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Correction: 5-Heptadecylresorcinol attenuates oxidative damage and mitochondria-mediated apoptosis through activation of the SIRT3/FOXO3a signaling pathway in neurocytes
Jie
Liu
a,
Yu
Wang
a,
Yiming
Hao
a,
Zongwei
Wang
a,
Zihui
Yang
a,
Ziyuan
Wang
a and
Jing
Wang
*ab
aChina-Canada Joint Lab of Food Nutrition and Health (Beijing), Beijing Technology & Business University (BTBU), Beijing 100048, China. E-mail: wangjing@th.btbu.edu.cn
bBeijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Technology & Business University, Beijing 100048, China
First published on 26th March 2020
Abstract
Correction for ‘5-Heptadecylresorcinol attenuates oxidative damage and mitochondria-mediated apoptosis through activation of the SIRT3/FOXO3a signaling pathway in neurocytes’ by Jie Liu et al., Food Funct., 2020, DOI: 10.1039/c9fo03028j.
The authors regret the incorrect version of Fig. 4 was included in the original article. The correct version of Fig. 4 is presented below.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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| Fig. 4 AR-C17 prevents oxidative damage and mitochondria-mediated apoptosis through the SIRT3-FOXO3a signaling pathway. Cells were incubated with or without 30 μM SIRT3 inhibitor (3-TYP) for 12 h. They were then incubated with AR-C17 for another 48 h, and finally exposed to 250 μM H2O2. (A) The effect of AR-C17 on the protein expression of SIRT3 and FOXO3a. (B) The effect of AR-C17 and cotreatment with 3-TYP on cell viability. (C) The effect of AR-C17 and cotreatment with 3-TYP on protein expression of SIRT3 and FOXO3a. (D) The effect of AR-C17 and cotreatment with 3-TYP on cell apoptosis. Data are presented as the means ± SD (n = 3). Results marked with the same letters are not significantly different (P < 0.05). | ||
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