Post-Ischemic Housing Conditions Influence On Gene Transcription And Translation After Permanent Focal Brain Ischemia In Rats
(2004)- Abstract
- Enriched environment (EE) housing significantly ameliorates neurological deficits induced by cortical brain ischemia without changing infarction size, suggesting that EE-related functional benefits are associated with neuronal plasticity events in the remaining tissue. Brain-derived neurotrophic factor (BDNF), nerve growth factor-induced gene A (NGFI-A) and corticosteroid receptors (mineralocorticoid receptor, MR; glucocorticoid receptor, GR) have been demonstrated to be involved in brain plasticity. The purpose of this thesis was to determine if post-ischemic housing conditions had a significant effect on transcription and/or translation of BDNF, NGFI-A and corticosteroid receptors. We found that BDNF gene was down regulated in EE-housed... (More)
- Enriched environment (EE) housing significantly ameliorates neurological deficits induced by cortical brain ischemia without changing infarction size, suggesting that EE-related functional benefits are associated with neuronal plasticity events in the remaining tissue. Brain-derived neurotrophic factor (BDNF), nerve growth factor-induced gene A (NGFI-A) and corticosteroid receptors (mineralocorticoid receptor, MR; glucocorticoid receptor, GR) have been demonstrated to be involved in brain plasticity. The purpose of this thesis was to determine if post-ischemic housing conditions had a significant effect on transcription and/or translation of BDNF, NGFI-A and corticosteroid receptors. We found that BDNF gene was down regulated in EE-housed rats when compared to the rats housed in standard cages at 2~12 days after cortical brain ischemia in peri-infarct cortex, contralateral cortex and bilateral hippocampus. The protein level of BDNF in the ipsilateral frontal cortex was lower in the EE-housed rats than the standard environment (SE)-housed rats at 12d postischemia. The mRNA expression of NGFI-A showed a similar pattern of BDNF except for an increase at 30 d after induction of brain ischemia in EE-housed rats. Ischemia-induced reduction of GR was prevented in the rats housed in EE condition. There was no difference between EE- and SE-housed animals in MR gene expression. Gene expressions, however, are very complex in housing conditions and postischemia. Whether EE-related gene transcription and/or translation reported in this thesis are linked with EE-induced functional benefits to brain ischemia, further studies need be conducted. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/467190
- author
- Zhao, Li-Ru LU
- supervisor
- opponent
-
- Eriksson, Peter
- organization
- publishing date
- 2004
- type
- Thesis
- publication status
- published
- subject
- keywords
- rats, brain-derived neurotrophic factor, mRNA, nerve growth factor-induced gene A, corticosteroid receptors, in situ hybridization, Neurologi, neurophysiology, Neurology, neuropsychology, brain ischemia, enriched environment, neuropsykologi, neurofysiologi
- pages
- 71 pages
- publisher
- Department of Clinical Neuroscience, Lund University
- defense location
- Segerfalksalen, Wallenberg Neurocentrum
- defense date
- 2004-09-15 10:15:00
- ISBN
- 91-628-6171-9
- language
- English
- LU publication?
- yes
- additional info
- Article: I. Zhao LR, Mattsson B, Johansson BB. Environmental influence on brain-derived neurotrophic factor messenger RNA expression after middle cerebral artery occlusion in spontaneously hypertensive rats. Neuroscience. 2000;97:177-184. Article: II Zhao LR, Risedal A, Wojcik A, Hejzlar J, Johansson BB, Kokaia Z.Enriched environment influences brain-derived neurotrophic factor levels in rat forebrain after focal stroke. Neurosci Lett. 2001; 305: 169-172. Article: III. Dahlqvist P, Zhao L, Johansson IM, Mattsson B, Johansson BB, Seckl JR, Olsson T. Environmental enrichment alters nerve growth factor-induced gene A and glucocorticoid receptor messenger RNA expression after middle cerebral artery occlusion in rats. Neuroscience.1999; 93: 527-535. The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Laboratory for Experimental Brain Research (013041000)
- id
- e6a24cb9-3a1a-4b11-91f1-3152114bb8fb (old id 467190)
- date added to LUP
- 2016-04-04 10:20:47
- date last changed
- 2025-04-04 15:13:43
@phdthesis{e6a24cb9-3a1a-4b11-91f1-3152114bb8fb, abstract = {{Enriched environment (EE) housing significantly ameliorates neurological deficits induced by cortical brain ischemia without changing infarction size, suggesting that EE-related functional benefits are associated with neuronal plasticity events in the remaining tissue. Brain-derived neurotrophic factor (BDNF), nerve growth factor-induced gene A (NGFI-A) and corticosteroid receptors (mineralocorticoid receptor, MR; glucocorticoid receptor, GR) have been demonstrated to be involved in brain plasticity. The purpose of this thesis was to determine if post-ischemic housing conditions had a significant effect on transcription and/or translation of BDNF, NGFI-A and corticosteroid receptors. We found that BDNF gene was down regulated in EE-housed rats when compared to the rats housed in standard cages at 2~12 days after cortical brain ischemia in peri-infarct cortex, contralateral cortex and bilateral hippocampus. The protein level of BDNF in the ipsilateral frontal cortex was lower in the EE-housed rats than the standard environment (SE)-housed rats at 12d postischemia. The mRNA expression of NGFI-A showed a similar pattern of BDNF except for an increase at 30 d after induction of brain ischemia in EE-housed rats. Ischemia-induced reduction of GR was prevented in the rats housed in EE condition. There was no difference between EE- and SE-housed animals in MR gene expression. Gene expressions, however, are very complex in housing conditions and postischemia. Whether EE-related gene transcription and/or translation reported in this thesis are linked with EE-induced functional benefits to brain ischemia, further studies need be conducted.}}, author = {{Zhao, Li-Ru}}, isbn = {{91-628-6171-9}}, keywords = {{rats; brain-derived neurotrophic factor; mRNA; nerve growth factor-induced gene A; corticosteroid receptors; in situ hybridization; Neurologi; neurophysiology; Neurology; neuropsychology; brain ischemia; enriched environment; neuropsykologi; neurofysiologi}}, language = {{eng}}, publisher = {{Department of Clinical Neuroscience, Lund University}}, school = {{Lund University}}, title = {{Post-Ischemic Housing Conditions Influence On Gene Transcription And Translation After Permanent Focal Brain Ischemia In Rats}}, url = {{https://lup.lub.lu.se/search/files/5517198/1693113.pdf}}, year = {{2004}}, }