» Articles » PMID: 24069608

Microtubule-associated Proteins in Mesial Temporal Lobe Epilepsy with and Without Psychiatric Comorbidities and Their Relation with Granular Cell Layer Dispersion

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2013 Sep 27
PMID 24069608
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Despite strong association between epilepsy and psychiatric comorbidities, biological substrates are unknown. We have previously reported decreased mossy fiber sprouting in mesial temporal lobe epilepsy (MTLE) patients with psychosis and increased in those with major depression. Microtubule associated proteins (MAPs) are essentially involved in dendritic and synaptic sprouting.

Methods: MTLE hippocampi of subjects without psychiatric history, MTLE + major depression, and MTLE + interictal psychosis derived from epilepsy surgery and control necropsies were investigated for neuronal density, granular layer dispersion, and MAP2 and tau immunohistochemistry.

Results: Altered MAP2 and tau expression in MTLE and decreased tau expression in MTLE with psychosis were found. Granular layer dispersion correlated inversely with verbal memory scores, and with MAP2 and tau expression in the entorhinal cortex. Patients taking fluoxetine showed increased neuronal density in the granular layer and those taking haloperidol decreased neuronal density in CA3 and subiculum.

Conclusions: Our results indicate relations between MAPs, granular layer dispersion, and memory that have not been previously investigated. Differential MAPs expression in human MTLE hippocampi with and without psychiatric comorbidities suggests that psychopathological states in MTLE rely on differential morphological and possibly neurochemical backgrounds. This clinical study was approved by our institution's Research Ethics Board (HC-FMRP no. 1270/2008) and is registered under the Brazilian National System of Information on Ethics in Human Research (SISNEP) no. 0423.0.004.000-07.

Citing Articles

Tauopathy and Epilepsy Comorbidities and Underlying Mechanisms.

Hwang K, Vaknalli R, Addo-Osafo K, Vicente M, Vossel K Front Aging Neurosci. 2022; 14:903973.

PMID: 35923547 PMC: 9340804. DOI: 10.3389/fnagi.2022.903973.


Verbal memory dysfunction is associated with alterations in brain transcriptome in dominant temporal lobe epilepsy.

Busch R, Yehia L, Bazeley P, Seyfi M, Blumcke I, Hermann B Epilepsia. 2020; 61(10):2203-2213.

PMID: 32945555 PMC: 8525612. DOI: 10.1111/epi.16673.


Central nervous system lymphatic unit, immunity, and epilepsy: Is there a link?.

Noe F, Marchi N Epilepsia Open. 2019; 4(1):30-39.

PMID: 30868113 PMC: 6398113. DOI: 10.1002/epi4.12302.


Targeting neurodegeneration to prevent post-traumatic epilepsy.

Ali I, Silva J, Liu S, Shultz S, Kwan P, Jones N Neurobiol Dis. 2018; 123:100-109.

PMID: 30099094 PMC: 6348126. DOI: 10.1016/j.nbd.2018.08.006.


Do Patients With Temporal Lobe Epilepsy and Cognitive Decline Have Alzheimer's Disease or Chronic Traumatic Encephalopathy (CTE)?.

Barr W Epilepsy Curr. 2017; 17(2):96-98.

PMID: 28490998 PMC: 5416868. DOI: 10.5698/1535-7511.17.2.96.


References
1.
Houser C . Granule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy. Brain Res. 1990; 535(2):195-204. DOI: 10.1016/0006-8993(90)91601-c. View

2.
Yang C, Wang G, Wang H, Liu Z, Wang X . Cytoskeletal alterations in rat hippocampus following chronic unpredictable mild stress and re-exposure to acute and chronic unpredictable mild stress. Behav Brain Res. 2009; 205(2):518-24. DOI: 10.1016/j.bbr.2009.08.008. View

3.
SCHEIBEL M, CRANDALL P, SCHEIBEL A . The hippocampal-dentate complex in temporal lobe epilepsy. A Golgi study. Epilepsia. 1974; 15(1):55-80. DOI: 10.1111/j.1528-1157.1974.tb03997.x. View

4.
Dalmagro C, Velasco T, Bianchin M, Martins A, Guarnieri R, Cescato M . Psychiatric comorbidity in refractory focal epilepsy: a study of 490 patients. Epilepsy Behav. 2012; 25(4):593-7. DOI: 10.1016/j.yebeh.2012.09.026. View

5.
Law A, Weickert C, Hyde T, Kleinman J, Harrison P . Reduced spinophilin but not microtubule-associated protein 2 expression in the hippocampal formation in schizophrenia and mood disorders: molecular evidence for a pathology of dendritic spines. Am J Psychiatry. 2004; 161(10):1848-55. DOI: 10.1176/ajp.161.10.1848. View