Department of Pharmaceutical Analysis and Analytical Chemistry, College of Pharmacy, Harbin Medical University, Harbin 150081, China.
Key Laboratory of Chinese Materia Medica, Ministry of Education, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Int J Mol Sci. 2023 Oct 22;24(20):15457. doi: 10.3390/ijms242015457.
(Gouteng in Chinese, GT) is the main medicine in many traditional recipes in China. It is commonly used to alleviate central nervous system (CNS) disorders, although its mechanism in Alzheimer's disease is still unknown. This study was designed to predict and validate the underlying mechanism in AD treatment, thus illustrating the biological mechanisms of GT in treating AD. In this study, a PPI network was constructed, KEGG analysis and GO analysis were performed, and an "active ingredient-target-pathway" network for the treatment of Alzheimer's disease was constructed. The active ingredients of GT were screened out, and the key targets were performed by molecular docking. UHPLC-Q-Exactive Orbitrap MS was used to screen the main active ingredients and was compared with the network pharmacology results, which verified that GT did contain the above ingredients. A total of targets were found to be significantly bound up with tau, Aβ, or Aβ and tau through the network pharmacology study. Three SH-SY5Y cell models induced by okadaic acid (OA), NaSO, and HO were established for in vitro validation. We first found that GT can reverse the increase in the hyperphosphorylation of tau induced by OA to some extent, protecting against ROS damage. Moreover, the results also indicated that GT has significant neuroprotective effects. This study provides a basis for studying the potential mechanisms of GT in the treatment of AD.
钩藤(Gouteng in Chinese, GT)是中国许多传统方剂中的主要药物。它通常用于缓解中枢神经系统(CNS)紊乱,尽管其在阿尔茨海默病中的作用机制尚不清楚。本研究旨在预测和验证其在 AD 治疗中的潜在机制,从而阐明 GT 治疗 AD 的生物学机制。在本研究中,构建了 PPI 网络,进行了 KEGG 分析和 GO 分析,并构建了用于治疗阿尔茨海默病的“活性成分-靶标-通路”网络。筛选出 GT 的活性成分,并进行分子对接。采用 UHPLC-Q-Exactive Orbitrap MS 筛选主要活性成分,并与网络药理学结果进行比较,验证 GT 确实含有上述成分。通过网络药理学研究发现,共有靶点与 tau、Aβ 或 Aβ 和 tau 有明显的结合。通过建立 OA、NaSO 和 HO 诱导的三种 SH-SY5Y 细胞模型进行体外验证。我们首先发现 GT 可以在一定程度上逆转 OA 诱导的 tau 过度磷酸化的增加,从而起到保护 ROS 损伤的作用。此外,结果还表明 GT 具有显著的神经保护作用。本研究为研究 GT 治疗 AD 的潜在机制提供了依据。