Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells

Human lung tissue, directly exposed to the environmental oxidants and toxicants, is apt to be harmed to bring about acute or chronic oxidative insults. The nuclear factor erythroid 2-related factor 2 (Nrf2) represents a central cellular defense mechanism, and is a target for developing agents agains...

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Main Authors: Ming-Xing Zhou, Guo-Hui Li, Bin Sun, You-Wei Xu, Ai-Ling Li, Yan-Ru Li, Dong-Mei Ren, Xiao-Ning Wang, Xue-Sen Wen, Hong-Xiang Lou, Tao Shen
Format: Article
Language:English
Published: Elsevier 2018-04-01
Series:Redox Biology
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231717305773
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spelling doaj-9fc457dbc1c542008057c77280c366ac2020-11-25T01:59:00ZengElsevierRedox Biology2213-23172018-04-0114154163Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cellsMing-Xing Zhou0Guo-Hui Li1Bin Sun2You-Wei Xu3Ai-Ling Li4Yan-Ru Li5Dong-Mei Ren6Xiao-Ning Wang7Xue-Sen Wen8Hong-Xiang Lou9Tao Shen10Key Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaDepartment of Pharmacy, Jinan Maternity and Child Care Hospital, Jinan, PR ChinaNational Glycoengineering Research Center, Shandong University, Jinan 250012, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR ChinaKey Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, Jinan, PR China; Correspondence to: School of Pharmaceutical Sciences, Shandong University, 44 Wenhua Xi Road, Jinan 250012, PR China.Human lung tissue, directly exposed to the environmental oxidants and toxicants, is apt to be harmed to bring about acute or chronic oxidative insults. The nuclear factor erythroid 2-related factor 2 (Nrf2) represents a central cellular defense mechanism, and is a target for developing agents against oxidative insult-induced human lung diseases. Our previous study found that the EtOH extract of Cinnamomum chartophyllum protected human bronchial epithelial cells against oxidative insults via Nrf2 activation. In this study, a systemic phytochemical investigation of the aerial parts of C. chartophyllum led to the isolation of thirty chemical constituents, which were further evaluated for their Nrf2 inducing potential using NAD(P)H: quinone reductase (QR) assay. Among these purified constituents, a sesquiterpenoid bearing α, β-unsaturated ketone group, 3S-(+)-9-oxonerolidol (NLD), and a diphenyl sharing phenolic groups, 3, 3â², 4, 4â²-tetrahydroxydiphenyl (THD) significantly activated Nrf2 and its downstream genes, NAD(P)H quinone oxidoreductase 1 (NQO-1), and γ-glutamyl cysteine synthetase (γ-GCS), and enhanced the nuclear translocation and stabilization of Nrf2 in human lung epithelial cells. Importantly, NLD and THD had no toxicities under the Nrf2 inducing doses. THD also demonstrated a potential of interrupting Nrf2-Keap1 proteinâprotein interaction (PPI). Furthermore, NLD and THD protected human lung epithelial cells against sodium arsenite [As(III)]-induced cytotoxicity. Taken together, we conclude that NLD and THD are two novel Nrf2 activators with potential application of preventing acute and chronic oxidative insults in human lung tissue. Keywords: Cinnamomum chartophyllum, Nrf2 activator, Arsenic, Oxidative insulthttp://www.sciencedirect.com/science/article/pii/S2213231717305773
collection DOAJ
language English
format Article
sources DOAJ
author Ming-Xing Zhou
Guo-Hui Li
Bin Sun
You-Wei Xu
Ai-Ling Li
Yan-Ru Li
Dong-Mei Ren
Xiao-Ning Wang
Xue-Sen Wen
Hong-Xiang Lou
Tao Shen
spellingShingle Ming-Xing Zhou
Guo-Hui Li
Bin Sun
You-Wei Xu
Ai-Ling Li
Yan-Ru Li
Dong-Mei Ren
Xiao-Ning Wang
Xue-Sen Wen
Hong-Xiang Lou
Tao Shen
Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
Redox Biology
author_facet Ming-Xing Zhou
Guo-Hui Li
Bin Sun
You-Wei Xu
Ai-Ling Li
Yan-Ru Li
Dong-Mei Ren
Xiao-Ning Wang
Xue-Sen Wen
Hong-Xiang Lou
Tao Shen
author_sort Ming-Xing Zhou
title Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
title_short Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
title_full Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
title_fullStr Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
title_full_unstemmed Identification of novel Nrf2 activators from Cinnamomum chartophyllum H.W. Li and their potential application of preventing oxidative insults in human lung epithelial cells
title_sort identification of novel nrf2 activators from cinnamomum chartophyllum h.w. li and their potential application of preventing oxidative insults in human lung epithelial cells
publisher Elsevier
series Redox Biology
issn 2213-2317
publishDate 2018-04-01
description Human lung tissue, directly exposed to the environmental oxidants and toxicants, is apt to be harmed to bring about acute or chronic oxidative insults. The nuclear factor erythroid 2-related factor 2 (Nrf2) represents a central cellular defense mechanism, and is a target for developing agents against oxidative insult-induced human lung diseases. Our previous study found that the EtOH extract of Cinnamomum chartophyllum protected human bronchial epithelial cells against oxidative insults via Nrf2 activation. In this study, a systemic phytochemical investigation of the aerial parts of C. chartophyllum led to the isolation of thirty chemical constituents, which were further evaluated for their Nrf2 inducing potential using NAD(P)H: quinone reductase (QR) assay. Among these purified constituents, a sesquiterpenoid bearing α, β-unsaturated ketone group, 3S-(+)-9-oxonerolidol (NLD), and a diphenyl sharing phenolic groups, 3, 3â², 4, 4â²-tetrahydroxydiphenyl (THD) significantly activated Nrf2 and its downstream genes, NAD(P)H quinone oxidoreductase 1 (NQO-1), and γ-glutamyl cysteine synthetase (γ-GCS), and enhanced the nuclear translocation and stabilization of Nrf2 in human lung epithelial cells. Importantly, NLD and THD had no toxicities under the Nrf2 inducing doses. THD also demonstrated a potential of interrupting Nrf2-Keap1 proteinâprotein interaction (PPI). Furthermore, NLD and THD protected human lung epithelial cells against sodium arsenite [As(III)]-induced cytotoxicity. Taken together, we conclude that NLD and THD are two novel Nrf2 activators with potential application of preventing acute and chronic oxidative insults in human lung tissue. Keywords: Cinnamomum chartophyllum, Nrf2 activator, Arsenic, Oxidative insult
url http://www.sciencedirect.com/science/article/pii/S2213231717305773
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