体育学刊
體育學刊
체육학간
Journal of Physical Education
2012年
1期
129~133
,共null页
运动生物化学 低氧训练 脑红蛋白 低氧诱导因子-1α 细胞凋亡基因 大鼠
運動生物化學 低氧訓練 腦紅蛋白 低氧誘導因子-1α 細胞凋亡基因 大鼠
운동생물화학 저양훈련 뇌홍단백 저양유도인자-1α 세포조망기인 대서
sports biochemistry; hypoxic training; neuroglobin; hypoxia induced factor-1α ; apoptotic gene; rat
探讨常压下模拟低氧(氧体积分数13.6%)训练对大鼠脑组织Ngb、HIF-1α、Bax和Bcl-2的影响,为运动和低氧适应提供理论参考。将50只9周龄雄性SD大鼠随机分为低住安静组、低住低练组、高住安静组、高住低练组和高住高练低练组,每组10只。训练组大鼠进行跑台训练,强度为常氧下35 m/min、低氧下30 m/min,持续运动1 h/d,5 d/周,持续4周。实验结束后,采用ELISΑ试剂盒分别检测大鼠脑组织Ngb、HIF-1α、Bax和Bcl-2水平,并计算Bax与Bcl-2的比值。结果发现:(1)与低住安静组比较,低住低练组HIF-1α、Bax和Bax/Bcl-2均升高(P〈0.05或P〈0.01);高住安静、高住低练和高住高练低练组的Ngb、HIF-1α、Bax和Bcl-2均升高(P〈0.05或P〈0.01)。(2)与低住低练组相比,高住安静、高住低练和高住高练低练组的HIF-1α和Bcl-2均升高(P〈0.01);高住低练和高住高练低练组的Bax/Bcl-2降低(P〈0.01);高住高练低练组的Ngb升高(P〈0.01)。(3)与高住安静组相比,高住低练组和高住高练低练组的HIF-1α、Bcl-2均升高(P〈0.05或P〈0.01);高住高练低练组的Ngb升高(P〈0.01),Bax/Bcl-2降低(P〈0.05)。(4)与高住低练组相比,高住高练低练组Bcl-2升高(P〈0.01)。(5)Ngb表达和HIF-1α表达呈正相关(r=0.563,P〈0.01);Ngb表达与Bax/Bcl-2变化呈正相关(r=0.486,P〈0.01);HIF-1α表达与Bax/Bcl-2变化呈正相关(r=0.353,P〈0.05)。结果表明:单纯训练刺激会引起大鼠脑组织HIF-1α升高,单纯低氧刺激会引起大鼠脑组织Ngb和HIF-1α升高,当训练和低氧这两种因素相互结合时,Ngb和HIF-1α的升高更明显。高住高练低练对大鼠脑组织Bcl-2的影响要大于高住低练。Ngb和HIF-1α的升高,使Bax/Bcl-2向着有利于神经元存活的方向发展,提示Ngb和HIF-1α参与了中枢神经系统的缺氧耐受和自我保护。
探討常壓下模擬低氧(氧體積分數13.6%)訓練對大鼠腦組織Ngb、HIF-1α、Bax和Bcl-2的影響,為運動和低氧適應提供理論參攷。將50隻9週齡雄性SD大鼠隨機分為低住安靜組、低住低練組、高住安靜組、高住低練組和高住高練低練組,每組10隻。訓練組大鼠進行跑檯訓練,彊度為常氧下35 m/min、低氧下30 m/min,持續運動1 h/d,5 d/週,持續4週。實驗結束後,採用ELISΑ試劑盒分彆檢測大鼠腦組織Ngb、HIF-1α、Bax和Bcl-2水平,併計算Bax與Bcl-2的比值。結果髮現:(1)與低住安靜組比較,低住低練組HIF-1α、Bax和Bax/Bcl-2均升高(P〈0.05或P〈0.01);高住安靜、高住低練和高住高練低練組的Ngb、HIF-1α、Bax和Bcl-2均升高(P〈0.05或P〈0.01)。(2)與低住低練組相比,高住安靜、高住低練和高住高練低練組的HIF-1α和Bcl-2均升高(P〈0.01);高住低練和高住高練低練組的Bax/Bcl-2降低(P〈0.01);高住高練低練組的Ngb升高(P〈0.01)。(3)與高住安靜組相比,高住低練組和高住高練低練組的HIF-1α、Bcl-2均升高(P〈0.05或P〈0.01);高住高練低練組的Ngb升高(P〈0.01),Bax/Bcl-2降低(P〈0.05)。(4)與高住低練組相比,高住高練低練組Bcl-2升高(P〈0.01)。(5)Ngb錶達和HIF-1α錶達呈正相關(r=0.563,P〈0.01);Ngb錶達與Bax/Bcl-2變化呈正相關(r=0.486,P〈0.01);HIF-1α錶達與Bax/Bcl-2變化呈正相關(r=0.353,P〈0.05)。結果錶明:單純訓練刺激會引起大鼠腦組織HIF-1α升高,單純低氧刺激會引起大鼠腦組織Ngb和HIF-1α升高,噹訓練和低氧這兩種因素相互結閤時,Ngb和HIF-1α的升高更明顯。高住高練低練對大鼠腦組織Bcl-2的影響要大于高住低練。Ngb和HIF-1α的升高,使Bax/Bcl-2嚮著有利于神經元存活的方嚮髮展,提示Ngb和HIF-1α參與瞭中樞神經繫統的缺氧耐受和自我保護。
탐토상압하모의저양(양체적분수13.6%)훈련대대서뇌조직Ngb、HIF-1α、Bax화Bcl-2적영향,위운동화저양괄응제공이론삼고。장50지9주령웅성SD대서수궤분위저주안정조、저주저련조、고주안정조、고주저련조화고주고련저련조,매조10지。훈련조대서진행포태훈련,강도위상양하35 m/min、저양하30 m/min,지속운동1 h/d,5 d/주,지속4주。실험결속후,채용ELISΑ시제합분별검측대서뇌조직Ngb、HIF-1α、Bax화Bcl-2수평,병계산Bax여Bcl-2적비치。결과발현:(1)여저주안정조비교,저주저련조HIF-1α、Bax화Bax/Bcl-2균승고(P〈0.05혹P〈0.01);고주안정、고주저련화고주고련저련조적Ngb、HIF-1α、Bax화Bcl-2균승고(P〈0.05혹P〈0.01)。(2)여저주저련조상비,고주안정、고주저련화고주고련저련조적HIF-1α화Bcl-2균승고(P〈0.01);고주저련화고주고련저련조적Bax/Bcl-2강저(P〈0.01);고주고련저련조적Ngb승고(P〈0.01)。(3)여고주안정조상비,고주저련조화고주고련저련조적HIF-1α、Bcl-2균승고(P〈0.05혹P〈0.01);고주고련저련조적Ngb승고(P〈0.01),Bax/Bcl-2강저(P〈0.05)。(4)여고주저련조상비,고주고련저련조Bcl-2승고(P〈0.01)。(5)Ngb표체화HIF-1α표체정정상관(r=0.563,P〈0.01);Ngb표체여Bax/Bcl-2변화정정상관(r=0.486,P〈0.01);HIF-1α표체여Bax/Bcl-2변화정정상관(r=0.353,P〈0.05)。결과표명:단순훈련자격회인기대서뇌조직HIF-1α승고,단순저양자격회인기대서뇌조직Ngb화HIF-1α승고,당훈련화저양저량충인소상호결합시,Ngb화HIF-1α적승고경명현。고주고련저련대대서뇌조직Bcl-2적영향요대우고주저련。Ngb화HIF-1α적승고,사Bax/Bcl-2향착유리우신경원존활적방향발전,제시Ngb화HIF-1α삼여료중추신경계통적결양내수화자아보호。
The authors probed into the effects of hypoxic(13.6% oxygen content) training simulated under a normal pressure on brain tissues Ngb,HIF-1α,Bax and Bcl-2 of rats,so as to provide a theoretical reference for exercising and hypoxic adaptation.The authors divided 50 9 weeks old male SD rats randomly into a living low calm group,a living low training low group,a living high calm group,a living high training low group and a living high training high and low group;each group contained 10 rats.The rats in training groups were trained on a treadmill for 4 weeks at an intensity of 35m/min under a normal oxygen condition or 30m/min under a hypoxic condition,1h/d(continuous exercising),5d/week.After the experiment was finished,an ELISA kit was used to respectively measure the levels of brain tissues Ngb,HIF-1α,Bax and Bcl-2 of the rats,and the ratio of Bax to Bcl-2 was calculated.The authors revealed the following findings: 1) as compared with living low calm group,the HIF-1α,Bax and Bax/Bcl-2 of the rats in living low training low group increased(P〈0.05 or P〈0.01);the Ngb,HIF-1α,Bax and Bcl-2 of the rats in living high calm group,living high training low group and living high training and high and low group in-creased(P〈0.05 or P〈0.01);2) as compared with living high calm group,the HIF-1α and Bcl-2 of the rats in living high calm group,living high training low group and living high training and high and low group increased(P〈0.01);the Bax/Bcl-2 of the rats in living high training low group and living high training and high and low graoup de-creased(P〈0.01);the Ngb of the rats in living high training and high and low group increased(P〈0.01);3) as com-pared with living high calm group,the HIF-1α and Bcl-2 of the rats in living high training low group and living high training and high and low group increased(P〈0.05 or P〈0.01);the Ngb of the rats in living high training and high and group increased(P〈0.01),while their Bax/Bcl-2 decreased(P〈0.05);4) as compared with living high training low group,the Bcl-2 of the rats in living high training and high and low group increased(P〈0.01);5) Ngb expres-sion and HIF-1α expression showed a positive correlation(r=0.563,P〈0.01);Ngb expression and Bax/Bcl-2 varia-tion showed a positive correlation(r=0.486,P〈0.01);HIF-1α expression and Bax/Bcl-2 variation showed a positive correlation(r=0.353,P〈0.05).The findings indicated the followings: training stimulation alone would cause the in-crease of brain tissue HIF-1 of rats;hypoxic stimulation alone would cause the increase of brain tissues Ngb and HIF-1α of rats;when such two factors as training and hypoxia were mutually combined,the increase of Ngb and HIF-1α would be more significant;the effects of living high training high and low on brain tissue Bcl-2 of rats were more significant than the effects of living high training low;the increase of Ngb and HIF-1α enabled Bax/Bcl-2 to develop in the direction favorable for neuron survival,which suggested that Ngb and HIF-1α had participated in the hypoxic tolerance and self protection of the central nervous system.