Wang Mingzhu, Li Jianhua, Gui Mingtai, Lu Bo, Yao Lei, Zhou Xunjie, Shi Moyi, Hu Liang, Fu Deyu
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Academy of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Evid Based Complement Alternat Med. 2022 May 27;2022:9599090. doi: 10.1155/2022/9599090. eCollection 2022.
Obesity is recognized as not only a major contributing factor to cardiovascular diseases but also an independent risk factor for end-stage renal disease. Previous studies have found that Huoxue Qianyang Qutan Recipe (HQQR) could reduce urinary microalbumin in patients with obesity-related hypertension (OBH). However, the renal protective activity of HQQR in OBH and its molecular targets involved remains ambiguous. In this work, we investigate the mechanism of HQQR against OBH-induced early renal damage using integrating network pharmacology and experimental validation-based strategy. First, via network pharmacology, IL-6 is identified as one of the key targets of HQQR against early renal damage in hypertension, and inhibition of inflammation is a crucial process. Second, in in vivo experiments, HQQR can lower blood pressure, lose weight, and restore metabolic abnormalities in OBH rats, which could be associated with the effects on protecting early renal damage. Finally, in the mechanism, HQQR increases SIRT1 mRNA and protein expression consistent with reduction of NF-B acetylation and suppressed the p65-mediated inflammatory signaling pathway. As a result, HQQR robustly inhibits OBH-induced renal inflammation by reducing IL-6 mRNA and protein levels in the renal tissue and the release of IL-6 in serum of OBH rats. This study aims to provide a multimethod (network pharmacology-animal experiment) and multilevel (component-target-pathway) strategy for the prevention and treatment of OBH-induced target organ damage by traditional Chinese medicine.
肥胖不仅被认为是心血管疾病的主要促成因素,也是终末期肾病的独立危险因素。先前的研究发现,活血潜阳祛痰方(HQQR)可降低肥胖相关性高血压(OBH)患者的尿微量白蛋白。然而,HQQR对OBH的肾脏保护活性及其涉及的分子靶点仍不明确。在本研究中,我们采用整合网络药理学和基于实验验证的策略,研究HQQR对抗OBH诱导的早期肾损伤的机制。首先,通过网络药理学,白细胞介素-6(IL-6)被确定为HQQR对抗高血压早期肾损伤的关键靶点之一,抑制炎症是一个关键过程。其次,在体内实验中,HQQR可降低OBH大鼠的血压、减轻体重并恢复代谢异常,这可能与保护早期肾损伤的作用有关。最后,在机制方面,HQQR增加沉默信息调节因子1(SIRT1)mRNA和蛋白表达,与核因子-κB(NF-κB)乙酰化减少一致,并抑制p65介导的炎症信号通路。结果,HQQR通过降低肾组织中IL-6 mRNA和蛋白水平以及OBH大鼠血清中IL-6的释放,强烈抑制OBH诱导的肾脏炎症。本研究旨在为中医药防治OBH诱导的靶器官损伤提供一种多方法(网络药理学-动物实验)和多层次(成分-靶点-通路)的策略。