A network pharmacology approach to elucidate the anti-inflammatory effects of ellagic acid

被引:7
作者
Hoang, Skyler H. [1 ]
Dao, Hue [1 ]
Lam, Emerson My [2 ]
机构
[1] Rutgers State Univ, Dept Cell Biol & Neurosci, Piscataway, NJ 08854 USA
[2] Ton Duc Thang Univ, Fac Pharm, Ho Chi Minh City, Vietnam
关键词
Ellagic acid (EA); inflammation; molecular dynamics simulation; network pharmacology; NF-KAPPA-B; CHRONIC INFLAMMATION; OXIDATIVE STRESS; TNF-ALPHA; EXPRESSION; GROWTH; CELLS; DISEASE; MECHANISMS; SECRETION;
D O I
10.1080/07391102.2023.2240417
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ellagic acid (EA) is a naturally occurring polyphenolic compound found in various fruits and vegetables like strawberries, raspberries, pomegranates, and nuts such as pecans and walnuts. With its antioxidant properties, EA has shown potential health benefits, although further research is necessary to fully comprehend its effects, mechanisms, and safe and effective application as a complementary medicine. Notably, there is accumulating evidence of EA's anti-inflammatory effects; however, the precise underlying mechanism remains unclear. To investigate the anti-inflammatory properties of EA, a network pharmacology approach was employed. The study identified 52 inflammation-related targets of EA and revealed significant signaling pathways and relevant diseases associated with inflammation through GO and KEGG analysis. Furthermore, topological analysis identified 10 important targets, including AKT1, VEGFA, TNF, MAPK3, ALB, SELP, MMP9, MMP2, PTGS2, and ICAM1. Molecular docking and molecular dynamics simulations were conducted, indicating that AKT1, PTGS2, VEGFA, and MAPK3 are the most likely targets of EA, as evidenced by their molecular mechanics Poisson-Boltzmann surface area binding energy calculations. In summary, this study not only confirmed the anti-inflammatory effects of EA observed in previous research but also identified the most probable targets of EA.Communicated by Ramaswamy H. Sarma
引用
收藏
页码:7409 / 7420
页数:12
相关论文
共 80 条
[1]   Matrix Metalloproteinase-9 (MMP-9) induced disruption of intestinal epithelial tight junction barrier is mediated by NF-κB activation [J].
Al-Sadi, Rana ;
Engers, Jessica ;
Haque, Mohammad ;
King, Steven ;
Al-Omari, Deemah ;
Ma, Thomas Y. .
PLOS ONE, 2021, 16 (04)
[2]   Ellagic Acid as a Tool to Limit the Diabetes Burden: Updated Evidence [J].
Amor, Antonio J. ;
Gomez-Guerrero, Carmen ;
Ortega, Emilio ;
Sala-Vila, Aleix ;
Lazaro, Iolanda .
ANTIOXIDANTS, 2020, 9 (12) :1-26
[3]  
Attilio Peter, 2010, AANA J, V78, P453
[4]  
Baliga M.S., 2019, DIETARY INTERVENTION, P79, DOI [DOI 10.1016/B978-0-12-814466, 10.1016/B978-0-12- 814466-4.00007-0, DOI 10.1016/B978-0-12-814466-4.00007-0]
[5]   Anti-inflammatory potential of ellagic acid, gallic acid and punicalagin A&B isolated from Punica granatum [J].
BenSaad, Lamees A. ;
Kim, Kah Hwi ;
Quah, Chin Chew ;
Kim, Wee Ric ;
Shahimi, Mustafa .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2017, 17
[6]   Chronic inflammatory diseases are stimulated by current lifestyle: how diet, stress levels and medication prevent our body from recovering [J].
Bosma-den Boer, Margarethe M. ;
van Wetten, Marie-Louise ;
Pruimboom, Leo .
NUTRITION & METABOLISM, 2012, 9
[7]   ICAM-1: A master regulator of cellular responses in inflammation, injury resolution, and tumorigenesis [J].
Bui, Triet M. ;
Wiesolek, Hannah L. ;
Sumagin, Ronen .
JOURNAL OF LEUKOCYTE BIOLOGY, 2020, 108 (03) :787-799
[8]   Experimental Evidence of the Antitumor, Antimetastatic and Antiangiogenic Activity of Ellagic Acid [J].
Ceci, Claudia ;
Lacal, Pedro M. ;
Tentori, Lucio ;
De Martino, Maria Gabriella ;
Miano, Roberto ;
Graziani, Grazia .
NUTRIENTS, 2018, 10 (11)
[9]   P-selectin mediates adhesion of leukocytes, platelets, and cancer cells in inflammation, thrombosis, and cancer growth and metastasis [J].
Chen, M ;
Geng, JG .
ARCHIVUM IMMUNOLOGIAE ET THERAPIAE EXPERIMENTALIS, 2006, 54 (02) :75-84
[10]   cytoHubba: identifying hub objects and sub-networks from complex interactome [J].
Chin, Chia-Hao ;
Chen, Shu-Hwa ;
Wu, Hsin-Hung ;
Ho, Chin-Wen ;
Ko, Ming-Tat ;
Lin, Chung-Yen .
BMC SYSTEMS BIOLOGY, 2014, 8