Resveratrol increases sirtuin 1 expression in peripheral blood mononuclear cells of premature infants and inhibits the oxidative stress induced by hyperoxia in vivo

YANG Xi, DONG Wen-Bin, LI Qing-Ping, KANG Lan, LEI Xiao-Ping, ZHANG Lian-Yu, LU You-Ying, ZHAI Xue-Song

Chinese Journal of Contemporary Pediatrics ›› 2016, Vol. 18 ›› Issue (1) : 72-77.

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Chinese Journal of Contemporary Pediatrics ›› 2016, Vol. 18 ›› Issue (1) : 72-77. DOI: 10.7499/j.issn.1008-8830.2016.01.015
EXPERIMENTAL RESEARCH

Resveratrol increases sirtuin 1 expression in peripheral blood mononuclear cells of premature infants and inhibits the oxidative stress induced by hyperoxia in vivo

  • YANG Xi, DONG Wen-Bin, LI Qing-Ping, KANG Lan, LEI Xiao-Ping, ZHANG Lian-Yu, LU You-Ying, ZHAI Xue-Song
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Abstract

Objective To explore the effect of resveratrol on the levels of sirtuin 1 (SIRT1) and reactive oxygen species (ROS) in peripheral blood mononuclear cells (PBMCs) of premature infants exposed to hyperoxia. Methods Peripheral blood and isolated PBMCs from premature infants (gestational age <32 weeks) without oxygen supplement were collected and were randomly assigned into four groups: control, air+resveratrol, hyperoxia, and hyperoxia + resveratrol. The PBMCs were cultured in vitro for 48 hours, then the ROS content in PBMCs was measured by laser scanning confocal microscopy. Malondialdehyde (MDA) content in the medium was measured by the whole spectrum spectrophotometer. SIRT1 positioning was assessed by immunofluorescence. SIRT1 expression levels in PBMCs were measured by Western bolt. Results Compared with the control group, the level of SIRT1 in the air+resveratrol group increased significantly (P<0.05). The levels of ROS and MDA and the SIRT1 transposition rate in the hyperoxia group increased significantly, while the expression level of SIRT1 decreased significantly compared with the control group (P<0.05). The levels of ROS and MDA and the SIRT1 transposition rate decreased significantly (P<0.05), and the expression level of SIRT1 increased significantly in the hyperoxia+resveratrol group (P<0.05). Conclusions Resveratrol can increase SIRT1 expression in PBMCs and inhibit SIRT1 shuttle from nucleus to cytoplasm in order to increase the ability of antioxidative stress in premature infants exposed to hyperoxia, thereby reducing the oxidative stress injury in premature infants.

Key words

Resveratrol / Sirtuin 1 / Oxidative stress / Peripheral blood mononuclear cell

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YANG Xi, DONG Wen-Bin, LI Qing-Ping, KANG Lan, LEI Xiao-Ping, ZHANG Lian-Yu, LU You-Ying, ZHAI Xue-Song. Resveratrol increases sirtuin 1 expression in peripheral blood mononuclear cells of premature infants and inhibits the oxidative stress induced by hyperoxia in vivo[J]. Chinese Journal of Contemporary Pediatrics. 2016, 18(1): 72-77 https://doi.org/10.7499/j.issn.1008-8830.2016.01.015

References

[1] Sureshbabu A, Syed MA, Boddupalli CS, et al. Conditional overexpression of TGFβ1 promotes pulmonary inflammation, apoptosis and mortality via TGFβR2 in the developing mouse lung[J]. Respir Res, 2015, 16: 4.
[2] Bhandari V. Postnatal inflammation in the pathogenesis of bronchopulmonary dysplasia[J]. Birth Defects Res A Clin Mol Teratol, 2014, 100(3): 189-201.
[3] Volonte D, Zou H, Bartholomew JN, et al. Oxidative stressinduced inhibition of Sirt1 by caveolin-1 promotes p53-dependent premature senescence and stimulates the secretion of interleukin 6 (IL-6)[J]. J Biol Chem, 2015, 290(7): 4202-4214.
[4] Wang SJ, Zhao XH, Chen W, et al. Sirtuin 1 activation enhances the PGC-1α/mitochondrial antioxidant system pathway in status epilepticus[J]. Mol Med Rep, 2015, 11(1): 521-526.
[5] Nogueiras R, Habegger KM, Chaudhary N, et al. Sirtuin 1 and sirtuin 3: physiological modulators of metabolism[J]. Physiol Rev, 2012, 92(3): 1479-1514.
[6] Meng C, Liu JL, Du AL. Cardioprotective effect of resveratrol on atherogenic diet-fed rats[J]. Int J Clin Exp Pathol, 2014, 7(11): 7899-7906.
[7] Sinclair DA, Guarente L. Small-molecule allosteric activators of sirtuins[J]. Annu Rev Pharmacol Toxicol, 2014, 54: 363-380.
[8] Ruan Y, Dong C, Patel J, et al. SIRT1 suppresses doxorubicininduced cardiotoxicity by regulating the oxidative stress and p38MAPK pathways[J]. Cell Physiol Biochem, 2015, 35(3): 1116-1124.
[9] Zhang L, Guo X, Xie W, et al. Resveratrol exerts an antiapoptotic effect on human bronchial epithelial cells undergoing cigarette smoke exposure[J]. Mol Med Rep, 2015, 11(3): 1752-1758.
[10] Li J, Feng L, Xing Y, et al. Radioprotective and antioxidant effect of resveratrol in hippocampus by activating Sirt1[J]. Int J Mol Sci, 2014, 15(4): 5928-5939.
[11] Nicoletti NF, Rodrigues-Junior V, Santos AA Jr, et al. Protective effects of resveratrol on hepatotoxicity induced by isoniazid and rifampicin via SIRT1 modulation[J]. J Nat Prod, 2014, 77(10): 2190-2195.
[12] Yun JM, Chien A, Jialal I, et al. Resveratrol up-regulates SIRT1 and inhibits cellular oxidative stress in the diabetic milieu: mechanistic insights[J]. J Nutr Biochem, 2012, 23(7): 699-705.
[13] 车忠丽, 董文斌, 李清平, 等. PKCβ/P66Shc 氧化应激通路 在高氧诱导人肺泡上皮细胞活性氧簇产生中的作用[J]. 中国 当代儿科杂志, 2015, 17(3): 275-280.
[14] 张玲萍, 董文斌, 李清平, 等. p47phox 介导早产儿氧暴露后 体内活性氧簇产生的机制[J]. 中华实用儿科临床杂志, 2015, 30(2): 127-130.
[15] 卢美燕, 董文斌. 氧化应激在高体积分数氧肺损伤中的作用[J]. 实用儿科临床杂志, 2012, 27(22): 1763-1765.
[16] 张春艳, 董文斌, 李清平, 等. 白藜芦醇上调人肺泡上皮细 胞SIRT1 表达抑制高氧诱导的细胞凋亡[J]. 细胞与分子免疫 学杂志, 2015, 31(5): 590-595.
[17] 车忠丽, 董文斌, 李清平, 等. PKCβ/p66Shc 氧化应激通路 介导高氧诱导人肺泡上皮细胞凋亡的作用[J]. 临床儿科杂 志, 2013, 31(11): 1066-1069.
[18] Lau AW, Liu P, Inuzuka H, et al. SIRT1 phosphorylation by AMP-activated protein kinase regulates p53 acetylation[J]. Am J Cancer Res, 2014, 4(3): 245-255.
[19] Iyer S, Han L, Bartell SM, et al. Sirtuin1 (Sirt1) promotes cortical bone formation by preventing β-catenin sequestration by FoxO transcription factors in osteoblast progenitors[J]. J Biol Chem, 2014, 289(35): 24069-24078.
[20] Hori YS, Kuno A, Hosoda R, et al. Regulation of FOXOs and p53 by SIRT1 modulators under oxidative stress[J]. PLoS One, 2013, 8(9): e73875.
[21] Kim YH, Hwang JH, Kim KS, et al. NAD(P)H: quinone oxidoreductase 1 activation reduces blood pressure through regulation of endothelial nitric oxide synthase acetylation in spontaneously hypertensive rats[J]. Am J Hypertens, 2015, 28(1): 50-57.
[22] Tanno M, Sakamoto J, Miura T, et al. Nucleocytoplasmic shuttling of the NAD+-dependent histone deacetylase SIRT1[J]. J Biol Chem, 2007, 282(9): 6823-6832.
[23] Morris KC, Lin HW, Thompson JW, et al. Pathways for ischemic cytoprotection: role of sirtuins in caloric restriction, resveratrol, and ischemic preconditioning[J]. J Cereb Blood Flow Metab, 2011, 31(4): 1003-1019.
[24] Verdin E, Dequiedt F, Kasler HG. Class II histone deacetylases: versatile regulators[J]. Trends Genet, 2003, 19(5): 286-293.
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