RETRACTED: Environmental Experience Modulates Ischemia-Induced Amyloidogenesis and Enhances Functional Recovery (Retracted article. See vol. 32, pg. 863, 2015)

被引:25
作者
Briones, Teresita L. [1 ]
Rogozinska, Magdalena [1 ]
Woods, Julie [1 ]
机构
[1] Univ Illinois, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
A beta oligomers; beta-secretase amyloid cleaving enzyme (BACE); enriched environment; learning and memory; water maze; AMYLOID PRECURSOR PROTEIN; ENRICHMENT IMPROVES COGNITION; CEREBRAL-ARTERY OCCLUSION; TRAUMATIC BRAIN-INJURY; BETA PEPTIDE; SYNAPTIC PLASTICITY; HIPPOCAMPAL REGION; LEARNING-CAPACITY; DENDRITIC GROWTH; GENE-EXPRESSION;
D O I
10.1089/neu.2008.0707
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
In this study, we examined whether ischemia-induced amyloidogenesis could be modulated by environmental "experience,'' and whether this modulation is associated with improved cognitive functioning. Rats were subjected to either global ischemia or sham surgery and then were randomly assigned to either enriched environment housing (EE) or socially paired housing (controls). After 14 days of differential environmental housing, the rats were tested in the water maze. Our results show decreased C-terminal fragments of the beta-amyloid precursor protein (beta APP) and decreased amyloid beta (A beta) load in the ischemic EE rats compared to the ischemic control animals. In addition, A beta oligomerization was significantly decreased in the ischemic EE animals compared to the ischemic control rats. Further, significantly increased levels of neprilysin, but not insulin-degrading enzyme, amyloid-degrading enzymes, were seen in the ischemic EE rats compared to the ischemic control animals. Behavioral analyses showed that ischemic EE rats performed significantly better on the memory task compared to the ischemic control group. These results suggest that use of multi-sensory environmental enrichment following cerebral ischemia may reduce the accumulation of A beta peptide in the more pathologic oligomeric form, and consequently may enhance functional recovery.
引用
收藏
页码:613 / 625
页数:13
相关论文
共 69 条
[1]  
Abramov AY, 2003, J NEUROSCI, V23, P5088
[2]   Expression of amyloid precursor protein mRNA isoforms in rat brain is differentially regulated during postnatal maturation and by cholinergic activity [J].
Apelt, J ;
Schliebs, R ;
Beck, M ;
Rossner, S ;
Bigl, V .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1997, 15 (01) :95-112
[3]   Environmental enrichment improves cognition in aged Alzheimer's transgenic mice despite stable β-amyloid deposition [J].
Arendash, GW ;
Garcia, MF ;
Costa, DA ;
Cracchiolo, JR ;
Wefes, IM ;
Potter, H .
NEUROREPORT, 2004, 15 (11) :1751-1754
[4]   Accelerated accumulation of N- and C-terminal βAPP fragments and delayed recovery of microtubule-associated protein 1B expression following stroke in aged rats [J].
Badan, I ;
Dinca, I ;
Buchhold, B ;
Suofu, Y ;
Walker, L ;
Gratz, M ;
Platt, D ;
Kessler, CH ;
Popa-Wagner, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 19 (08) :2270-2280
[5]   GLIAL EXPRESSION OF THE BETA-AMYLOID PRECURSOR PROTEIN (APP) IN GLOBAL-ISCHEMIA [J].
BANATI, RB ;
GEHRMANN, J ;
WIESSNER, C ;
HOSSMANN, KA ;
KREUTZBERG, GW .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1995, 15 (04) :647-654
[6]   COMPARISON OF GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE AND 28S-RIBOSOMAL RNA GENE-EXPRESSION AS RNA LOADING CONTROLS FOR NORTHERN BLOT ANALYSIS OF CELL-LINES OF VARYING MALIGNANT POTENTIAL [J].
BHATIA, P ;
TAYLOR, WR ;
GREENBERG, AH ;
WRIGHT, JA .
ANALYTICAL BIOCHEMISTRY, 1994, 216 (01) :223-226
[7]   Sensorimotor and cognitive deficits after transient middle cerebral artery occlusion in the mouse [J].
Bouet, Valentine ;
Freret, Thomas ;
Toutain, Jerome ;
Divoux, Didier ;
Boulouard, Michel ;
Schumann-Bard, Pascale .
EXPERIMENTAL NEUROLOGY, 2007, 203 (02) :555-567
[8]   REDUCTION OF NEUROLOGICAL DAMAGE BY A PEPTIDE SEGMENT OF THE AMYLOID BETA/A4 PROTEIN-PRECURSOR IN A RABBIT SPINAL-CORD ISCHEMIA MODEL [J].
BOWES, MP ;
MASLIAH, E ;
OTERO, DAC ;
ZIVIN, JA ;
SAITOH, T .
EXPERIMENTAL NEUROLOGY, 1994, 129 (01) :112-119
[9]  
Briones T L, 2000, Biol Res Nurs, V1, P299, DOI 10.1177/109980040000100406
[10]  
Briones Teresita L, 2005, Biol Res Nurs, V6, P167, DOI 10.1177/1099800404271328