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Published on: July 5, 2017
Phylloquinone improves endothelial function, inhibits cellular senescence, and vascular inflammation
Anna Kieronska-Rudek1,2,3, Agnieszka Kij1, Anna Bar1
1Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, Krakow, Poland.
Phylloquinone (PK) and menaquinones (MK), vitamin K compounds, show similar vasoprotective effects. Both inhibit vascular inflammation and cell senescence, suggesting PK offers comparable vascular benefits to MK.
Area of Science:
- Biochemistry
- Cardiovascular Research
- Nutritional Science
Background:
- Vitamin K compounds, including phylloquinone (PK) and menaquinones (MK), are vital nutrients.
- Vascular dysfunction is a significant health concern, and understanding protective mechanisms is crucial.
- Previous studies suggested menaquinones possess vasoprotective properties.
Purpose of the Study:
- To investigate the vasoprotective potential of phylloquinone (PK) in various models of vascular dysfunction.
- To compare the effects of PK and MK on endothelial function, inflammation, and cellular senescence.
- To explore the vascular conversion of PK to menaquinone-4 (MK-4).
Main Methods:
- In vivo studies using ApoE/LDLR-/- mice fed with PK or MK.
- In vitro studies on isolated aorta and cultured vascular cells (endothelial and smooth muscle cells).
- Assessment of endothelial function, TNF-induced vasorelaxation, inflammation (NFκB activation), and cell senescence.
Main Results:
- Both PK and MK significantly improved endothelial function in ApoE/LDLR-/- mice over 8 weeks.
- PK and MK equally prevented TNF-induced impairment of vasorelaxation in isolated aortas.
- PK and MK demonstrated comparable anti-senescence effects by reducing DNA damage and anti-inflammatory activity via NFκB modulation in vascular cells.
Conclusions:
- Phylloquinone (PK) and menaquinones (MK) exhibit similar vasoprotective effects.
- These effects are partly attributed to the inhibition of cellular senescence and inflammation in the vascular wall.
- The vascular conversion of PK to MK-4 suggests a potential role for MK in PK's vasoprotective actions.
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