2020
DOI: 10.3389/fphar.2020.00762
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Hyperoside Protects Human Umbilical Vein Endothelial Cells Against Anticardiolipin Antibody-Induced Injury by Activating Autophagy

Abstract: Anticardiolipin antibody (aCL), an important characterization of antiphospholipid syndrome, shows an intense association with vascular endothelial injury. Hyperoside is a flavonoid extracted from medicinal plants traditionally used in Chinese medicines, displaying anti-inflammatory, anti-cancer, and anti-oxidative properties in various diseases. Recent studies have shifted the focus on the protective effects of hyperoside on vascular endothelial injury. However, little is known about the mechanisms involved. I… Show more

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Cited by 13 publications
(9 citation statements)
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“…16 For example, Hyp suppresses inflammation effectively in mice with acute lung injury, 17 and Hyp protects human umbilical vein endothelial cells against aCL-induced damage by triggering autophagy. 18 In addition, the protective effects of Hyp against RPL have also been described, and Hyp is confirmed to attenuate pregnancy loss by activating autophagy and inhibiting inflammation in a rat model. 19 Also, it is reported that Hyp exerts an inhibitory effect on NLRP3 inflammasome activation in human and mouse macrophages.…”
Section: Introductionmentioning
confidence: 93%
“…16 For example, Hyp suppresses inflammation effectively in mice with acute lung injury, 17 and Hyp protects human umbilical vein endothelial cells against aCL-induced damage by triggering autophagy. 18 In addition, the protective effects of Hyp against RPL have also been described, and Hyp is confirmed to attenuate pregnancy loss by activating autophagy and inhibiting inflammation in a rat model. 19 Also, it is reported that Hyp exerts an inhibitory effect on NLRP3 inflammasome activation in human and mouse macrophages.…”
Section: Introductionmentioning
confidence: 93%
“… 72 Researchers also found that hyperoside could help to against the vascular endothelial injury induced by anticardiolipin antibody in human umbilical vein endothelial cells (HUVECs) via activating mammalian target of rapamycin (mTOR)-mediated autophagy. 73 Hyperoside protected HUVECs against H 2 O 2 damage, at least partially, by activating the extra cellular signal-regulated protein kinase (ERK) signaling pathway. 74 Hyperoside suppressed vascular inflammatory processes induced by high glucose (HG) in HUVECs and in C57BL/6 mice.…”
Section: Pharmacologic Effectmentioning
confidence: 99%
“…When HUVECs were pretreated with hyperoside (10, 20, 50 mM) for 24 h, the secretion of proinflammatory cytokines, such as IL-1b and IL-8, and endothelial adhesion cytokines such as TF, ICAM1, and VCAM1, was significantly reduced. Mechanistically, hyperoside activated autophagy and suppressed the mTOR/S6K and TLR4/Myd88/NF-k B signalling transduction pathways [ 66 ].…”
Section: Antioxidant Treatment In Aps Patients: the State Of The Artmentioning
confidence: 99%