Your browser doesn't support javascript.
loading
Effects of enriched environment on the expression of ß-amyloid and transport-related proteins LRP1 and RAGE in chronic sleep-deprived mice.
Yuan, Ren; Yisen, Zhang; Xiu, Wang; Wei, Tang; Wei, Wang.
Affiliation
  • Yuan R; Department of Neurology, Affiliated Xinhua Hospital of Dalian University, Dalian, Liaoning Province, China.
  • Yisen Z; Department of Neurology, Affiliated Xinhua Hospital of Dalian University, Dalian, Liaoning Province, China.
  • Xiu W; Department of Clinical Laboratory, Wuhan Children's Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Hubei Province, China.
  • Wei T; Department of Neurology, Affiliated Xinhua Hospital of Dalian University, Dalian, Liaoning Province, China.
  • Wei W; Department of Basic Medicine, School of Medicine of Dalian University, Dalian, Liaoning Province, China.
Transl Neurosci ; 14(1): 20220301, 2023 Jan 01.
Article de En | MEDLINE | ID: mdl-37692085
ABSTRACT
Sleep plays an important role in the learning process and memory consolidation, and sleep deprivation (SD) leads to inadequate memory consolidation and plays an important role in brain development and plasticity. SD increases ß-amyloid levels while impairing cognitive function. We explored the effect of enriched environment (EE) on ß-amyloid and transporter protein LRP1 and receptor for advanced glycosylation end-products (RAGE) expression in chronic sleep deprived mice. We randomly divided mice into four groups (n = 10), the standard environment group (Ctrl group), the sleep deprivation group (SD group), the enriched environment intervention group (EE group), and the sleep deprivation plus environmental enrichment intervention group (SD + EE group). A modified multi-platform SD model was used to sleep deprive the mice for 19 h per day. Five hours of EE intervention was performed daily in the EE group and the SD + EE group, respectively. The behavioral measurements of mice were performed by Y-maze method and new object recognition; the expression levels of Aß1-42, LRP1, and RAGE in prefrontal cortex and hippocampus of mice were measured by immunofluorescence; the expression levels of LRP1 and RAGE in prefrontal cortex and hippocampus were detected by Western blot. The results showed that EE could effectively ameliorate the effects of SD on cognitive impairment, reduce SD induced Aß deposition, and decrease the expression of RAGE, while increase the expression of LRP1.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Transl Neurosci Année: 2023 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Transl Neurosci Année: 2023 Type de document: Article Pays d'affiliation: Chine