期刊文献+

兔脑激光间质热毁损及血脑屏障急性期改变 被引量:2

Observing thermal injury of rabbit brain in laser interstitial themotherapy and evaluating changed structure of blood brain barrier in acute stage
原文传递
导出
摘要 目的 观察激光间质加热(laser interstitial thermotherapy,LITT)后兔脑毁损组织与周边脑组织的超微病理改变,评估Lrrr后急性期的血脑屏障(blood brain barrier,BBB)开放性。方法浙江大学动物实验中心提供新西兰大门兔共70只,经随机筛选设LITTA组(2W,600S,20只)及B组(15W,100S,20只),应用直体定向技术插入半导体激光光纤,分别对兔右侧前脑实行立体定向间质加热,另随机设甘露醇灌注组和假手术对照组各15只。透射电镜下观察LITT后3h,6h,12h,24h的中心热毁损灶及靶周边脑组织BBB的超微形态学的改变;酶联免疫吸附法测定相应不同时间的S100B蛋白变化;另检测脑脊液白蛋白与血清白蛋白比值(BBB系数)。实验数据作单因素方差分析,组间均数比较用q检验。结果接触激光光纤前端成为加热毁损灶,以细胞坏死为主,细胞膜结构损伤,线粒体、内质网等细胞器膨胀,线粒体嵴消失,胞浆稀疏等。形态学改变明显于对照组。热能传导至周边,可见部分细胞发生不同时期的凋亡改变。急性期内可见内皮细胞肿胀、血管基膜模糊断裂、周围间隙增宽、缝隙结构破坏,且S100B蛋白及BBB系数在LITT组明显升高,BBB开放的时程较甘露醇灌注组长。但24h后LITT组开始恢复,S100B与BBB系数较LITT组的差异具有统计学意义(P=0.0087)。结论利用立体定向技术半导体激光加热兔脑组织的毁损灶,急性期内可导致明确的细胞组织损伤,BBB结构破坏,小功率加热组血脑屏障开放时程较大功率组缩短。提示利用小功率半导体激光可形成精确安全的脑毁损灶,为功能神经外科发展提供了新思路。 Objective To observe ultramicro pathologic change of rabbit brain central damaged tissue and peripheral tissue 'after LITT, to evaluate the changed structure of blood brain barrier (BBB) of peripheral tissue in acute stage. Method Seventy Newzealand rabbits were randomly screened from Zhejiang University Animal Experiment Center. By stereotaxic technique, semiconductor surgica laser fibers were inserted into right frontal lobes and heat treated to randomly build LITT Group A (2W, 600 s, n = 20) and LITT Group B (15 W, 100 s, n = 20) brain damaged models successfully. Other 15 nomal rabbits were randomly distributed as mannitol perfusion group and fake operation group. The ultramicro structures in central theruaodamaged tissue were observed with transmission electro microscope 'after LITT 3 h, 6 h, 12 h, 24 b. In peripheral tissue, ultramicro morphologie changes of brain vessels and BBB were evaluated. S100B protein in serum and BBB indexe were measured at different stages post LITT. Experimental data were treated as one-factor analysis of variance and q test. Results The brain damage center connected the tip of laser fiber and turn into thennodamage tissue. The main structure changes were cytoclasis, damnification of cell membrum, swelling of cell organelle such as mitochondrion, endoplasmicreticulum, disappearance of mitochondfion and sparseness of cytoplasm in local tissure. Heat energy conducted to damage peripheral tissue, some cells occured apoptosis in different stage. In aeute stage after LITT, contracted capillary, vessel, ancreted red cell, swell endothelium cell, broken base membrum, wide around clearance and destroyed aperture structure were identified. The levels of serum S100B and BBB indexe dramatically rised. The opening time of BBB in peripheral tissue was longer than mannital peffusion group. However at 24 h post LITT, they began to recover in Group A. The difference of serum S100B and BBB indexe between Group A and Group B has statistical significance ( P = 0. 0087). Conclusions With semiconductor laser heat treatment and stereotaxic techniqe, definite ceils cytoclasis, cell membrance structures and chondriosome damage could be performed obviously in rabbit brain thermotherapy point. Apoptosis could be found in peripheral tissue, BBB could be opened in an acute stage. The opening time course of BBB was shortened in those LITT eases with small power. It shew us a new method to perform a safe and exact damage zone of brain for functional neurosurgery.
出处 《中华急诊医学杂志》 CAS CSCD 北大核心 2009年第12期1243-1247,共5页 Chinese Journal of Emergency Medicine
基金 基金项目:国家自然科学基金(30672207) 浙江省医约卫生科学研究基金(2007A091)
关键词 激光 血脑屏障 加热 S100蛋白 电镜 立体定向 脑毁损 Laser Blood brain barrier Thermotherapy S100 protein Electron microscope Stereotaxis Brain damage Rabbit
  • 相关文献

参考文献13

  • 1Brown TE, True C, Mclaufin RL,et al. Laser radiation. II. Long-term effects of laser radiation on certain intracranial structures[J]. Neurology, 1967,17(8) :789-796.
  • 2石键,张建民,吴群,赵洪洋.红外热像测温在胶质瘤模型热疗研究中的应用[J].中华物理医学与康复杂志,2007,29(2):88-90. 被引量:4
  • 3Kapural M, Krizanac-Bengez LJ, Barnett G, et al. Serum S100beta as a possible marker of blood-brain-barrier disruption[J]. Brain Res, 2002, 940( 1/2):102-104.
  • 4刘如恩,赵洪洋.多功能动物立体定位仪的制作[J].中华神经外科杂志,2003,19(6):471-472. 被引量:7
  • 5Sehulze PC, Vitzthum HE, Goldammer A, et al. Laser-induced ther motherapy of neoplastic lesions in the brain-underlying tissue alterations MRI-monitoring and clinical applicability [ J ]. Acta Neurochir, 2004 146(8) :803-812.
  • 6Sehwabe B, Kahn T, Harth T, et al. Laser-induced thermal lesions in the human brain: short- and long-term appearance on MRI[J]. J Comput Assist Tomogr, 1997, 21(5) :818-825.
  • 7Impaeratore C, Germano A, Avella D, et al. Effects of the radical scavenger AVS on behavioral and BBB changes after experimental subarachnoid hemorrhage[J]. Life Sci,2000, 66(9) :779-790.
  • 8Rapoport SI. Osmotic opening of the blood-brain barrier: principles, mechanism, and therapeutic applications [J]. Cell Mol Neuorbiol, 2000, 20(2) :217-230.
  • 9余樱,张兆辉,杨波,曾庆杏.溶血磷脂酸对血脑屏障通透性的影响及其机制[J].中华急诊医学杂志,2006,15(12):1109-1112. 被引量:8
  • 10陈一招,徐如祥,杨志林,徐宗俊,姜晓丹,蔡颖谦.高温对血脑屏障内皮细胞紧密连接的作用及其机制[J].中华创伤杂志,2003,19(9):540-543. 被引量:6

二级参考文献37

  • 1张培林 张培林 主编.被膜、脑脊液和脑屏障[A].张培林,主编.神经解剖学:第1版[C].北京:人民卫生出版社,1995.506—510.
  • 2MeCarthy KD, de Vellis J. Preparation of separate astroglial and oligdendroglial cell cultures from rat cerebral tissue. J Cell Biol, 1980,85:890-902.
  • 3Hurst RD, Fritz IB. Propemes of an immortalised vascular endothelial/glioma cell co-culture model of the blood-brain barrier. J Cell Physiol, 1996, 167:81-88.
  • 4Scott PA, Bicknell R. The isolation and culture of microvascular endothelium. J Cell Sci, 1993,105:269 -273.
  • 5Schneeberger EE, Lynch RD. Structure, function, and regulation of cellular tight junctions. Am J Physiol, 1992, 262:L647-L661.
  • 6Raub TJ. Signal tranduction and glial cell modulation of cultured brain microvessel endothelial cell tight junctions. Am J Physiol,1996,271:C495- C503.
  • 7Youakim A, Ahdieh M. Interferon-gamma decreases barrier function in T84 cells by reducing ZO-1 levels and disrupting apical actin.Am J Physiol, 1999, 276: G1279-G1288.
  • 8Sambrook J, Fritsch EF, Maniatis T, et al. Molecular Cloning: a Laboratory Manual. 2nd ed. New York: Cold spring hartmr laboratory press, 1989. 332.
  • 9Sharma HS, Westman J, Nyberg F. Pathophysiology of brain edema and cell changes following hyperthermic brain injury. Prog Brain Res,1998:115:351 -412.
  • 10Denker BM, Nigam SK. Molecular structure and assembly of the tight junction. Am J Physiol. 1998,274: F1-F9.

共引文献21

同被引文献26

  • 1徐昌盛,刘文革.热射病研究进展[J].中华急诊医学杂志,2005,14(7):609-611. 被引量:35
  • 2赵灵,林小华,李永波,韦玉文,侯玉宇,楚磊.山莨菪碱对重型弥漫性轴索损伤患者血浆NSE、ET及CGRP含量的影响[J].中华急诊医学杂志,2006,15(3):209-212. 被引量:2
  • 3余樱,张兆辉,杨波,曾庆杏.溶血磷脂酸对血脑屏障通透性的影响及其机制[J].中华急诊医学杂志,2006,15(12):1109-1112. 被引量:8
  • 4张弩,陈大庆,朱烈烈,李永领,张荣.颅脑创伤患者血清胶质纤维酸性蛋白和神经元特异性烯醇化酶的变化[J].中华急诊医学杂志,2007,16(11):1194-1196. 被引量:2
  • 5Kerwin AJ,Schinco MA,Tepas JJ,et al.The use of 23.4% hypertonic saline for the management of elevated intracranial pressure in patients with severe traumatic brain injury:a pilot study[J].J Trauma,2009,67 (2):277-282.
  • 6Torre-Healy A,Marko NF,Weil RJ.Hyperosmolar therapy for intracranial hypertension[J].Neurocrit Care,2012,17 (1):117-130.
  • 7Mortazavi MM,Romeo AK,Deep A,et al.Hypertonic saline for treating raised intracranial pressure:literature review with metaanalysis[J].Neurosurg,2012,116 (1):210-221.
  • 8Brain Trauma Foundation,American Association of Neurological Surgeons,Congress of Neurological Surgeons.Guidelines for the management of severe traumatic brain injury[J].J Neurotrauma,2007,24 Suppl 1:S1-106.
  • 9Stubbe HD.Salt or sugar on the brain:does it matter except for taste[J].Crit Care Med,2011,39 (3):601-602.
  • 10Kamel H,Navi BB,Nakagawa K,et al.Hypertonic saline versus mannitol for the treatment of elevated intracranial pressure:a metaanalysis of randomized clinical trials[J].Crit Care Med,2011,39 (3):554-559.

引证文献2

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部