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Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells

Cortex Eucommiae (Du-zhong) is the dried bark of the Eucommia ulmoides Oliv. The natural products identified from Du-zhong include lignans, iridoids, flavonoids, polysaccharides, terpenes, and proteins, Liu et al. (2012). Lignans, the main bioactive components, were protective against hypertensive r...

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Autores principales: Jing, Xian, Huang, Wei-Hua, Tang, Yong-Jun, Wang, Ya-Qin, Li, Hui, Tian, Ying-Ying, Chen, Yao, Zhou, Hong-Hao, Ouyang, Dong-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478362/
https://www.ncbi.nlm.nih.gov/pubmed/26170892
http://dx.doi.org/10.1155/2015/987973
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author Jing, Xian
Huang, Wei-Hua
Tang, Yong-Jun
Wang, Ya-Qin
Li, Hui
Tian, Ying-Ying
Chen, Yao
Zhou, Hong-Hao
Ouyang, Dong-Sheng
author_facet Jing, Xian
Huang, Wei-Hua
Tang, Yong-Jun
Wang, Ya-Qin
Li, Hui
Tian, Ying-Ying
Chen, Yao
Zhou, Hong-Hao
Ouyang, Dong-Sheng
author_sort Jing, Xian
collection PubMed
description Cortex Eucommiae (Du-zhong) is the dried bark of the Eucommia ulmoides Oliv. The natural products identified from Du-zhong include lignans, iridoids, flavonoids, polysaccharides, terpenes, and proteins, Liu et al. (2012). Lignans, the main bioactive components, were protective against hypertensive renal injury in spontaneous hypertensive rats in our previous study, Li et al. (2012). Moreover, Eucommia lignans also diminished aldose reductase (AR) overexpression in the kidney, Li et al. (2012). However, the pathological mechanism underlying the protective effects of Eucommia lignans remains unknown. Cellular proliferation was reported to contribute to important pathological changes in hypertensive renal injuries, and increased angiotensin II (Ang II) expression was reported to be essential for target-organ damage during hypertension. Ang II is the main effective peptide in the renin-angiotensin system and is considered to be a key mediator in the development of hypertensive nephropathy, Rüster and Wolf (2011). Our preliminary results showed that Eucommia lignans had inhibitory effects on Ang II-induced proliferation of rat mesangial cells. In the present study, we investigated the effects of Eucommia ulmoides on Ang II-induced proliferation and apoptosis of rat mesangial cells. Cell cycle-related genes P21 and P27, and cell apoptosis-related genes Bax and Bcl-2, were determined.
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spelling pubmed-44783622015-07-13 Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells Jing, Xian Huang, Wei-Hua Tang, Yong-Jun Wang, Ya-Qin Li, Hui Tian, Ying-Ying Chen, Yao Zhou, Hong-Hao Ouyang, Dong-Sheng Evid Based Complement Alternat Med Research Article Cortex Eucommiae (Du-zhong) is the dried bark of the Eucommia ulmoides Oliv. The natural products identified from Du-zhong include lignans, iridoids, flavonoids, polysaccharides, terpenes, and proteins, Liu et al. (2012). Lignans, the main bioactive components, were protective against hypertensive renal injury in spontaneous hypertensive rats in our previous study, Li et al. (2012). Moreover, Eucommia lignans also diminished aldose reductase (AR) overexpression in the kidney, Li et al. (2012). However, the pathological mechanism underlying the protective effects of Eucommia lignans remains unknown. Cellular proliferation was reported to contribute to important pathological changes in hypertensive renal injuries, and increased angiotensin II (Ang II) expression was reported to be essential for target-organ damage during hypertension. Ang II is the main effective peptide in the renin-angiotensin system and is considered to be a key mediator in the development of hypertensive nephropathy, Rüster and Wolf (2011). Our preliminary results showed that Eucommia lignans had inhibitory effects on Ang II-induced proliferation of rat mesangial cells. In the present study, we investigated the effects of Eucommia ulmoides on Ang II-induced proliferation and apoptosis of rat mesangial cells. Cell cycle-related genes P21 and P27, and cell apoptosis-related genes Bax and Bcl-2, were determined. Hindawi Publishing Corporation 2015 2015-06-10 /pmc/articles/PMC4478362/ /pubmed/26170892 http://dx.doi.org/10.1155/2015/987973 Text en Copyright © 2015 Xian Jing et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jing, Xian
Huang, Wei-Hua
Tang, Yong-Jun
Wang, Ya-Qin
Li, Hui
Tian, Ying-Ying
Chen, Yao
Zhou, Hong-Hao
Ouyang, Dong-Sheng
Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title_full Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title_fullStr Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title_full_unstemmed Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title_short Eucommia ulmoides Oliv. (Du-Zhong) Lignans Inhibit Angiotensin II-Stimulated Proliferation by Affecting P21, P27, and Bax Expression in Rat Mesangial Cells
title_sort eucommia ulmoides oliv. (du-zhong) lignans inhibit angiotensin ii-stimulated proliferation by affecting p21, p27, and bax expression in rat mesangial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478362/
https://www.ncbi.nlm.nih.gov/pubmed/26170892
http://dx.doi.org/10.1155/2015/987973
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