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美罗培南联合血必净注射液治疗脓毒症协同作用的代谢组学研究

Metabolomic Insights Into the Synergistic Effect of Biapenem in Combination With Xuebijing Injection Against Sepsis.

作者信息

Liu Li-Wei, Shi Ying-Ying, Li Zhuo-Lun, Zuo Li-Hua, Tang Meng, Jing Zi-Wei, Zhao Hong-Yu, Xue Peng, Zhou Lin, Du Qiu-Zheng, Zhang Xiao-Jian, Sun Zhi

机构信息

Department of Pharmacy, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Henan Key Laboratory of Precision Clinical Pharmacy, Zhengzhou University, Zhengzhou, China.

出版信息

Front Pharmacol. 2020 Apr 22;11:502. doi: 10.3389/fphar.2020.00502. eCollection 2020.

Abstract

The drug combination of biapenem (BIPM) and xuebijing injection (XBJ) is commonly applied for the treatment of sepsis in China. However, the potential synergistic mechanism is still enigmatic. There have been no studies focused on the plasma metabolome alterations in sepsis after the intervention of this combination. In this work, an untargeted metabolomics approach was performed by liquid chromatography-mass spectrometry coupled with multivariate statistical analysis to provide new insights into the synergistic effect of BIPM in combination with XBJ. We characterized the metabolic phenotype of sepsis and described metabolic footprint changes in septic rats responding to XBJ and BIPM individually and in combination, in addition to histopathological and survival evaluation. A total of 91 potential biomarkers of sepsis were identified and 32 disturbed metabolic pathways were constructed. Among these biomarkers, 36 metabolites were reversely regulated by XBJ, mainly including glycerophospholipids, sphingolipids, free fatty acids (FFAs), bile acids and acylcarnitines; 42 metabolites were regulated by BIPM, mainly including amino acids, glycerophospholipids, and acylcarnitines; 72 metabolites were regulated after XBJ-BIPM combination treatment, including most of the 91 potential biomarkers. The results showed that the interaction between XBJ and BIPM indeed exhibited a synergistic effect by affecting some key endogenous metabolites, 15 metabolites of which could not be regulated when XBJ or BIPM was used alone. Compared with Model group, 13, 22, and 27 metabolic pathways were regulated by XBJ, BIPM, and XBJ-BIPM combination, respectively. It suggested that many more endogenous metabolites and metabolic pathways were significantly regulated after combination treatment compared with XBJ or BIPM monotherapy. Metabolisms of lipids, amino acids, acylcarnitines, and bile acids were common pathways involved in the synergistic action of XBJ and BIPM. This study was the first to employ metabolomics to elucidate the synergistic effect and decipher the underlying mechanisms of BIPM in combination with XBJ against sepsis. The results provide some support for clinical application of antibiotics in combination with traditional Chinese medicines and have important implications for the treatment of sepsis in clinic.

摘要

在中国,比阿培南(BIPM)与血必净注射液(XBJ)联合用药常用于治疗脓毒症。然而,其潜在的协同作用机制仍不清楚。此前尚无研究聚焦于该联合用药干预后脓毒症患者血浆代谢组的变化。在本研究中,采用液相色谱 - 质谱联用结合多变量统计分析的非靶向代谢组学方法,以深入了解BIPM与XBJ联合使用的协同效应。除了组织病理学和生存评估外,我们还对脓毒症的代谢表型进行了表征,并描述了脓毒症大鼠对XBJ、BIPM单独用药及联合用药的代谢足迹变化。共鉴定出91个脓毒症潜在生物标志物,并构建了32条受干扰的代谢途径。在这些生物标志物中,36种代谢物受XBJ反向调节,主要包括甘油磷脂、鞘脂、游离脂肪酸(FFA)、胆汁酸和酰基肉碱;42种代谢物受BIPM调节,主要包括氨基酸、甘油磷脂和酰基肉碱;72种代谢物在XBJ - BIPM联合治疗后受到调节,包括91个潜在生物标志物中的大部分。结果表明,XBJ与BIPM之间的相互作用确实通过影响一些关键内源性代谢物表现出协同效应,其中15种代谢物在单独使用XBJ或BIPM时无法被调节。与模型组相比,XBJ、BIPM和XBJ - BIPM联合用药分别调节了13、22和27条代谢途径。这表明与XBJ或BIPM单药治疗相比,联合治疗后有更多的内源性代谢物和代谢途径受到显著调节。脂质、氨基酸、酰基肉碱和胆汁酸的代谢是XBJ和BIPM协同作用涉及的常见途径。本研究首次采用代谢组学阐明BIPM与XBJ联合抗脓毒症的协同效应并解读其潜在机制。研究结果为抗生素与中药联合的临床应用提供了一定支持,对临床脓毒症治疗具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c365/7189733/b571f15a9e2f/fphar-11-00502-g001.jpg

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