首页> 外文期刊>Vascular Health and Risk Management >Vasa vasorum anti-angiogenesis through H2O2, HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract ( Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
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Vasa vasorum anti-angiogenesis through H2O2, HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract ( Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain

机译:山竹果皮乙醇提取物(Garcinia mangostana Linn)在高胆固醇饮食中通过H 2 O 2 ,HIF-1α,NF-κB和iNOS抑制脉管血管生成鼠褐家鼠Wistar菌株

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Background: Oxidative stress in atherosclerosis produces H2O2 and triggers the activation of nuclear factor kappa beta (NF-κB) and increase of inducible nitric oxide synthase (iNOS). The formation of vasa vasorum occurs in atherosclerosis. Vasa vasorum angiogenesis is mediated by VEGFR-1 and upregulated by hypoxia-inducible factor-1α (HIF-1α). The newly formed vasa vasorum are fragile and immature and thus increase plaque instability. It is necessary to control vasa vasorum angiogenesis by using mangosteen pericarp antioxidant. This study aims to demonstrate that mangosteen pericarp ethanolic extract can act as vasa vasorum anti-angiogenesis through H2O2, HIF-1α, NF-κB, and iNOS inhibition in rats given a hypercholesterol diet. Methods: This was a true experimental laboratory, in vivo posttest with control group design, with 20 Rattus norvegicus Wistar strain rats divided into five groups (normal group, hypercholesterol group, and hypercholesterol groups with certain doses of mangosteen pericarp ethanolic extract: 200, 400, and 800 mg/kg body weight). The parameters of this study were H2O2 measured by using colorimetric analysis, as well as NF-κB, iNOS, and HIF-1α, which were measured by using immunofluorescence double staining and observed with a confocal laser scanning microscope in aortic smooth muscle cell. The angiogenesis of vasa vasorum was quantified from VEGFR-1 level in aortic tissue and confirmed with hematoxylin and eosin staining. Results: Analysis of variance test and Pearson’s correlation coefficient showed mangosteen pericarp ethanolic extract had a significant effect ( P 2O2, HIF-1α, NF-κB, and iNOS inhibition in hypercholesterol-diet-given R. norvegicus Wistar strain. Conclusion: Mangosteen pericarp ethanolic extract 800 mg/kg body weight is proven to decrease vasa vasorum angiogenesis. Similar studies with other inflammatory parameters are encouraged to clarify the mechanism of vasa vasorum angiogenesis inhibition by mangosteen pericarp ethanolic extract.
机译:背景:动脉粥样硬化中的氧化应激产生H 2 O 2 ,并触发核因子κβ(NF-κB)的激活和诱导型一氧化氮合酶(iNOS)的增加。脉管血管的形成发生在动脉粥样硬化中。血管新生血管由VEGFR-1介导,并由缺氧诱导因子1α(HIF-1α)上调。新形成的脉管血管脆弱且不成熟,因此增加了斑块的不稳定性。必须使用山竹果皮抗氧化剂来控制脉管血管新生。本研究旨在证明山竹果皮乙醇提取物可通过抑制H 2 O 2 ,HIF-1α,NF-κB和iNOS抑制血管新生。大鼠给予高胆固醇饮食。方法:这是一个真实的实验实验室,具有对照组的体内后测试,将20只褐家鼠Wistar品系大鼠分为五组(正常组,高胆固醇组和高胆固醇组),并配以一定剂量的山竹果皮果皮乙醇提取物:200、400 ,以及800 mg / kg体重)。这项研究的参数是通过比色分析测量的H 2 O 2 以及通过免疫荧光测量的NF-κB,iNOS和HIF-1α双重染色,并用共聚焦激光扫描显微镜在主动脉平滑肌细胞中观察。血管的血管新生由主动脉组织中的VEGFR-1水平定量,并用苏木精和曙红染色证实。结果:方差分析和Pearson相关系数分析显示,山竹果皮乙醇提取物具有显着的作用(P 2 O 2 ,HIF-1α,NF-κB和iNOS抑制高胆固醇血症。结论:罗汉果皮果皮乙醇提取物800 mg / kg体重可减轻血管脉管血管生成,并通过其他炎症参数的类似研究来阐明山竹果皮乙醇对脉管血管生成的抑制作用。提取。

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