School of Pharmacy, Shenyang Pharmaceutical University, No.103 Wenhua Road, Shenhe District, Shenyang 110016, China.
School of Pharmacy, Shenyang Pharmaceutical University, No.103 Wenhua Road, Shenhe District, Shenyang 110016, China.
J Pharm Biomed Anal. 2024 Jan 5;237:115765. doi: 10.1016/j.jpba.2023.115765. Epub 2023 Oct 4.
Alzheimer's disease (AD) threatens elderly human health and still lacks effective treatment. Our previous work showed that LGZGD possessed a neuroprotective effect on the Aβ-induced neurotoxicity in differentiated PC12 cells, indicating that LGZGD may be a potential drug for treatment of AD. However, its pharmacodynamic substances which show anti-inflammatory and anti-oxidant stress activities are still unrevealed. This research aims to reveal the pharmacodynamic substances of LGZGD on Aβ-induced PC12 cell model of AD based on a spectrum-effect relationship study by using HPLC-FT-ICR-MS method and multivariate statistical analysis. Firstly, the chemical composition spectra of different combinations of LGZGD were recorded by HPLC-FT-ICR MS. Subsequently, Aβ-induced PC12 cell model of AD was established and pharmacodynamic experiments were conducted to evaluate their anti-inflammatory and anti-oxidant activities, respectively. Finally, the potential pharmacodynamic substances were screened out through spectrum-effect relationship study accompanied by multivariate statistical analysis including bivariate correlation analysis (BCA), grey relational analysis (GRA), principal component analysis (PCA), partial least squares regression analysis (PLSR). As a result, a total of 96 chemical consistents in different combinations of LGZGD were discovered. Among them, 7 components such as isoglabrolide, licorice saponin E2, licorice saponin N2 and licoisoflavanone were directly linked with the anti-inflammatory effects, and 14 constituents such as tumulosic acid, polyporenic acid C, dehydrotumulosic acid, dehydropachymic acid, and pachymic acid were directly correlated with the anti-oxidative stress activities. In conclusion, we combined the HPLC-FT-ICR-MS spectra with pharmacodynamic indicators to develop the spectrum-effect relationships of LGZGD for the first time, and successfully revealed its potential pharmacodynamic substances in the treatment of AD from the anti-inflammatory and antioxidant pathways in the cell model.
阿尔茨海默病(AD)威胁着老年人的健康,目前仍然缺乏有效的治疗方法。我们之前的工作表明,LGZGD 对 Aβ诱导的分化 PC12 细胞神经毒性具有神经保护作用,表明 LGZGD 可能是治疗 AD 的潜在药物。然而,其具有抗炎和抗氧化应激活性的药效物质仍未被揭示。本研究旨在基于 HPLC-FT-ICR-MS 方法和多变量统计分析,通过谱效关系研究,揭示 LGZGD 对 Aβ诱导的 AD 模型 PC12 细胞的药效物质。首先,通过 HPLC-FT-ICR-MS 记录不同组合的 LGZGD 的化学成分谱。随后,建立 Aβ诱导的 AD 模型 PC12 细胞,并进行药效学实验,分别评价其抗炎和抗氧化活性。最后,通过谱效关系研究,结合多元统计分析,包括双变量相关分析(BCA)、灰色关联分析(GRA)、主成分分析(PCA)、偏最小二乘回归分析(PLSR),筛选出潜在的药效物质。结果发现,LGZGD 不同组合中共发现 96 种化学成分。其中,7 种成分,如异甘草素、甘草皂苷 E2、甘草皂苷 N2 和甘草异黄酮,与抗炎作用直接相关,14 种成分,如土莫酸、多孔菌酸 C、去氢土莫酸、脱水巴曲酸和巴曲酸,与抗氧化应激活性直接相关。总之,我们首次将 HPLC-FT-ICR-MS 光谱与药效指标相结合,建立了 LGZGD 的谱效关系,从细胞模型的抗炎和抗氧化途径成功揭示了其治疗 AD 的潜在药效物质。