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针康法对糖尿病缺血性脑卒中大鼠神经功能缺损及胰岛素抵抗机制的研究
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摘要
目的
     观察针康法对糖尿病缺血性脑卒中大鼠运动功能;血清糖脂代谢;血清NF-κKB-p65、 TNF-α、IL-1β;脑缺血皮质区及骨骼肌NF-κB-p65、TNF-α、IL-1β蛋白;骨骼肌IRS-1、 PI3K基因的表达,探讨针康法对于改善糖尿病缺血性脑卒中大鼠神经功能缺损和胰岛素抵抗的相关机制。
     方法
     建立糖尿病缺血性脑卒中大鼠模型,将192只大鼠按随机数字法分为6组:空白组、假手术组、模型组、针刺组、康复组、针康组,每组各32只。每组按3、7、14、21天再分为4亚组,每组8只。空白组、假手术组、模型组不进行任何干预,针刺组采用头穴丛刺结合体针治疗,康复组采用跑台训练,针康组采用针刺结合跑台训练治疗。各时间点运用平衡木试验观察大鼠神经功能变化;采用全自动生化分析仪测血TG、TC含量;酶联免疫吸附法测FINS及血清NF-κB-p65、TNF-α、IL-1β含量;免疫组化法检测脑缺血皮质区及骨骼肌NF-KB-p65、TNF-α、IL-1β蛋白表达;Real-Time PCR检测骨骼肌IRS-1mRNA、PI3K mRNA的表达。
     结果
     1平衡木试验评分:与假手术组比较,各时间点、各组平衡木试验评分明显增高(P<0.01)。与模型组比较,术后3天、7天、14天康复组评分降低(P<0.05),术后3天、7天、14天、21天针康组评分降低(P<0.05)。与针刺组、康复组比较,术后14天、21天针康组评分降低(P<0.05)。
     2糖脂代谢:①空腹血糖(FPG):术后14天、21天,与空自组比较,其余各组大鼠FPG均明显增加(P<0.01);与假手术组、模型组比较,针康组FPG明显降低(P<0.01):与针刺组比较,针康组FPG降低(P<0.05)。②血清胰岛素(FINS):与空白组比较,术后14天、21天其余各组大鼠IFINS均明显增加(P<0.01);与假手术组、模型组比较,术后21天,康复组FINS明显降低(P<0.01);术后14天、21天,针康组FINS明显降低(P<0.01)。与针刺组比较,术后14天、21天针康组FINS降低(P<0.05)。③胰岛素敏感指数其自然对数(IAI):与空白组比较,术后14天、21天其余各组大鼠IAI均明显降低(P<0.01);与假手术组比较,术后21天康复组IAIt增加(P<0.05),术后14天、21天针康组IAI均明显增加(P<0.01);与模型组比较,术后14天康复组IAI上升(P<0.05),术后14天、21天,针康组IAI均明显上升(P<0.01);与针刺组比较,术后14天、21天,针康组IAI均上升(P<0.05)。④甘油三酯(TG):与空白组比较,术后14天、21天其余各组大鼠TG均明显增加(P<0.01);与假手术组、模型组比较,术后21天针康组TG下降(P<0.05)。⑤胆固醇(TC):与空白组比较,术后14天、21天其余各组大鼠TC均明显增加(P<0.01);与假手术组、模型组比较,术后14天、21天针康组TC均下降(P<0.05);与模型组比较,术后21天康复组TC下降。
     3血清NF-κB-p65、TNF-α、IL-1β含量:与空白组、假手术组比较,术后各时间点其余各组大鼠血清NF-κB-p65、TNF-α、IL-1β含量均明显增加(P<0.01),假手术组较空白组含量增加(P<0.01)。血清NF-κB-p65与模型组比较,术后各天针康组含量降低(P<0.05)。与针康组比较,术后7天针刺组(P<0.01)、康复组(P<0.05)含量降低不如针康组明显。血清TNF-α与模型组比较,术后7天、14天,针刺组、康复组、针康组含量均明显降低(P<0.01),术后21天康复组含量降低(P<0.05),针康组含量明显降低(P<0.01)。与针康组比较,术后7天、14天针刺组、康复组含量降底不如针康组(P<0.05)。血清IL-1β与模型组比较,针刺组术后3天、7天含量降低(P<0.05);康复组术后3天、14天含量降低(P<0.05);针康组术后各时间点含量均明显降低(P<0.01)。与针刺组比较,针康组术后21天含量降低(P<0.05)。
     4缺血区皮层NF-κB-p65、TNF-α、IL-1β的表达:与空白组、假手术组比较,术后各时间点NF-κB-p65、TNF-α、IL-1β阳性细胞数均明显增加(P<0.01),假手术组较空白组数量增加(P<0.01)。缺血区皮层NF-κB-p65与模型组比较,针康组术后各时间点阳性细胞数降低显著(P<0.01)。与针刺组、康复组比较,针康组术后3天、21天阳性细胞数降低(P<0.05)。缺血区皮层TNF-α与模型组比较,针康组术后各时间点数量明显降低(P<0.01)。与针刺组比较,针康组术后7天数量明显降低(P<0.01),术后3天、21天数量降低(P<0.05)。与康复组比较,针康组术后14天数量降低(P<0.05)。缺血区皮层IL-1β的表达与模型组比较,针康组术后3天、7天、14天数量明显降低(P<0.01),数量降低(P<0.05)。与针刺组、康复组比较,针康组术后3天、7天含量降低(P<0.05)。
     5骨骼肌NF-κB-p65、TNF-α、IL-1β的表达:术后21天,与空白组比较,各组NF-κB-p65、TNF-α、IL-1β光密度值明显增加(P<0.01);与假手术组及模型组比较,针刺组、康复组、针康组NF-κB-p65光密度值均明显降低有显著意义(P<0.01);与针刺组、康复组比较,针康组光密度值明显降低(P<0.01)。与假手术组及模型组比较,针刺组、康复组、针康组TNF-α光密度值均明显降低(P<0.01);与针刺组、康复组比较,针康组TNF-α光密度值明显降低(P<0.01)。与假手术组及模型组比较,针刺组、康复组、针康组IL-1β光密度值均明显降低(P<0.01);与针刺组、康复组比较,康复组IL-1β光密度值降低(P<0.05)。
     6骨骼肌IRS-1mRNA表达:术后21天各组均有IRS-1mRNA的表达,空白组较其他各组表达明显(P<0.01);与假手术组、模型组比较,针刺组、康复组、针康组IRS-1mRNA的表达水平明显增高(P<0.01);与针刺组比较,康复组IRS-1mRNA表达增加(P<0.05),针康组IRS-1mRNA表达水平明显增加(P<0.01);与康复组比较,针康组IRS-1mRNA表达增加(P<0.05)。
     7骨骼肌PI3KmRNA表达:术后21天各组均有PI3KmRNA的表达,空白组较其他各组表达明显(P<0.01);与假手术组、模型组比较,针刺组、康复组、针康组PI3KmRNA的表达水平明显增高(P<0.01);与针刺组、康复组比较,针康组IRS-1mRNA表达增加(P<0.05)。
     结论:
     1.针康法能够促进糖尿病缺血性脑卒中大鼠神经功能的康复,针康法优于单纯针刺或康复。
     2.针康法能够降低糖尿病缺血性脑卒中大鼠糖脂代谢水平,增加胰岛素敏感指数,逆转糖代谢异常,使病态机体得到改善。
     3.针康法能够降低糖尿病缺血性脑卒中大鼠血清、脑缺血区皮质NF-κB-p65、 TNF-α、IL-1β的含量,进而减少缺血区脑组织炎症的损伤,起到脑保护作用。
     4.针康法能够减少糖尿病缺血性脑卒中大鼠骨骼肌NF-κB-p65、TNF-α、IL-1β的蛋白表达,缓解微炎状态,使骨骼肌的胰岛素敏感性增加,改善胰岛素抵抗。
     5.针康法能使糖尿病缺血性脑卒中大鼠骨骼肌IRS-1mRNA、PI3KmRNA的含量增加,针康法可能通过IRS-1/PI3K信号转导通路改善骨骼肌对胰岛素的抵抗。
Objective
     To observe the effects of cluster needling of acupuncture combined with treadmill training in Motor function metabolism of serum glucolipid、NF-κB-p65、TNF-α and IL-1β in serum、ischemic region of cerebral cortex and skeletal muscle NF-κB-p65、TNF-α、IL-1β protein and skeletal muscle IRS-1and PI3K expression of gene in rats with Diabetes ischemic stroke. To discuss the probable mechanism applied to improve the neurological function defects and IR in rats.
     Method
     Establish rat diabetes ischemic stroke model. To randomly divide192rats into six groups, which are Sham operation group, Model group, Acupuncture group, Rehabilitation group and Blank group. And then each group was divided into four subgroups in accordance with the3rd,7th,14th,21st days (n=8). No intervention was given to Sham operation group, Blank group and Model group, while the Acupuncture group was treated with head combined with body acupuncture therapy, the Rehabilitation group was treated with treadmill training, Acupuncture combined with rehabilitation group was treated with acupuncture treatment combined with treadmill training. Each time the changing of rats' neurological function was observed. TG、TC content were evaluated by net screen test. FINS、NF-KB-p65、TNF-α、IL-1β content were evaluated by ELISA. Ischemic region of cerebral cortex and skeletal muscle NF-κB-p65、TNF-α、IL-1β were evaluated by SABC. And the Real-Time PCR staining was used to observe the expression of skeletal muscle's IRS-1mRNA、PI3K mRNA.
     Results
     1. Scores of Balance Beam test:Compared with Sham operation group, the score of each group was significantly improved at each point (p<0.01). The3rd,7th,14th,21st day after the modeling, the score of Acupuncture combined with rehabilitation group dropped down (p<0.05). And compared with Acupuncture group and Rehabilitation group, the score of Acupuncture combined with rehabilitation group dropped down (p<0.05) on the14th and21st day after the modeling.
     2.Metabolism of glucolipid:①FPG:Compared with the blank group, the FPG of the remaining groups have been significantly improved on the14th and21st day after the modeling (p<0.01). The FPG of the Acupuncture combined with the rehabilitation group decreased clearly which compared with the Sham operation group and the Model group (p<0.01).And the Acupuncture combined with rehabilitation group's FPG had been decreased compared with the Acupuncture group (p<0.05).②FINS:Compared with the blank group, the FINS of the remaining groups have been significantly improved on the14th and21st day after the modeling (p<0.01).Compared with the Sham operation group and the Model group, the FINS of the Rehabilitation group decreased clearly on the21st day after the modeling (p<0.01). The acupuncture combined with rehabilitation group's FINS decreased clearly (p<0.01). And the FINS of acupuncture combined with rehabilitation group's FINS had a decrease compared with the acupuncture group (p<0.05).③IAI:Compared with the blank group, the IAI of the remaining groups was significantly reduced on the14th and21st day after the modeling (p<0.01). Compared with the sham operation group, the IAI of the rehabilitation group increased clearly on the21st day after the modeling (p<0.05). The acupuncture combined with rehabilitation group's IAI decreased clearly on the14th and21st day after the modeling (p<0.01). And the IAI of acupuncture group's IAI was been decreased compared with the model group (p<0.05). The.acupuncture combined with rehabilitation group's IAI decreased clearly on the14th and21st day after the modeling (p<0.01). Compared with the acupuncture group, the IAI of the acupuncture combined with rehabilitation group had a decrease on the14th and21st days after the modeling (p<0.05).④TG:Compared with the blank group, the TG of the remaining groups was significantly reduced on the14th and21st day after the modeling (p<0.01). Compared with the sham operation group and the model group, the TG of the acupuncture combined with rehabilitation group dropped down on the21st day after the modeling (p<0.05).⑤TC: Compared with the blank group, the TC of the remaining groups was significantly decreased on the14th and21st day after the modeling (p<0.01). Compared with the sham operation group and the model group, the TC of the acupuncture combined with rehabilitation group dropped down on the14th and21st day after the modeling (p<0.05). Compared with the model group, the TC of the acupuncture group dropped down on the21st days after the modeling.
     3. The content of NF-κB-p65、TNF-α、IL-1β in serum:Compared with the blank group and the sham operation group, the NF-κB-p65、TNF-α IL-1β content in serum of the remaining groups was significantly decreased on each point after the modeling (p<0.01). Compared with the model group,the content of the NF-KB-p65、TNF-α、IL-1β in serum of the which acupuncture combined with rehabilitation group have been decreased (p<0.01). Compared with the acupuncture combined with rehabilitation group, the NF-KB-p65contents of the acupuncture group decreased (p<0.01) and the rehabilitation group (p<0.05) are not clearer than acupuncture combined with rehabilitation group on the7th day after the modeling. The content's decrease of the acupuncture group is not clearer than acupuncture combined with rehabilitation group on the14th and21st day after the modeling. Compared with the model group, the TNF-α content of the acupuncture group,the rehabilitation group、 the acupuncture combined with rehabilitation group have been decreased (p<0.01) on the7th and14st day after the modeling, the content of the rehabilitation group(p<0.05) and the acupuncture combined with rehabilitation group(p<0.01) decreased on the21th day after the modeling。Compared with the acupuncture combined with rehabilitation group, The content's decrease of the acupuncture group and the rehabilitation group is not clearer than it on the7th and14st day after the modeling(p<0.05). Compared with the model group, the IL-1β content of the acupuncture group have been decreased (p<0.05) on the3th and7st day after the modeling; the rehabilitation group decreased (p<0.05) on the3th and14st day; the acupuncture combined with rehabilitation group decreased (p<0.01) on every day. Compared with the acupuncture group, the acupuncture combined with rehabilitation group decreased (p<0.05)on the21st day.
     4. The expression of NF-κB-p65、TNF-α、IL-1β around ischemic cortex:Compared with the sham operation group and the blank group, there was a significant increase of NF-κB-p65、TNF-α、IL-1β expression in the remaining groups on each point (P<0.01). Compared with blank group, the sham group have been increased (P<0.01). Compared with model group, the NF-KB-p65expression reduced in acupuncture combined with rehabilitation group on every day after modeling (p<0.01). Compared with acupuncture group and rehabilitation group, expression reduced in acupuncture combined with rehabilitation group on3rd and2st day after modeling (p<0.05). Compared with model group, the TNF-α expression reduced in acupuncture combined with rehabilitation group on every day after modeling (p<0.01). Compared with acupuncture group, expression reduced in acupuncture combined with rehabilitation group on7rd (p<0.01) and3rd,21st(p<0.05) day after modeling, Compared with rehabilitation group, expression reduced in acupuncture combined with rehabilitation group on14st (p<0.05) day after modeling。Compared with model group, the IL-1β expression reduced in acupuncture combined with rehabilitation group on3rd、7th、14th day (p<0.01) and21rd day(p<0.05). Compared with acupuncture group and rehabilitation group, expression reduced in acupuncture combined with rehabilitation group on3rd,7th (p<0.05).
     5.The expression of skeletal muscle NF-κB-p65/TNF-α IL-1β:On the21st day after modeling, compared with the blank group,there was a significant decrease of NF-κB-p65、 TNF-α、IL-1β expression in the remaining groups (P<0.01), compared with the sham operation group and the blank group,there was a significant increase of NF-κB-p65、TNF-α IL-1β expression in the remaining groups expect of the blank group (P<0.01), compared with acupuncture group, the expression had a significant reduce in rehabilitation group (p<0.05), the expression reduced clearly in acupuncture combined with rehabilitation group (p<0.01), compared with rehabilitation group, the expression reduced in acupuncture combined with rehabilitation group (p<0.05).
     6. The expression of skeletal muscle IRS-1mRNA:On the21st day after modeling, there was the skeletal muscle IRS-1mRNA expression in every group there was a significant decrease of IRS-1mRNA expression in blank group than any others (P<0.01), compared with the sham operation group and the blank group,there was a significant increase of IRS-1mRNA expression in the remaining groups expect of the blank group (P<0.01), compared with acupuncture group, the expression decreased in rehabilitation group (p<0.05),the expression decreased more clearly in acupuncture combined with rehabilitation group (p<0.01), compared with rehabilitation group, the expression decreased in acupuncture combined with rehabilitation group (p<0.05).
     7. The expression of skeletal muscle PI3KmRNA:On the21st day after modeling, there was the skeletal muscle PI3KmRNA expression in every group. There was a significant decrease of PI3KmRNA expression in blank group than any others (P<0.01), compared with the sham operation group and the blank group, there was a significant decrease of PI3KmRNA expression in the remaining groups expect of the blank group (P<0.01). Compared with rehabilitation group and acupuncture group, the expression decreased in acupuncture combined with rehabilitation group (p<0.05).
     Conclusion
     1. Acupuncture and rehabilitation can promote the recovery of neural function of rats after diabetes ischemic stroke, and its effect is superior to the rehabilitation or acupuncture.
     2. Acupuncture and rehabilitation can demote the glucolipid metabolism of rats after diabetes ischemic stroke, making insulin more sensitive, and reverse metabolize abnormal, to improve diseased organism status.
     3. Acupuncture and rehabilitation can demote the NF-κB-p65、TNF-α and IL-1β in brain serum and cerebral ischemic region of rats after diabetes ischemic stroke, and then demote inflammation of ischemic region of cerebral issue and protect the brain.
     4. Acupuncture and rehabilitation can demote the expression of skeletal muscle NF-κB-p65、TNF-α、IL-1β protein in cerebral ischemic region of rats with diabetes ischemic stroke, to help relieve inflammation, making insulin in skeletal muscle more sensitive and demote insulin resistance.
     5. Acupuncture and rehabilitation can promote the expression of skeletal muscle IRS-1mRNA、PI3KmRNA protein in cerebral ischemic region of rats with diabetes ischemic stroke. Improvements demote the insulin resistance of skeletal muscle probability by IRS-1/PI3K signal transduction pathway.
引文
[1]王永炎,栗德林.今日中医内科(下卷)[M].北京:人民卫生出版社,1999:654.
    [2]林兰.中西医结合糖尿病学[M].北京:中国医药科技出版社,1999:318.
    [3]张海燕.2型糖尿病并发脑梗死的危险因素研究[J].第四军医大学学报,2008,29(5):477.
    [4]Kaarisalo MM, Rih l, Sivenius J, et al. Diabetes worsens the outcome of acute ischemic stroke[J].Diabetes Res Clin Pract,2005,69(3):293-298.
    [5]向红丁.住院病例高血压与糖尿病慢性并发症患病率的研究[J].中华流行病学杂志,2003,24(9):819.
    [6]Baird TA, Parsons MW, Barber PA, et al. The influence of diabetes mellitus and hyperglycaemia on stroke incidence and outcome[J].J Clin Neurosci,2002,9:618-626.
    [7]Giorda CB, Avogaro A, Maggini M, et al. Incidence and risk factors for stroke in type 2 diabetic patients:The DAI Study[J]. Stroke,2007,38:1154-1160.
    [8]Kissela BM, Khoury J, Kleindorfer D, et al. Epidemiology of ischemic stroke in patients with diabetes:the greater Cincinnati/Northern Kentucky Stroke Study [J].Diabetes Care,2005,28:355.
    [9]Megherbi SE, Milan C, Minier D, et al. Association between diabetes and stroke on survival and functional outcome 3 months after stroke:data from the European Biomed[J].Stroke,2003,34: 688.
    [10]Bokura H, Kobayashi S, Yamaguchi S, et aLClinical characteristics and prognosis in stroke patients with diabetes mellitus:retrospective evaluation using the Japanese Standard Stroke Registry database (JSSRS)[J]. Brain and Nerve,2006,58:135-139.
    [11]王维治,罗祖明主编.神经病学[M].第5版.北京:人民卫生出版社,2004,147-153.
    [12]Stegmayr B, Asplund K, Kuulasmaa K et al. Stroke incidence and mortality correlated to stroke risk factors in the WHO MONICA Project [J].Stroke,2001,4(28):1362-1367.
    [13]李琳.糖尿病并发缺血性脑卒中研究进展[J].中西医结合心脑血管病杂志,2004,8(2):35-38.
    [14]郭瑜建.胰岛素抵抗与缺血性脑血管病.国外医学·脑血管疾病分册,1998,6(2):28.
    [15]何丽彬,周旭光,孙伟峰,等.胰岛素抵抗及其与缺血性脑血管病关系的研究[J].黑龙江医学,2001,25(3):165-167.
    [16]Capes SE, Hunt D, Malmberg K, et al.Stress hyperglycemia and prognosis of stroke in nondiabetic and diabetic patients:a systematic overview. Stroke.2001,32(10):2426-2432.
    [17]Alvarez-Sabin J, Molina CA, Montaner J, et al. Effects of admission hyperglycemia on stroke outcome in reperfused tissue plasminogen activator-treated patients. Stroke,2003,34(5): 1235-1241.
    [18]Bruno A, Biller J, Adams Hp Jr, et al.Acute blood level and outcome from ischemic stroke.Trial of ORG 10172 in Acute Stroke Treatment (TOAST)investigators.Neurology,1999,52(2):280-284.
    [19]Quinones, M.J., S.B. Nicholas, and C.J. Lyon, Insulin resistance and the endothelium.Curr Diab Rep,2005.5(4):p.246-53.
    [20]Ruggeri, Z.M., Von Willebrand factor, platelets and endothelial cell interactions. J Thromb Haemost,2003.1(7):p.1335-42.
    [21]Anderson RE, Tan WK, Martin HS, et al.Effects of glucose and PaO2 modulation on cortical intracellular acidosis, NADH redox state, and infarction in the ischemic penumbra.Stroke,1999, 30(1):160-170.
    [22]Plengvidhya N, Leelawatana R, Pratipanawatr Tet al. Thailand diabetes registry project:prevalence and risk factors of stroke in Thai diabetic patients[J]. J Med Assoc Thai,2006,1:49-53.
    [23]Kaarisalo, M.M., et al., Diabetes worsens the outcome of acute ischemic stroke.Diabetes Res Clin Pract,2005.69(3):p.293-8.
    [24]DCCT Research Group. Effect of intensive diabetes management on macrOovascular events and risk_factors in the Diabetes Control and Complications Trial. Am J Cardiol,1995.75(14):p. 894-903.
    [25]过阳,曼淑梅,郭津津,等.糖化低密度脂蛋白、氧化低密度脂蛋白与脑梗死的关系[J].临床神经病学杂志,1997,10(6):355-357.
    [26]庞素华,黄文龙.糖尿病合并脑梗塞脑血管舒缩反应能力的研究[J].临床荟萃,1998,13(17):772-773.
    [27]柴伟栋,陈家伟.糖尿病内皮依赖性舒张减弱及其发生机制[J].国外医学内分泌学分册1999,19(2):62-65.
    [28]De Vriese AS, Verbeuren TJ, Vande Vcorde J, et al. Endothelia dysfunction in diabetes. Br J Pharmaca 1.2000,130:963-974.
    [29]Koga, M., et al., Relationship between circulating vascular cell adhesion molecule-1 and microvascular complications in type 2 diabetes mellitus. Diabet Med,1998.15(8):p.661-7.
    [30]戚晓坤.糖尿病与脑梗死[J].继续医学教育,2005,19(9):52-53.
    [31]吴毅,吴军发.2型糖尿病患者的康复治疗与评价[J].中国临床康复,2002,6(15):2202-03.
    [32]Shinozaki K, Naritomi H, Shimizu T, et al.Role of insulin resistance associated with compensatory hyperinsulinemia in ischemic stroke[J].Stroke,1996,27(1):37-43.
    [33]Lyons, T.J., et al., Decrease in skin collagen glycation with improved glycemic control in patients with insulin-dependent diabetes mellitus. J Clin Invest,1991.87(6):p.1910-5.
    [34]McCall, A.L., et al., Effects of hypoglycemia and diabetes on fuel metabolism by rat brain microvessels. Am J Psiol,1988.254(3 Pt 1):p. E272-8.
    [35]陈新勇,吴富东.头针针刺病灶侧和非病灶侧对中风患者脑血流的影响[J].上海针灸杂志,2011,30(9):586-588.
    [36]庞国军,张挺,王可博.头针抽提法治疗脑卒中偏瘫疗效观察[J].上海针灸杂志2012,31(1):11-20.
    [37]吴向琼,李庄.头体针治疗急性期脑梗塞45例疗效观察[J].深圳中西医结合杂志,2012,22(5):285-287,295.
    [38]柴英芳.头针配合体针治疗中风后遗症463例[J],现代中医药,2009,29(6):49-51.
    [39]曾沛金,黎高林.头针结合康复训练对脑卒中患者平衡功能障碍的临床研究[J].中国医药导刊,2012,14(12):2034-2035.
    [40]王利春,刘海燕,王庆海等.针刺内关穴联合康复训练治疗中风后手部痉挛临床研究[J].中西医结合心脑血管病杂志,2011,9(6):689-690.
    [41]林奕君.巨刺法结合康复训练改善脑卒中上肢痉挛的临床研究.福建中医药大学硕士学位论文,2010.
    [42]王红梅.电针治疗中风后遗症[J].中国民族民间医药,2010,100.
    [43]彭慧渊,何希俊,赵明华.电针对脑卒中后抑郁患者日常生活活动能力及生存质量影响[J].上海针灸杂志,2010,29(7):425-427.
    [44]刘克英,泰培森,刘秀梅等.电针阳明经穴治疗缺血性脑卒中及经颅彩色多普勒超声观察[J].中国针灸,2000,20(12):735-737.
    [45]张红星.头针对中风病患者血液流变性、血脂、载脂蛋白的影响[J].中国中医急症,2003,12(5):409-410.
    [46]胡葵,李嘉.针灸治疗肥胖型NIDDM的临床研究[J].上海针灸杂志,2001,20(4):8-9.
    [47]谌剑飞,马雅玲,蔡绍华等.针刺对糖尿病的抗凝与逆转胰岛素抵抗的作用[J].上海针灸杂志.2001,20(4):5-7.
    [48]王玲,刘筱慧.针刺养阴通络法治疗糖尿病性脑梗死临床疗效观察[J].实用中西医结合杂志,2004,4(4):9-10.
    [49]方慧,陈艺.中药合针刺治疗糖尿病脑梗死临床研究[J].浙江中西医结合杂志,2007,17(15):273-274.
    [50]孙志,马丽,韩海荣.针灸对2型糖尿病大鼠胰岛素、抵抗素的作用研究[J].北京中医药大学学报,2010:33(10):718-20.
    [51]梁凤霞,王华,陈泽斌.“双固一通”针法对糖尿病大鼠血清IL-6的影响[J].中国中医药信息杂志,2007,14(1):28-29.
    [52]周逸平,王月兰,汪克明等.针刺心经经脉对自发性高血压大鼠血压及生化指标的影响[J].中国中医药科技,1996,3(6):6-8.
    [53]祁燕,张泳南,谢自敬.针刺对2型糖尿病大鼠胰岛素抵抗的作用[J].中国临床康复,2006,11(20):166-170.
    [54]许娌綵,许能贵,易玮等.针刺对实验性胰岛素抵抗模型血脂及氧自由基代谢的影响[J].现代生物医学进展.2009,9(9):2234-2236:1657-1659.
    [55]薛莉,吉学群,于颂华等.针刺对2型糖尿病大鼠胰岛素抵抗影响的实验研究[J].天津中医药,2004,21(6):479.
    [56]李嘉,袁锦虹.针灸治疗非胰岛素依赖型糖尿病肥胖型的临床观察及作用机理研究[M].南京中医药大学2000届针灸专业硕博士论文.
    [57]张通.急性脑卒中早期康复的研究[J].中国康复医学杂志,2001,16(5):266-272.
    [58]倪朝民.急性脑卒中的早期康复及功能训练时间[J].中国临床康复,2002,6(3):54.
    [59]燕铁斌,窦祖林.实用瘫痪康复[M].人民卫生出版社,2000:205-271.
    [60]Mitchell UH, Myrer JW, Hopkins JT, et al.Neurophy Biological reflex mechanisms'lack of contribution to the success of PNF stretches[J].Sport Rehabil,2009,18(3):343-357.
    [61]缪鸿石.康复医学理论与实践[M].上海,上海科学技术出版社,2000.
    [62]黄永禧,王宁华.中风患者运动再学习方法的原理和应用.中国康复医学杂志[J].1996,11(1):184-185.
    [63]白震民,王安利,李胜志.运动对胰岛素抵抗模型大鼠骨骼肌GLUT4和PKBβmRNA表达的影响[J].北京体育大学学报.2010,33(6):44-46。
    [64]Cesari M, Penninx BS, Pahor M,etc.Inflammatory markers and physical performance in older persons:the InCHIANTI study[J]. J Gerontol Biol Sci Med Sci,2004,59A:242-248.
    [65]Christian P. Fischer Peter Plomga, etc. Endurance training reduces the contraction-induced interleukin-6 mRNA expression in human skeletal muscle[J].Am J Physiol Endoerinol Metab, 2004,287:E1189-1194.
    [66]Straczkkowski M, Kowalska 1, Dzierfis-Straczkowsko S, et c.Changes in tumor necrosis factor-alpha syslem and sensitivity during an exercise training program in obese women with normal and impaired glucose tolerance[J].Eud Endoctnol,2001,145:273-280.
    [67]戴筱英.糖尿病患者餐后不同时间运动的降糖效果[J].中华护理杂志2001,6(12):914-915.
    [68]孙莉敏,胡永善,吴毅社区糖尿病患者运动干预效果评价[J].中国康复医学杂志,2002,17(2):93-96.
    [69]Sreekumar R, Nair KS. Skeletal muscle mitochondrial dysfunction&diabetel [J].Indian J Med Res, 2007,125(3):399-410.
    [70]Archuletaty,Lemieux A m, Vitoon S, et al. Oxidant stress induced loss of IRS-1 and IRS-2 proteins in rat skeletal muscle:Role of p38 MAPK [J]. Free Radical Biology and Medicine 2009, 47(10):1486-1493.
    [71]Zhang Q, Carter E A, Bang-Yi Ma, et al. Molecular mechanism(s) of burn-induced insulin resistance in murine skeletal muscle:Role of IRS phosphorylation [J].Life Sciences,2005,77(24): 3068-3077.
    [72]邵月.耐力运动对糖尿病大鼠血清脂联素、总胆固醇、甘油三酷和胰岛素抵抗指数的影响[J].中国老年学杂志,2012,1(32):318-320.
    [73]周云枫.黄芪多糖对2型糖尿病大鼠肾组织胰岛素信号转导的影响[J].武汉大学学报,2005,26(2):139-143.
    [74]Philippe Gual. Positive and negative regulation of insulin signaling through IRS-1 phosphorylation [J]. Biochimie,2005(1):99-109.
    [75]Tanti J F, Gual P, Gremeaux T, et al. Alteration in insulin action:role of IRS-1 serine phosphorylation in the retroregulation of insulin signalling[J].Annales d Endocrinologie2004,65 (1):43-48.
    [76]许国喜,沈飞.运动对胰岛素抵抗大鼠骨骼肌IRS-1与Tyr磷酸化及氧化应激的影响[J]。西安体育学院学报,2012,1(29):89-93.
    [77]林枫.耐力训练对STZ诱导糖尿病大鼠背根神经节内NF-κB活性的调节作用.硕士毕业论文,南京医科大学,2005.
    [78]Huang J, Upadhyay UM, Tamargo RJ:Inflammation in stroke and focal cerebral ischemia[J]. Surg Neurol,2006,66:232-245.
    [79]Chamorro, A. and J. Hallenbeck, The harms and benefits of inflammatory and immune responses in vascular disease. Stroke,2006.37(2):p.291-3.
    [80]Wang HK, Park UJ, Kim SY, et al. Free radical production in CA 1 neurons induces MIP-1{alpha} expression, microglia recruitment, and delayed neuronal death after transient forebrain ischemia [J].J Neurosci,2008,28:1721-1727.
    [81]Candelario-Jalil E, Yang Y, Rosenberg G.Diverse roles of matrix metalloproteinases and tissue inhibitors of metalloproteinases in neuroinflammation and cerebral ischemia [J]. Neuroscience, 2009,158:983-994.
    [82]Vahedi K, Hofmeijer J, Juettler E, et al. Early decompressive surgery in malignant infarction of the middle cerebral artery:a pooled analysis of three randomised controlled trials [J]. Lancet Neurol, 2007,6:215-222.
    [83]任丽,孙善全.缺血性脑水肿的病理生理研究进展[J].国外医学神经病学:神经外科学分册,2003,30(5):423-427.
    [84]周鸿雁,毛海峰,王一蓉,等.脑缺血损伤的研究进展[J].湖南文理学院学报(自然科版),2005.17(2):73-75.
    [85]Lambertsen KL, Biber K, Finsen B. Inflammatory cytokines in experimental and human stroke[J]. J Cereb Blood Flow Metab.2012; 32(9):1677-1698.
    [86]Whitney NP, Eidem TM, Peng H, et al. Inflammation mediates varying effects in neurogenesis: relevance to the pathogenesis of brain injury and neurodegenerative disorders[J]. J Neurochem, 2009,108(6):1343-1359.
    [87]Ahmad M, Graham SH. Inflammation After Stroke:Mechanisms and Therapeutic Approaches[J]. Transl Stroke Res,2010,1(2):74-84.
    [88]Wang Q, Tang XN, Yenari MA.The inflammatory response in stroke[J]. JNeuroimmunol,2007, 184(1-2):53-68.
    [89]Zhao B Q, Wang S, Kim H Y, et al. Role of matrix metalloproteinases in delayed cortical responses after stroke[J]. Nature Medicine 2006,12(4):441-445.
    [90]段春艳,陈元,李定祥,等.滋阴活血解毒方对局灶性脑缺血模型大鼠血清IL-1β、IL-8、TNF-α含量的影响[J].湖南中医药大学学报,2011,21(1):36-39.
    [91]Yang GY, Schielke GP, Gong C, et al. Expression of tumor necrosis factor-alpha and intercellu adhesion molecule-1 after focal cerebral ischemia in interleukin-1 beta converting enzyme deficient mice[J].J Cereb Blood Flow Metab,1999,19(10):1109-17.
    [92]Sriram K, O'Callaghan JP:Divergent roles for tumor necrosis factor-alpha in the brain. J Neuroimmune Pharmacol 2007,2:140-153.
    [93]Amantea D, Nappi G, Bernardi G, Bagetta G, Corasaniti MT:Post-ischemic braindamage: pathophysiology and role of inflammatory mediators. Febs J 2009,276:13-26.
    [94]Gong C, Qin Z, Betz AL, Liu XH, Yang GY. Cellular localization of tumor necrosis factor alpha following focal cerebral ischemia in mice. Brain Res.1998; 80:1-8.
    [95]Intiso D, Zarrelli MM, Lagioia q et al. Tumor necrosis factor alpha serum levels and inflammatory response in acute ischemic stroke patients [J].Neurol Sci,2004,24:390-396.
    [96]Hallenbeck JM The many faces of tumor necrosis factor in stroke [J].Nat Med,2002,8:1363-1368.
    [97]Rosenzweig HL, Minami M, Lessov NS, et al. Endotoxin preconditioning protects against the cytotoxic effects of TNFalpha after stroke:a novel role for TNFalpha in LPS-ischemic tolerance [J]. J Cereb Blood Flow Metab,2007,27:1663-1674.
    [98]王丽平,边垠,李建媛,等.针刺对急性脑梗塞患者血清肿瘤坏死因子的影响[J],中国针灸,2002,22(2):117-118.
    [99]郭壮丽,裴海涛.头针对急性脑缺血再灌注大鼠脑内肿瘤坏死因子-α表达影响的实验研究[J].针刺研究.2004,29(2):94-97.
    [100]任平,马贤德,关洪全.眼针疗法对急性局灶性脑缺血再灌注大鼠模型血清中TNF-a含量的影响明.中医药导报.2010,16(7):96-97.
    [101]谌剑飞,粱浩荣,马雅玲,等.针刺对糖尿病并发急性脑梗塞血浆自细胞介素-6及肿瘤坏死因子α水平的影响[J].中国中西医结合急救杂志,2001,8(2):92.
    [102]Allan S M, Tyrrell P J, Rothwell N J. lnterleukin-1 and neuronal injury[J]/Nat Rev Immunol,2005, 5(8):629-640.
    [103]Hu S, Peterson PK, Chao CC, Cytokine-mediated neuronal apoptosis[J].Neurochem Int,1997, 30(4-5):427-431.
    [104]Touzani O, Boutin H, Chuquet J, et al. Potential mechanisms of interleukin-1 involvement in cerebral ischaemia[J]. J Neuroimmunol.1999,100(1-2):203-215.
    [105]Rothwell NJ, Luheshi GN:Interleukin 1 in the brain:biology, pathology and therapeutic target. Trends Neurosci 2000,23:618-625.
    [106]Yamasaki Y, Matsuura N, Shozuhara H, Onodera H, Itoyama Y, Kogure K: Interleukin-1 as a pathogenetic mediator of ischemic brain damage in rats. Stroke 1995,26:676-680 (discussion 681).
    [107]Huang FP, Wang ZQ, Wu DC, et al.Early NFkappaB activation is inhibited during focal cerebral ischemia in interleukin-1beta-converting enzyme deficient:mice[J].Neurosci Res,2003,73: 698-707.
    [108]郭永明,梁宪如,杜元灏,等.醒脑开窍针法对局灶性脑缺血大鼠脑组织及血清IL-1含量的影响[J].上海针灸杂志,2004,23(8):35-37.
    [109]刘宗超,周官恩NF-κB与脑缺血[J].中风与神经疾病杂志,2005,22(1):88-90.
    [110]Malek R, Borowicz KK, Jargiello M, et al. Role of NF-kB in the central nervous system. Pharmacol Rep,2007,59:25-33.
    [111]Zhang HL, Gu ZL, Savitz SI, et al. Neuropro tective effects of prostagl andinA(1) in rat models of permanent focal cerebral ischemi a are associated with nuclear factor-kappa B inhibition and peroxisome proliferator-activ ated receptor-gamma up-regulation. J Neurosci Res,2008,86: 1132-1141.
    [112]Yi JH, Park SW, Kapadia R, et al. Role of transcription factors in mediating post-ischemic cerebral inflammation and brain damage. Neurochem Int,2007.50:1014-1027.
    [113]StePhensonD, Yin, TSmalstigEB, HsuMA, PnaettaJ, LittleS, ClemensJ. Transcfiption factor nuclear factor-kappa B is actived in neurons after focalcerebral ischemia[J].Jceerb Blood Flow Metba. 2000,20(3):592-603.
    [114]Ritchie ME. Nuclear factor 2 kappa B is selectively and markedly activated in humans with unstable angina pectoris[J].Circulation,1998,98(17):1707-1713.
    [115]孔立红,刘胜洪,毛娟娟,等.电针对脑缺血大鼠NF-κB及TNF-a表达的影响[J].中国康复医学杂志,2009,24(8):711-714.
    [116]李秀钧,邬云红.糖尿病是一种炎症性疾病?[J].中华内分泌代谢杂2003,19(4):251-253.
    [117]Ross R. Atherosclerosis:an inflammatory disease[J].N Engl J Med.1999.340(2):115-126.
    [118]Ding C, He Q, Li PA, et al. Diabetes increases expression of IC AM after a brief period of cerebral ischemia[J].Neuroimmunology,2005,161:61-67.
    [119]O, Harre J A.Prevalence and forms of neuropathic morbidity in 800 diabetes[J].Ir J Med Sci,1994, 163:132-135.
    [120]谷春华,刘囡杰,杨立波,等.代谢综合征临床研究进展[J].中国中医药信息杂志,2004,11(6):548-560.
    [121]薛冰,母义明NF-κB信号转导通路与胰岛素抵抗[J].辽宁中医药大学学报.2012,8(14):68-71.
    [122]Peter J Bamees, Michael Karin.Nuclear factor-kB-a pivotal transcri -ption factor in chronic inflammatory diseases[J].N Engl J Med,1997,336(15):1066-1071.
    [123]李秀钧.胰岛素抵抗综合征[M].北京:人民卫生出版社,59-69.
    [124]潘长玉,尹士男.胰岛素抵抗-2型糖尿病发病机制的重要因素[J].中华内分泌代谢杂志,2000,16(1):56-57.
    [125]Cusi K, Maezono K, Oaman A et al. Insulin resistance differentially affects the pi3-kinase-and MAP kinase-me-diated signaling in human muscle [J]. J Clin Invest,2000,105:311-320.
    [126]Sun XJ, rothenberg P, Kahn CR, et al. Structure of the insulin receptor substrate IRS-1 defines a unique signal transduction protein. Nature,1991,352(6630):73-77
    [127]Tanti JF, Gremeaux T, Grillo S, et al. Overexpression of constitutively active form of phosphatidylinlsitol 3-kinase is sufficient to promote Glut4 translocation in adipocytes. J Biol Chem, 1996,271:25227-25232.
    [128]Tamemoto H, Kadowaki T, Tobe K, et al.Insulin resistance and growth retardation in mice lacking insulin receptor substrate-1 [J].Nature,1994,372(6502):182-186.
    [129]White MF, Kahn CR. The insulin signaling system. J Biol Chem,1994,269(1):1-4.
    [130]Osaki M, Oshimura M, Ito H. PI3K-Akt pathway:its functions and alterations in human cancer. Apoptosis,2004,9(6):667-676
    [131]Kampmann U, Christensen B, Nielsen TS, et al. GLUT4 and UBC9 Protein Expression Is Reduced in Muscle from Type 2 Diabetic Patients with Severe Insulin Resistance. PLoS ONE,2011,6(11): e27854.
    [132]王艳军,尤雪娜,PI3K, P70S6K在胰岛素抵抗大鼠脂肪中的表达及其意义.中国老年学杂志,2008,28(3):559-561.
    [133]Kadowaki T. Insights into insulin resistance and type 2 diabetes from knockout mouse models. J Clin Invest,2000,106(4):459-466.
    [134]李焱,炎症与胰岛素抵抗.中华糖尿病杂志,2005,13(2):81-82.
    [135]何积源.慢性炎症与代谢综合征[M].内科,2010,5(1):67-70.
    [136]Wilkinson2Berka JL, Kelly DJ, Koerner SM, et al.ALT-946 and an inoguanidine, inhibitors of advanced glycation, improve sever nephropathy in the diabetic transgenic (mREN-2) 27 rats [J].Diabetes,2002,51(11):3283-3289.
    [137]李光伟,潘孝仁,Stephen L, et al检测人群胰岛素敏感性的一项新指数,中华内科杂志1993,32(10):656-660.
    [138]Schmittgen T D, Livak K J. Analyzing real-time PCR data by the comparative C(T) method[J]. Nat Protoc.2008.3(6):1101-8.
    [139]Tseng C P, Cheng A J, chang J T, et al. Quantitative analysis of multidrug-resistance mdrl gene etpression in head and neck cancer by real-time RT-PCR[J]. Jpn J Cancer Res,2002,93(11):1230-6.
    [140]MC GARRY J D. Banting lecture 2001:dysregulation of fatty acid metabolism in the etiology of type 2 diabetes[J].Diabetes.2002,51(1):7-18.
    [141]蒋升,谢自敬,张莉.链脲佐菌素诱导1型糖尿病大鼠模型稳定性观察.[J].中国比较医学杂志.2006.16:16-18.
    [142]王拥军,卢德宏,崔丽瑛,等.现代神经病学进展.北京:科学技术文献出版社,2004.7.
    [143]SmithML, Bendek G, Dahlgren N, etal. Models for studying long-term recovery following forebrain ischemia in the rat:A 2-vessel occlusion model. Acta Neurol Scand,1984,69:385.
    [144]马学玲,徐荣,刘亢丁.局灶性脑缺血实验动物模型原理及适用范围[J].武警医学2005,16(2):131-134.
    [145]刘亢丁,苏志强,李逸平,等.实验性局灶性脑缺血再灌注动物模型的改进与评价[J].中风与神经疾病杂志,1997,14:87-89.
    [146]辛世萌,刘远洪,聂志余.栓线长度,直径及大鼠体重与栓线法大鼠局灶性脑缺血模型关系的研究.[J].大连医科大学学报,200022:105-107.
    [147]唐强,朱路文.脑缺血大鼠康复方法研究进展[J].中国康复医学杂志,2011,26(11):1091-1093.
    [148]王希佳,刘庆宪,宋永建,等.糖尿病合并脑梗死60例临床分析[J].浙江临床医学,2004,2(6):4:31-34.
    [149]屈传强,郭洪志.糖尿病中枢神经病变特征及发病机制新进展[J].临床神经病学杂志,2003,3(16):18-22.
    [150]李光伟.胰岛素敏感性评估及其在临床研究中的应用[J].中华内分泌代谢杂志2000,16(3):198-200.
    [151]Acalovschi D, Wiest T, Hartmann M, et al. Multiple levels of regulation of the interleukin-6 system in stroke [J]. Stroke,2003,34:1864-1869.
    [152]Zhao, H., G.K. Steinberg, and R.M. Sapolsky, General versus specific actions of mild-moderate hypothermia in attenuating cerebral ischemic damage. J Cereb Blood Flow Metab,2007.27(12):p. 1879-94.
    [153]张桂兰,蔡玉洁,血液中炎症因子水平对于急性脑缺血性卒中预后的评估[J].医学理论与实践,2014,27(2):181-183.
    [154]Gabriel C, Justicia C, Camins A, et al. Activation of nuclear factor-kappa B in the rat brain after transient focal ischemia. Brain Res Mol Brain Res 1999; 65(1):61-9.
    [155]Nurmi A, Lindsberg PJ, Koistinaho M, et al.Nuclear factor-kappa B contributes to infarction after permanent focal ischemia.Stroke 2004; 35(4):987-91.
    [156]Liu T, Clark RK, et al.Tumor necrosis factor-a expression in ischemic neurons[J].Stroke,1994, 25:1481-1488.
    [157]Czemak B J, Sarma V, Bless N M, et al.In vitro and in vivo dependency of chemokine generation on CSa and TNF-a[J].Immunol,1999,162(4):2321-2325.
    [158]Hara H, Fink K, Endres M, et a 1. Attenuation trasient focol cerebral ischemic injury in transgenic m expressing a mutant ICE inhibitory protein[J]. Cereb Blood Fliw Metab,1997,17(4):370-375.
    [159]Lin HY, Huang CC, Chang KF.Lipopolysaccharide preconditioning reduces neuroinflammation against hypoxic ischemia and provides long-term outcome of neuroprotection in neonatal rat [J].Pediatr Res,2009,66(3):254-259.
    [160]Zaremba J, Losy J.Cytokines in clinical and experimental ischemic stroke. [J].Neurol Neurochir Pol,2004,38:57-62.
    [161]Qin B, Anderson RA, A deliK. Tumor necrosis factor-di rectly stimulates the overproduction of hepatic apolipoprote in B100-containing VLDL via impairment of hepatic insulin signaling [J].Am J Physiol G astrointest Liver Physiol,2008,294:G 1120-1129.
    [162]张健颖,张颖冬.缺血性脑损害病理生理过程的炎症反应[J].中华脑血管病杂志(电子版),2011,5(2):122-131.
    [163]Pola R. Inflammatory markers for ischaemic stroke[J]. Thromb Haemost 2009,101(5):800-801.
    [164]Moskowitz MA, Lo EH, Iadecola C. The Science of Stroke:Mechanisms in Search of Treatments[J]. Neuron 2010.67(2):181-198.
    [165]Denes A, Thornton P, Rothwell N J, et al. Inflammation and brain injury:acute cerebral ischaemia, peripheral and central inflammation[J].Brain Behav lmmun,2010,24(5):708-723.
    [166]俞悦,刘柏炎.脑缺血后炎症反应对神经发生的影响.国际脑血管病杂志,2011,19(10): 797-800.
    [167]Nilupul Perera, M., et al., Inflammation following stroke. J Clin Neurosci,2006.13(1):p.1-8.
    [168]Huang CY, Fujimura M, Noshita N, et aLSOD1 down-regulates NF-kappaB and c-Myc expression in mice after transient focal cerebral ischemia [J].J Cereb Blood Flow Metab,2001,21:163-173.
    [169]Nurmi A, Lindsberg PJ, Koistinaho M, et al. Nuclear factor-kappaB contributes to infarction after permanent focal ischemia [J]. Stroke,2004,35:987-991.
    [170]Taylor, C.T., A.L. Dzus&S. P. Colgan. Autocrine regulation of epithelial permeability by hypoxia: role for polarized release of tumor necrosis factor alpha [J].Gastroenterol,1998,114:657-668.
    [171]Kunz A, Abe T, Hochrainer K, et aLNuclear factor-kappaB activation and postischemic inflammation are suppressed in CD36-null mice after middle cerebral artery occlusion [J]. Neurosci,2008,28:1649-1658.
    [172]马惠芳,图娅.“十二井穴”针法对局灶性脑缺血大鼠脑皮质及血清肿瘤坏死因子-α含量的影响[J].针刺研究,2006,31(1):35-42.
    [173]Loddick SA,Rothwell NJ.Mechanisms of tumor necrosis factor alpha action on neurodey eneration: interaction with insulin-like gruwth factor [J].Prol Nstl Acad Sci USA,1999,96(17):9449-9451.
    [174]周晓磊,张鹏,核因子-κB信号途径与胰岛素抵抗关系的研究进展[J].天津医科大学学报.2020(1):77-80.
    [175]Sriwijitkam ol A, Christ-Roberts C, Berria R, et al. Reduced skeletal muscle inhibitor of kappaB beta content is associated with insulin resistance in subjects with type 2 diabetes:reversal by exercise training[J].Diabetes,2006,55:760-767.
    [176]Zhang H, Park Y, Wu J, etc. Role of TNF-alpha in vascular dysf unction[J].Clin Sci (Lond),2009, 116(3):219-2130.
    [177]Phillips MD, Flynn MG, McFarlin BK, et al. Resistive exercise blunts LPS-stimulated TNF-alpha and IL-1 beta [J].Int J Sports Med,2008,29(2):102-109.
    [178]Zhang JZ, Jing L, Ma AL, et al.Hyperglycemia increased brain ischemia injury through extracellular signalregulated protein kinase [J].Pathol Res Pract,2006,202:31-36.
    [179]Gang Y, Juanjuan D, Tao W. Tissue Kallikrein Reverses Insulin Resistance and Attenuates Nephropathy in Diabetic Rats by Activation of Pathosphatidylinositol 3-Kinase/Protein Kinase B and Adenosine5'-Monophosphate-Activated Protein Kinase Signaling Pathways [J]. Endocninology,2007,148; 2016-2026.

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