6-姜辣素通过PPARδ在HUVECs、HEK293和分化的3T3-L1细胞中正常化高血压相关生物标志物的表达

IF 3.5 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL PPAR Research Pub Date : 2018-12-16 eCollection Date: 2018-01-01 DOI:10.1155/2018/6485064
Yong-Jik Lee, Yoo-Na Jang, Yoon-Mi Han, Hyun-Min Kim, Hong Seog Seo
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引用次数: 12

摘要

高血压是世界范围内发病率高、死亡率高的疾病。此外,各种因素,如遗传易感性、生活方式因素、与血压有关的器官异常等,都与高血压的发生有关。然而,目前很少有治疗高血压的药物是没有副作用的。虽然生姜对高血压的治疗作用已经确立,但其确切的机制尚未阐明。因此,本研究旨在评价生姜的主要成分之一6-姜辣素的降压机制,为开发无副作用的高血压新药提供依据。通过逆转录聚合酶链反应(RT-PCR)、western blotting和免疫细胞化学染色对人脐静脉内皮细胞(HUVECs)、人胚胎肾细胞(HEK293细胞)和小鼠前脂肪细胞(3T3-L1细胞)高血压相关生物标志物进行检测,鉴定6-姜辣素的降压作用及其机制。油红O染色法观察分化3T3-L1细胞的脂质积累情况。6-姜辣素升高huvec细胞内皮一氧化氮合酶(eNOS)蛋白磷酸化水平,降低血管细胞粘附蛋白1 (VCAM1)和肿瘤坏死因子α (TNFα)水平。在HEK293细胞中,6-姜辣素可降低上皮钠通道(ENaC)蛋白的表达。6-姜辣素处理可减轻分化3T3-L1细胞的脂质积累。这些作用是通过过氧化物酶体增殖物激活受体δ (PPARδ)调节的。6-姜辣素可通过PPARδ改善huvec、HEK293和分化3T3-L1细胞中参与高血压发展的生物标志物的表达。
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6-Gingerol Normalizes the Expression of Biomarkers Related to Hypertension via PPARδ in HUVECs, HEK293, and Differentiated 3T3-L1 Cells.

Hypertension is a disease with a high prevalence and high mortality rates worldwide. In addition, various factors, such as genetic predisposition, lifestyle factors, and the abnormality of organs related to blood pressure, are involved in the development of hypertension. However, at present, there are few available drugs for hypertension that do not induce side effects. Although the therapeutic effects of ginger on hypertension are well established, the precise mechanism has not been elucidated. Therefore, this study was designed to evaluate the antihypertensive mechanism of 6-gingerol, one of the main ingredients of ginger, and to assist in the development of new drugs for hypertension without side effects. The antihypertensive effects and mechanism of 6-gingerol were identified through reverse transcription polymerase chain reaction (RT-PCR), western blotting, and immunocytochemical staining for biomarkers involved in hypertension in human umbilical vein endothelial cells (HUVECs), human embryonal kidney cells (HEK293 cells), and mouse preadipocytes (3T3-L1 cells). The lipid accumulation in differentiated 3T3-L1 cells was evaluated by using Oil Red O staining. 6- Gingerol increased the level of phosphorylated endothelial nitric oxide synthase (eNOS) protein but decreased that of vascular cell adhesion protein 1 (VCAM1) and tumor necrosis factor alpha (TNFα) in HUVECs. In HEK293 cells, the expression of the epithelial sodium channel (ENaC) protein was reduced by 6-gingerol. Lipid accumulation was attenuated by 6-gingerol treatment in differentiated 3T3-L1 cells. These effects were regulated via peroxisome proliferator-activated receptor delta (PPARδ). 6-Gingerol ameliorated the expression of biomarkers involved in the development of hypertension through PPARδ in HUVECs, HEK293, and differentiated 3T3-L1 cells.

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来源期刊
PPAR Research
PPAR Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.20
自引率
3.40%
发文量
17
审稿时长
12 months
期刊介绍: PPAR Research is a peer-reviewed, Open Access journal that publishes original research and review articles on advances in basic research focusing on mechanisms involved in the activation of peroxisome proliferator-activated receptors (PPARs), as well as their role in the regulation of cellular differentiation, development, energy homeostasis and metabolic function. The journal also welcomes preclinical and clinical trials of drugs that can modulate PPAR activity, with a view to treating chronic diseases and disorders such as dyslipidemia, diabetes, adipocyte differentiation, inflammation, cancer, lung diseases, neurodegenerative disorders, and obesity.
期刊最新文献
Clinical Relevance and Drug Modulation of PPAR Signaling Pathway in Triple-Negative Breast Cancer: A Comprehensive Analysis. Mangiferin and EGCG Compounds Fight Against Hyperlipidemia by Promoting FFA Oxidation via AMPK/PPARα. Systemic and Lung Inflammation and Oxidative Stress Associated With Behavioral Changes Induced by Inhaled Paraquat Are Ameliorated by Carvacrol. Interaction between Nuclear Receptor and Alpha-Adrenergic Agonist Subtypes in Metabolism and Systemic Hemodynamics of Spontaneously Hypertensive Rats. Shared Mechanisms in Pparγ1sv and Pparγ2 Expression in 3T3-L1 Cells: Studies on Epigenetic and Positive Feedback Regulation of Pparγ during Adipogenesis.
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