Epilepsy Research
Volume 32, Issue 3 , Pages 335-344, November 1998

Synaptophysin immunohistochemistry densitometry measurement in resected human hippocampus: implication for the etiology of hippocampal sclerosis

  • Keith G Davies

      Affiliations

    • Epi-Care Center, Baptist Memorial Hospital, 930 Madison Avenue, Suite 700, Memphis, TN 38103, USA
    • Semmes-Murphey Clinic, Memphis, TN, USA
    • Department of Neurosurgery, University of Tennessee, Memphis, TN, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 901 5222660; fax: +1 901 5222665; e-mail kgdavies@pol.net
  • ,
  • John B Schweitzer

      Affiliations

    • Department of Pathology, University of Tennessee, Memphis, TN, USA
    • Department of Anatomy and Neurobiology, University of Tennessee, Memphis, TN, USA
  • ,
  • Mark R Looney

      Affiliations

    • Department of Pathology, University of Tennessee, Memphis, TN, USA
  • ,
  • Andrew J Bush

      Affiliations

    • Department of Preventive Medicine, University of Tennessee, Memphis, TN, USA
  • ,
  • F.Curtis Dohan Jr.

      Affiliations

    • Department of Pathology, University of Tennessee, Memphis, TN, USA
  • ,
  • Bruce P Hermann

      Affiliations

    • Department of Neurology, University of Wisconsin, Madison, WI, USA

Received 22 December 1997; received in revised form 13 March 1998; accepted 17 March 1998.

Abstract 

Synaptophysin (SY) is a protein expressed at presynaptic vesicles. SY immunohistochemistry (IHC) was undertaken in surgically resected hippocampal specimens from 25 patients with intractable epilepsy. All were investigated with chronic ictal EEG videotelemetry, which showed a temporal onset in each case, and all had normal magnetic resonance imaging (MRI). The density of reaction product of SY IHC was used to generate optical density (OD) measurements as an estimate of synaptic density in CA1 and CA4 fields (ODCA1 and ODCA4), and inner third and outer two-thirds of the molecular layer of the dentate gyrus (ODIML and ODOML). There was significant correlation between ODCA1 (r=0.619, P=0.001) and ODCA4 (r=0.639, P=0.001) and onset age of epilepsy. There was no correlation between ODCA1 and duration of epilepsy. There was correlation between ODCA4 and duration (r=−0.412, P=0.041), but partial correlations showed no significant correlation between ODCA4 and duration when controlling for onset, although correlation between ODCA4 and onset when controlling for duration remained significant (r=0.536, P<0.01). Univariate ANOVA revealed onset age to be the only predictor of ODCA1 and ODCA4. Chronological age and duration were not predictors. There was no correlation between ODIML or ODOML and either onset age or duration. ODIML and ODOML were not predicted by onset age, duration or chronological age. These findings support the hypothesis that the major cause of hippocampal sclerosis is an age specific insult rather than the result of repeated seizures.

Keywords:  Epilepsy, Hippocampal sclerosis, Immunohistochemistry, Optical density, Synaptophysin, Temporal lobectomy

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PII: S0920-1211(98)00032-1

Epilepsy Research
Volume 32, Issue 3 , Pages 335-344, November 1998