Key Laboratory of Digital Quality Evaluation of Chinese Materia Medica of State Administration of TCM and Engineering & Technology Research Center for Chinese Materia Medica Quality of Guangdong Province, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou 510405, China.
Phytomedicine. 2022 Jan;95:153777. doi: 10.1016/j.phymed.2021.153777. Epub 2021 Sep 27.
Diabetic nephropathy (DN) is a severe diabetic complication that is the principal cause of end-stage kidney disease worldwide. Huang-Lian-Jie-Du Decoction (HLJDD) is widely used to treat diabetes clinically. However, the nephroprotective effects and potential mechanism of action of HLJDD against DN have not yet been fully elucidated.
This study aimed to investigate the potential roles of HLJDD in DN and elucidate its mechanisms in db/db mice.
An integrated strategy of network pharmacology, pharmacodynamics, molecular biology, and metabolomics was used to reveal the mechanisms of HLJDD in the treatment of DN. First, network pharmacology was utilized to predict the possible pathways for DN using the absorbed ingredients of HLJDD in rat plasma in silico. Then, combined with histopathological examination, biochemical evaluation immunohistochemistry/immunofluorescence assay, western blot analysis, and UPLC-Q-Orbitrap HRMS/MS-based metabolomics approach were applied to evaluate the efficacy of HLJDD against DN and its underlying mechanisms in vivo.
In silico, network pharmacology indicated that the AGEs/RAGE pathway was the most prominent pathway for HLJDD against DN. In vivo, HLJDD exerted protective effects against DN by ameliorating glycolipid metabolic disorders and kidney injury. Furthermore, we verified that HLJDD protected against DN by regulating the AGEs/RAGE/Akt/Nrf2 pathway for the first time. In addition, 22 potential biomarkers were identified in urine, including phenylalanine metabolism, tryptophan metabolism, glucose metabolism, and sphingolipid metabolism.
These findings suggest that HLJDD ameliorates DN by regulating the AGEs/RAGE/Akt/Nrf2 pathway and metabolic profiling.
糖尿病肾病(DN)是一种严重的糖尿病并发症,是全球终末期肾病的主要原因。黄连解毒汤(HLJDD)广泛用于临床治疗糖尿病。然而,HLJDD 对 DN 的肾保护作用及其潜在作用机制尚未完全阐明。
本研究旨在探讨 HLJDD 在 DN 中的潜在作用,并阐明其在 db/db 小鼠中的作用机制。
采用网络药理学、药效学、分子生物学和代谢组学的综合策略,揭示 HLJDD 治疗 DN 的机制。首先,利用网络药理学在计算机上预测 HLJDD 在大鼠血浆中吸收成分治疗 DN 的可能途径。然后,结合组织病理学检查、生化评价、免疫组织化学/免疫荧光检测、Western blot 分析和基于 UPLC-Q-Orbitrap HRMS/MS 的代谢组学方法,评估 HLJDD 对 DN 的疗效及其在体内的作用机制。
计算机模拟表明,AGEs/RAGE 通路是 HLJDD 治疗 DN 的最主要通路。体内,HLJDD 通过改善糖脂代谢紊乱和肾脏损伤发挥对 DN 的保护作用。此外,我们首次验证了 HLJDD 通过调节 AGEs/RAGE/Akt/Nrf2 通路来防治 DN。此外,在尿液中鉴定出 22 个潜在的生物标志物,包括苯丙氨酸代谢、色氨酸代谢、葡萄糖代谢和鞘脂代谢。
这些发现表明,HLJDD 通过调节 AGEs/RAGE/Akt/Nrf2 通路和代谢谱来改善 DN。