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无膜干细胞与磷酸吡哆醛协同增强阿尔茨海默病小鼠模型的认知功能。

Membrane-Free Stem Cells and Pyridoxal 5'-Phosphate Synergistically Enhance Cognitive Function in Alzheimer's Disease Mouse Model.

作者信息

Choi Ji Myung, Park Hye Sook, He Mei Tong, Kim Young Sil, Kim Hyun Young, Lee Ah Young, Cho Eun Ju

机构信息

Department of Food Science and Nutrition, Pusan National University, Busan 46241, Korea.

Department of Food Science and Biotechnology, Kyungsung University, Busan 48434, Korea.

出版信息

Antioxidants (Basel). 2022 Mar 21;11(3):601. doi: 10.3390/antiox11030601.

Abstract

Accumulation of amyloid beta (Aβ) is a major pathological hallmark of Alzheimer's disease (AD). In this study, we evaluated the protective effect of membrane-free stem cell extract (MFSCE), which is a component of adipose-tissue-derived stem cells, on cognitive impairment in Aβ-injected AD mice. The ICR mice were i.c.v. injected with Aβ and then treated with MFSCE for 14 days (i.p.). The Aβ-injected mice showed deficits in spatial and object perception abilities, whereas treatment with MFSCE inhibited Aβ-induced learning and memory impairment in the T-maze, novel object recognition, and Morris water maze tests. Moreover, Aβ-induced lipid peroxidation and nitric oxide overproduction were attenuated by treatment with MFSCE. These antioxidant effects of MFSCE were related to the inhibition of the apoptotic signaling pathway. In particular, the combination treatment of MFSCE and pyridoxal 5'-phosphate (PLP) showed greater suppression of Bax and cleaved caspase-3 protein expression compared to the MFSCE- or PLP-only treatment. Furthermore, the MFSCE and PLP combination significantly downregulated the amyloidogenic-pathway-related protein expressions, such as amyloid precursor protein, presenilin 1, and presenilin 2. Therefore, the MFSCE and PLP combination may synergistically prevent Aβ-induced neuronal apoptosis and amyloidogenesis, which contributes to cognitive improvement and has potential therapeutic implications for AD patients.

摘要

β淀粉样蛋白(Aβ)的积累是阿尔茨海默病(AD)的主要病理标志。在本研究中,我们评估了无膜干细胞提取物(MFSCE)(脂肪组织来源干细胞的一种成分)对注射Aβ的AD小鼠认知障碍的保护作用。将ICR小鼠脑室内注射Aβ,然后腹腔注射MFSCE治疗14天。注射Aβ的小鼠在空间和物体感知能力方面表现出缺陷,而MFSCE治疗在T迷宫、新物体识别和莫里斯水迷宫试验中抑制了Aβ诱导的学习和记忆障碍。此外,MFSCE治疗减轻了Aβ诱导的脂质过氧化和一氧化氮过量产生。MFSCE的这些抗氧化作用与凋亡信号通路的抑制有关。特别是,与单独使用MFSCE或吡哆醛5'-磷酸(PLP)治疗相比,MFSCE和PLP联合治疗对Bax和裂解的半胱天冬酶-3蛋白表达的抑制作用更强。此外,MFSCE和PLP联合显著下调了淀粉样蛋白生成途径相关蛋白的表达,如淀粉样前体蛋白、早老素1和早老素2。因此,MFSCE和PLP联合可能协同预防Aβ诱导的神经元凋亡和淀粉样蛋白生成,这有助于改善认知,对AD患者具有潜在的治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212b/8945526/a58341bb7382/antioxidants-11-00601-g001.jpg

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