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A mouse model of the 15q13.3 microdeletion syndrome shows prefrontal neurophysiological dysfunctions and attentional impairment

Nilsson, Simon R O (author)
The State University of New York,University of Cambridge
Celada, Pau (author)
CIBER Salud Mental (CIBERSAM)
Fejgin, Kim (author)
H. Lundbeck A/S
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Thelin, Jonas (author)
Lund University,Lunds universitet,Neuronano Research Center (NRC),Forskargrupper vid Lunds universitet,Lund University Research Groups,H. Lundbeck A/S
Nielsen, Jacob (author)
H. Lundbeck A/S
Santana, Noemí (author)
CIBER Salud Mental (CIBERSAM)
Heath, Christopher J. (author)
Open University
Larsen, Peter H. (author)
H. Lundbeck A/S
Nielsen, Vibeke (author)
H. Lundbeck A/S
Kent, Brianne A. (author)
University of Cambridge
Saksida, Lisa M. (author)
University of Cambridge
Stensbøl, Tine B. (author)
H. Lundbeck A/S
Robbins, Trevor W. (author)
University of Cambridge
Bastlund, Jesper F. (author)
H. Lundbeck A/S
Bussey, Timothy J. (author)
University of Cambridge
Artigas, Francesc (author)
CIBER Salud Mental (CIBERSAM)
Didriksen, Michael (author)
H. Lundbeck A/S
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 (creator_code:org_t)
2016-03-17
2016
English 13 s.
In: Psychopharmacologia. - : Springer Science and Business Media LLC. - 0033-3158. ; 233:11, s. 2151-2163
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Rationale: A microdeletion at locus 15q13.3 is associated with high incidence rates of psychopathology, including schizophrenia. A mouse model of the 15q13.3 microdeletion syndrome has been generated (Df[h15q13]/+) with translational utility for modelling schizophrenia-like pathology. Among other deficits, schizophrenia is characterised by dysfunctions in prefrontal cortical (PFC) inhibitory circuitry and attention. Objectives: The objective of this study is to assess PFC-dependent functioning in the Df(h15q13)/+ mouse using electrophysiological, pharmacological, and behavioural assays. Method: Experiments 1–2 investigated baseline firing and auditory-evoked responses of PFC interneurons and pyramidal neurons. Experiment 3 measured pyramidal firing in response to intra-PFC GABAAreceptor antagonism. Experiments 4–6 assessed PFC-dependent attentional functioning through the touchscreen 5-choice serial reaction time task (5-CSRTT). Experiments 7–12 assessed reversal learning, paired-associate learning, extinction learning, progressive ratio, trial-unique non-match to sample, and object recognition. Results: In experiments 1–3, the Df(h15q13)/+ mouse showed reduced baseline firing rate of fast-spiking interneurons and in the ability of the GABAAreceptor antagonist gabazine to increase the firing rate of pyramidal neurons. In assays of auditory-evoked responses, PFC interneurons in the Df(h15q13)/+ mouse had reduced detection amplitudes and increased detection latencies, while pyramidal neurons showed increased detection latencies. In experiments 4–6, the Df(h15q13)/+ mouse showed a stimulus duration-dependent decrease in percent accuracy in the 5-CSRTT. The impairment was insensitive to treatment with the partial α7nAChR agonist EVP-6124. The Df(h15q13)/+ mouse showed no cognitive impairments in experiments 7–12. Conclusion: The Df(h15q13)/+ mouse has multiple dysfunctions converging on disrupted PFC processing as measured by several independent assays of inhibitory transmission and attentional function.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

15q13.3
Animal model
Chrna7
Cognition
Copy number variation
Neurophysiology
Prefrontal cortex

Publication and Content Type

art (subject category)
ref (subject category)

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