Effects of hypothermia and lamotrigine on trace-conditioned learning after global cerebral ischemia in rabbits

Jae Young Kwon, Andreas Bacher, Donald J. Deyo, Marjorie Grafe, John F. Disterhoft, Tatsuo Uchida, Mark Zornow

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Acquisition of the trace-conditioned eye blink response (CR) is mediated by a variety of brain structures, including the cerebellum, the hippocampus, and brain stem nuclei. We examined the effects of a neuronal sodium channel antagonist (lamotrigine) on the ability of rabbits to acquire an eye blink CR after 6.5 min of cerebral ischemia. New Zealand white rabbits (n = 31) were randomly assigned to sham (S), normothermic ischemia (N), hypothermic (30°C) ischemia(H), or lamotrigine (50 mg/kg) treated (L) groups. In the N, H, and L groups, 6.5 min of global cerebral ischemia was produced using an inflatable neck tourniquet. Trace conditioning was started on the 7th postischemic day. The conditioned stimulus consisted of a tone (85 dB, 6 kHz) presented for 100 ms. The unconditioned stimulus was an air puff (150 ms duration) directed at the cornea. The interval between the end of the conditioned stimulus and the start of the unconditioned stimulus (the trace interval, TI) was 300 ms in duration. A trace-conditioned response was defined as an eye blink that was initiated during the TI. Eighty trials were delivered daily for 15 days. Neurologic deficits were greatest in the N group, and these animals had fewer CRs (149 ± 157) than animals in the S (509 ± 214) or H (461 ± 149) groups (P <0.05 by analysis of variance). Animals in the L group had a total number of CRs (380 ± 253) that was intermediate between the S and N groups. Histologic evidence of neural injury was greatest in the N group. This study demonstrates that a brief episode of cerebral ischemia results in the impairment of this test of neurobehavioral function. Both hypothermia and lamotrigine were able to attenuate the impairment of eye blink trace- conditioned responses produced by cerebral ischemia.

Original languageEnglish (US)
Pages (from-to)105-113
Number of pages9
JournalExperimental Neurology
Volume159
Issue number1
DOIs
StatePublished - Sep 1999
Externally publishedYes

Fingerprint

Hypothermia
Brain Ischemia
Learning
Rabbits
Ischemia
Tourniquets
Aptitude
Sodium Channels
Neurologic Manifestations
Cornea
Cerebellum
Brain Stem
Hippocampus
Analysis of Variance
Neck
Air
lamotrigine
Wounds and Injuries
Brain

Keywords

  • Brain
  • Conditioned response
  • Hypothermia
  • Ischemia
  • Lamotrigine
  • Rabbits

ASJC Scopus subject areas

  • Neurology
  • Neuroscience(all)

Cite this

Effects of hypothermia and lamotrigine on trace-conditioned learning after global cerebral ischemia in rabbits. / Kwon, Jae Young; Bacher, Andreas; Deyo, Donald J.; Grafe, Marjorie; Disterhoft, John F.; Uchida, Tatsuo; Zornow, Mark.

In: Experimental Neurology, Vol. 159, No. 1, 09.1999, p. 105-113.

Research output: Contribution to journalArticle

Kwon, Jae Young ; Bacher, Andreas ; Deyo, Donald J. ; Grafe, Marjorie ; Disterhoft, John F. ; Uchida, Tatsuo ; Zornow, Mark. / Effects of hypothermia and lamotrigine on trace-conditioned learning after global cerebral ischemia in rabbits. In: Experimental Neurology. 1999 ; Vol. 159, No. 1. pp. 105-113.
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