Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases

Cardiovascular disease (CVD) is the leading cause of death worldwide, in both developed and developing countries. According to the WHO report, the morbidity and mortality caused by CVD will continue to rise with the estimation of death going up to 22.2 million in 2030. NADPH oxidase (NOX)-derived...

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Main Authors: M. Sofiullah, Siti Sarah, Murugan, Dharmani Devi, Abd Muid, Suhaila, Wu, Yuan Seng, Syed Abdul Kadir, Sharifah Zamiah, Abas, Razif, Adib Ridzuan, Nurul Raudzah, Zamakshshari, Nor Hisam, Choy, Ker Woon
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Published: MDPI 2023
Online Access:http://psasir.upm.edu.my/id/eprint/109100/
https://www.mdpi.com/1420-3049/28/3/1047
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Institution: Universiti Putra Malaysia
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spelling my.upm.eprints.1091002024-10-14T03:40:36Z http://psasir.upm.edu.my/id/eprint/109100/ Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases M. Sofiullah, Siti Sarah Murugan, Dharmani Devi Abd Muid, Suhaila Wu, Yuan Seng Syed Abdul Kadir, Sharifah Zamiah Abas, Razif Adib Ridzuan, Nurul Raudzah Zamakshshari, Nor Hisam Choy, Ker Woon Cardiovascular disease (CVD) is the leading cause of death worldwide, in both developed and developing countries. According to the WHO report, the morbidity and mortality caused by CVD will continue to rise with the estimation of death going up to 22.2 million in 2030. NADPH oxidase (NOX)-derived reactive oxygen species (ROS) production induces endothelial nitric oxide synthase (eNOS) uncoupling and mitochondrial dysfunction, resulting in sustained oxidative stress and the development of cardiovascular diseases. Seven distinct members of the family have been identified of which four (namely, NOX1, 2, 4 and 5) may have cardiovascular functions. Currently, the treatment and management plan for patients with CVDs mainly depends on the drugs. However, prolonged use of prescribed drugs may cause adverse drug reactions. Therefore, it is crucial to find alternative treatment options with lesser adverse effects. Natural products have been gaining interest as complementary therapy for CVDs over the past decade due to their wide range of medicinal properties, including antioxidants. These might be due to their potent active ingredients, such as flavonoid and phenolic compounds. Numerous natural compounds have been demonstrated to have advantageous effects on cardiovascular disease via NADPH cascade. This review highlights the potential of natural products targeting NOX-derived ROS generation in treating CVDs. Emphasis is put on the activation of the oxidases, including upstream or downstream signalling events. MDPI 2023-01-20 Article PeerReviewed M. Sofiullah, Siti Sarah and Murugan, Dharmani Devi and Abd Muid, Suhaila and Wu, Yuan Seng and Syed Abdul Kadir, Sharifah Zamiah and Abas, Razif and Adib Ridzuan, Nurul Raudzah and Zamakshshari, Nor Hisam and Choy, Ker Woon (2023) Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases. Molecules, 28 (3). art. no. 1047. pp. 1-24. ISSN 1420-3049 https://www.mdpi.com/1420-3049/28/3/1047 10.3390/molecules28031047
institution Universiti Putra Malaysia
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content_provider Universiti Putra Malaysia
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description Cardiovascular disease (CVD) is the leading cause of death worldwide, in both developed and developing countries. According to the WHO report, the morbidity and mortality caused by CVD will continue to rise with the estimation of death going up to 22.2 million in 2030. NADPH oxidase (NOX)-derived reactive oxygen species (ROS) production induces endothelial nitric oxide synthase (eNOS) uncoupling and mitochondrial dysfunction, resulting in sustained oxidative stress and the development of cardiovascular diseases. Seven distinct members of the family have been identified of which four (namely, NOX1, 2, 4 and 5) may have cardiovascular functions. Currently, the treatment and management plan for patients with CVDs mainly depends on the drugs. However, prolonged use of prescribed drugs may cause adverse drug reactions. Therefore, it is crucial to find alternative treatment options with lesser adverse effects. Natural products have been gaining interest as complementary therapy for CVDs over the past decade due to their wide range of medicinal properties, including antioxidants. These might be due to their potent active ingredients, such as flavonoid and phenolic compounds. Numerous natural compounds have been demonstrated to have advantageous effects on cardiovascular disease via NADPH cascade. This review highlights the potential of natural products targeting NOX-derived ROS generation in treating CVDs. Emphasis is put on the activation of the oxidases, including upstream or downstream signalling events.
format Article
author M. Sofiullah, Siti Sarah
Murugan, Dharmani Devi
Abd Muid, Suhaila
Wu, Yuan Seng
Syed Abdul Kadir, Sharifah Zamiah
Abas, Razif
Adib Ridzuan, Nurul Raudzah
Zamakshshari, Nor Hisam
Choy, Ker Woon
spellingShingle M. Sofiullah, Siti Sarah
Murugan, Dharmani Devi
Abd Muid, Suhaila
Wu, Yuan Seng
Syed Abdul Kadir, Sharifah Zamiah
Abas, Razif
Adib Ridzuan, Nurul Raudzah
Zamakshshari, Nor Hisam
Choy, Ker Woon
Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
author_facet M. Sofiullah, Siti Sarah
Murugan, Dharmani Devi
Abd Muid, Suhaila
Wu, Yuan Seng
Syed Abdul Kadir, Sharifah Zamiah
Abas, Razif
Adib Ridzuan, Nurul Raudzah
Zamakshshari, Nor Hisam
Choy, Ker Woon
author_sort M. Sofiullah, Siti Sarah
title Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
title_short Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
title_full Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
title_fullStr Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
title_full_unstemmed Natural bioactive compounds targeting NADPH oxidase pathway in cardiovascular diseases
title_sort natural bioactive compounds targeting nadph oxidase pathway in cardiovascular diseases
publisher MDPI
publishDate 2023
url http://psasir.upm.edu.my/id/eprint/109100/
https://www.mdpi.com/1420-3049/28/3/1047
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