牛蒡子素在脉络膜新生血管发病机制中的抗血管生成作用

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Aimi Shirakawa , Hiroto Yasuda , Shinsuke Nakamura , Yuichi Takajo , Satoshi Inamasu , Satoshi Yomoda , Shimpei Watanabe , Yoshiki Kuse , Masamitsu Shimazawa
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引用次数: 0

摘要

新生血管性年龄相关性黄斑变性(nAMD)是一种以脉络膜新生血管(CNV)为特征的眼部疾病,可导致严重的视力损害。牛蒡素是一种天然木脂素化合物,具有抗炎和血管正常化作用。在此,我们研究了牛蒡子素对CNV形成的抗血管生成作用。激光诱导CNV模型小鼠在激光照射前5天口服牛蒡素100 mg/kg,每天1次。口服牛蒡子素可抑制CNV的形成、血管渗漏和CNV病变中内皮细胞的增殖。30 μM剂量的牛蒡子素可减弱血管内皮生长因子(VEGF)诱导的人视网膜微血管内皮细胞(HRMECs)的增殖。此外,arctigenin抑制Src的磷酸化,Src参与VEGF信号传导。牛蒡子素还能抑制vegf诱导的线粒体呼吸激活。这些发现表明,每天摄入牛蒡子素可能对nAMD有有益的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The anti-angiogenic effects of arctigenin on choroidal neovascularization pathogenesis
Neovascular age-related macular degeneration (nAMD) is an ocular disease characterized by choroidal neovascularization (CNV), resulting in severe visual impairment. Arctigenin is a natural lignan compound from Arctium lappa L. and has anti-inflammatory and vascular normalizing effects. Here, we investigated the anti-angiogenic effects of arctigenin on CNV formation. Laser-induced CNV model mice were orally administered arctigenin at 100 mg/kg once a day for 5 days before laser irradiation. Oral administration of arctigenin suppressed CNV formation, vascular leakage, and the proliferation of endothelial cells in the CNV lesions. Treatment with arctigenin at 30 μM attenuated vascular endothelial growth factor (VEGF)-induced cell proliferation of human retinal microvascular endothelial cells (HRMECs). Moreover, arctigenin suppressed the phosphorylation of Src, which is involved in VEGF signaling. Arctigenin also inhibited VEGF-induced mitochondrial respiratory activation. These findings suggested that daily intake of arctigenin may have beneficial effects on nAMD.
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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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