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伤灶局部亚低温、引流治疗对创伤性脑损伤时Na^+、脑含水量及TNF-α的变化 被引量:2

Treatment effects of focus hypothermia and drainage on traumatic brain injury of Sprague-dawley rats
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摘要 目的研究伤灶局部引流、伤灶局部亚低温联合治疗对SD大鼠创伤性脑损伤后脑水含量、Na+含量、肿瘤坏死因子变化的影响,以探讨伤灶局部引流、伤灶局部亚低温对创伤性脑损伤的治疗作用及可能机制。方法采用自由落体打击装置造成大鼠创伤性脑损伤,分别在伤后30min开始实施伤灶局部引流、25℃循环水对伤灶脑组织进行局部降温至(31.5±0.5)℃,而对假脑外伤组及脑外伤模型组不降温,各组在相应时间点断头处死;采用干湿重法测伤灶脑组织含水量,原子吸收火焰分光光度法测Na+含量,采用RT-PCR法检测伤灶区脑组织中肿瘤坏死因子基因表达情况、免疫组化实验检测其蛋白水平。结果(1)脑含水量:FH组、FD组、FDH组伤灶区脑组织含水量分别低于M组,差异有统计学意义(P<0.05);FDH组水含量低于FD组和FH组,差异有统计学意义(P<0.05)。(2)脑组织钠含量:脑组织钠离子变化与含水量变化一致。(3)伤灶区脑组织TNF-αmRNA含量:FH组、FD组、FDH组伤灶区脑组织TNF-αmRNA含量分别低于M组,差异有统计学意义(P<0.05);FDH组TNF-αmRNA含量低于FD组和FH组,差异有统计学意义(P<0.05)。(4)伤灶区脑组织中TNF-α蛋白含量趋势TNF-αmRNA变化一致。(5)引流量:FD组、FDH组引流量分别为(0.230 8±0.035 6)g(、0.345 6±0.069 2)g。结论伤灶局部亚低温、伤灶局部引流分别单独或联合均对创伤性脑损伤有治疗作用,并且联合治疗组疗效胜于单一治疗组。这种治疗效果可能是通过直接引流出水肿液和脑脊液、减轻脑水肿、减轻炎症反应等途径发挥作用。 Objective To investigate the effect of the focus hypothermia group, the focus drainage group, the group of united focus hypothermia and focus drainage on traumatic brain injury of Sprague-dawley rats and its mechanism. Methods Feeney's model was used to produce traumatic brain injury in Sprague-dawley rats. After half an hour, both the focus hypothermia group and the group of united focus hypothermia and drainage were received focus brain hypothermia with 25℃ circling water except for the model group, the sham operation group and the focus drainage group. The injured rats were sacrificed at preconcerted time. Results Water content of the focus hypothermia group, the focus drainage group as well as the united group was markedly less than that of model group (P 〈0.05). The concentration of brain sodium coincided with that of water content (P〈0. 05). Expression of TNF- α mRNA in the brain tissue of the focus hypothermia group, the focus drainage group, the united group were less than those of model group (P〈0.05). Compared with traumatic model group, TNF-α protein amount decreased significantly (P〈0.05). Conclusion The focus hypothermia group, the focus drainage group, the group of united local hypothermia and local drainage showed great effect on traumatic brain edema. Its mechanism may be anti-express TNF-α, decreasing brain edema.
出处 《重庆医学》 CAS CSCD 2006年第9期818-820,共3页 Chongqing medicine
关键词 引流 亚低温 创伤性脑损伤 肿瘤坏死因子 联合治疗 drainage hypothermia traumatic brain injury TNF-α ; united treatment
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参考文献9

  • 1Clifton GL, Miller ER, Choi SC, et al. Lack of effect of induction of hypothermia after acute brain injury[J]. N Engl J Med,2001,344(8):556
  • 2王光伟,刘运生,梁有明,屈洪涛,李创华.重型颅脑外伤局灶低温疗法的实验研究[J].医学临床研究,2004,21(6):616-619. 被引量:4
  • 3梁有明,刘运生,李创华,王光伟,屈洪涛.局灶低温治疗大鼠脑外伤对脑组织氧自由基影响的研究[J].中国耳鼻咽喉颅底外科杂志,2004,10(5):257-259. 被引量:12
  • 4罗超,刘运生.亚低温的并发症[J].国外医学(神经病学.神经外科学分册),2004,31(1):38-42. 被引量:17
  • 5徐如祥.创伤性脑水肿研究进展[J].中国现代神经疾病杂志,2004,4(3):141-145. 被引量:19
  • 6Cao M, Lisheng H, Shouzheng S. Resolution of brain edema in severe brain injury at controlled high and low intracranial pressures[J]. J Neurosurg, 1984,61(4): 707
  • 7Unterberg AW, Stover J, Kress B, et al. Edema and brain trauma[J]. Neuroscience,2004,129(4): 1021
  • 8Vitarbo EA, Chatzipanteli K, Kinoshita K, et al. Tumor necrosis factor alpha expression and protein levels after fluid percussion injury in rats: the effect of injury severity and brain temperature[J]. Neurosurgery, 2004, 55(2):416
  • 9Morganti-Kossmann MC, Rancan M, Stahel PF, et al.Inflammatory response in acute traumatic brain injury: a double-edged sword[J]. Curr Opin Crit Care, 2002,8(2):101

二级参考文献33

  • 1Polderman KH, Peerdeman SM, Girbes AR. Hypophosphatemia and hypomagnesemia induced by cooling in patients with severe head injury.J Neurosurg, 2001 , 94(5) :697 - 705.
  • 2Shiozaki T, Hayakata T, Taneda M, et al. A multicenter prospective randomized controlled trial of the efficacy of mild hypothermia for severely head injured patients with low intracranial pressure. Mild Hypethermia Study Group in Japan. J Neurosurg, 2001,94(1) : 50 -54.
  • 3Shiozaki T, Kato A, Taneda M, et al. Little benefit from mild hypothermia therapy for severely head injured patients with low intracranial pressure. J Neurosurg, 1999, 91(2) : 185 - 191.
  • 4Wong KC. Physiology and pharmacology of hypothermia. West J Med,1983,138 : 227 - 232.
  • 5Kaufman HH, Timberlake G, Voelker J, et al. Medical complications of head injury. Med Clin North Am, 1993, 77:43-60.
  • 6Schwab S, Georgiadis D, Berrouschot J, et al. Feasibility and safety of moderate hypothermia after massive hemispheric infarction. Stroke,2001, 32(9) :2033 - 2035.
  • 7Koht A, Cane R, Cerullo LJ. Serum potassium levels during prolonged hypothermia. Intensive Care Med, 1983 ;9(5) :275 - 277.
  • 8Clifton GL, Miller ER, Choi SC, et al. Lack of effect of induction of hypothermia after acute brain injury. N Engl J Med,2001,344(8) :556-563.
  • 9Tokutomi T, Morimoto K, Miyagi T, et al. Optimal temperature for the management of severe traumatic brain injury: effect of hypothermia on intracranial pressure, systemic and intracranial hemodynamics, and metabolism. Neurosurgery, 2003,52 ( 1 ) : 102 - 111 ; discussion 111 -112.
  • 10Bernard SA, MacC Jones B, Buist MD. Experience with prolonged induced hypothermia in severe head injury. Crit Care, 1999,3: 167-172.

共引文献43

同被引文献19

  • 1肖国民,危静.大鼠脑损伤后核因子-κB与肿瘤坏死因子-α的表达[J].浙江医学,2005,27(1):27-29. 被引量:8
  • 2罗超,刘运生,彭形,赵贤军,李玉斌,徐立新.伤灶局部亚低温及伤灶局部引流治疗大鼠创伤性脑损伤[J].创伤外科杂志,2006,8(4):340-343. 被引量:3
  • 3樊兴娟,柯开富,姜正林,王国华.人参皂苷单体对大鼠局灶性脑缺血再灌注的神经保护研究[J].中华医学杂志,2006,86(29):2071-2074. 被引量:16
  • 4樊兴娟,姜正林,王国华,柯开富.人参总皂苷对大鼠脑缺血再灌注的神经保护研究[J].交通医学,2006,20(6):662-664. 被引量:6
  • 5Morganti-Kossmann MC, Ranean M, Stahel PF, et al. Inflammatory response in acute traumatic brain injury: a double-edged sword[J]. Curr Opin Crit Care, 2002,8 (2) : 101-103.
  • 6Grossman KJ, Goss CW, Stein DG. Effects of progesterone on the inflammatory response to brain injury in the rat[J]. Brain Res, 2004,1008 (1) : 29-31.
  • 7Feeney DM, Boyeson MG, Linn RT, et al. Responses to cortical injury:I. Methodology and local effects of contu- sions in the rat[J]. Brain Res,1981,211(1) :67-69.
  • 8Oshima T, Lee S, Sato A, et al. TNF-alpha contributes to axonal sprouting and functional recovery following traumatic brain inj ury[J]. Brain Res, 2009,1290 (1) : 102-104.
  • 9Marini H, Altavilla D, Bellomo M, et al. Modulation of IL1 beta gene expression by lipid peroxidation inhibition after kainic acid-induced rat brain injury[J]. Exp Neurol, 2004,188(1) : 178-180.
  • 10Folkersma H, Breve J J, Tilders FJ, et al. Cerebral microdialysis of interleukin (IL)-lbeta and IL-6:extraction efficiency and production in the acute phase after severe traumatic brain injury in rats[J]. Acta Neurochir, 2008, 150(12) :1277-1279.

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