Saikosaponin D attenuates inflammatory response and cell apoptosis of lipopolysaccharide-induced lung epithelial cells.


Journal

The clinical respiratory journal
ISSN: 1752-699X
Titre abrégé: Clin Respir J
Pays: England
ID NLM: 101315570

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 28 07 2023
received: 03 02 2023
accepted: 03 08 2023
medline: 5 10 2023
pubmed: 25 8 2023
entrez: 24 8 2023
Statut: ppublish

Résumé

Acute lung injury (ALI) is a prevalent complication of sepsis with high mortality rate. Saikosaponin D (SSD) is a triterpenoid saponin that has been reported to alleviate sepsis-triggered renal injury in mice. Nonetheless, the therapeutic effect of SSD on sepsis-evoked ALI is unclarified. Lipopolysaccharide (LPS) from Escherichia coli 055:B5 was utilized to stimulate lung epithelial cell line MLE-12. A mouse model of sepsis was established. CCK-8 assay was employed for determining cytotoxicity. ELISA was utilized for determining proinflammatory cytokine production. Flow cytometry and western blotting were implemented for evaluating cell apoptosis. Hematoxylin-eosin staining was conducted for histologic analysis of murine lung tissues. SSD alleviated LPS-triggered inflammation and cell apoptosis of MLE-12 cells. SSD treatment ameliorated the pathological damages, inflammatory response, and cell apoptosis in the lungs of septic mice. SSD protects against sepsis-triggered ALI by inhibiting inflammation and cell apoptosis in MLE-12 cells and septic mouse mice.

Sections du résumé

BACKGROUND BACKGROUND
Acute lung injury (ALI) is a prevalent complication of sepsis with high mortality rate. Saikosaponin D (SSD) is a triterpenoid saponin that has been reported to alleviate sepsis-triggered renal injury in mice. Nonetheless, the therapeutic effect of SSD on sepsis-evoked ALI is unclarified.
METHODS METHODS
Lipopolysaccharide (LPS) from Escherichia coli 055:B5 was utilized to stimulate lung epithelial cell line MLE-12. A mouse model of sepsis was established. CCK-8 assay was employed for determining cytotoxicity. ELISA was utilized for determining proinflammatory cytokine production. Flow cytometry and western blotting were implemented for evaluating cell apoptosis. Hematoxylin-eosin staining was conducted for histologic analysis of murine lung tissues.
RESULTS RESULTS
SSD alleviated LPS-triggered inflammation and cell apoptosis of MLE-12 cells. SSD treatment ameliorated the pathological damages, inflammatory response, and cell apoptosis in the lungs of septic mice.
CONCLUSION CONCLUSIONS
SSD protects against sepsis-triggered ALI by inhibiting inflammation and cell apoptosis in MLE-12 cells and septic mouse mice.

Identifiants

pubmed: 37619985
doi: 10.1111/crj.13688
pmc: PMC10542997
doi:

Substances chimiques

Lipopolysaccharides 0
saikosaponin D UR635J3F00
Saponins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1017-1024

Subventions

Organisme : Natural Science Key Project of Bengbu Medical College
ID : 2021byzd157
Organisme : Natural Science Key Project of Bengbu Medical College
ID : BYKY2019118ZD

Informations de copyright

© 2023 The Authors. The Clinical Respiratory Journal published by John Wiley & Sons Ltd.

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Auteurs

Lijie Song (L)

Department of Emergency medical, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.

Guoyu Lu (G)

Department of Emergency medical, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.

Yanyan Tao (Y)

Department of Emergency medical, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.

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Classifications MeSH