Oren-gedoku-to inhibits calcification of human aortic valve interstitial cells in vitro and aortic valve in spontaneously hypertensive rats in vivo

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Zaiqiang Yu , Shihu Men , Kazuyuki Daitoku , Tadaatsu Imaizumi , Masahito Minakawa , Kazuhiko Seya
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引用次数: 0

Abstract

Despite being the most common adult heart valve disease in developed countries, no medicinal treatment exists for calcific aortic valve stenosis (CAS). We previously demonstrated that tumor necrosis factor (TNF)-α promotes aortic valve calcification (AVC) via the bone morphogenic protein (BMP) 2-alkaline phosphatase (ALP) pathway. In the present study, we aimed to investigate the effects of Kampo, a traditional Japanese herbal medicine, on TNF-α-induced AVC involving CAS progression. We confirmed that Oren-gedoku-to (OGT, 10–100 μg/mL) strongly and dose-relatedly inhibited HAVIC calcification induced by TNF-α (30 ng/mL). OGT significantly inhibited TNF-α-induced BMP2 expression, p65 NF-κB phosphorylation, and ALP activation in HAVICs. Notably, two crude drugs from OGT [Coptis rhizome (CR), and Phellodendron bark (PB)] exhibited inhibitory effects akin to those of OGT. Berberine, mainly contained in CR and PB, also inhibited TNF-α induced HAVIC calcification, BMP2 expression, and p65 NF-κB phosphorylation. Further, OGT significantly prevented accelerated AVC in spontaneously hypertensive rats in vivo. Our results suggest that OGT and its component, berberine, can effectively prevent AVC acceleration both in vitro and in vivo.
oren - gedokuto体外抑制人主动脉瓣间质细胞钙化,体内抑制自发性高血压大鼠主动脉瓣钙化
尽管钙化性主动脉瓣狭窄(CAS)是发达国家最常见的成人心脏瓣膜疾病,但目前尚无药物治疗方法。我们之前已经证明肿瘤坏死因子(TNF)-α通过骨形态发生蛋白(BMP) 2-碱性磷酸酶(ALP)途径促进主动脉瓣钙化(AVC)。在本研究中,我们旨在研究日本传统中草药甘布对TNF-α-诱导的AVC涉及CAS进展的影响。我们证实了orengedoku -to (OGT, 10-100 μg/mL)对TNF-α (30 ng/mL)诱导的HAVIC钙化具有强烈且剂量相关的抑制作用。OGT显著抑制TNF-α-诱导的肝纤维化患者BMP2表达、p65 NF-κB磷酸化和ALP激活。值得注意的是,从OGT中提取的两种药材[黄连(Coptis rhizome, CR)和黄柏树皮(Phellodendron bark, PB)]表现出与OGT相似的抑制作用。主要存在于CR和PB中的小檗碱还能抑制TNF-α诱导的HAVIC钙化、BMP2表达和p65 NF-κB磷酸化。此外,OGT在体内显著阻止自发性高血压大鼠AVC加速。我们的研究结果表明,OGT及其成分小檗碱在体外和体内都能有效地防止AVC加速。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
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