2015
DOI: 10.1016/j.brainres.2015.10.019
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Equal effects of typical environmental and specific social enrichment on posttraumatic cognitive functioning after fimbria-fornix transection in rats

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Cited by 7 publications
(4 citation statements)
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“…Previous studies have demonstrated that either the enriched environment or exercise could be promising strategies in enhancing learning and memory as well as upregulation of the BDNF/TrkB signaling pathway, thus highlighting their therapeutic potential [26][27][28]. It has been shown that, compared to a single intervention, combined exercise and enriched environment interventions yield better effects in healthy animals [29][30][31][32].…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies have demonstrated that either the enriched environment or exercise could be promising strategies in enhancing learning and memory as well as upregulation of the BDNF/TrkB signaling pathway, thus highlighting their therapeutic potential [26][27][28]. It has been shown that, compared to a single intervention, combined exercise and enriched environment interventions yield better effects in healthy animals [29][30][31][32].…”
Section: Introductionmentioning
confidence: 99%
“…Studies have concluded that EE has a more profound effect on cognitive improvement compared to social enrichment (SE) alone following insult or injury, but both SE and EE improve cognition beyond standard housing conditions (SC) (i.e. no form of enrichment) (Gajhede Gram, Gade, Wogensen, Mogensen, & Mala, 2015; Sozda et al, 2010). We have previously shown in young rats that four months of EE, and not SE, is sufficient to improve learning ability and enhance metabotropic glutamate receptor-dependent long-term potentiation (mGluR-LTP) via a mechanism involving activation of p70S6 kinase (p70S6K) in hippocampus (Hullinger et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…In addition to the aforementioned effects of EE and SE under physiological conditions, both interventions have been demonstrated to have therapeutic effects under pathological conditions. In this regard, both EE and SE induce recovery in various models of central nervous system injury (Berrocal et al, 2007;Gajhede Gram et al, 2015;Lajud et al, 2018). Moreover, EE increases AHN in mouse models of Down syndrome (Chakrabarti et al, 2011;Pons-Espinal et al, 2013), Alzheimer's disease (Levi and Michaelson, 2007;Mirochnic et al, 2009;Valero et al, 2011;Llorens-Martin et al, 2013;Marlatt et al, 2013), Huntington's disease (Lazic et al, 2006), diabetes (Pamidi and Nayak, 2014), ischemia (Rojas et al, 2013), and chronic pain (Zheng et al, 2017), after cranial irradiation (Garbugino et al, 2016), and during physiological aging (Kempermann et al, 1998(Kempermann et al, , 2002Kempermann, 2008Kempermann, , 2015Speisman et al, 2013).…”
Section: Discussionmentioning
confidence: 99%