## Abstract C57BL/6 mice consistently outperform DBA/2 mice in a range of hippocampal‐dependent spatial learning behaviors. We recorded evoked responses from the dentate gyrus of awake, freely‐moving mice and measured synaptic plasticity (LTP) and performance in a hippocampal‐dependent task in indi
Differential involvement of the dorsal hippocampus in passive avoidance in C57bl/6J and DBA/2J mice
✍ Scribed by Petra J.J. Baarendse; Gerard van Grootheest; René F. Jansen; Anton W. Pieneman; Sven Ove Ögren; Matthijs Verhage; Oliver Stiedl
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 333 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1050-9631
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The inferior performance of DBA/2 mice when compared to C57BL/6 mice in hippocampus‐dependent behavioral tasks including contextual fear conditioning has been attributed to impaired hippocampal function. However, DBA/2J mice have been reported to perform similarly or even better than C57BL/6J mice in the passive avoidance (PA) task that most likely also depends on hippocampal function. The apparent discrepancy in PA versus fear conditioning performance in these two strains of mice was investigated using an automated PA system. The aim was to determine whether these two mouse strains utilize different strategies involving a different contribution of hippocampal mechanisms to encode PA. C57BL/6J mice exhibited significantly longer retention latencies than DBA/2J mice when tested 24 h after training irrespective of the circadian cycle. Dorsohippocampal NMDA receptor inhibition by local injection of the selective antagonist DL‐2‐amino‐5‐phosphonovaleric acid (AP5, 3.2 μg/mouse) before training resulted in impaired PA retention in C57BL/6J but not in DBA/2J mice. Furthermore, nonreinforced pre‐exposure to the PA system before training caused a latent inhibition‐like reduction of retention latencies in C57BL/6J, whereas it improved PA retention in DBA/2J mice. These pre‐exposure experiments facilitated the discrimination of hippocampal involvement without local pharmacological intervention. The results indicate differences in PA learning between these two strains based on a different NMDA receptor involvement in the dorsal hippocampus in this emotional learning task. We hypothesize that mouse strains can differ in their PA learning performance based on their relative ability to form associations on the basis of unisensory versus multisensory contextual/spatial cues that involve hippocampal processing. © 2007 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Hippocampal and amygdaloid neuroplasticity are important substrates for Pavlovian fear conditioning. The hippocampus has been implicated in trace fear conditioning. However, a systematic investigation of the significance of the trace interval has not yet been performed. Therefore, this
## Abstract The two inbred strains of mice C57BL/6 (alcohol‐preferring) and DBA/2 (alcohol‐avoiding) mice have been shown to differ significantly in their preference for alcohol (EtOH). We have previously demonstrated the differences in the density and the affinity of cannabinoid (CB1) receptors in
The two inbred strains of mice C57BL/6 and DBA/2 mice have been shown to differ significantly in their preference for alcohol (EtOH). These strains of mice have been employed to study various aspects of pharmacological and behavioral effects of EtOH. We have previously demonstrated that chronic EtOH
Glycinergic neurons in the cochlear nucleus (CN) of C57BL/6J (C57) and CBA/CaJ (CBA) mice were studied by using immunocytochemical and receptor-binding techniques. Adult C57 mice exhibit progressive cochlear pathology as they age, whereas aging CBA mice retain good hearing. In the CN of old C57 mice