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ORIGINAL RESEARCH

Mechanisms of Panax Ginseng on Treating Sepsis by RNA-Seq Technology

ORCID Icon, , , , , , & show all
Pages 7667-7678 | Received 12 Nov 2022, Accepted 16 Dec 2022, Published online: 23 Dec 2022
 

Abstract

Purpose

To explore the potential active targets and mechanisms of Panax Ginseng in the treatment of sepsis using network pharmacology and RNA-seq technology.

Patients and Methods

Patients with sepsis and healthy volunteers were collected according to SEPSIS 3.0, and their peripheral blood was used for RNA-seq analysis. The active ingredients and targets of Panax Ginseng were obtained using the TCMSP database, PPI and GO analysis were performed for disease-drug intersection targets. Then, we used Meta-analysis to screen core genes. Finally, single-cell RNA-seq was used to perform cell localization analysis on core genes.

Results

RNA-seq analysis collected 4521 sepsis-related genes, TCMSP database obtained 86 Panax Ginseng active ingredients and their 294 active targets. PPI and GO analysis showed intersection targets were closely linked, and mainly involved in cellular response to chemical stress, response to drug and molecule of bacterial origin, etc. Then, core targets, IL1B, ALOX5, BCL2 and IL4R, were sorted by Meta-analysis, and all four genes have high expression in the sepsis survivor group compared to the sepsis non-survivor group; single-cell RNA-seq revealed that IL1B was mainly localized in macrophages, ALOX5 was mainly localized in macrophages and B cells, BCL2 was mainly localized in natural killer cells, T cells and B cells, IL4R was widely distributed in immune cells. Finally, according to the correspondence between the active ingredients and targets of Panax Ginseng in TCMSP database, we found that Ginsenoside rh2 regulates the expression of IL1B, Ginsenoside rf regulates the expression of IL1B and IL4R, Kaempferol regulates the expression of ALOX5 and BCL2, and β-sitosterol regulates the expression of BCL2.

Conclusion

Ginsenoside rh2, Ginsenoside rf, Kaempferol and β-sitosterol may produce anti-sepsis effects by regulating the expression of IL1B, ALOX5, BCL2 and IL4R, thus improving the survival rate of sepsis patients.

Data Sharing Statement

We intend to share individual deidentified participant data. The RNA-seq data from 23 septic patients and 10 healthy volunteers are available in the China National GeneBank

DataBase (CNGBdb) and can be found below: https://db.cngb.org/, under the accession: CNP0002611.

Acknowledgments

The study was supported by Doctoral Research Initiation Fund of Affiliated Hospital of Southwest Medical University [grant number 20119].

Disclosure

The authors report no conflicts of interest in this work.