李方晖, 刘承宜, 杨海平, 韦恩秀, 刘延莹. 2012: 高糖诱导成肌细胞应激的低强度单色光调节的实验研究. 体育科学, 32(8): 40-48,54. DOI: 10.16469/j.css.2012.08.002
    引用本文: 李方晖, 刘承宜, 杨海平, 韦恩秀, 刘延莹. 2012: 高糖诱导成肌细胞应激的低强度单色光调节的实验研究. 体育科学, 32(8): 40-48,54. DOI: 10.16469/j.css.2012.08.002
    LI Fang-hui, LIU Cheng-yi, YANG Hai-ping, WEI En-xiu, LIU Yan-ying. 2012: Experimental Study on Low-intensity Monochromatic Light Modulation of High Glucose-induced Myoblast Stress. China Sport Science, 32(8): 40-48,54. DOI: 10.16469/j.css.2012.08.002
    Citation: LI Fang-hui, LIU Cheng-yi, YANG Hai-ping, WEI En-xiu, LIU Yan-ying. 2012: Experimental Study on Low-intensity Monochromatic Light Modulation of High Glucose-induced Myoblast Stress. China Sport Science, 32(8): 40-48,54. DOI: 10.16469/j.css.2012.08.002

    高糖诱导成肌细胞应激的低强度单色光调节的实验研究

    Experimental Study on Low-intensity Monochromatic Light Modulation of High Glucose-induced Myoblast Stress

    • 摘要: 背景和目的:低强度单色光(LIL)疗法广泛应用于运动损伤防护。研究LIL对高糖(HG)诱导的成肌细胞应激的调节作用及其机制。方法:C2C12成肌细胞在不同浓度的葡萄糖中培养,其中22.5和90.0mmol/L浓度分别作为正糖组(NG)和HG组。随后用强度为I mW/cm2的发光二极管640±15nm红光(RLED)照射N天(I*N)(I=0.035,0.067;N=1,2,3)(每天15min)。细胞用浓度为1~100μmol/L的白藜芦醇(RES)在NG中预处理细胞M h(RES1-100/M)(M=6,12,24),随后更换为NG/HG继续培养72h。细胞的各个指标用常规方法检测。结果:1)NG组细胞的增殖速率最快。2)0.035*3不能调节NG组细胞增殖,但I*N(I=0.035,0.067;N=1,2,3)分别在第3和4天显著促进HG组细胞增殖。3)RES5-100/6、RES1-100/12和RES1-30/24显著促进HG组细胞增殖,且RES10/12显著促进NG组细胞增殖。4)0.035*3显著地增加了sirtuin 1(SIRT1)、锰超氧化物歧化酶(MnSOD)和肌源性胰岛素样生长因子(mIGF-1)mRNA转录,降低了叉头框蛋白3a(FOXO3a)、p27和细胞死亡介导因子(BIM)mRNA转录;RES10/12显著增加SIRT1和Mn-SOD mRNA转录,降低了p27mRNA转录,但对FOXO3a和BIM mRNA转录没有明显影响。5)HG在第4和72h分别增加和减少烟酰胺腺嘌呤二核苷酸辅酶与其还原形式比值(NAD+/NADH)及SIRT1蛋白表达,但分别被0.035*1和0.035*3所康复。结论:22.5mmol/L葡萄糖浓度组的C2C12成肌细胞处于增殖特异的内稳态,不能被红光调节,但可以被白藜芦醇促进。红光通过激活mIGF-1/SIRT1/FOXO3a信号通路促进90.0mmol/L浓度组C2C12成肌细胞增殖特异的内稳态建立。

       

      Abstract: Background and Objective:Low intensity monochromatic light(LIL) therapy was widely applied in athletic training.The LIL modulation of high glucose(HG) induced myoblast stress and its mechanism was studied in this paper.Study Design/Materials and Methods:C2C12 myoblasts were cultivated in glucose at different concentrations including 22.5(NG) and 90.0(HG) mmol/L and then irradiated with red light at 640±15 nm from light-emitting diode array(RLED) at I mW/cm2 for 15 min once a day for N days(I*N)(I=0.035,0.067;N=1,2,3),respectively.They were also pretreated with resveratrol(RES) at 1-100 μmol/L for M h(RES1-100/M)(M=6,12,24) in NG and then cultivated at NG/HG for 3 days.The cellular parameters were routinely assessed.Results:1)The proliferation peaked in NG.2)0.035*3 did not modulate the proliferation in NG,but I*N(I=0.035,0.067;N=1,2,3) significantly improved the proliferation in HG on the 3rd and 4th day,respectively.3)RES5-100/6,RES1-100/12 and RES1-30/24 significantly promoted the proliferation in HG,and moreover,RES10/12 significantly promoted the proliferation in NG.4)0.035*3 significantly increased the mRNA expression of sirtuin 1(SIRT1),manganese superoxide dismutase(MnSOD) and muscular insulin-like growth factor-1(mIGF-1),but significantly decreased the one of forkhead class O 3a(FOXO3a),p27 and Bcl-2 interacting mediator of cell death(BIM).RES10/12 significantly increased SIRT1 mRNA expression,significantly decreased p27 mRNA expression,but did not modulate the mRNA expression of FOXO3a and BIM.5)HG significantly increased at the 4th h but decreased at the 72nd h the ratio of nicotinamide adenine dinucleotide(NAD+) and its reduced form NADH and SIRT1,which were recovered by 0.035*1 and 0.035*3,respectively.Conclusions:The proliferation of C2C12 myoblasts may be in proliferation-specific homeostasis in glucose at concentrations 22.5 mmol/L group,in which the proliferation may not be modulated by red light,but may be promoted by resveratrol.The establishment of proliferation-specific homeostasis in glucose at concentrations 90.0 mmol/L group may be promoted by red light through mIGF-1/SIRT1/FOXO3a pathways.

       

    /

    返回文章
    返回