Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis

Background: Atherosclerosis is an inflammatory disease well known as the leading cause of Cardiovascular Diseases (CVDs). Astaxanthin (ATX) is a reddish pigment that belongs to the family of xanthophylls, which are oxygenated derivatives of carotenoids. Aim: In this study, we aimed to investigate th...

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Main Authors: Barizi, Anis Zuhaida Mamnun, Shamsol Azman, Ain Nabila Syahira, Saad, Muhamad Fikri Shazlan, Abdullah, Muhammad Nazrul Hakim, Lim, Vuanghao, Yong, Yoke Keong
Format: Article
Language:English
Published: Wolters Kluwer - Medknow Publications and Media 2024
Online Access:http://psasir.upm.edu.my/id/eprint/117204/
http://psasir.upm.edu.my/id/eprint/117204/1/117204.pdf
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author Barizi, Anis Zuhaida Mamnun
Shamsol Azman, Ain Nabila Syahira
Saad, Muhamad Fikri Shazlan
Abdullah, Muhammad Nazrul Hakim
Lim, Vuanghao
Yong, Yoke Keong
author_facet Barizi, Anis Zuhaida Mamnun
Shamsol Azman, Ain Nabila Syahira
Saad, Muhamad Fikri Shazlan
Abdullah, Muhammad Nazrul Hakim
Lim, Vuanghao
Yong, Yoke Keong
author_sort Barizi, Anis Zuhaida Mamnun
building UPM Institutional Repository
collection Online Access
description Background: Atherosclerosis is an inflammatory disease well known as the leading cause of Cardiovascular Diseases (CVDs). Astaxanthin (ATX) is a reddish pigment that belongs to the family of xanthophylls, which are oxygenated derivatives of carotenoids. Aim: In this study, we aimed to investigate the targets and mechanisms involved in treating atherosclerosis using network pharmacology and molecular approaches. Materials and Methods: The genes targeted by ATX were predicted using Swiss Target Prediction, BATMAN-TCM, and Super-Pred databases, while genes associated with atherosclerosis were retrieved from DigSee, GAD, GeneCards, and OMIM databases. The interactions between ATX and atherosclerosis genes were identified through protein–protein interaction analysis, Gene Ontology (GO) enrichment analysis, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Results: The results revealed a total of 240 ATX-related genes and 4,977 atherosclerosis-related genes, with 172 overlapping genes identified. Six core genes were obtained: SRC, AKT1, MAPK3, HDAC1, PIK3R1, and RXRA. These results were further validated through the molecular docking approach, where all six core targets exhibit low binding energy, suggesting strong binding affinity, with PIK3R1 having the best binding affinity among them. Conclusion: Our study provides novel insights into the potential application of ATX in the management of atherosclerosis.
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spelling upm-1172042025-05-02T01:18:07Z http://psasir.upm.edu.my/id/eprint/117204/ Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis Barizi, Anis Zuhaida Mamnun Shamsol Azman, Ain Nabila Syahira Saad, Muhamad Fikri Shazlan Abdullah, Muhammad Nazrul Hakim Lim, Vuanghao Yong, Yoke Keong Background: Atherosclerosis is an inflammatory disease well known as the leading cause of Cardiovascular Diseases (CVDs). Astaxanthin (ATX) is a reddish pigment that belongs to the family of xanthophylls, which are oxygenated derivatives of carotenoids. Aim: In this study, we aimed to investigate the targets and mechanisms involved in treating atherosclerosis using network pharmacology and molecular approaches. Materials and Methods: The genes targeted by ATX were predicted using Swiss Target Prediction, BATMAN-TCM, and Super-Pred databases, while genes associated with atherosclerosis were retrieved from DigSee, GAD, GeneCards, and OMIM databases. The interactions between ATX and atherosclerosis genes were identified through protein–protein interaction analysis, Gene Ontology (GO) enrichment analysis, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Results: The results revealed a total of 240 ATX-related genes and 4,977 atherosclerosis-related genes, with 172 overlapping genes identified. Six core genes were obtained: SRC, AKT1, MAPK3, HDAC1, PIK3R1, and RXRA. These results were further validated through the molecular docking approach, where all six core targets exhibit low binding energy, suggesting strong binding affinity, with PIK3R1 having the best binding affinity among them. Conclusion: Our study provides novel insights into the potential application of ATX in the management of atherosclerosis. Wolters Kluwer - Medknow Publications and Media 2024-06 Article PeerReviewed text en cc_by_4 http://psasir.upm.edu.my/id/eprint/117204/1/117204.pdf Barizi, Anis Zuhaida Mamnun and Shamsol Azman, Ain Nabila Syahira and Saad, Muhamad Fikri Shazlan and Abdullah, Muhammad Nazrul Hakim and Lim, Vuanghao and Yong, Yoke Keong (2024) Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis. Pharmacognosy Research, 16 (3). pp. 626-637. ISSN 0976-4836; eISSN: 0974-8490 https://phcogres.com/article/2024/16/3/105530pres16374 10.5530/pres.16.3.74
spellingShingle Barizi, Anis Zuhaida Mamnun
Shamsol Azman, Ain Nabila Syahira
Saad, Muhamad Fikri Shazlan
Abdullah, Muhammad Nazrul Hakim
Lim, Vuanghao
Yong, Yoke Keong
Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title_full Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title_fullStr Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title_full_unstemmed Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title_short Network pharmacology and molecular docking approaches of Astaxanthin (ATX) against atherosclerosis
title_sort network pharmacology and molecular docking approaches of astaxanthin (atx) against atherosclerosis
url http://psasir.upm.edu.my/id/eprint/117204/
http://psasir.upm.edu.my/id/eprint/117204/
http://psasir.upm.edu.my/id/eprint/117204/
http://psasir.upm.edu.my/id/eprint/117204/1/117204.pdf