The Combination of Natural Compounds Escin-Bromelain-Ginkgo Biloba-Sage Miltiorrhiza (EBGS) Reduces Platelet Adhesion to TNFα-Activated Vascular Endothelium through FAK Signaling.
Humans
Platelet Adhesiveness
/ drug effects
Signal Transduction
/ drug effects
Tumor Necrosis Factor-alpha
/ metabolism
Endothelium, Vascular
/ drug effects
Blood Platelets
/ metabolism
Salvia miltiorrhiza
/ chemistry
Focal Adhesion Kinase 1
/ metabolism
Human Umbilical Vein Endothelial Cells
/ metabolism
Plant Extracts
/ pharmacology
EBGS
bromelain
endothelial cells
escin
ginkgo biloba
platelet adhesion
sage miltiorrhiza
tumor necrosis factor α
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
26 Aug 2024
26 Aug 2024
Historique:
received:
25
07
2024
revised:
22
08
2024
accepted:
25
08
2024
medline:
14
9
2024
pubmed:
14
9
2024
entrez:
14
9
2024
Statut:
epublish
Résumé
Thrombosis is a key process that determines acute coronary syndrome and ischemic stroke and is the leading cause of morbidity and mortality in the world, together with cancer. Platelet adhesion and subsequent activation and aggregation are critical processes that cause thrombus formation after endothelial damage. To date, high hopes are associated with compounds of natural origin, which show anticoagulant action without undesirable effects and can be proposed as supportive therapies. We investigated the effect of the new combination of four natural compounds, escin-bromelain-ginkgo biloba-sage miltiorrhiza (EBGS), on the initial process of the coagulation cascade, which is the adhesion of platelets to activated vascular endothelium. Our results demonstrated that EBGS pretreatment of endothelial cells reduces platelet adhesion even in the presence of the monocyte-lymphocyte population. Our data indicate that EBGS exerts its effects by inhibiting the transcription of adhesion molecules, including P-selectin, platelet membrane glycoprotein GP1b, integrins αV and β3, and reducing the secretion of the pro-inflammatory cytokines interleukin 6, interleukin 8, and the metalloproteinases MMP-2 and MMP-9. Furthermore, we demonstrated that EBGS inhibited the expression of focal adhesion kinase (FAK), strictly involved in platelet adhesion, and whose activity is correlated with that of integrin β3. The results shown in this manuscript suggest a possible inhibitory role of the new combination EBGS in the reduction in platelet adhesion to activated endothelium, thus possibly preventing coagulation cascade initiation.
Identifiants
pubmed: 39273200
pii: ijms25179252
doi: 10.3390/ijms25179252
pii:
doi:
Substances chimiques
Tumor Necrosis Factor-alpha
0
Focal Adhesion Kinase 1
EC 2.7.10.2
Plant Extracts
0
PTK2 protein, human
EC 2.7.10.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : PO FESR Sicilia 2014/2020
ID : 08TP1041100162