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Investigating the impact of environmental enrichment on proteome and neurotransmitter-related profiles in an animal model of Alzheimer's disease.
Nam, Yunkwon; Kim, Sujin; Park, Yong Ho; Kim, Byeong-Hyeon; Shin, Soo Jung; Leem, Seol Hwa; Park, Hyun Ha; Jung, Gukhwa; Lee, Jeongbeen; Kim, Hyung-Gun; Yoo, Doo-Han; Kim, Hak Su; Moon, Minho.
Afiliação
  • Nam Y; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Kim S; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Park YH; Research Institute for Dementia Science, Konyang University, Daejeon, South Korea.
  • Kim BH; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Shin SJ; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Leem SH; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Park HH; Research Institute for Dementia Science, Konyang University, Daejeon, South Korea.
  • Jung G; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Lee J; Department of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
  • Kim HG; NeuroVis Inc., Cheonan, South Korea.
  • Yoo DH; NeuroVis Inc., Cheonan, South Korea.
  • Kim HS; NeuroVis Inc., Cheonan, South Korea.
  • Moon M; Research Institute for Dementia Science, Konyang University, Daejeon, South Korea.
Aging Cell ; : e14231, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38952076
ABSTRACT
Alzheimer's disease (AD) is a neurodegenerative disorder associated with behavioral and cognitive impairments. Unfortunately, the drugs the Food and Drug Administration currently approved for AD have shown low effectiveness in delaying the progression of the disease. The focus has shifted to non-pharmacological interventions (NPIs) because of the challenges associated with pharmacological treatments for AD. One such intervention is environmental enrichment (EE), which has been reported to restore cognitive decline associated with AD effectively. However, the therapeutic mechanisms by which EE improves symptoms associated with AD remain unclear. Therefore, this study aimed to reveal the mechanisms underlying the alleviating effects of EE on AD symptoms using histological, proteomic, and neurotransmitter-related analyses. Wild-type (WT) and 5XFAD mice were maintained in standard housing or EE conditions for 4 weeks. First, we confirmed the mitigating effects of EE on cognitive impairment in an AD animal model. Then, histological analysis revealed that EE reduced Aß accumulation, neuroinflammation, neuronal death, and synaptic loss in the AD brain. Moreover, proteomic analysis by liquid chromatography-tandem mass spectrometry showed that EE enhanced synapse- and neurotransmitter-related networks and upregulated synapse- and neurotransmitter-related proteins in the AD brain. Furthermore, neurotransmitter-related analyses showed an increase in acetylcholine and serotonin concentrations as well as a decrease in polyamine concentration in the frontal cortex and hippocampus of 5XFAD mice raised under EE conditions. Our findings demonstrate that EE restores cognitive impairment by alleviating AD pathology and regulating synapse-related proteins and neurotransmitters. Our study provided neurological evidence for the application of NPIs in treating AD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article