glycogen synthase kinase-3. METHODS: We undertook a literature search of recent relevant journal articles, book chapter and reviews on neurodegeneration and neuroprotection in BD. Search words entered were 'brain-derived neurotrophic factor,''Bcl-2,''mitogen-activated protein kinases,''neuroprotection,''calcium,''bipolar disorder,''mania,' and 'depression.' RESULTS: The most consistent and replicated findings in the pathophysiology of BD may be classified as follows: i) calcium dysregulation, ii) mitochondrial/endoplasmic reticulum dysfunction, iii) glial and neuronal death/atrophy and iv) loss of neurotrophic/plasticity effects in brain areas critically involved in mood regulation. In addition, the evidence supports that treatment with mood stabilizers; in particular, lithium restores these pathophysiological changes. CONCLUSION: Bipolar disorder is associated with impairments in neurotrophic, cellular plasticity and resilience pathways as well as in neuroprotective processes. The evidence supports that treatment with mood stabilizers, in particular lithium, restores these pathophysiological changes. Studies that attempt to prevent (intervene before the onset of the molecular and cellular changes), treat (minimize severity of these deficits over time), and rectify (reverse molecular and cellular deficits) are promising therapeutic strategies for developing improved treatments for bipolar disorder. SN - 1600-0447 UR - https://www.unboundmedicine.com/medline/citation/22676371/Translating_neurotrophic_and_cellular_plasticity:_from_pathophysiology_to_improved_therapeutics_for_bipolar_disorder_ L2 - https://doi.org/10.1111/j.1600-0447.2012.01889.x DB - PRIME DP - Unbound Medicine ER -