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Quantitative expression and localization of GABAB receptor protein subunits in hippocampi from patients with refractory temporal lobe epilepsy.
Sheilabi, Mariam A; Battacharyya, Dev; Caetano, Laura; Thom, Maria; Reuber, Markus; Duncan, John S; Princivalle, Alessandra P.
Afiliación
  • Sheilabi MA; Biomolecular Sciences Research Centre, Sheffield Hallam University, Howard Street, Sheffield, S1 1WB, UK.
  • Battacharyya D; Neurosurgery, Sheffield Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK.
  • Caetano L; Biomolecular Sciences Research Centre, Sheffield Hallam University, Howard Street, Sheffield, S1 1WB, UK.
  • Thom M; Department of Neuropathology, Institute of Neurology, UCL, Queen Square, London, UK.
  • Reuber M; Academic Neurology Unit, University of Sheffield, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK.
  • Duncan JS; Department of Clinical and Experimental Epilepsy, Institute of Neurology, UCL, Queen Square, London, UK.
  • Princivalle AP; Biomolecular Sciences Research Centre, Sheffield Hallam University, Howard Street, Sheffield, S1 1WB, UK; Division of Neuroscience, Department of Pharmacology, Medical School, University of Birmingham, Birmingham, B15 2TT, UK. Electronic address: a.p.princivalle@shu.ac.uk.
Neuropharmacology ; 136(Pt A): 117-128, 2018 07 01.
Article en En | MEDLINE | ID: mdl-28782512
This study investigates GABAB protein expression and mRNA levels in three types of specimens. Two types of specimens from patients with temporal lobe epilepsy (TLE), secondary to hippocampal sclerosis, sclerotic hippocampal samples (TLE-HS), and tissue from the structurally preserved non-spiking ipsilateral superior temporal gyrus (TLE-STG) removed from the same patient during epilepsy surgery; and third specimen is hippocampal tissue from individuals with no history of epilepsy (post-mortem controls, PMC). mRNA expression of GABAB subunits was quantified in TLE-HS, TLE-STG and PMC specimens by qRT-PCR. Qualitative and quantitative Western blot (WB) and immunohistochemistry techniques were employed to quantify and localize GABAB proteins subunits. qRT-PCR data demonstrated an overall decrease of both GABAB1 isoforms in TLE-HS compared to TLE-STG. These results were mirrored by the WB findings. GABAB2 mRNA and protein were significantly reduced in TLE-HS samples compared to TLE-STG; however they appeared to be upregulated in TLE-HS compared to the PMC samples. Immunohistochemistry (IHC) showed that GABAB proteins were widely distributed in PMC and TLE-HS hippocampal sections with regional differences in the intensity of the signal. The higher expression of mature GABAB protein in TLE-HS than PMC is in agreement with previous studies. However, these findings could be due to post-mortem changes in PMC specimens. The TLE-STG samples examined here represent a better 'control' tissue compared to TLE-HS samples characterised by lower than expected GABAB expression. This interpretation provides a better explanation for previous functional studies suggesting reduced inhibition in TLE-HS tissue due to attenuated GABAB currents. This article is part of the "Special Issue Dedicated to Norman G. Bowery".
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de GABA-B / Epilepsia del Lóbulo Temporal / Epilepsia Refractaria / Hipocampo Tipo de estudio: Qualitative_research Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Neuropharmacology Año: 2018 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de GABA-B / Epilepsia del Lóbulo Temporal / Epilepsia Refractaria / Hipocampo Tipo de estudio: Qualitative_research Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Neuropharmacology Año: 2018 Tipo del documento: Article Pais de publicación: Reino Unido