Saponins from Allium macrostemon Bulbs Attenuate Endothelial Inflammation and Acute Lung Injury via the NF-κB/VCAM-1 Pathway.
Li LiuLiang QiuJing XueChao ZhongManman QinYifeng ZhangChuanming XuYanfei XieJun YuPublished in: Molecules (Basel, Switzerland) (2024)
Endothelial inflammation is a multifaceted physiological process that plays a pivotal role in the pathogenesis and progression of diverse diseases, encompassing but not limited to acute lung infections like COVID-19, coronary artery disease, stroke, sepsis, metabolic syndrome, certain malignancies, and even psychiatric disorders such as depression. This inflammatory response is characterized by augmented expression of adhesion molecules and secretion of pro-inflammatory cytokines. In this study, we discovered that saponins from Allium macrostemon bulbs (SAMB) effectively inhibited inflammation in human umbilical vein endothelial cells induced by the exogenous inflammatory mediator lipopolysaccharide or the endogenous inflammatory mediator tumor necrosis factor-α, as evidenced by a significant reduction in the expression of pro-inflammatory factors and vascular cell adhesion molecule-1 (VCAM-1) with decreased monocyte adhesion. By employing the NF-κB inhibitor BAY-117082, we demonstrated that the inhibitory effect of SAMB on VCAM-1 expression may be attributed to the NF-κB pathway's inactivation, as characterized by the suppressed IκBα degradation and NF-κB p65 phosphorylation. Subsequently, we employed a murine model of lipopolysaccharide-induced septic acute lung injury to substantiate the potential of SAMB in ameliorating endothelial inflammation and acute lung injury in vivo. These findings provide novel insight into potential preventive and therapeutic strategies for the clinical management of diseases associated with endothelial inflammation.
Keyphrases
- lps induced
- inflammatory response
- lipopolysaccharide induced
- oxidative stress
- endothelial cells
- cell adhesion
- poor prognosis
- toll like receptor
- signaling pathway
- coronary artery disease
- metabolic syndrome
- acute kidney injury
- binding protein
- sars cov
- coronavirus disease
- nuclear factor
- rheumatoid arthritis
- atrial fibrillation
- intensive care unit
- percutaneous coronary intervention
- pi k akt
- high glucose
- cell proliferation
- escherichia coli
- cardiovascular disease
- liver failure
- physical activity
- biofilm formation
- vascular endothelial growth factor
- cystic fibrosis
- type diabetes
- uric acid
- brain injury
- coronary artery bypass grafting
- aortic valve
- transcatheter aortic valve replacement
- pseudomonas aeruginosa
- cerebral ischemia