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Int J Mol Sci. 2019 Oct 5;20(19). pii: E4936. doi: 10.3390/ijms20194936.

Ginsenoside Rb1 Attenuates High Glucose-Induced Oxidative Injury via the NAD-PARP-SIRT Axis in Rat Retinal Capillary Endothelial Cells.

Author information

1
School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China. fanchunlan77@163.com.
2
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. maqing988@163.com.
3
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. xm_dreaming@163.com.
4
Institute of Chinese Materia Medica, Shaanxi Provincial Academy of Traditional Chinese Medicine, Xi'an 710003, Shaanxi, China. qy0508@163.com.
5
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. yizhang714@163.com.
6
School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China. 20170941210@bucm.edu.cn.
7
School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China. byc1206@163.com.
8
School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China. tangmk@bucm.edu.cn.

Abstract

(1) Aims: The present study aimed to observe the effects of Ginsenoside Rb1 on high glucose-induced endothelial damage in rat retinal capillary endothelial cells (RCECs) and to investigate the underlying mechanism. (2) Methods: Cultured RCECs were treated with normal glucose (5.5 mM), high glucose (30 mM glucose), or high glucose plus Rb1 (20 μM). Cell viability, lactate dehydrogenase (LDH) levels, the mitochondrial DNA copy number, and the intracellular ROS content were measured to evaluate the cytotoxicity. Superoxide dismutase (SOD), catalase (CAT), nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX), poly(ADP-ribose) polymerase (PARP), and sirtuin (SIRT) activity was studied in cell extracts. Nicotinamide adenine dinucleotide (NAD+)/NADH, NADPH/NADP+, and glutathione (GSH)/GSSG levels were measured to evaluate the redox state. The expression of nicotinamide mononucleotide adenylyltransferase 1 (NMNAT1), SIRT1, and SIRT3 was also evaluated after Rb1 treatment. (3) Results: Treatment with Rb1 significantly increased the cell viability and mtDNA copy number, and inhibited ROS generation. Rb1 treatment increased the activity of SOD and CAT and reduced the activity of NOX and PARP. Moreover, Rb1 enhanced both SIRT activity and SIRT1/SIRT3 expression. Additionally, Rb1 was able to re-establish the cellular redox balance in RCECs. However, Rb1 showed no effect on NMNAT1 expression in RCECs exposed to high glucose. (4) Conclusion: Under high glucose conditions, decreases in the reducing power may be linked to DNA oxidative damage and apoptosis via activation of the NMNAT-NAD-PARP-SIRT axis. Rb1 provides an advantage during high glucose-induced cell damage by targeting the NAD-PARP-SIRT signaling pathway and modulating the redox state in RCECs.

KEYWORDS:

Ginsenoside Rb1; NAD+; PARP; high glucose; retinal capillary endothelial cells; sirtuin

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