The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway

Calcific aortic valve disease (CAVD) is an active pathobiological process that involves fibrosis and calcification of aortic valve leaflets, thereby causing cardiac hemodynamic changes and eventually heart failure. Cell proliferation changes at the initial stage of CAVD are an important target for p...

Full description

Bibliographic Details
Main Authors: Yuming Huang, Ming Liu, Chungeng Liu, Nianguo Dong, Liang Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2022.871748/full
_version_ 1828366420339064832
author Yuming Huang
Ming Liu
Chungeng Liu
Nianguo Dong
Liang Chen
author_facet Yuming Huang
Ming Liu
Chungeng Liu
Nianguo Dong
Liang Chen
author_sort Yuming Huang
collection DOAJ
description Calcific aortic valve disease (CAVD) is an active pathobiological process that involves fibrosis and calcification of aortic valve leaflets, thereby causing cardiac hemodynamic changes and eventually heart failure. Cell proliferation changes at the initial stage of CAVD are an important target for pharmaceutical intervention. This study aimed to investigate whether andrographolide (AGP) could inhibit the proliferation of valve interstitial cells (VICs) in vitro and in vivo to delay the process of CAVD. Cell proliferative factors were tested in both healthy and CAVD aortic valve samples. Cell cycle, cell growth, and calcification of VICs were assessed using flow cytometry, CCK8 assay, EdU staining, and Alizarin Red S staining. The expression of cell proliferative factors and osteogenic factors were quantified by qRT-PCR or immunofluorescence staining. The interaction between AGP and ERK (extracellular regulated protein kinases) was detected by molecular docking. In addition, a high-fat diet-fed animal model was used to verify the effect of AGP on CAVD in vivo. In conclusion, we found that AGP ameliorates aortic valve incrassation by inhibiting cell proliferation via the MAPK-ERK signaling pathway. Therefore, AGP is a promising drug that prevents the occurrence of CAVD via regulating cell proliferation.
first_indexed 2024-04-14T05:44:50Z
format Article
id doaj.art-5a59f4badd6b44f5b60a4974a85ad79b
institution Directory Open Access Journal
issn 1663-9812
language English
last_indexed 2024-04-14T05:44:50Z
publishDate 2022-04-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Pharmacology
spelling doaj.art-5a59f4badd6b44f5b60a4974a85ad79b2022-12-22T02:09:20ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122022-04-011310.3389/fphar.2022.871748871748The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK PathwayYuming Huang0Ming Liu1Chungeng Liu2Nianguo Dong3Liang Chen4Department of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, ChinaDepartment of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaDepartment of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaDepartment of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaDepartment of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, ChinaCalcific aortic valve disease (CAVD) is an active pathobiological process that involves fibrosis and calcification of aortic valve leaflets, thereby causing cardiac hemodynamic changes and eventually heart failure. Cell proliferation changes at the initial stage of CAVD are an important target for pharmaceutical intervention. This study aimed to investigate whether andrographolide (AGP) could inhibit the proliferation of valve interstitial cells (VICs) in vitro and in vivo to delay the process of CAVD. Cell proliferative factors were tested in both healthy and CAVD aortic valve samples. Cell cycle, cell growth, and calcification of VICs were assessed using flow cytometry, CCK8 assay, EdU staining, and Alizarin Red S staining. The expression of cell proliferative factors and osteogenic factors were quantified by qRT-PCR or immunofluorescence staining. The interaction between AGP and ERK (extracellular regulated protein kinases) was detected by molecular docking. In addition, a high-fat diet-fed animal model was used to verify the effect of AGP on CAVD in vivo. In conclusion, we found that AGP ameliorates aortic valve incrassation by inhibiting cell proliferation via the MAPK-ERK signaling pathway. Therefore, AGP is a promising drug that prevents the occurrence of CAVD via regulating cell proliferation.https://www.frontiersin.org/articles/10.3389/fphar.2022.871748/fullCAVDandrographolidecell proliferationvalve interstitial cellMAPK /ERK2 pathway
spellingShingle Yuming Huang
Ming Liu
Chungeng Liu
Nianguo Dong
Liang Chen
The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
Frontiers in Pharmacology
CAVD
andrographolide
cell proliferation
valve interstitial cell
MAPK /ERK2 pathway
title The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
title_full The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
title_fullStr The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
title_full_unstemmed The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
title_short The Natural Product Andrographolide Ameliorates Calcific Aortic Valve Disease by Regulating the Proliferation of Valve Interstitial Cells via the MAPK-ERK Pathway
title_sort natural product andrographolide ameliorates calcific aortic valve disease by regulating the proliferation of valve interstitial cells via the mapk erk pathway
topic CAVD
andrographolide
cell proliferation
valve interstitial cell
MAPK /ERK2 pathway
url https://www.frontiersin.org/articles/10.3389/fphar.2022.871748/full
work_keys_str_mv AT yuminghuang thenaturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT mingliu thenaturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT chungengliu thenaturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT nianguodong thenaturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT liangchen thenaturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT yuminghuang naturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT mingliu naturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT chungengliu naturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT nianguodong naturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway
AT liangchen naturalproductandrographolideamelioratescalcificaorticvalvediseasebyregulatingtheproliferationofvalveinterstitialcellsviathemapkerkpathway