Cognitive impairment in spontaneously hypertensive rats

Role of central nicotinic receptors. Part II

Mahanandeeshwar Gattu, Alvin V Terry, James R. Pauly, Jerry J. Buccafusco

Research output: Contribution to journalArticle

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Abstract

The adult spontaneously hypertensive rat (SHR) has been shown to exhibit a decrease in the expression and nicotine-stimulated function of brain nicotinic acetylcholine receptors, factors that could play a role in the impaired ability of this strain in the performance of learning and memory- related tasks. The purpose of this study was to determine whether either or both the impaired task performance and the loss of nicotinic receptors is directly related to the presence of the hypertensive state. To address this issue, two experimental approaches were taken. In the first series, 4-week- old pre-hypertensive SHR were tested in two phases of a water maze (spatial memory) task, and their performance was compared with that of two age- matched normotensive strains, Wistar Kyoto (WKY) and Wistar rats. During phase 1, SHR and WKY rats were not different in their ability to learn the task. In contrast, during phase 2 (subsequent series of trials after a 4 day inter-phase period), where rats were required to find a new platform location, SHR exhibited significantly impaired performance compared to both WKY and Wistar normotensive controls. In a single trial passive avoidance paradigm, SHR again displayed significantly reduced avoidance behavior as compared with both WKY and Wistar rats. In consecutive coronal sections the density of [3H]cytisine binding sites was decreased in pre-hypertensive SHR by up to 18% in about 40% of the brain regions examined, with the deficits particularly apparent in frontal cortex (layers 4-6), posterior subiculum, several thalamic regions, and the interpeduncular nucleus. In the second series, age-matched SHR and WKY were treated with the antihypertensive agent hydralazine administered in the drinking water beginning at 4 weeks of age. Hydralazine prevented the development of hypertension in adult SHR, but did not forestall the reduced expression of brain nicotinic receptors, nor the impairment in learning- and memory-related tasks normally observed in untreated adults with established hypertension. Moreover, the magnitude of nicotine-stimulated rubidium efflux from cortical and striatal synaptosomes in vitro was significantly reduced in samples derived from hydralazine- treated SHR as compared with those from hydralazine-treated, or untreated WKY. These results support the contention that the hypertensive state does not directly contribute to the reduced expression of nicotinic receptors in SHR. Therefore, the SHR may provide an important genetic model for the study of the role of central nicotinic receptors in cognitive and learning abnormalities.

Original languageEnglish (US)
Pages (from-to)104-114
Number of pages11
JournalBrain Research
Volume771
Issue number1
DOIs
StatePublished - Oct 10 1997

Fingerprint

Nicotinic Receptors
Inbred SHR Rats
Hydralazine
Inbred WKY Rats
Aptitude
Task Performance and Analysis
Learning
Nicotine
Brain
Cognitive Dysfunction
Rubidium
Avoidance Learning
Hypertension
Corpus Striatum
Synaptosomes
Genetic Models
Frontal Lobe
Drinking Water
Antihypertensive Agents
Hippocampus

Keywords

  • Autoradiography
  • Learning and memory
  • Nicotinic receptor
  • Passive avoidance
  • Rubidium efflux
  • Spontaneously hypertensive rat
  • Water maze

ASJC Scopus subject areas

  • Neuroscience(all)
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

Cite this

Cognitive impairment in spontaneously hypertensive rats : Role of central nicotinic receptors. Part II. / Gattu, Mahanandeeshwar; Terry, Alvin V; Pauly, James R.; Buccafusco, Jerry J.

In: Brain Research, Vol. 771, No. 1, 10.10.1997, p. 104-114.

Research output: Contribution to journalArticle

Gattu, Mahanandeeshwar ; Terry, Alvin V ; Pauly, James R. ; Buccafusco, Jerry J. / Cognitive impairment in spontaneously hypertensive rats : Role of central nicotinic receptors. Part II. In: Brain Research. 1997 ; Vol. 771, No. 1. pp. 104-114.
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