Cargando…

Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells

Hypertension is a major risk factor for the development of cardiovascular diseases. This study aimed to elucidate whether the natural product mixture No-ap (NA) containing Pine densiflora, Annona muricate, and Monordica charantia, or its single components have inhibitory effects on hypertension-rela...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Eun Young, Kim, Tae Yang, Hong, Gwan Ui, Kang, Hanna, Lee, Jung-Yun, Park, Jae Yeo, Kim, Se-Chan, Kim, Young Ho, Chung, Myung-Hee, Kwon, Young-In, Ro, Jai Youl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384670/
https://www.ncbi.nlm.nih.gov/pubmed/30678135
http://dx.doi.org/10.3390/molecules24030414
_version_ 1783397032075984896
author Hong, Eun Young
Kim, Tae Yang
Hong, Gwan Ui
Kang, Hanna
Lee, Jung-Yun
Park, Jae Yeo
Kim, Se-Chan
Kim, Young Ho
Chung, Myung-Hee
Kwon, Young-In
Ro, Jai Youl
author_facet Hong, Eun Young
Kim, Tae Yang
Hong, Gwan Ui
Kang, Hanna
Lee, Jung-Yun
Park, Jae Yeo
Kim, Se-Chan
Kim, Young Ho
Chung, Myung-Hee
Kwon, Young-In
Ro, Jai Youl
author_sort Hong, Eun Young
collection PubMed
description Hypertension is a major risk factor for the development of cardiovascular diseases. This study aimed to elucidate whether the natural product mixture No-ap (NA) containing Pine densiflora, Annona muricate, and Monordica charantia, or its single components have inhibitory effects on hypertension-related molecules in Angiotensin II (Ang II)-stimulated H9C2 cells. Individual functional components were isolated and purified from NA using various columns and solvents, and then their structures were analyzed using ESI–MS, (1)H-NMR, and (13)H-NMR spectra. H9C2 cells were stimulated with 300 nM Ang II for 7 h. NA, telmisartan, ginsenoside, roseoside (Roseo), icariside E4 (IE4), or a combination of two components (Roseo and IE4) were administered to the cells 1 h before Ang II stimulation. The expression and activity of hypertension-related molecules or oxidative molecules were determined using RT-PCR, western blot, and ELISA. Ang II stimulation increased the expression of Ang II receptor 1 (AT1), tumor necrosis factor-α (TNF-α), monocyte chemoattractant protein-1 (MCP-1), tumor growth factor-β (TGF-β) mRNA, and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity and the levels of hydrogen peroxide (H(2)O(2)) and superoxide anion (•O(2)(−)) and reduced anti-oxidant enzyme activity. NA significantly improved the expression or activities of all hypertension-related molecules altered in Ang II-stimulated cells. Roseo or IE4 pretreatment either decreased or increased the expression or activities of all hypertension-related molecules similar to NA, but to a lesser extent. The pretreatment with a combination of Roseo and IE4 (1:1) either decreased or increased the expression of all hypertension-related molecules, compared to each single component, revealing a synergistic action of the two compounds. Thus, the combination of single components could exert promising anti-hypertensive effects similar to NA, which should be examined in future animal and clinical studies.
format Online
Article
Text
id pubmed-6384670
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-63846702019-02-23 Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells Hong, Eun Young Kim, Tae Yang Hong, Gwan Ui Kang, Hanna Lee, Jung-Yun Park, Jae Yeo Kim, Se-Chan Kim, Young Ho Chung, Myung-Hee Kwon, Young-In Ro, Jai Youl Molecules Article Hypertension is a major risk factor for the development of cardiovascular diseases. This study aimed to elucidate whether the natural product mixture No-ap (NA) containing Pine densiflora, Annona muricate, and Monordica charantia, or its single components have inhibitory effects on hypertension-related molecules in Angiotensin II (Ang II)-stimulated H9C2 cells. Individual functional components were isolated and purified from NA using various columns and solvents, and then their structures were analyzed using ESI–MS, (1)H-NMR, and (13)H-NMR spectra. H9C2 cells were stimulated with 300 nM Ang II for 7 h. NA, telmisartan, ginsenoside, roseoside (Roseo), icariside E4 (IE4), or a combination of two components (Roseo and IE4) were administered to the cells 1 h before Ang II stimulation. The expression and activity of hypertension-related molecules or oxidative molecules were determined using RT-PCR, western blot, and ELISA. Ang II stimulation increased the expression of Ang II receptor 1 (AT1), tumor necrosis factor-α (TNF-α), monocyte chemoattractant protein-1 (MCP-1), tumor growth factor-β (TGF-β) mRNA, and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity and the levels of hydrogen peroxide (H(2)O(2)) and superoxide anion (•O(2)(−)) and reduced anti-oxidant enzyme activity. NA significantly improved the expression or activities of all hypertension-related molecules altered in Ang II-stimulated cells. Roseo or IE4 pretreatment either decreased or increased the expression or activities of all hypertension-related molecules similar to NA, but to a lesser extent. The pretreatment with a combination of Roseo and IE4 (1:1) either decreased or increased the expression of all hypertension-related molecules, compared to each single component, revealing a synergistic action of the two compounds. Thus, the combination of single components could exert promising anti-hypertensive effects similar to NA, which should be examined in future animal and clinical studies. MDPI 2019-01-23 /pmc/articles/PMC6384670/ /pubmed/30678135 http://dx.doi.org/10.3390/molecules24030414 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hong, Eun Young
Kim, Tae Yang
Hong, Gwan Ui
Kang, Hanna
Lee, Jung-Yun
Park, Jae Yeo
Kim, Se-Chan
Kim, Young Ho
Chung, Myung-Hee
Kwon, Young-In
Ro, Jai Youl
Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title_full Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title_fullStr Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title_full_unstemmed Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title_short Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells
title_sort inhibitory effects of roseoside and icariside e4 isolated from a natural product mixture (no-ap) on the expression of angiotensin ii receptor 1 and oxidative stress in angiotensin ii-stimulated h9c2 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384670/
https://www.ncbi.nlm.nih.gov/pubmed/30678135
http://dx.doi.org/10.3390/molecules24030414
work_keys_str_mv AT hongeunyoung inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT kimtaeyang inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT honggwanui inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT kanghanna inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT leejungyun inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT parkjaeyeo inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT kimsechan inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT kimyoungho inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT chungmyunghee inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT kwonyoungin inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells
AT rojaiyoul inhibitoryeffectsofroseosideandicarisidee4isolatedfromanaturalproductmixturenoapontheexpressionofangiotensiniireceptor1andoxidativestressinangiotensiniistimulatedh9c2cells