Key Laboratory of Neuroscience, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou 511436, China.
Department of Traditional Chinese Medicine, School of Medicine, Xiamen University, Xiamen 361102, China.
Oxid Med Cell Longev. 2019 Nov 3;2019:8340192. doi: 10.1155/2019/8340192. eCollection 2019.
Alzheimer's disease (AD) is a common neurodegenerative disease, characterized by cognitive dysfunction; however, the therapeutic strategies are not fully understood. Huang-Lian-Jie-Du-Decoction (HLJDD) is a famous traditional Chinese herbal formula that has been widely used clinically to treat dementia. Recently, according to previous study and our clinical practice, we generate a new modification of HLJDD (named modified-HLJDD). In this study, we indicated that modified-HLJDD attenuated learning and memory deficiencies in A oligomer-induced AD model, and we confirmed the exact metabolites in modified-HLJDD solution, as compared with HLJDD by UHPLC-Q-TOF-MS. Using GC-Q-TOF/MS-based metabolomics, we identified adenosine as the potential significant metabolite, responsible for modified-HLJDD regulating energy metabolism and synaptic plasticity in AD model. We also revealed that the potential underlying mechanism of modified-HLJDD in AD model may involve NMDA receptor-mediated glutamatergic transmission and adenosine/ATPase/AMPK cascade. Moreover, we also indicated the differential gut microbiota which mainly involved , , , and at the phylum level upon modified-HLJDD treatment in AD model. Based on the correlation of metabolomic analysis with microbiome analysis, we clarified that is the most affected microbiota with adenosine upon modified-HLJDD treatment in AD model. Thus, our study suggests that modified-HLJDD may serve as a potential therapeutic drug in treating AD.
阿尔茨海默病(AD)是一种常见的神经退行性疾病,其特征是认知功能障碍;然而,其治疗策略尚未完全阐明。黄连解毒汤(HLJDD)是一种著名的中药方剂,已广泛应用于临床治疗痴呆。最近,根据既往研究和我们的临床实践,我们对 HLJDD 进行了新的改良(命名为改良-HLJDD)。在这项研究中,我们表明改良-HLJDD 可减轻 Aβ寡聚体诱导的 AD 模型中的学习和记忆缺陷,并且我们通过 UHPLC-Q-TOF-MS 证实了改良-HLJDD 溶液中的确切代谢物与 HLJDD 相比。使用基于 GC-Q-TOF/MS 的代谢组学,我们确定腺苷是潜在的重要代谢物,负责调节 AD 模型中的能量代谢和突触可塑性。我们还揭示了改良-HLJDD 在 AD 模型中的潜在作用机制可能涉及 NMDA 受体介导的谷氨酸能传递和腺苷/ATP 酶/AMPK 级联。此外,我们还表明,在 AD 模型中,经改良-HLJDD 治疗后,肠道微生物群主要涉及门水平的 、 、 、 。基于代谢组学分析与微生物组分析的相关性,我们阐明了在改良-HLJDD 治疗 AD 模型中,腺苷对 影响最大。因此,我们的研究表明,改良-HLJDD 可能是治疗 AD 的一种潜在治疗药物。