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基于代谢组学和脂质组学的综合分析揭示了补肾填髓方在 Aβ1-42 诱导的阿尔茨海默病大鼠模型中的神经保护作用机制。

Integrated Metabolomic and Lipidomic Analysis Reveals the Neuroprotective Mechanisms of Bushen Tiansui Formula in an A1-42-Induced Rat Model of Alzheimer's Disease.

机构信息

Department of Integrated Traditional Chinese & Western Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China.

Department of Integrated Traditional Chinese and Western Medicine, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.

出版信息

Oxid Med Cell Longev. 2020 Jun 19;2020:5243453. doi: 10.1155/2020/5243453. eCollection 2020.

Abstract

Bushen Tiansui Formula (BSTSF) is a traditional Chinese medicine prescription. It has been widely applied to treat Alzheimer's disease (AD) in the clinic; however, the mechanisms underlying its effects remain largely unknown. In this study, we used a rat AD model to study the effects of BSTSF on cognitive performance, and UPLC-MS/MS-based metabolomic and lipidomic analysis was further performed to identify significantly altered metabolites in the cerebral cortices of AD rats and determine the effects of BSTSF on the metabolomic and lipidomic profiles in the cerebral cortices of these animals. The results revealed that the levels of 47 metabolites and 30 lipids primarily associated with sphingolipid metabolism, glycerophospholipid metabolism, and linoleic acid metabolism were significantly changed in the cerebral cortices of AD rats. Among the altered lipids, ceramides, phosphatidylethanolamines, lysophosphatidylethanolamines, phosphatidylcholines, lysophosphatidylcholines, phosphatidylserines, sphingomyelins, and phosphatidylglycerols showed robust changes. Moreover, 34 differential endogenous metabolites and 21 lipids, of which the levels were mostly improved in the BSTSF treatment group, were identified as potential therapeutic targets of BSTSF against AD. Our results suggest that lipid metabolism is highly dysregulated in the cerebral cortices of AD rats, and BSTSF may exert its neuroprotective mechanisms by restoring metabolic balance, including that of sphingolipid metabolism, glycerophospholipid metabolism, alanine, aspartate, and glutamate metabolism, and D-glutamine and D-glutamate metabolism. Our data may lead to a deeper understanding of the AD-associated metabolic profile and shed new light on the mechanism underlying the therapeutic effects of BSTSF.

摘要

补肾填髓方(BSTSF)是一种中药方剂。它已广泛应用于临床治疗阿尔茨海默病(AD),但其作用机制仍知之甚少。在这项研究中,我们使用 AD 大鼠模型研究 BSTSF 对认知表现的影响,并进一步进行基于 UPLC-MS/MS 的代谢组学和脂质组学分析,以鉴定 AD 大鼠大脑皮质中明显改变的代谢物,并确定 BSTSF 对这些动物大脑皮质代谢组学和脂质组学图谱的影响。结果表明,AD 大鼠大脑皮质中 47 种代谢物和 30 种脂质的水平主要与鞘脂代谢、甘油磷脂代谢和亚油酸代谢有关。在改变的脂质中,神经酰胺、磷脂酰乙醇胺、溶血磷脂酰乙醇胺、磷脂酰胆碱、溶血磷脂酰胆碱、磷脂酰丝氨酸、鞘磷脂和磷脂酰甘油显示出强烈的变化。此外,还鉴定出 34 种差异内源性代谢物和 21 种脂质,其中 BSTSF 治疗组的水平大多提高,这些代谢物和脂质可能是 BSTSF 治疗 AD 的潜在治疗靶点。我们的结果表明,AD 大鼠大脑皮质中的脂质代谢严重失调,BSTSF 可能通过恢复代谢平衡发挥其神经保护机制,包括鞘脂代谢、甘油磷脂代谢、丙氨酸、天冬氨酸和谷氨酸代谢以及 D-谷氨酰胺和 D-谷氨酸代谢。我们的数据可能会深入了解 AD 相关的代谢特征,并为 BSTSF 的治疗效果的机制提供新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2a/7322593/0ec0853755aa/OMCL2020-5243453.001.jpg

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