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<em>Panax notoginseng</em> saponins alleviates advanced glycation end product‑induced apoptosis by upregulating SIRT1 and antioxidant expression levels in HUVECs
Author(s) -
Bo Yang,
Jian Zhang,
S Gonccedil alves Z,
Wu Quing,
Hua Zhao,
Li Chuanwei,
YuKang Cao
Publication year - 2020
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2020.9229
Subject(s) - panax notoginseng , apoptosis , umbilical vein , glycation , advanced glycation end product , chemistry , superoxide dismutase , malondialdehyde , nitric oxide , viability assay , pharmacology , oxidative stress , biochemistry , medicine , receptor , pathology , alternative medicine , organic chemistry , in vitro
The present study examined whether saponins (PNS) alleviated advanced glycation end product (AGE)-induced apoptosis in human umbilical vein endothelial cells (HUVECs). HUVECs were incubated with 300 µg/ml AGEs alone or AGEs and PNS (0.05, 0.5 or 1 mg/ml) for 48 h. The results of the present study demonstrated that PNS effectively promoted cell viability, inhibited apoptosis and suppressed the activity of caspase-3 in AGE-induced HUVECs. The activities of monocyte chemoattractant protein-1 and malondialdehyde were reduced, and superoxide dismutase activity was increased following treatment with PNS. Furthermore, PNS significantly increased the expression of silent information regulator 1 (SIRT1) and transforming growth factor (TGF)-β1 proteins, and suppressed the expression of inducible nitric oxide synthase and cyclooxyggenase-2 proteins in AGE-induced HUVECs. Therefore, the present study demonstrated that PNS reduced AGE-induced apoptosis by upregulating SIRT1 and antioxidants in HUVECs. The present findings suggest that the PNS may as an important pharmacological agent for AGE-induced cardiovascular injury.

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