Seizure susceptibility and epileptogenesis are decreased in transgenic rats overexpressing neuropeptide Y

Neuroscience. 2002;110(2):237-43. doi: 10.1016/s0306-4522(01)00581-4.

Abstract

Functional studies in epileptic tissue indicate that neuropeptide Y and some of its peptide analogs potently inhibit seizure activity. We investigated seizure susceptibility in transgenic rats overexpressing the rat neuropeptide Y gene under the control of its natural promoter. Seizures were induced in adult transgenic male rats and their wild-type littermates by i.c.v. injection of 0.3 microg kainic acid or by electrical kindling of the dorsal hippocampus. Transgenic rats showed a significant reduction in the number and duration of electroencephalographic seizures induced by kainate by 30% and 55% respectively (P<0.05 and 0.01). Transgenic rats were also less susceptible to epileptogenesis than wild-type littermates as demonstrated by a 65% increase in the number of electrical stimuli required to induce stage 5 seizures (P<0.01). This phenotype was associated with a strong and specific expression of neuropeptide Y mRNA in area CA1, a brain area involved in the seizure network. We conclude that endogenous neuropeptide Y overexpression in the rat hippocampus is associated with inhibition of seizures and epileptogenesis suggesting that this system may be a valuable target for developing novel antiepileptic treatments.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Electric Stimulation
  • Electroencephalography / drug effects
  • Epilepsy / chemically induced
  • Epilepsy / genetics*
  • Epilepsy / physiopathology
  • Epilepsy, Temporal Lobe / metabolism*
  • Epilepsy, Temporal Lobe / physiopathology
  • Excitatory Amino Acid Agonists / pharmacology
  • Gene Expression Regulation / physiology
  • Genetic Predisposition to Disease / genetics*
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Hippocampus / physiopathology
  • Kindling, Neurologic / drug effects
  • Kindling, Neurologic / genetics
  • Male
  • Neurons / drug effects
  • Neurons / metabolism*
  • Neuropeptide Y / genetics*
  • Promoter Regions, Genetic / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation / genetics*

Substances

  • Excitatory Amino Acid Agonists
  • Neuropeptide Y
  • RNA, Messenger