Echinacoside improves the memory impairment of senescence accelerated mouse‐prone 8 (SAMP8) mice via inhibiting glial activation

Background Cognitive impairment, a common aging‐related pathology, is a risk factor for dementia. Echinacoside (ECH), derived from the traditional Chinese medicine Cistanche deserticola, shows anti‐aging properties including anti‐inflammation, oxidative stress reduction, and neuronal protection. Des...

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Veröffentlicht in:Alzheimer's & dementia 2024-12, Vol.20 (S6), p.n/a
Hauptverfasser: Zhou, Rong, Tian, Ge, Yu, Jing, Wang, Rui, Guo, Xingzhi, Li, Rui
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Sprache:eng
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Zusammenfassung:Background Cognitive impairment, a common aging‐related pathology, is a risk factor for dementia. Echinacoside (ECH), derived from the traditional Chinese medicine Cistanche deserticola, shows anti‐aging properties including anti‐inflammation, oxidative stress reduction, and neuronal protection. Despite its benefits, the beneficial impact of ECH on age‐related cognitive decline remains unclear. Senescence accelerated mouse‐prone 8 (SAMP8) mice, known for rapid aging and related pathologies in the brain like glial activation, neuro‐inflammation, neuron loss, and cognitive decline, are ideal for this study. The purpose of this study is to investigate the effect of ECH effects on cognitive functions in SAMP8 mice. Methods Six‐month‐old male SAMP8 mice (n = 8∼9) were used as the model group, while age‐matched senescence‐accelerated mouse resistant 1 (SAMR1) mice were used as normal controls. After adaptation in the specific pathogen free (SPF) room for one week, we administered ECH intragastrically to the SAMP8 mice daily for two months, and the control group was administered with saline. Behavioral tests, including open field test and Morris water maze, were performed to assess the mood and memory function of the SAMP8 mice. After that, all mice were sacrificed by intraperitoneal perfusion to extract brain tissues for western blotting and immunofluorescence. Results ECH‐treated SAMP8 mice showed significantly reduced escape latency in the Morris water maze compared to controls, indicating improved cognitive abilities (P
ISSN:1552-5260
1552-5279
DOI:10.1002/alz.085863