Densities of parvalbumin-immunoreactive neurons in non-malformed hippocampal sclerosis-temporal neocortex and in cortical dysplasias
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16459206
DOI
10.1016/j.brainresbull.2005.10.008
PII: S0361-9230(05)00430-2
Knihovny.cz E-resources
- MeSH
- Biomarkers MeSH
- Diagnosis, Differential MeSH
- Child MeSH
- Adult MeSH
- Epilepsy, Temporal Lobe metabolism pathology physiopathology MeSH
- Epilepsy metabolism pathology physiopathology MeSH
- Gliosis metabolism pathology physiopathology MeSH
- Hippocampus abnormalities metabolism pathology MeSH
- Immunohistochemistry MeSH
- Interneurons metabolism pathology MeSH
- Infant MeSH
- Middle Aged MeSH
- Humans MeSH
- Nervous System Malformations * MeSH
- Adolescent MeSH
- Parvalbumins metabolism MeSH
- Cell Count MeSH
- Child, Preschool MeSH
- Temporal Lobe abnormalities metabolism pathology MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Infant MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Parvalbumins MeSH
The changes in density of inhibitory parvalbumin-immunoreactive interneurons were quantitatively studied by immunohistochemistry in a series of human neocortical samples comprising the spectrum of malformations of cortical development (MCD) encountered in epilepsy surgery and the non-malformed hippocampal sclerosis-temporal neocortex in patients with refractory temporal lobe epilepsy. The highest relative density of parvalbumin-immunoreactive cells was obtained in the control samples (n = 21). The number of parvalbumin-immunoreactive neurons was significantly decreased in non-malformed hippocampal sclerosis-temporal neocortex (n = 73, 80.5% of control values). In a proportion of the latter samples as well as in two controls we observed patchy regions of absence of parvalbumin staining. The total counts of parvalbumin-immunoreactive cells in all the categories of MCD - "mild MCD" (n = 25), focal cortical dysplasia type I (n = 19) and type II (n = 15) - were decreased representing 72.4%, 55.0% and 12.2% of control values, respectively. Significantly different parvalbumin-immunoreactive cell densities were demonstrated between the focal cortical dysplasia types IIA and IIB. In "mild MCD", we observed a more pronounced decrease of parvalbumin-immunoreactive cells in the infragranular layers. No significant differences were revealed between the temporal and extratemporal examples of analogous MCD types. This study provides evidence for reduction of inhibitory parvalbumin-immunoreactive interneurons in the epileptic neocortex affected by MCD as well as in morphologically unaffected epileptic temporal neocortex, thus representing a possible mechanism for their epileptogenicity.
References provided by Crossref.org