Matches in SemOpenAlex for { <https://semopenalex.org/work/W2124079851> ?p ?o ?g. }
- W2124079851 endingPage "3106" @default.
- W2124079851 startingPage "3095" @default.
- W2124079851 abstract "Abstract Epileptiform activity was previously described [ Luhmann et al . (1998 ) Eur.J. Neurosci ., 10, 3085–3094] in the neocortex of the adult rat following freeze lesioning of the newborn neocortex. After a survival time of 3 months, a small area of dysplastic cortex surrounded by histologically normal (exofocal) neocortex was observed. The dysplastic cortex is characterized by the formation of a small sulcus and a three‐ to four‐layered architecture. Two questions are addressed here: (i) is the hyperexcitability associated with changes in binding to major excitatory and inhibitory transmitter receptors in the dysplastic cortex?; and (ii) do such changes also occur in the exofocal cortex? Alterations in binding to glutamatergic N ‐methyl‐ d ‐aspartate (NMDA), (±)‐α‐amino‐3‐hydroxy‐5‐methylisoxazole‐4‐propionic acid (AMPA), kainate and GABA A and GABA B (γ‐aminobutyric acid) receptors are demonstrated with quantitative in vitro receptor autoradiography by using the ligands [ 3 H]MK‐801, [ 3 H]AMPA, [ 3 H]kainate, [ 3 H]muscimol and [ 3 H]baclofen, respectively. In the dysplastic cortex, the binding to NMDA, AMPA and kainate receptors is significantly increased, whereas the binding to GABA A and GABA B receptors is reduced. Exofocal areas of the lesioned hemisphere show an imbalance between excitatory and inhibitory receptor binding with an up‐regulation of the binding to AMPA and kainate, and a down‐regulation to GABA A receptors. The binding to GABA B and NMDA receptors is not significantly changed in the exofocal areas. The imbalance between excitatory and inhibitory receptors may cause the hyperexcitability, as previously found in the identical experimental model, and may also induce epileptiform activity in the human cortex with migration disorders." @default.
- W2124079851 created "2016-06-24" @default.
- W2124079851 creator A5065994712 @default.
- W2124079851 creator A5069216487 @default.
- W2124079851 creator A5070715804 @default.
- W2124079851 creator A5087646992 @default.
- W2124079851 date "1998-10-01" @default.
- W2124079851 modified "2023-10-03" @default.
- W2124079851 title "Characterization of neuronal migration disorders in neocortical structures: quantitative receptor autoradiography of ionotropic glutamate, GABA<sub>A</sub>and GABA<sub>B</sub>receptors" @default.
- W2124079851 cites W111104 @default.
- W2124079851 cites W1564385970 @default.
- W2124079851 cites W1574239291 @default.
- W2124079851 cites W1964168449 @default.
- W2124079851 cites W1965417826 @default.
- W2124079851 cites W1967519027 @default.
- W2124079851 cites W1973182368 @default.
- W2124079851 cites W1986903653 @default.
- W2124079851 cites W1991893040 @default.
- W2124079851 cites W1992792117 @default.
- W2124079851 cites W1993442791 @default.
- W2124079851 cites W1993837919 @default.
- W2124079851 cites W1996858420 @default.
- W2124079851 cites W2005417728 @default.
- W2124079851 cites W2010132442 @default.
- W2124079851 cites W2027203408 @default.
- W2124079851 cites W2033106534 @default.
- W2124079851 cites W2033959417 @default.
- W2124079851 cites W2034131096 @default.
- W2124079851 cites W2034377493 @default.
- W2124079851 cites W2036209909 @default.
- W2124079851 cites W2038480095 @default.
- W2124079851 cites W2039738625 @default.
- W2124079851 cites W2039872800 @default.
- W2124079851 cites W2039917407 @default.
- W2124079851 cites W2047543957 @default.
- W2124079851 cites W2047714465 @default.
- W2124079851 cites W2054064374 @default.
- W2124079851 cites W2054653910 @default.
- W2124079851 cites W2055590786 @default.
- W2124079851 cites W2060523026 @default.
- W2124079851 cites W2061556807 @default.
- W2124079851 cites W2063045558 @default.
- W2124079851 cites W2068851283 @default.
- W2124079851 cites W2073627392 @default.
- W2124079851 cites W2074382776 @default.
- W2124079851 cites W2074683128 @default.
- W2124079851 cites W2077059819 @default.
- W2124079851 cites W2077506421 @default.
- W2124079851 cites W2077630079 @default.
- W2124079851 cites W2081678712 @default.
- W2124079851 cites W2084106471 @default.
- W2124079851 cites W2091393718 @default.
- W2124079851 cites W2101124030 @default.
- W2124079851 cites W2107970548 @default.
- W2124079851 cites W2109301124 @default.
- W2124079851 cites W2121090033 @default.
- W2124079851 cites W2121454764 @default.
- W2124079851 cites W2124980980 @default.
- W2124079851 cites W2130215954 @default.
- W2124079851 cites W2131234693 @default.
- W2124079851 cites W2133239469 @default.
- W2124079851 cites W2136427434 @default.
- W2124079851 cites W2152110988 @default.
- W2124079851 cites W2154447884 @default.
- W2124079851 cites W2157031808 @default.
- W2124079851 cites W2160987264 @default.
- W2124079851 cites W2164930173 @default.
- W2124079851 cites W2171584675 @default.
- W2124079851 cites W2314512523 @default.
- W2124079851 cites W2335025908 @default.
- W2124079851 cites W2488889860 @default.
- W2124079851 cites W65079823 @default.
- W2124079851 cites W77091309 @default.
- W2124079851 doi "https://doi.org/10.1046/j.1460-9568.1998.00322.x" @default.
- W2124079851 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9786204" @default.
- W2124079851 hasPublicationYear "1998" @default.
- W2124079851 type Work @default.
- W2124079851 sameAs 2124079851 @default.
- W2124079851 citedByCount "81" @default.
- W2124079851 countsByYear W21240798512012 @default.
- W2124079851 countsByYear W21240798512014 @default.
- W2124079851 countsByYear W21240798512015 @default.
- W2124079851 countsByYear W21240798512016 @default.
- W2124079851 countsByYear W21240798512017 @default.
- W2124079851 countsByYear W21240798512019 @default.
- W2124079851 countsByYear W21240798512020 @default.
- W2124079851 countsByYear W21240798512021 @default.
- W2124079851 countsByYear W21240798512023 @default.
- W2124079851 crossrefType "journal-article" @default.
- W2124079851 hasAuthorship W2124079851A5065994712 @default.
- W2124079851 hasAuthorship W2124079851A5069216487 @default.
- W2124079851 hasAuthorship W2124079851A5070715804 @default.
- W2124079851 hasAuthorship W2124079851A5087646992 @default.
- W2124079851 hasConcept C112592302 @default.
- W2124079851 hasConcept C115955781 @default.
- W2124079851 hasConcept C160268369 @default.
- W2124079851 hasConcept C168258287 @default.
- W2124079851 hasConcept C169760540 @default.