2019
DOI: 10.1016/j.abb.2018.11.016
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SIRT1 activation promotes angiogenesis in diabetic wounds by protecting endothelial cells against oxidative stress

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Cited by 35 publications
(29 citation statements)
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“…Topical applications of resveratrol to the wounded area of diabetic mice stimulated proliferation and inhibited apoptosis of endothelial cells, leading to accelerated wound healing, while either SIRT1 inhibitor or knockout of SIRT1 abolished the benefits of resveratrol in wound healing [125]. SIRT1-mediated benefits of resveratrol in diabetic wound healing can also be attributable to protection of endothelial cells from oxidative stress [201]. In addition, studies in mice indicate that resveratrol accelerates cutaneous wound healing by upregulation of vascular endothelial growth factor mediated by activation of at least two antioxidant enzymes (thioredoxin-1 and heme oxygenase-1) [123].…”
Section: Woundmentioning
confidence: 99%
“…Topical applications of resveratrol to the wounded area of diabetic mice stimulated proliferation and inhibited apoptosis of endothelial cells, leading to accelerated wound healing, while either SIRT1 inhibitor or knockout of SIRT1 abolished the benefits of resveratrol in wound healing [125]. SIRT1-mediated benefits of resveratrol in diabetic wound healing can also be attributable to protection of endothelial cells from oxidative stress [201]. In addition, studies in mice indicate that resveratrol accelerates cutaneous wound healing by upregulation of vascular endothelial growth factor mediated by activation of at least two antioxidant enzymes (thioredoxin-1 and heme oxygenase-1) [123].…”
Section: Woundmentioning
confidence: 99%
“…ERK is a MAPK that has a crucial role in the maintenance of cellular homeostasis, acting in stress and proliferative responses [72] at least in part through Nrf2 activation [73]. Nrf2 is a crucial factor involved in oxidative stress protection mechanisms [74]. Given that, it is involved in the regulation of anti-inflammatory and cell survival genes such as phase II detoxifying/antioxidant enzymes as catalase [75].…”
mentioning
confidence: 99%
“…Notably, diabetic ZDF‐C rats also showed a significant decrease in the levels of sirtuin‐1 (SIRT‐1) (Figure E). SIRT‐1 has been shown to protect against ROS‐mediated oxidative damage in arteries by suppressing NADPH oxidase activation . In fact, inhibition of SIRT‐1 significantly increased vascular superoxide production and enhanced NADPH oxidase activity and mRNA expression of NOX‐4 in aortic rings .…”
Section: Resultsmentioning
confidence: 99%
“…Actually, SIRT‐1 protects against ROS‐mediated oxidative damage by suppressing NOXs activation in the vascular wall . Likewise SIRT‐1 activation also increased the expression levels of the Nuclear factor‐E2 related factor 2 (Nrf2) and its antioxidant target in human endothelial cells …”
Section: Introductionmentioning
confidence: 99%