针灸对HIBD模型幼鼠NF-κb、Caspase-3蛋白表达的影响
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
背景
     新生儿缺氧缺血性脑病(hypoxic-ischemic brain damage, HIBD)是指由于围生期窒息、缺氧所导致的脑缺氧缺血性损害,临床出现一系列神经系统异常的表现。常见于严重窒息的足月新生儿,严重者可死于新生儿早期,幸存者多留有神经系统损伤后后遗症,如智能低下、脑瘫、癫痫、共济失调等。是围生期脑损伤的最重要原因。
     大量研究表明HIBD的发病原因及发病机制极为复杂,多方面综合因素有关,但存在共同的病理变化,即脑部缺氧缺血,引起脑区神经细胞凋亡,并且神经元细胞凋亡的发生与HIBD患儿的预后有着密切的联系。神经细胞凋亡受一系列基因表达的调控,表现在缺血损伤后许多基因转录翻译,这些基因编码合成的蛋白质产物直接或间接参与了脑缺血后神经元凋亡过程。在参与调控神经元凋亡的基因和蛋白质产物中,核因子κB (nuclear factor-κB, NF-κB)和caspase-3备受关注。
     针灸作为祖国医学的重要主成部分,在小儿脑瘫临床研究方面,取得了较好的成绩,明显改善了脑瘫患儿的神经功能缺损症状,但基础研究方面,开展较少,具体机制尚不清楚。本课题组,前期观察到了早期针灸干预缺血缺氧损伤的病理模型,可以对脑组织单胺类神经递质与氨基酸含量,以及细胞凋亡相关的Bax与Bcl-2造成影响。缺血缺氧损伤后的病理改变机制,甚为复杂,针灸干预可能是多方面的综合作用,借此,本研究在前期工作基础上,观察早期针灸干预对核因子-κB (nuclear factor-κB, NF-kB)和caspase-3基因表达的影响,试图从多方面探讨针灸对于新生儿缺血缺氧性脑病的作用机制。
     目的
     观察针刺结合艾灸督脉对脑瘫模型幼鼠运动功能、平衡功能、学习记忆功能及脑组织神经细胞凋亡相关NF-Kb、Caspase-3蛋白表达的影响,探讨早期针灸治疗小儿脑瘫凋亡相关的作用机制,为针灸疗法的临床应用提供客观的科学依据。
     方法
     (一)HIBD模型造模方法
     SPF级7日龄新生SD幼鼠,在室温26℃环境下,用皮筋在手术台上固定造模组幼鼠的四肢及头部,在乙醚吸入浅麻醉下,小心剪开颈部皮肤,分离迷走神经并暴露左侧颈总动脉,用细丝线双线结扎该动脉并中间离断,造成永久性断流。缝合好皮肤后放入37℃恒温水浴容器中恢复2h,然后密闭容器,整个手术时间控制在5min内,保证实验幼鼠皮肤红润。如果动物出血或者呼吸抑制,则弃去不用。以1.0L/min流速将含8%氧气的92%氮氧混合气持续通入缺氧箱中,缺氧箱置于水温37℃的恒温水浴锅内,缺氧2.5h,1h后作行为测定。
     (二)分组及治疗方法
     1.正常组:仅同方式抓取,不做造模及治疗干预。
     2.假手术组:麻醉后分离左颈总动脉,但不结扎,术后亦不作低氧处理
     3.模型组:进行造模,不做治疗干预。
     4.针刺组:所有需要针刺治疗的小鼠针四肢及头部穴位。以直径2mm,长20mm的针灸针,先在“内关”、“涌泉”速刺不留针,然后针四肢及头部穴位。四肢穴位“曲池”、“足三里”穴针1分深左右,头部穴位“百会”、“颞Ⅰ针”平刺,进针后觉针下沉紧即可,留针10min。
     5.针刺+艾灸组:针刺基础上结合艾灸督脉,温和灸“督脉”10分钟。
     (三)定位方法:
     穴位定位参照《实验针灸学》,结合人与动物骨度类比:“督脉”为尾根与肛门之间的凹陷中;顶骨正中定“百会”;外耳道口直上0.8cm处模拟“颞Ⅰ针”;桡骨近端的关节外侧,离腕关节约3mm左右的尺桡骨缝间取“内关”;“曲池”位于桡骨近端的关节外侧前方的凹陷中;“足三里”在膝关节后外侧,腓骨小头下约5mm处;后肢掌心前正中取“涌泉”。
     (四)治疗时间
     手术当天称重,术后1d休息,术后2d检测悬吊试验和斜坡试验,术后3d开始治疗6天,术后9d检测悬吊试验和斜坡试验,术后10再次治疗6天,术后16d检测悬吊试验和斜坡试验,术后18d称重。
     (五)指标观测
     1.行为运动能力及学习记忆能力测试:悬吊试验、斜坡试验、Y迷宫试验
     2.脑组织病理学形态:HE染色病理检查
     3.脑组织中NF-Kb、Caspase-3蛋白表达:免疫组化法测结果
     1.造模情况:死亡率18/54=33.3%,成功率33/54=61.11%
     2.体重变化
     治疗前各组幼鼠体重比较,差异无统计学意义(P>0.05),说明各组幼鼠之间体重均衡,组间具有可比性。治疗后,自身前后比较:五组的治疗后体重均高于治疗前,差异有统计学意义(P<0.05);组间比较,差异有统计学意义(P<0.05);进行两两比较后,模型组体重明显低于其他组,差异有统计学意义(P<0.05);进行两次体重测量的差值进行比较,组间差异有统计学意义(P<0.05);两两比较后,正常组、假手术组、针刺结合艾灸组比较差异无统计学意义(P>0.05);模型组、单纯针刺组明显低于其他三组,差异有统计学意义(P<0.05);单纯针刺组高于模型组,差异有统计学意义(P<0.05);
     3.悬吊试验
     相同时间点,不同组间悬吊时间比较:治疗前,模型组、单纯针刺组、针刺结合艾灸组都低于正常组与假手术组(P<0.05);第一阶段治疗后,模型组、单纯针刺组、针刺结合艾灸组仍全部低于正常组与假手术组(P<0.05);但针刺结合艾灸组高于模型组及单纯针刺组(P<0.05);第二阶段治疗后,模型组、单纯针刺组、针刺结合艾灸组仍全部低于正常组与假手术组(P<0.05);但针刺结合艾灸组高于模型组及单纯针刺组(P<0.05);单纯针刺组高于模型组(P<0.05)。
     同一组别,不同时间点悬吊时间比较:各组幼鼠治疗前、第一阶段治疗后、与第二阶段治疗后悬吊时间比较,差异有统计学意义(P<0.05);分别进行两两比较,五组均存在:幼鼠悬吊时间第一阶段治疗后高于治疗前,第二阶段高于第一阶段,差异均有统计学意义(P<0.05)。
     4.斜坡试验
     相同时间点,不同组间斜坡时间比较:治疗前,模型组、单纯针刺组、针刺结合艾灸组都低于正常组与假手术组(P<0.05);第一、二阶段治疗后,模型组、单纯针刺组、针刺结合艾灸组仍全部低于正常组与假手术组(P<0.05);但针刺结合艾灸组高于模型组及单纯针刺组(P<0.05);单纯针刺组高于模型组(P<0.05)。
     同一组别,不同时间点斜坡时间比较:各组幼鼠治疗前、第一阶段治疗后、与第二阶段治疗后悬吊时间比较,差异有统计学意义(P<0.05);分别进行两两比较,五组均存在:幼鼠斜坡时间第一阶段治疗后高于治疗前,第二阶段高于第一阶段,差异均有统计学意义(P<0.05)。
     5.Y迷宫结果
     各组幼鼠Y迷宫正确次数不同,差异有统计学意义(P<0.05),进行两两比较,除正常组与假手术组比较,差异无统计学意义(P>0.05)外,其余组间两两比较,差异均有统计学意义(P<0.05);由高到低依次为针刺+艾灸组、单纯针刺组、模型组。
     6.脑组织病理改变
     脑组织常规石蜡切片:HE染色,神经细胞胞浆呈淡紫色,核呈蓝黑色。正常组及假手术组神经细胞结构正常,胞浆丰富,胞核清晰可见,海马锥体细胞3-4层,相邻细胞间排列紧密。模型组皮层变薄,大部分神经元变性,体积变小,核固缩成不规则形,核仁消失,胞核与胞浆界限模糊。单纯针刺组有少量神经细胞变性,体积变小,核固缩少见。单纯针刺结合艾灸组神经细胞排列仍不整齐,少量神经元变性。针刺结合艾灸组神经细胞形态、排列基本正常,仅有少量的神经细胞变性,零星可见极少量损伤细胞,海马锥体细胞1-3层,相邻细胞排列比较紧密。
     7.各组大鼠脑皮质正常神经细胞数目的比较
     与正常组比较,模型组脑皮质正常神经细胞数目低于正常组及假手术组,差异具有统计学意义(P<0.05);与模型组比较,针刺组、针灸组高于模型组正常神经细胞数目,差异具有统计学意义(P<0.05);针刺组与针灸组比较,差异无统计学意义(P>0.05)。
     8.脑组织NF-Kb蛋白表达
     光密度值,与正常组比较,模型组脑组织NF-Kb蛋白表达高于正常组及假手术组,差异具有统计学意义(P<0.05);与模型组比较,针刺组、针灸组低于模型组,差异具有统计学意义(P<0.05);针刺组与针灸组比较,差异无统计学意义(P>0.05)。
     9.脑组织Caspase-3蛋白表达
     正常组及假手术组,仅在皮层个别区域有少量Caspase-3阳性细胞。模型组中,皮层出现明显的Caspase-3免疫阳性细胞,其平均光密度值与正常组比较,差异有统计学意义(P<0.05);针刺及针灸治疗后Caspase-3蛋白表达较模型组明显减少,差异有统计学意义(P<0.05);针刺组和针灸组间Caspase-3表达,差异无统计学意义(P>0.05)。
     结论
     1.缺血缺氧性损伤引起了幼鼠脑神经细胞凋亡,并且与细胞凋亡NF-κB、caspase-3基因表达密切相关。
     2.早期针灸干预对脑瘫幼鼠肌力(悬吊试验),平衡能力(斜坡试验)、学习记忆功能(Y迷宫)均有促进作用,并且针刺结合艾灸优于单纯针刺组。
     3.早期针灸干预对影响了脑瘫幼鼠脑组织病理形态学改变,治疗后,变性神经细胞数量显著减少,零星可见一些损伤细胞,海马锥体细胞层细胞形态、排列基本正常。
     4.早期针灸干预对脑瘫幼鼠脑组织神经细胞凋亡NF-κB、caspase-3基因表达具有良性调节作用,可能是针灸疗法治疗小儿脑瘫的作用机制。
Background
     Neonatal hypoxic-ischemic brain damage (HIBD) is due to asphyxia caused cerebral blood supply and gas exchange impairment caused by a brain injury, a serious disease endangering the health of newborn lives, have a higher morbidity and mortality, also one of the important reasons contributed to children's mental retardation, cerebral palsy and other neurological disabilities. The causes and pathogenesis of HIBD are more complex; more and more evidence has showed that apoptosis is also involved and plays a unique role. The occurrence of neuronal apoptosis and prognosis in children is closely linked. At the molecular level, apoptosis is affected by many genes and the regulation of cytokines, nuclear factor-κB and caspase-3 are the research focus.
     Acupuncture and moxibustion are the important part of traditional Chinese medicine.They are very useful for children with cerebral palsy. We have did a lot of work in clinical research, but a little work in experiment research. We could not understand clearly the specific mechanism of acupuncture and moxibustion. For of all the reasons, our team investigated the effect of acupuncture and moxibustion under governor vessel treatment on movement function, balance function, study and memery function, and brain NF-Kb, Caspase-3 expressing in the HIBD rats. Attempts to explore the mechanism of acupuncture and moxibustion for hypoxic-ischemic brain damage from various aspects.
     Objective
     To investigate the effect of acupuncture and moxibustion under governor vessel treatment on movement function, balance function, study and memery function, and brain NF-Kb、Caspase-3 expressing in the CP rats. Meanwhile, to understand the mechanism of early acupuncture and moxibustion treatment for CP, and to provide the theoretical basis for the promotion of early acupuncture and moxibustion treatment in clinical use for children with cerebral palsy.
     Methods
     1. Established a simulation model of perinatal asphyxia HIBD
     2. The animals were randomly divided into five groups:normal group, sham group, model group, simple acupuncture group and acupuncture with moxibustion group. We developed a treatment timetable with acupoints reference from (Study of experimental acupuncture), combining human and animal bones analogy: acupoints taken for treatment include parietal bone center for'Baihui' external ear canal, straight 0.8cm simulate take'Temporal 1 needle'; radial bone proximal lateral aspect from the wrist off 3cm or so take'Neiguan' radius proximal lateral joint when elbow is flexed take'Quchi'; anterior aspect of lower leg under the fibular head and about 5mm take'Zusanli' hind legs before the middle of the sole take'Yongquan'. After treatment for two stages, separately carry out tests for HIBD mouse model on behavior motor ability and on learning and memory ability, and then after mice were sacrificed, examine the model mouse brain tissue and related gene expression targets.
     3. Hanging test, Slope test and Y maze test were used for valuing neuroethology function in different groups.
     The method of immunohistochemistry was used to observe the HIDB mouse dynamic expression of apoptosis regulatory proteins NF-Kb and Caspase-3.
     Results
     1. Modeling results
     Mortality rate:33.3%, Success rate:61.11%
     2. Change of weight
     Multiple comparison results showed that:the normal group, sham operation group, acupuncture group, acupuncture and moxibustion group were no significant difference between the four groups, model group and acupuncture group was no statistical difference neither. The first four groups compared with the other groups, P<0.01, both statistically significant weight gain can be considered the first four group weight gain more than two groups. Area group F=15.897, P>0.05, shows that factors between area group was not statistically significant.
     Before intervention, there were no significant difference among five groups. After intervention, the weight of rats were heavier than before. Model group was lighter than other groups. From heavy to light, the order was normal group, sham operation group, acupuncture and moxibustion group, acupuncture group and model group.
     3. Hanging test
     Before intervention, model group, acupuncture group and acupuncture with moxibustion group were worse than normal group and sham operation group.
     After the first treatment, the situation was the same as before., but acupuncture with moxibustion group was better than acupuncture group
     After the second treatment, model group, acupuncture group and acupuncture with moxibustion group were also worse than normal group and sham operation group. From better to worse,the order was acupuncture and moxibustion group, acupuncture group and model group.
     After intervention, the valu of Hanging test were better than before in five groups.
     4. Slope test
     Before intervention, model group, acupuncture group and acupuncture with moxibustion group were worse than normal group and sham operation group.
     After the first treatment, the situation was the same as before., but acupuncture with moxibustion group was better than acupuncture group
     After the second treatment, model group, acupuncture group and acupuncture with moxibustion group were also worse than normal group and sham operation group. From better to worse, the order was acupuncture and moxibustion group, acupuncture group and model group.
     After intervention, the valu of Slope test were better than before in five groups.
     5. Y maze test
     The times of right movement, there were significant difference among five groups. From better to worse, the order was acupuncture and moxibustion group, acupuncture group, model group, normal group and sham operation group.
     6. Pathological changes in brain tissue
     HE staining:normal light microscope under 10X20 times for each section were observed within 5 View pathological changes after cerebral ischemia. Each group were pathological changes in rat brain:brain tissue of paraffin, HE staining, nerve cells of pale red, blue-black nuclear was. Normal control group and the sham operation group structure of the normal cortical brain cells, clear nucleus, cytoplasm-rich, interstitial edema-free performance, hippocampal pyramidal cells in 2 to 3 layers, closely arranged, round and large nucleus, clear nucleolus. Model group, cortical thinning, part of the neuronal degeneration and smaller, the nucleus and cytoplasm of ambiguous nuclear fast shrunk triangles or irregular, nucleoli disappear. Reduce hippocampal pyramidal cell layer, arranged in sparse, irregular, smaller cell volume, nuclear condensation phenomenon can be seen. Acupuncture group, acupuncture combined with moxibustion group, there are different degrees of nerve cell degeneration, but significantly reduced the number of nerve cell degeneration, sporadic seen a number of injured cells, hippocampal pyramidal cell layer of cell morphology, arrangement normal.
     7. Counting of normal nerve cells in brain cortex
     Model group was worse than normal group and sham operation group.
     Acupuncture with moxibustion group and acupuncture group were better than model group. There were no significant difference between acupuncture with moxibustion group and acupuncture group.
     8. Expressing of proteins NF-Κb
     Model group was worse than normal group and sham operation group.
     Acupuncture with moxibustion group and acupuncture group were better than model group. There were no significant difference between acupuncture with moxibustion group and acupuncture group.
     9. Expressing of proteins Caspase-3
     Model group was worse than normal group and sham operation group.
     Acupuncture with moxibustion group and acupuncture group were better than model group. There were no significant difference between acupuncture with moxibustion group and acupuncture group.
     Conclusion
     1. Hypoxic-ischemic brain injury in rats caused neural cell apoptosis. There were clsed relationship between neural cell apoptosis and expressing of proteins NF-Κb and Caspase-3.
     2. The therapy of early combining acupuncture with moxibustion was useful for the improvement of neural function, and acupuncture with moxibustion group was better than acupuncture group.
     3. The therapy of early combining acupuncture could improve the pathological changes in brain tissue.
     4. The therapy of early combining acupuncture has positive regulation in the expressing of proteins NF-Kb and Caspase-3.
引文
[1]袁青.靳三针问答图解.广东经济出版社.2003:23-35
    [2]陈秀洁,李树春.小儿脑性瘫痪的定义、分型和诊断条件[J].中华物理医学与康复杂志,2007,29(5):309
    [3]Sundrum R, Logan S, Wallace A, etal. Cerebral palsy and socioeconomics tatus:A ret rospective cohort study[J]. Arch Dis Child,2005,90:15-18
    [4]林庆,李松,刘建蒙,等.我国六省(区)小儿脑性瘫痪患病率及临床类型的调查分析[J].中华儿科杂志,2001,39:613-615
    [5]Cans C. Surveillance of cerebral palsy in Europe:a collaboration of cerebral palsy surveys and registers.Surveillance of Cerebral Palsy in Europe(SCPE)[J].Dev Med Child Neurol,2000,42(12):816-824
    [6]陈秀洁,李树春.小儿脑性瘫痪的定义、分型和诊断条件[J].中华物理医学与康复杂志,2007,29(5):309
    [7]Han TR, Bang MS,Lim JY, etal. Risk factors of cerebral palsy in preterm infants[J]. Am J Phys Med Rehabil,2002,81(4):297-303
    [8]Gibbs RS. The relationship between infections and adverse pregnancy outcomes:an overview[J]. Ann Periodontol,2001,6(1):153-163
    [9]李松,林庆,刘建蒙,等.中国六省及自治区小儿脑性瘫痪患病状况的调查[J].中华医学杂志,2001,81(20):1220-1223
    [10]钟佑泉,吴惧,吴康敏,等.四川乐山地区308例脑性瘫痪儿童危险因素的病例对照研究[J].中华预防医学杂志,2002,36(5):323-326
    [11]Schendel DE, Schuchat A, Thorsen P. Public health issues related to infection in pregnancy and cerebral palsy[J]. Ment Retard Dev Disabil Res Rev, 2002,8(1):39-45
    [12]Schendel DE. Infection in pregnancy and cerebral palsy [J]. J Am Med Womens Assoc,2001,56(3):105-108
    [13]Minagawa K, Tsuji Y, Ueda H, et al. Possible correlation between high levels of IL-18 in the cord blood of preterm infants and neonata ldevelopment of periventricular leukom alacia and cerebral palsy[J]. Cytokine,2002,17:164-170
    [14]Stanley F, Blair E, Alberman E.Cerebral Palsies:Epidemiology and Causal Pathways[M]. London:Cambridge:Cambridge University Press,2000
    [15]Palmer L. Antenatal antecedents of moderate and severe cerebral palsy [J].Paediatric and Perinatal Epidemiology,1995,9(2):171-184
    [16]Schneider H. Birth asphyxia-an unsolved problem of perinatal medicine [J].Z Geburtshilfe Neonatol,2001,205(6):205-212
    [17]Yagev Y, Koren G. Eating Fish During Pregnancy:Risk of Exposure to ToxicLevels of Methylmercury[J]. Canadian Family Physician,2002,48: 1619-1621
    [18]Dolk H, Pattenden, Johnson A. Cerebral Palsy, lowbirth weight and socioeconomic deprivation:inequalities in a major cause of childhood disability[J]. Paediatric and Perinatal Epidemiology,2001,15:359-363
    [19]陈惠金.早产儿脑室周围白质软化[J].中国实用儿科杂志,2001,16(7):433-434
    [20]Gururaj A, Sztriha L, Dawodu A, etal. CT and MRI patterns of hypoxic ischemic brain damage following perinatal asphyxia [J]. J Trop Pediatr,2002,48(1):529
    [21]Legido A, Katsetos CD. Cerebral palsy:new pathogenetic concepts[J]. Rev Neurol,2003,36(2):157-165
    [22]吴仕孝.胎儿窘迫与宫内复苏新生儿窒息的诊断与急救[J].中国实用妇科与产科杂志,2000;16(1):18
    [23]徐发林,朱长连.脑发育过程与缺血缺氧性脑损伤的关系[J].国际儿科学杂志,2008,35(1)10
    [24]邢莹.神经分子生物学[M].郑州:河南医科大学出版社,1999;129-134
    [25]陈健,江莲,武秀华等.缺氧缺血时新生大鼠脑中谷氨酸含量的变化及[J].河北医科大学学报2004,25(1)21-24
    [26]韩济生主编.神经科学纲要[M].北京:北京医科大学&协和医科大学联合出版社,1993:351-395
    [27]Frank MG, Neonatal treatments with the serotonin uptake inhibitors clomipramine and zimelidine, but not the noradrenaline uptake inhibitor desipramine [J].Disrupt sleep patterns in adult rats, Brain Res,1997,768: 287-293
    [28]Potenza MN, Hollander E. Pathologic gambling and impulse control disorders. Neuropsychopharmacology;2002.14 (25):43
    [29]黄克维,吴丽娟.临床神经病理学[M].北京:人民军医出版社,1999;1-2
    [30]陈健,江莲,武秀华等.缺氧缺血时新生大鼠脑中谷氨酸含量的变化及[J].河北医科大学学报2004,25(1)21-24
    [31]MargotC. La Pointe Molecular regulation Of the brain natriuretic Peptide gene. Peptides,2005;26(6):944-956
    [32]Zhenggang Zhang, Michael Chopp, Anton Goussev et al.Cereral vessels express interleukin 1 B after focal cerebral ischemia. Brain Research, 1998:784:210-217
    [33]Shuying Lin, Lir-Wan Fan, Yi Pang, et al. IGF-1 protects oligodendrocyte progenitor cells and improves neurological functions following cerebral hypoxia-ischemia in the neonatal rat Brain Research,2005;1063(1):15-26
    [34]Evangelia Spandou, Stamatia et al. Hypoxia-ischemia affects erythropoietin and erythropoietin receptor expression pattern in the neonatal rat brain Brain Research,2004;1021(2):167-172
    [35]Gustafson K, Hegherg H,Bengtsson BA,et al.Possible protective role of growth hormone in hypoxicischemia in neonatal rats. Pediatr Res,1999;45(3):318
    [36]Xiao Y.Xia, Tomoake Ikeda, et al.Heat shock protein 72 expression and microtubule-associated protein 2 disappearance after hypoxia-ischemia in the developing rat brain, American Journal of Obstertics and Gynecology,1999; 180(50:1254-1256
    [37]周军平,魏根福,严彭钧等.新生儿缺氧缺血性脑病血浆与脑脊液内皮紊变化及临床意义临床儿科杂志[J],1997;15(1):19-20
    [38]Ohkuma H, Parney I, Megyest J, et al.Antisense Preptoendothelinoligo DNA therapy for vasospasm in a canine model of subar achnoid hemorrhage. J Neurosurg,1999; 90(5):1105-1114
    [39]Franceschini G, Tenconi, E. Barreca Endocrine abnormalities and outcome of ischaemic stroke Biomedecine & Pharmacotherapy,2001; 55(8):458-465
    [40]Dawson, V. L;Dawson, T. M. Nitricoxideneurotoxicity. J. Chem.Neuroanat.1996; 10:179-190
    [41]Bscotle Fe, GhheMy, Price WJ, et al. Endothelin levels inscease in rat focal and glolal ischemia. J Cenele Blood Flow Metale,1994; 14:337-342
    [42]史源,李华强,潘凤等,新生儿缺飘缺血性脑病内源性一氧化碳的变化[J].中华儿科杂志.1999:7(8):499-500
    [43]Tsu ji, M, Higuchi, Y, Shiraishi K, et al. Protective effect of aminoguanidine on hypoxic-ischemic brain damage and temporal profile of brain nitric oxide in neonatal rat. Pediatr. Res.2000;47:79-83
    [44]Erecinska, M;Cherian, S;Silver, I. A, Energy metabolism in mammalian brain during development. Prog. Neurobiol,2004;73:397-445
    [45]李占魁,陈玺,李瑞林等.新生儿缺氧缺血性脑病血浆与脑脊液降钙素基因相关肤 的研究.小儿急救医学[J],2000;7(3):131-132
    [46]Christodoulides N, Dusante W, Krall MH, et al. Vascular smooth muscle cell hame oxygease generate guanylyl cyclase-stimulatory cahan monoxi de. Ci culation.1995;91:2306-2309
    [47]王辉.国内脑瘫的研究近况[J].中国康复医学杂志,2004;19(8):637-640
    [48]卓大宏.中国康复医学[M].北京:华夏出版社,1991
    [49]Palisano RJ, Snider LM, Orlin MN. Recent advances in physical and occupational therapy for children with cerebral palsy[J]. Semin Pediatr Neurol,2004,11(1):66-77
    [50]董志文,范艳萍,唐伟,等.头针结合鲍巴斯疗法治疗小儿脑性瘫痪80例临床观察[J].针灸临床杂志,2002,18(8):25-26
    [51]吴卫红.脑瘫儿童特殊教育的方式:引导式教育[J].中国康复理论与实践,2003,9(5):259-260
    [52]Deluca SC, Echols K, Law CR, etal. Intensive pediatric constraint induced therapy for children with cerebral palsy:randomized, controlled, crossovertrial[J].J Child Neurol,2006,21(11):931-938
    [53]王权辉,王彬.强制性诱导运动治疗脑卒中后上肢运动功能障碍的疗效观察[J].中国康复医学杂志,2006,21(3):276
    [54]Charles JR, Wolf SL, Schneider JA, etal. Efficacy of a child friendly form of constraint induced movement therapy in hemiplegic cerebral palsy:a randomized control trial[J].Dev Med Child Neurol,2006,48(8):635-642
    [55]Sokolov PL, Dremova GV, Samsonova SV. Hippotherapy as a method for complex rehabilitation of patients with late residual stage of infantile cerebral palsy[J].Zh Nevrol Psikhiatr Im S S K or sakova,2002,102(10):42-45
    [56]Sterba JA. Does horseback riding therapy or therapist directed hippotherapy rehabilitate children with cerebral palsy[J].Dev Med Child Neurol,2007,49(1):68-73
    [57]Cherng RJ, Liao HF, Leung HWC, etal. The effectiveness of therapeutic horseback riding in children with spastic cerebral palsy[J]. Adapt Phys Act Q,2004,21 (2):103-121
    [58]Piggot J, Paterson J, Hocking C. Particpation in home treatment programs for children with cerebral plasy:a compelling challenge[J]. Qual Health Res,2002,12 (8):1112-1129
    [59]Ahlborg L, Andersson C, Julin P. Whole body vibration training compared with resistance training:effect on spasticity, muscle streng than dmotor performance in adults with cerebral palsy[J]. J Rehabil Med,2006,8(5):302-308
    [60]Dodd KJ, Taylor NF, Damiano DL. A systematic review of the effectiveness of strength training programs for people with cerebral palsy [J]. Arch Phys Med Rehabil,2002,83(8):1157-1164
    [61]Dodd KJ, Taylor NF, Graham HK. A randomized clinical trial of strength training in young people with cerebral palsy[J].Dev Med Child Neurol, 2003,45(10):652-657
    [62]Akhutina T, Foreman N, Krichevets A, etal. Improving spatial function ing in children with cerebral palsy using computerized and traditional game tasks[J]. Disabil Rehabil,2003,25(24):1361-1371
    [63]Ho CL, Holt KG, Saltzman E, etal. Functional electrical stimulation changes dynamic resources in children with spastic cerebral palsy [J]. Phys Ther,2006,86 (7):987-1000
    [64]Orlin MN, Pierce SR, Stackhouse CL, etal. Immediate effect of percutaneous in tramuscular stimulation during gait in children with cerebral palsy:a feasibility study[J].Dev Med Child Neurol,2005,47(10):684-690
    [65]Petrofsky JS, Petrofsky D. A simple device to assess and train motor coordination[J].J Med Eng Technol,2004,28(2):67-73
    [66]Bryanton C, Boss J, Brien M, etal. Feasibility, motivation, and selective motor control:virtual reality compared to conventional homeexercise in children with cerebral palsy[J].Cyberpsychol Behav,2006,9(2):123-128
    [67]Ledebt A, Becher J, Kapper J, etal. Balance training with visualfeedback in children with hemiplegic cerebral palsy.effect on stance and gait[J]. Motor Control,2005,9(4):459-468
    [68]李温仁,倪国坛.高压氧医学[M].上海:上海科学技术出版社,1998
    [69]樊凌冰.小儿脑性瘫痪高压氧综合治疗的探讨[J].高压氧医学杂志,1996,5(1):17
    [70]Crenshaw S,Herzog R, Castagno P, etal. The efficacy of tone reducing features in orthotic sonthegait of children with spastic diplegic cerebralpalsy[J].J Pediatr Orthop,2000,20(2):210-216
    [71]易南,王冰水,李玲,等.不同类型的踝足矫形器对痉挛型脑瘫患儿行走功能的影响[J].中国康复医学杂志,2002,17(2):100-102
    [72]Basar P,Yilmaz S, Haberfellner H. Use of an innsbruck sensori motor activator and regulator(ISMAR)in the treatment of oral motor dysfunctions:a single case report[J]. Int J RehabilRes,2003,26(1):57-59
    [73]卜笑松,唐久来.脑性瘫痪动物模型研究进展.中国康复理论与实践[J].2007,13(12):1106-1108
    [74]Duncan J R, Cock ML, Scheerlinck J PY, et al. White matter injury after repeated endotoxin exposure in the preterm ovine fetus[J]. Pediatr Res,2002,52(6):941-949
    [75]Dom A, Brian K, Joey P, et al. Interleukin-10 administration and bacterial endotoxin-induced preterm birth in a rat model [J]. Obstet Gynecol,2001,98(3):476-480
    [76]Cai Z, Pan ZL, Pang Y, et al. Cytokine induction in fetal rat brains and brain injury in neonatal rats after maternal lipolysaccharide administration[J]. Pediatr Res,2000,47(1):64-72
    [77]Saliba E, Henrot A. Inflammatory mediators and neonatal brain damage [J]. Biol Neonate,2001,79(324):224-227
    [78]Calvert JW, Yin W, Patel M, et al. Hyperbaric oxygenation prevented brain injury induced by hypoxia-ischemia in a neonatal ratmodel [J]. Brain Res,2002,951 (1):1-8
    [79]Jansen EM, Low WC. Long-term effects of neonatal ischemichypoxic brain injury on sensorimotor and locomotor tasks in rats[J]. Behav Brain Res,1996,78 (2):189-194
    [80]Strata F, Coq JO, Byl N, et al. Effects of sensorimotor restriction and anoxia on gait and motor cortex organization:implications for arodent model of cerebral palsy[J]. Neuroscience,2004,129:141-156
    [81]Weiss J, Takizawa B, McGee A, et al. Neonatal hypoxia suppesses oligodendrocyte Nogo-A and increases axonal sprouting in a rodentmodel for human prematurity[J]. Exp Neurol,2004,189 (1):141-149
    [82]Uehara H, Yoshioka H, Kawase S, et al. A new model of white matter injury in neonatal rats with bilateral carotid artery occlusion[J]. Brain Res,1999, 837(122):213-220
    [83]Buatlid D. How bilirabin gets into the brain[J]. Clin Perinatal,1990, 17(2):449
    [84]孙叶强,李晓捷,吴军,等.胆红素致新生兔脑瘫动物模型的实验研究[J].中国康复,1999,14(2):65-67
    [85]Hennebert O, Marret S, Carmeliet P, et al. Role of tissue-derived plasminogen activator (t-PA) in an excitotoxic mouse model of neonatal white matter lesions[J]. J Neuropat hol Exp Neurol,2004,63(1):53-63
    [86]吴珊.大鼠痉挛性脑瘫模型的改建[J].中国康复,1998,13(3):103-104
    [87]于海波,刘永锋等.针刺结合音乐疗法治疗小儿脑瘫30例临床观察.中医杂志,2008:49(12):1093-1095
    [88]王琴玉.“靳三针疗法”治疗脑性瘫痪的主要学术特点.上海针灸杂志,2004:23(6):3-4
    [89]刘卫民,袁海斌等.靳三针对小儿脑瘫脑血流的影响.光明中医2007:22(8):33-34
    [90]刘振寰.针灸治疗脑性瘫痪效果评估:150例随机分组对照(J].中国临床康复,2004:8(6):1091-109
    [91]刘震寰.头针为主治疗小儿脑性瘫痪210例临床观察[J].中国针灸,1999,19(11):651-665
    [92]刘焕荣.针刺治疗小儿脑性瘫痪249例临床观察[J].中国针灸,1998,18(8):42
    [93]崔艳丽,王慧娟,白莉恒.针灸在小儿脑瘫康复中的应用[J].中外医疗,2008,27(32):95-96
    [94]张小莉.针刺夹脊为主治疗脑瘫354例疗效观察[J].中国针灸,2000,20(5):269
    [95]王琴玉,袁青.“靳三针”不同留针时间治疗脑性瘫痪的疗效对比.中国临床康复,2005:9(11)156-157
    [96]秦秀娣.汤氏头针治疗小儿脑瘫34例临床观察[J].辽宁中医杂志,2000,27(9):42
    [97]米署光.头针滞针法加体针速刺治疗小儿脑瘫362例临床观察[J].针灸临床杂志,2000,16(3):28-31
    [98]黄茂,范焕芳,施荣富,等.头针加体针对痉挛型脑瘫患儿骨代谢的影响[J].辽宁中医杂志,2006,33(10):1335.
    [99]张举玲,程立红,所闽娜,等.头、体针治疗小儿脑瘫肢体功能疗效观察[J].实用中西医结合临床,2007,7(1):30
    [100]徐东浩,施炳培,史惟,等.穴位注射治疗小儿脑性瘫痪40例[J].上海中医药杂志,2008,42(5):49-50
    [101]郑卫国,吴夏勃.点穴推拿治疗痉挛型脑瘫的临床观察[J].中国骨伤,2005,8(8):491-492.
    [102]赵鑫胤.循经推拿拮抗肌群为主治疗小儿脑性瘫痪性尖足30例[J].广西中医学院学报,2008,11(4):14-15
    [103]胡鸾,邰先桃,王春林.选择性脊柱推拿疗法治疗痉挛型小儿脑瘫的临床研究[J]. 云南中医学院学报,2009,32(1):43-45
    [104]宋西晓,汪东,赵小燕,等.循经按摩配合神经运动发育学疗法治疗小儿脑瘫32例[J].陕西中医,2009,30(7):872-873
    [105]贾广良,胡晓丽.王雪峰教授提出的“脊背六法”及其在脑瘫康复中应用[J].医学综述,2008,14(1):146-149
    [106]韩庆,张跃,梁艳萍.推拿配合功能训练治疗小儿脑瘫抬头不佳39例[J].新疆中医药,2002,20(6):36
    [107]史惟,王素娟,廖元贵,等.运动发育推拿法治疗小儿脑瘫[J].中国康复,2004,12(6):351-352
    [108]闻庆汉.推拿配合中药治疗脑瘫的体会[J].按摩与导引,2003,6(3):56-57
    [109]张奇,路素芹.综合康复疗法治疗小儿脑瘫62例[J].中原医刊,2004,9(17):24-25
    [110]杨颖,李润洁,曹春京.Bobath联合郁氏手法对脑瘫患儿运动功能的影响[J].中国医疗前沿,2008,3(21):36
    [111]张蕾.中药熏蒸治疗不随意运动型小儿脑瘫的临床观察[J].光明中医,2009,24(3):484-485
    [112]陈静.中药熏蒸对脑瘫患儿肌张力关节活动度的影响[J].中国实用神经疾病杂志,2007,10(7):105
    [113]余亚平,周红玲,董小丽,等.针刺配合功能训练治疗小儿脑性瘫痪疗效观察[J].现代中西医结合杂志,2005,14(1):66
    [114]幸小玲.头针联合穴位注射治疗小儿脑瘫42例[J].陕西中医,2008,29(7):880-881
    [115]姚国民,何素玉.针刺配合推拿治疗小儿脑瘫29例临床观察[J].国际中医中药杂志,2009,31(2):142-143
    [116]李艳玲,潘纪红.中西医结合治疗小儿脑瘫23例[J].现代中医药,2009,29(3):10-11
    [117]高明灿,王淑斌针刺对缺血缺氧性脑性瘫痪幼鼠脑细胞凋亡及含水量的干预效应[J].中国临床康复,2005,(21):132-133
    [118]袁青,马瑞玲,薛媛等.针刺对脑缺血小鼠脑组织胶质纤维酸性蛋白表达的影响.针刺研究[J].2004;29(2):90-93
    [119]刘伟,吴爱群,李宛青,高艳,侯晓强,汤善均.氦氖激光穴位照射对缺血缺氧新生大鼠脑神经元尼氏体与BDNF表达的影响[J].解剖学研究,2003;25(4):270-272,276
    [120]Rice, et al. The influence of immaturity on hypoxic-ischemic brain damage in the rat[J]. Annals of neurology,1981,9(2):131-1981,9 (2):131-141
    [121]Longa EZ, Weinstein PR, Carlson S, etal. Reversible middle cerebral artery occlusion with out craniotomy in rats[J]. Stroke,1989,20(1):84-91
    [122]骆仲达.电针督脉对缺血性脑损伤大鼠神经细胞凋亡的影响[J].安徽中医学院学报2002 21(6):28
    [123]田雁,林佩冲.颖三针合体针治疗中风后遗症60例体会[J].甘肃中医,2002,15(1):65-66
    [124]吴闻天.颞三针加体针治疗中风后遗症68例仁[J].河北中医,1999,21(4):234--235
    [125]易志龙,陈伟,陈春梅;等.颖三针加腹针疗法治疗中风后遗症50例疗效观察[J].针灸临床杂志,2005,21(2):18-19
    [126]Lawson IJ.Leukocyte migration into the central nervous system. Immune responses in the nervous system. Bro Scientific Publishers.1995;27-36
    [127]Clemens JA, Stephenson DT, Yin T, Smalstig EB, Panetta JA, Little SP. Drug-induced neuroprotection from global ischemia is associated with preventionof persistent but not transient activation of nuclear factor-kappaB in rats. Stroke.1998;29(3):677-82
    [128]冯春生,王虎山,李凇,谭毓铨.大鼠短暂局灶性脑缺血再灌注后核转录因子-kB的表达.中风与神经疾病杂志.2003;20(1):11-13.23
    [129]Schneider A, Martin-Villalba A,Weih F, Vogel J,Wirth T,Schwaninger M. NF-kappaB is activated and promotes cell death in focal cerebral ischemia.NatMed.1999:5(5):554-559
    [130]Collins T, Read MA, Neish M Z, et al.Transcriptional regulation of endothelialcell adhesion molecules:N F-kappaB and cytokine inducible enhancers. Faseb(FASEB)J.1995;9(10):899-909
    [131]陈燕启,刘德红,杨光田.大鼠急性全脑缺血再灌注时NF-к B表达及意义.医学临床研究.2004:21(7):772-774
    [132]Botchkina GI, Geimonen E, Bilof ML, et al. Loss of NF-kappaB activity during cerebral ischemia and TNF cytotoxicity. Mol Med.1999;5(6):372-81
    [133]Nicolas B, Catherine W, Michel L, et al. Activation of the nuclear factor-κ B is akey event in brain tolerance. J Neurosci.2001; 21 (13):4668-4677
    [134]田代实,王光海,郭国际.核因子кB在大鼠脑缺血耐受中的作用及其对细胞间黏附分子-1和Bcl-2表达的影响.中风与神经疾病杂志.2004;21(3):205-207
    [135]Perkins ND. The Rel/NF-kappa B family:friend and foe. Trends Biochem Sci.2000; 25 (9):434-440.32. Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, et al.The Ced-3/interleukinlbeta converting enzyme-like homolog Mch6 and the lamin-cleaving enzymeMch2alpha are substrates for the apoptotic mediator CPP32.J Biol Chem.1996;271(43):27099-27106
    [136]Nakajima W, Ishida A, Lange MS, et al. Apoptosis has a prolonged role in the neurodegeneration after hypoxic ischemia in thenewborn rat [J]. J Neurosci,2000,20(21):7994-8004
    [137]Srinivasula SM, Fernandes-Alnemri T, Zangrilli J, et al.The Ced-3/inter leukinlbeta converting enzyme-like homolog Mch6 and the lamin-cleaving enzymeMch2alpha are substrates for the apoptotic mediator CPP32. J Biol Chem.1996;271 (43):27099-27106
    [138]Schulz JB, Weller M, Moskowitz MA. Caspases as treatment targets in stroke andneurodegenerative diseases. Ann Neurol.1999;45(4):421-429.
    [139]Harrison DC, Davis RP, Bond BC, et al. Caspase mRNA expression in a ratmodel of focal cerebral ischemia. Brain Res Mol Brain Res.2001;89(1-2):133-146
    [140]LA, Wu YQ, Huang ZH, et al. Caspase activation and neuroprotection incaspase-3 deficient mice after in vivo cerebral ischemia and in vitro oxygenglucose deprivation. Proc Natl AcadSci USA.2002:99:15188-15193
    [141]曲喜英,张海风,祝其锋.H202对PC12细胞Caspase-3和NF-κ B P65基因表达的影响.武汉大学学报(医学版).2005;26(1):17-20

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700