Literature DB >> 19515491

Sulforaphane improves cognitive function administered following traumatic brain injury.

Pramod K Dash1, Jing Zhao, Sara A Orsi, Min Zhang, Anthony N Moore.   

Abstract

Recent studies have shown that sulforaphane, a naturally occurring compound that is found in cruciferous vegetables, offers cellular protection in several models of brain injury. When administered following traumatic brain injury (TBI), sulforaphane has been demonstrated to attenuate blood-brain barrier permeability and reduce cerebral edema. These beneficial effects of sulforaphane have been shown to involve induction of a group of cytoprotective, Nrf2-driven genes, whose protein products include free radical scavenging and detoxifying enzymes. However, the influence of sulforaphane on post-injury cognitive deficits has not been examined. In this study, we examined if sulforaphane, when administered following cortical impact injury, can improve the performance of rats tested in hippocampal- and prefrontal cortex-dependent tasks. Our results indicate that sulforaphane treatment improves performance in the Morris water maze task (as indicated by decreased latencies during learning and platform localization during a probe trial) and reduces working memory dysfunction (tested using the delayed match-to-place task). These behavioral improvements were only observed when the treatment was initiated 1h, but not 6h, post-injury. These studies support the use of sulforaphane in the treatment of TBI, and extend the previously observed protective effects to include enhanced cognition.

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Year:  2009        PMID: 19515491      PMCID: PMC2700200          DOI: 10.1016/j.neulet.2009.04.028

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  18 in total

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Journal:  Cancer Res       Date:  2002-09-15       Impact factor: 12.701

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Authors:  Ramesh Raghupathi
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Journal:  J Neurotrauma       Date:  2004-01       Impact factor: 5.269

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  47 in total

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Journal:  Mol Neurobiol       Date:  2011-04-19       Impact factor: 5.590

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Authors:  Raghavendar Chandran; TaeHee Kim; Suresh L Mehta; Eshwar Udho; Vishal Chanana; Pelin Cengiz; HwuiWon Kim; Chanul Kim; Raghu Vemuganti
Journal:  J Cereb Blood Flow Metab       Date:  2017-10-30       Impact factor: 6.200

5.  Sulforaphane Augments Glutathione and Influences Brain Metabolites in Human Subjects: A Clinical Pilot Study.

Authors:  Thomas W Sedlak; Leslie G Nucifora; Minori Koga; Lindsay S Shaffer; Cecilia Higgs; Teppei Tanaka; Anna M Wang; Jennifer M Coughlin; Peter B Barker; Jed W Fahey; Akira Sawa
Journal:  Mol Neuropsychiatry       Date:  2018-04-17

6.  Nrf2-ARE activator carnosic acid decreases mitochondrial dysfunction, oxidative damage and neuronal cytoskeletal degradation following traumatic brain injury in mice.

Authors:  Darren M Miller; Indrapal N Singh; Juan A Wang; Edward D Hall
Journal:  Exp Neurol       Date:  2014-11-26       Impact factor: 5.330

Review 7.  Pleiotropic role of PPARγ in intracerebral hemorrhage: an intricate system involving Nrf2, RXR, and NF-κB.

Authors:  Xiu-Rong Zhao; Nicole Gonzales; Jaroslaw Aronowski
Journal:  CNS Neurosci Ther       Date:  2014-11-28       Impact factor: 5.243

8.  Administration of the Nrf2-ARE activators sulforaphane and carnosic acid attenuates 4-hydroxy-2-nonenal-induced mitochondrial dysfunction ex vivo.

Authors:  Darren M Miller; Indrapal N Singh; Juan A Wang; Edward D Hall
Journal:  Free Radic Biol Med       Date:  2012-12-27       Impact factor: 7.376

9.  Sulforaphane protects primary cultures of cortical neurons against injury induced by oxygen-glucose deprivation/reoxygenation via antiapoptosis.

Authors:  Xuemei Wu; Jing Zhao; Shanshan Yu; Yanlin Chen; Jingxian Wu; Yong Zhao
Journal:  Neurosci Bull       Date:  2012-10-03       Impact factor: 5.203

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Authors:  Gerasimos P Sykiotis; Dirk Bohmann
Journal:  Sci Signal       Date:  2010-03-09       Impact factor: 8.192

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