Literature DB >> 17223364

Pre-training to find a hidden platform in the Morris water maze can compensate for a deficit to find a cued platform in a rat model of Parkinson's disease.

Claudio Da Cunha1, Samantha Wietzikoski, Evellyn C Wietzikoski, Marcio H C Silva, Jeff Chandler, Marcelo M Ferro, Roberto Andreatini, Newton S Canteras.   

Abstract

The bilateral intranigral infusion of 1 micromol 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in adult male Wistar rats caused a specific and partial loss of substantia nigra pars compacta (SNc) dopamine neurons, a partial depletion of striatal dopamine, and a deficit to learn the intra-maze cued version of the Morris water maze. Pre-training the SNc rats in the spatial version of the water maze or simply maintaining the animals on the water maze platform reversed this deficit. This improvement was even observed when the order of the extra-maze cues presented to the rats during pre-training of the spatial version was changed during training of the intra-maze cued version. However, this deficit was not reversed either by maintaining the animals on the platform if the spatial cues were surrounded and covered with a curtain or by swimming sessions in the maze without the escape platform and the curtain. These findings suggest that none of the following elements alone, learned during the spatial task pre-training, could help SNc rats learn the intra-maze cued task: improvement of swimming skills or knowledge of the existence of the escape platform; distance between the platform and the border of the pool; location of a particular extra-maze cue; relations among extra-maze cues. However, the simultaneous presence of the escape platform and extra-maze cues (irrespective of their relational configuration) during the pre-training sessions proved to be necessary for this improving effect to occur.

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Year:  2007        PMID: 17223364     DOI: 10.1016/j.nlm.2006.12.004

Source DB:  PubMed          Journal:  Neurobiol Learn Mem        ISSN: 1074-7427            Impact factor:   2.877


  6 in total

1.  The peroxisomal proliferator-activated receptor (PPAR) α agonist, fenofibrate, prevents fractionated whole-brain irradiation-induced cognitive impairment.

Authors:  Dana Greene-Schloesser; Valerie Payne; Ann M Peiffer; Fang-Chi Hsu; David R Riddle; Weiling Zhao; Michael D Chan; Linda Metheny-Barlow; Mike E Robbins
Journal:  Radiat Res       Date:  2014-01-07       Impact factor: 2.841

2.  Functional disconnection of the substantia nigra pars compacta from the pedunculopontine nucleus impairs learning of a conditioned avoidance task.

Authors:  Mariza Bortolanza; Evellyn C Wietzikoski; Suelen L Boschen; Patricia A Dombrowski; Mary Latimer; Duncan A A Maclaren; Philip Winn; Claudio Da Cunha
Journal:  Neurobiol Learn Mem       Date:  2010-06-01       Impact factor: 2.877

3.  Dorsal striatal dopamine depletion impairs both allocentric and egocentric navigation in rats.

Authors:  Amanda A Braun; Devon L Graham; Tori L Schaefer; Charles V Vorhees; Michael T Williams
Journal:  Neurobiol Learn Mem       Date:  2012-03-21       Impact factor: 2.877

4.  Partial lesion of the nigrostriatal dopamine pathway in rats impairs egocentric learning but not spatial learning or behavioral flexibility.

Authors:  Katharine M Seip-Cammack; James J Young; Megan E Young; Matthew L Shapiro
Journal:  Behav Neurosci       Date:  2017-02-20       Impact factor: 1.912

5.  Non-spatial pre-training in the water maze as a clinically relevant model for evaluating learning and memory in experimental TBI.

Authors:  Amy K Wagner; Samuel W Brayer; Max Hurwitz; Christian Niyonkuru; Huichao Zou; Michelle Failla; Patricia Arenth; Mioara D Manole; Elizabeth Skidmore; Edda Thiels
Journal:  Neurobiol Learn Mem       Date:  2013-07-18       Impact factor: 2.877

6.  Behavioral paradigms to evaluate PPAR modulation in animal models of brain injury.

Authors:  Dana Greene-Schloesser; Caroline I Schnegg; Mike E Robbins
Journal:  Methods Mol Biol       Date:  2013
  6 in total

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