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重庆医科大学附属第一医院神经内科
纸质出版日期:2016,
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[1]陈帅,李光勤,胡万群,唐杰,廖艳,黄妮.运动训练起始时间及强度对脑梗死大鼠神经功能的影响和机制研究[J].重庆医科大学学报,2016,41(01):44-50.
Chen Shuai, Li Guangqin, Hu Wanqun, et al. Effect of starting time and intensity of exercise training on neurological function after cerebral infarct in rats and its mechanism[J]. Journal of Chongqing Medical University, 2016,41(1):44-50.
[1]陈帅,李光勤,胡万群,唐杰,廖艳,黄妮.运动训练起始时间及强度对脑梗死大鼠神经功能的影响和机制研究[J].重庆医科大学学报,2016,41(01):44-50. DOI: 10.13406/j.cnki.cyxb.000857.
Chen Shuai, Li Guangqin, Hu Wanqun, et al. Effect of starting time and intensity of exercise training on neurological function after cerebral infarct in rats and its mechanism[J]. Journal of Chongqing Medical University, 2016,41(1):44-50. DOI: 10.13406/j.cnki.cyxb.000857.
目的 :观察不同运动训练起始时间及强度对脑梗死大鼠神经功能的变化及梗死侧海马脑源性神经营养因子(brainderived neurotrophic factor
BDNF)、5-羟色胺受体1A亚型(5-hydroxytryptamine receptor 1A subtyte
5-HT1A)表达的影响
并探讨运动训练促进脑梗死大鼠神经功能恢复的机制。方法:本研究共分3部分:1将成年雄性SD大鼠随机分为S1、I1、E1、E3、E5组;各组分别代表假手术1组
脑梗死1组
脑梗死1、3、5 d后运动训练组。每组5只
运动训练的强度为15 m/min。根据改良神经功能缺损程度评分(modified neurological severity scores
m NSS)及BDNF蛋白表达情况
确定脑梗死后运动训练的最佳起始时间。2在最佳起始时间的基础上
将大鼠随机分为S2、I2、L、M、H组;各组分别代表假手术2组
脑梗死2组
脑梗死低、中、高强度运动训练组。每组5只
L、M、H组运动训练强度分别为10 m/min、15 m/min、20 m/min
根据m NSS及BDNF蛋白表达情况
确定脑梗死后运动训练的最佳强度。3运用5-HT1A特异性受体拮抗剂WAY100635
观察5-HT1A对脑梗死后运动训练大鼠BDNF的影响。此部分实验将大鼠随机分为S3、I3、E、W组
各组分别代表假手术3组、脑梗死3组、运动训练组、WAY100635组。每组6只。运用Western blot和荧光定量PCR检测5-HT1A、BDNF蛋白及m RNA变化。结果:1 E1、E3、E5组较I1组m NSS明显降低(P<0.01)
E1、E3、E5各组的m NSS无统计学差异。E3、E5组的BDNF蛋白表达较I1组明显上调(P<0.05)
E3、E5组之间的表达无统计学差异。2M组的m NSS较I2组明显降低(P<0.01)
M组的BDNF蛋白水平较I2组表达明显升高(P<0.01)
但L、H组较I2组的m NSS及BDNF蛋白表达无统计学差异。脑梗死后运动训练的最佳强度为15 m/min。3E组的m NSS较I3组明显降低(P<0.05)
但W组较E组的m NSS无统计学差异。E组较I3组的5-HT1A、BDNF蛋白及m RNA水平均显著提高(P<0.05)
但W组的BDNF蛋白及m RNA水平较E组无统计学差异。结论:1运动训练可促进脑梗死后的神经功能恢复
上调5-HT1A及BDNF表达;2脑梗死后早期(1 d、3 d、5 d)进行运动训练有利于神经功能的恢复
并且脑梗死3 d或5 d后进行运动训练可有效上调BDNF表达水平;3中强度运动训练可有效促进神经功能恢复及BDNF表达;4脑梗死后运动训练促进BDNF表达的机制可能与5-HT1A无关。
Objective:To observe the effect of different starting time and intensities of exercise training on neurologic function change and the expression of brain-derived neurotrophic factor(BDNF) and 5-hydroxytryptamine receptor 1A subtyte(5-HT1A) in hippocampus after cerebral infarct in rats
and to discuss the mechanism of exercise training to improve neurological function recovery in cerebral infarction rats. Methods:The study has three parts:1 Adult male Sprague-Dawley(SD) rats were randomly divided into S1
I1
E1
E3 and E5 groups
namely sham group 1
infarct group 1
exercise training of day 1 after infarct group
exercise training of day 3 after infarct group and exercise training of day5 after infarct group respectively(five rats in each group;the intensity of exercise training was 15 m/min). The best starting time of exercise training after cerebral infarct was decided according to modified neurological severity scores(m NSS)and expression of BDNF protein. 2Basing on the best starting time and different intensities of exercise training
rats were randomly divided into S2
I2
L
M and H groups
namely sham group 2
infarct group 2
low-intensity exercise training after infarct group
moderate-intensity exercise training after infarct group and high-intensity exercise training after infarct group(five rats in each group;the intensity of L group
M group and H group was 10 m/min
15 m/min and 20 m/min respectively). The best intensity of exercise training after cerebral infarct was decided according to m NSS and expression of BDNF protein. 3WAY100635
a 5-HT1 A special receptor antagonist
was used to observe the effect of 5-HT1 A on BDNF in the rats of exercise training after cerebral infarct. In this part
rats were randomly divided into S3
I3
E and W groups
namely sham group 3
infarct group 3
exercise training group and WAY100635 group(5 rats in each group). Western blot and fluorogenic quantitative PCR were used to detect the protein and m RNA level of 5-HT1 A and BDNF. Results:1The m NSS was decreased in E1
E3 and E5 group than in I1 group(P<0.01)
without significant statistical differences between E1
E3 and E5 groups. The m NSS was also significantly up-regulated in E3 and E5 group than in I1 group(P<0.05)
without significant statistical differences between E3 and E5 groups. 2The m NSS was decreased in M group than in I2 group(P<0.01)
and the BDNF protein was up-regulated in M group than in I2 group(P<0.01)
without significant statistical differences in L
H and I2 groups. The best intensity of exercise training after cerebral infarct was 15 m/min. 3The m NSS was decreased in E group than in I3 group(P<0.05)
without significant statistical differences between E group and W group. The protein and m RNA level of 5-HT1 A and BDNF was significantly increased in E group than in I3 group(P<0.05)
without significant statistical differences between E group and W group. Conclusion:Exercise training can improve neurological function and up-regulate the expression of 5-HT1 A and BDNF after cerebral infarct. Early exercise training(day 1
day 3 or day 5)is benefit to neurological function recovery and it can up-regulate BDNF effectively day 3 or day 5 after cerebral infarct. Moderate intensity of exercise training can promote neurological function recovery and BDNF expression. The mechanism of exercise training which promote BDNF expression after cerebral infarct may be not related to 5-HT1 A.
脑梗死运动训练脑源性神经营养因子神经功能
cerebral infarctexercise trainingbrain-derived neurotrophic factorneurological function
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