2022
DOI: 10.1080/13880209.2022.2099430
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The effective constituent puerarin, from Pueraria lobata , inhibits the proliferation and inflammation of vascular smooth muscle in atherosclerosis through the miR-29b-3p/IGF1 pathway

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Cited by 17 publications
(7 citation statements)
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“… 33 , 34 In addition, a recent study on atherosclerosis showed that IGF1 pathway could regulate the inflammation and proliferation of vascular smooth muscle cells. 35 In AD-related disease, IGF1 has been reported to be positively correlated with an increased aortic diameters 36 in Turner syndrome, which is a common cause of AD. NOS3 is a key player in governing angiogenesis, and its aberrant expression will result in the dysfunction of vascular endothelium.…”
Section: Discussionmentioning
confidence: 99%
“… 33 , 34 In addition, a recent study on atherosclerosis showed that IGF1 pathway could regulate the inflammation and proliferation of vascular smooth muscle cells. 35 In AD-related disease, IGF1 has been reported to be positively correlated with an increased aortic diameters 36 in Turner syndrome, which is a common cause of AD. NOS3 is a key player in governing angiogenesis, and its aberrant expression will result in the dysfunction of vascular endothelium.…”
Section: Discussionmentioning
confidence: 99%
“…Li et al . [ 33 ] found that puerarin can inhibit the secretion of interleukin-6 and interleukin-8 by atherosclerotic vascular smooth muscle, mainly through the miR-29b-3p/IGF1 axis to inhibit inflammation. Tofacitinib inhibits the production of pro-inflammatory factors in rheumatoid arthritis synovial fibroblasts, in which IGF1 plays an important role [ 34 ].…”
Section: Discussionmentioning
confidence: 99%
“…Puerarin, an active monomer in Pueraria lobata, was reported to inhibit the proliferation and inflammation of VSMCs in atherosclerosis by reducing the expression of miR-29b-3p, thereby increasing the expression of insulin-like growth factor 1 (IGF1) (J. Li et al, 2023). Therefore, puerarin may have a beneficial effect in the treatment of atherosclerosis by regulating miRNA.…”
Section: Puerarinmentioning
confidence: 99%
“…In vitro: hVSMCs (J. Li et al, 2023) MKP-1 mitogen-activated protein kinase phosphatase 1, PTEN phosphatase and tensin homolog, ABCA1 ATP-binding cassette transporter A1, PCSK9 proprotein convertase subtilisin/kexin type 9, VLDLR very low-density lipoprotein receptor, KLF4 krüppel-like factor 4, DUSP5 dual specificity phosphatase 5, MGP matrix gla protein, MyD88 myeloid differentiation primary response 88, TLR4 toll-like receptor 4, SIRT1 sirtuin-1, p53 tumor protein 53, WNT5A wingless/integrated-5A, TPM1 tropomyosin 1, DDAH1 dimethylarginine dimethylaminohydrolase 1, HMGB1 high mobility group box 1, EZH2 enhancer of zeste homolog 2, Smad3 sma-and mad-related protein 3, STAT3 signal transducer and activator of transcription 3, IGF1 insulin-like growth factor 1, ApoE -/mice apolipoprotein e-knockout mice, RAW264.7 RAW 264.7 mouse leukemia macrophage cell line, HUVECs human umbilical vein endothelial cells, THP-1 human acute monocytic leukemia cell line, VSMCs vascular smooth muscle cells, HA-VSMCs human aortic vascular smooth muscle cells, HASMCs human airway smooth muscle cells, HAEC human aortic endothelial cells, SD rats sprague-dawley rats, RAECs rat aortic endothelial cells, VECs vascular endothelial cells, hVSMCs human vascular smooth muscle cells, TET2 tet methylcytosine dioxygenase 2.…”
Section: Conclusion and Prospectsmentioning
confidence: 99%