Pentylenetetrazol-kindling of seizures selectively decreases [3H]-citalopram binding in the CA-3 area of rat hippocampus

Neurosci Lett. 2002 Dec 19;335(1):49-53. doi: 10.1016/s0304-3940(02)01141-2.

Abstract

The present study was aimed at determining the changes in the 5-HT transporter activity, in different brain structures after pentylenetetrazol induced kindling of seizures. We examined [3H]-citalopram binding in the rat brain structures, and the neurodegenerative effects in the hippocampal formation using autoradiographic and immunohistochemical methods. A statistically significant and selective reduction in the binding of [3H]-citalopram was found in the CA3 field of the hippocampus (P=0.009), and a similar tendency, close to the significance level, in the dentate gyrus (P=0.05). This effect was accompanied by a loss of neurons and activation of microglia in the hippocampal formation. The present data suggest the important role for CA3- serotonergic innervation in pentylenetetrazol induced kindling of seizures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoradiography
  • Carrier Proteins / metabolism*
  • Citalopram / metabolism*
  • Convulsants
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Immunohistochemistry
  • Kindling, Neurologic
  • Male
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins*
  • Nerve Tissue Proteins*
  • Pentylenetetrazole
  • Rats
  • Rats, Wistar
  • Seizures / chemically induced
  • Seizures / metabolism*
  • Selective Serotonin Reuptake Inhibitors / metabolism*
  • Serotonin Plasma Membrane Transport Proteins
  • Tritium

Substances

  • Carrier Proteins
  • Convulsants
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin Uptake Inhibitors
  • Slc6a4 protein, rat
  • Citalopram
  • Tritium
  • Pentylenetetrazole