Yin Yihui, Zhang Kai, Wei Longyin, Chen Dongling, Chen Qian, Jiao Mingjie, Li Xinxin, Huang Jiaqi, Gong Zhexi, Kang Nianxin, Li Fei
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
School of Management, Beijing University of Chinese Medicine, Beijing, China.
Front Pharmacol. 2021 Nov 1;12:710976. doi: 10.3389/fphar.2021.710976. eCollection 2021.
Huolisu Oral Liquid (HLS), a well-known traditional Chinese medicine (TCM) prescription, is an over-the-counter drug that is registered and approved by the State Food and Drug Administration (Approval No. Z51020381). HLS has been widely applied in the clinical treatment of cognitive disorders and has effects on delaying aging. The antioxidant effects of HLS are closely related to its antiaging activities, but the underlying mechanisms are unclear. In this study, the potential antioxidant ingredients of HLS were screened based on serum pharmacochemistry and network pharmacology, and the potential mechanisms involved in HLS antioxidant effects were preliminarily explored. Further, the antioxidant effects of HLS were verified by and experiments. The results showed that potential antioxidant ingredients could affect the toxic advanced glycation end products-receptor for advanced glycation end products (TAGE-RAGE) signaling, mitogen-activated protein kinase (MAPK) signaling, interleukin (IL)-17 signaling, tumor necrosis factor (TNF) signaling, toll-like receptors (TLRs), cyclic adenosine monophosphate (cAMP) signaling, hypoxia-inducible factor (HIF)-1 signaling, and other related pathways by regulating GAPDH, AKT1, TP53, MAPK1, JUN, and other associated targets. Thus, HLS may reduce inflammation, control the release of inflammatory cytokines, and regulate mitochondrial autophagy and metabolic abnormalities to ultimately play an antioxidant role. This is the first study attempting to construct a multilevel network of "HLS-antioxidant targets" based on serum pharmacochemistry and network pharmacology to explore the relationship between HLS and antioxidation and the molecular mechanisms of antioxidation combined with bioinformatics functional analysis and lays a foundation for further elucidating the antioxidant mechanisms of HLS.
活力苏口服液(HLS)是一种著名的中药方剂,是经国家食品药品监督管理总局注册批准的非处方药(批准文号:Z51020381)。HLS已广泛应用于认知障碍的临床治疗,具有延缓衰老的作用。HLS的抗氧化作用与其抗衰老活性密切相关,但其潜在机制尚不清楚。本研究基于血清药物化学和网络药理学筛选HLS的潜在抗氧化成分,并初步探讨HLS抗氧化作用的潜在机制。此外,通过[具体实验名称1]和[具体实验名称2]实验验证了HLS的抗氧化作用。结果表明,潜在抗氧化成分可通过调节甘油醛-3-磷酸脱氢酶(GAPDH)、蛋白激酶B(AKT1)、肿瘤蛋白53(TP53)、丝裂原活化蛋白激酶1(MAPK1)、原癌基因c-Jun(JUN)等相关靶点,影响毒性晚期糖基化终末产物-晚期糖基化终末产物受体(TAGE-RAGE)信号通路、丝裂原活化蛋白激酶(MAPK)信号通路、白细胞介素(IL)-17信号通路、肿瘤坏死因子(TNF)信号通路、Toll样受体(TLRs)、环磷酸腺苷(cAMP)信号通路、缺氧诱导因子(HIF)-1信号通路等相关通路。因此,HLS可能通过减轻炎症、控制炎性细胞因子的释放以及调节线粒体自噬和代谢异常,最终发挥抗氧化作用。这是首次尝试基于血清药物化学和网络药理学构建“活力苏-抗氧化靶点”多层次网络,探索活力苏与抗氧化作用之间的关系以及抗氧化的分子机制,并结合生物信息学功能分析,为进一步阐明活力苏的抗氧化机制奠定基础。