» Articles » PMID: 23637826

Inhibition of Vascular Smooth Muscle Cell Proliferation by Gentiana Lutea Root Extracts

Overview
Journal PLoS One
Date 2013 May 3
PMID 23637826
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Gentiana lutea belonging to the Gentianaceae family of flowering plants are routinely used in traditional Serbian medicine for their beneficial gastro-intestinal and anti-inflammatory properties. The aim of the study was to determine whether aqueous root extracts of Gentiana lutea consisting of gentiopicroside, gentisin, bellidifolin-8-O-glucoside, demethylbellidifolin-8-O-glucoside, isovitexin, swertiamarin and amarogentin prevents proliferation of aortic smooth muscle cells in response to PDGF-BB. Cell proliferation and cell cycle analysis were performed based on alamar blue assay and propidium iodide labeling respectively. In primary cultures of rat aortic smooth muscle cells (RASMCs), PDGF-BB (20 ng/ml) induced a two-fold increase in cell proliferation which was significantly blocked by the root extract (1 mg/ml). The root extract also prevented the S-phase entry of synchronized cells in response to PDGF. Furthermore, PDGF-BB induced ERK1/2 activation and consequent increase in cellular nitric oxide (NO) levels were also blocked by the extract. These effects of extract were due to blockade of PDGF-BB induced expression of iNOS, cyclin D1 and proliferating cell nuclear antigen (PCNA). Docking analysis of the extract components on MEK1, the upstream ERK1/2 activating kinase using AutoDock4, indicated a likely binding of isovitexin to the inhibitor binding site of MEK1. Experiments performed with purified isovitexin demonstrated that it successfully blocks PDGF-induced ERK1/2 activation and proliferation of RASMCs in cell culture. Thus, Gentiana lutea can provide novel candidates for prevention and treatment of atherosclerosis.

Citing Articles

Uses of Molecular Docking Simulations in Elucidating Synergistic, Additive, and/or Multi-Target (SAM) Effects of Herbal Medicines.

Rigby S Molecules. 2024; 29(22).

PMID: 39598795 PMC: 11597140. DOI: 10.3390/molecules29225406.


Beauvericin Immunotoxicity Prevention by L. Flower In Vitro.

Di Matteo G, Cimbalo A, Manyes L, Mannina L Toxins (Basel). 2023; 15(9).

PMID: 37755964 PMC: 10535299. DOI: 10.3390/toxins15090538.


Regulatory mechanisms of Gentiopicroside on human diseases: a brief review.

Liu B, Pang F, Bi H, Guo D Naunyn Schmiedebergs Arch Pharmacol. 2023; 397(2):725-750.

PMID: 37632552 DOI: 10.1007/s00210-023-02672-6.


Active components and molecular mechanisms of Sagacious Confucius' Pillow Elixir to treat cognitive impairment based on systems pharmacology.

Hou Z, Yang X, Jiang L, Song L, Li Y, Li D Aging (Albany NY). 2023; 15(14):7278-7307.

PMID: 37517091 PMC: 10415554. DOI: 10.18632/aging.204912.


Encapsulation of Thymol in Gelatin Methacryloyl (GelMa)-Based Nanoniosome Enables Enhanced Antibiofilm Activity and Wound Healing.

Moghtaderi M, Bazzazan S, Sorourian G, Sorourian M, Akhavanzanjani Y, Noorbazargan H Pharmaceutics. 2023; 15(6).

PMID: 37376147 PMC: 10303142. DOI: 10.3390/pharmaceutics15061699.


References
1.
Sanchez I, Dynlacht B . New insights into cyclins, CDKs, and cell cycle control. Semin Cell Dev Biol. 2005; 16(3):311-21. DOI: 10.1016/j.semcdb.2005.02.007. View

2.
Waltenberger J . Modulation of growth factor action: implications for the treatment of cardiovascular diseases. Circulation. 1997; 96(11):4083-94. DOI: 10.1161/01.cir.96.11.4083. View

3.
Nickel T, Deutschmann A, Hanssen H, Summo C, Wilbert-Lampen U . Modification of endothelial biology by acute and chronic stress hormones. Microvasc Res. 2009; 78(3):364-9. DOI: 10.1016/j.mvr.2009.07.008. View

4.
Yang J, Liu L, Shi Y . Phytochemicals and biological activities of Gentiana species. Nat Prod Commun. 2010; 5(4):649-64. View

5.
Baba S, Barski O, Ahmed Y, OToole T, Conklin D, Bhatnagar A . Reductive metabolism of AGE precursors: a metabolic route for preventing AGE accumulation in cardiovascular tissue. Diabetes. 2009; 58(11):2486-97. PMC: 2768164. DOI: 10.2337/db09-0375. View