GSPE enhance eNOS expression through AMPK/SIRT1–KLF2 pathway and modulate blood pressure in ouabain induced hypertensive rats
スポンサーリンク
概要
- 論文の詳細を見る
Grape seed proanthocyanidin extracts (GSPE) belonging to polyphenols, possess various biological effects including anti-inflammation, anti-oxidant, anti-aging, anti-atherosclerosis and et al. GSPE is potential in regulating endothelial function. However, the underlying mechanism is not clear yet. In this study, by siRNA knocking down, we proved that GSPE increase endothelial nitric oxide synthase (eNOS) expression in human umbilical vessel cells (HUVECs) in vitro, which was attributed to its transcription factor Krüpple like factor 2 (KLF2) induction. Furthermore, GSPE activate 5'-AMP activated protein kinase (AMPK) and increase surtuin 1 (SIRT1) protein level, critical for KLF2 induction. We also illuminated the role of GSPE in hypertension treatment. By chronic administration of GSPE in ouabain induced hypertensive rats model, we access the effect of GSPE on blood pressure regulation and the possible mechanisms involved. After 5 weeks feeding, GSPE significantly block the ouabain induced blood pressure increase. The aortic NO production impaired by ouabain was improved. In conclusion, GSPE increase eNOS expression and NO production in an AMPK/SIRT1 dependent manner through KLF2 induction, and attenuate ouabain induced hypertension.
著者
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Gao Haiqing
Department Of Geriatrics Qi-lu Hospital Of Shandong University
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Feng Hua
Department Of Materia Medica Institute Of Dermatology Chinese Academy Of Medical Sciences & Peki
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Cui Xiaopei
Department of Geriatrics, Qilu Hospital of Shandong University
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Liu Xiangju
Department of Geriatrics, Qilu Hospital of Shandong University
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Zhao Shaohua
Department of Geriatrics, Qilu Hospital of Shandong University
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Gao Haiqing
Department of Geriatrics, Qilu Hospital of Shandong University
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Feng Hua
Department of Gastroenterology, Shandong Provincial Hospital
関連論文
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- GSPE enhance eNOS expression through AMPK/SIRT1–KLF2 pathway and modulate blood pressure in ouabain induced hypertensive rats