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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2002-7-8
pubmed:abstractText
Central administration of corticotropin-releasing hormone increases anxiety-like behaviour and arousal in rodents, and increased anxiety-like behaviour has been shown in mice overproducing corticotropin-releasing hormone on an elevated plus maze and in a dark-light emergence task. However, evidence is accumulating that measures obtained from different anxiety tasks may reflect different aspects of anxiety-like behaviour in animals. We therefore tested mice overproducing corticotropin-releasing hormone in a battery of paradigms, studying spontaneous behaviour after a mild stressor, tasks of innate anxiety-like behaviour (light-dark box), lick suppression (Vogel conflict), conditioned fear, and forced swimming. Exploratory behaviour was studied in a 16-hole board task. Furthermore, pain threshold, water intake, locomotor activity and sensorimotor learning/co-ordination were tested to control for confounding factors. In line with previous findings, increased anxiety-like behaviour of transgenic mice was observed in the light-dark box paradigm. However, no differences were seen in the conflict paradigm. Conditioned fear was decreased 1 h but not 24 h after conditioning in transgenic mice, and immobility was decreased [corrected] in forced swimming in corticotropin-releasing hormone overexpressors. Locomotor activity in a novel open field and on the hole board was reduced in transgenics. Exploratory behaviour (hole pokes) was reduced during initial exploration of an unfamiliar hole board. Moreover, sensorimotor performance on a rotorod was impaired, and water intake was reduced in corticotropin-releasing hormone overproducing mice, while no changes were seen in nociception. No differences in locomotor activity were seen in a second group of mice, tested in a familiar open field. When these animals were challenged with diazepam, transgenic mice were less susceptible to the sedative effects of the drug on locomotor activity. These data suggest that corticotropin-releasing hormone overproduction leads to specific effects in a subset of anxiety paradigms, and that these transgenic mice suffer from a motor deficit in addition to altered anxiety-like behaviour/arousal.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0953-816X
pubmed:author
pubmed:issnType
Print
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2007-15
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12099906-Animals, pubmed-meshheading:12099906-Anti-Anxiety Agents, pubmed-meshheading:12099906-Anxiety, pubmed-meshheading:12099906-Behavior, Animal, pubmed-meshheading:12099906-Brain, pubmed-meshheading:12099906-Brain Chemistry, pubmed-meshheading:12099906-Corticotropin-Releasing Hormone, pubmed-meshheading:12099906-Dark Adaptation, pubmed-meshheading:12099906-Diazepam, pubmed-meshheading:12099906-Drinking, pubmed-meshheading:12099906-Exploratory Behavior, pubmed-meshheading:12099906-Fear, pubmed-meshheading:12099906-Genetic Predisposition to Disease, pubmed-meshheading:12099906-Male, pubmed-meshheading:12099906-Mice, pubmed-meshheading:12099906-Mice, Transgenic, pubmed-meshheading:12099906-Motor Activity, pubmed-meshheading:12099906-Neurons, pubmed-meshheading:12099906-Pain Threshold, pubmed-meshheading:12099906-Photic Stimulation, pubmed-meshheading:12099906-Reaction Time, pubmed-meshheading:12099906-Stress, Physiological, pubmed-meshheading:12099906-Up-Regulation
pubmed:year
2002
pubmed:articleTitle
Effects of transgenic overproduction of CRH on anxiety-like behaviour.
pubmed:affiliation
Max Planck Institute of Psychiatry, Kraepelinstrasse 2-10, D-80804 Munich, Germany. mm.van_gaalen.pharm@med.vu.nl
pubmed:publicationType
Journal Article