Comparative effect of genistein and daidzein on the expression of MCP-1, eNOS, and cell adhesion molecules in TNF-α-stimulated HUVECs
We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expr...
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Published in | Nutrition research and practice Vol. 5; no. 5; pp. 381 - 388 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
한국영양학회
01.10.2011
The Korean Nutrition Society and the Korean Society of Community Nutrition |
Subjects | |
Online Access | Get full text |
ISSN | 1976-1457 2005-6168 2005-6168 |
DOI | 10.4162/nrp.2011.5.5.381 |
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Abstract | We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-α exposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally, NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs. |
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AbstractList | We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-α exposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally, NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs. We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-αexposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally,NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs. KCI Citation Count: 12 We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-α exposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally, NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs.We compared the effects of genistein and daidzein on the expression of chemokines, cell adhesion molecules (CAMs), and endothelial nitric oxide synthase (eNOS) in tumor necrosis factor (TNF)-α-stimulated human umbilical vascular endothelial cells (HUVECs). TNF-α exposure significantly increased expression of monocyte chemoattractant protein (MCP)-1, vascular adhesion molecule (VCAM)-1, and intercellular adhesion molecule-1. Genistein significantly decreased MCP-1 and VCAM-1 production in a dose-dependent manner, whereas CAM expression was not significantly lowered by genistein treatment. However, daidzein slightly decreased MCP-1 production. The effects of genistein and daidzein on MCP-1 secretion coincided with mRNA expression. Pre-treatment with either genistein or daidzein elevated eNOS expression and nitric oxide production disturbed by TNF-α exposure. A low concentration of isoflavones significantly inhibited nuclear factor (NF)κB activation, whereas a high dose slightly ameliorated these inhibitive effects. These results suggest that genistein had a stronger effect on MCP-1 and eNOS expression than that of daidzein. Additionally, NFκB transactivation might be partially related to the down-regulation of these mRNAs in TNF-α-stimulated HUVECs. |
Author | Cho, H.Y., Paik Institute for Clinical Research, Inje University, Busan, Republic of Korea Cho, C.W., Inje University, Gimhae, Republic of Korea Song, Y.S., Inje University, Gimhae, Republic of Korea Kim, M.J., Silla University, Busan, Republic of Korea Park, C.M., Inje University, Gimhae, Republic of Korea Chinzorig, Radnaabazar, Inje University, Gimhae, Republic of Korea |
AuthorAffiliation | 3 Department of Food and Nutrition, Silla University, Busan 617-736, Korea 2 Department of Smart Foods and Drugs, Inje University, 607 Obang-dong, Gimhae, Gyeongnam 621-749, Korea 1 Paik Institute for Clinical Research, Inje University, Busan 614-735, Korea 4 School of Biomedical and Biotechnology, Inje University, Gimhae, Gyeongnam 621-749, Korea |
AuthorAffiliation_xml | – name: 2 Department of Smart Foods and Drugs, Inje University, 607 Obang-dong, Gimhae, Gyeongnam 621-749, Korea – name: 3 Department of Food and Nutrition, Silla University, Busan 617-736, Korea – name: 1 Paik Institute for Clinical Research, Inje University, Busan 614-735, Korea – name: 4 School of Biomedical and Biotechnology, Inje University, Gimhae, Gyeongnam 621-749, Korea |
Author_xml | – sequence: 1 fullname: Cho, H.Y., Paik Institute for Clinical Research, Inje University, Busan, Republic of Korea – sequence: 2 fullname: Park, C.M., Inje University, Gimhae, Republic of Korea – sequence: 3 fullname: Kim, M.J., Silla University, Busan, Republic of Korea – sequence: 4 fullname: Chinzorig, Radnaabazar, Inje University, Gimhae, Republic of Korea – sequence: 5 fullname: Cho, C.W., Inje University, Gimhae, Republic of Korea – sequence: 6 fullname: Song, Y.S., Inje University, Gimhae, Republic of Korea |
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Keywords | MCP-1 cell adhesion molecules eNOS NFκB Genistein |
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SubjectTerms | cell adhesion molecules eNOS GENISTEIN GENISTEINA GENISTEINE MCP-1 NF kappa B Original Research 생활과학 |
Title | Comparative effect of genistein and daidzein on the expression of MCP-1, eNOS, and cell adhesion molecules in TNF-α-stimulated HUVECs |
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