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黄体酮减轻大鼠蛛网膜下腔出血后早期脑损伤 被引量:2

Progesterone attenuates early brain injury after subarachnoid hemorrhage in rats
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摘要 目的探讨黄体酮对蛛网膜下腔出血(SAH)后早期脑损伤(EBI)中细胞凋亡、血脑屏障(BBB)稳定性、脑水肿和死亡率方面的保护作用。方法 66只大鼠被随机分为假手术组、SAH+溶剂组、SAH+黄体酮组。于SAH模型制成后1h、6h和12h分别给予黄体酮(16毫克/千克体重)或等体积的溶剂。在SAH后24h分析不同组间大鼠在死亡率、神经功能评分、脑水肿、细胞凋亡、caspase-3及基质金属蛋白酶-9(MMP-9)表达水平的差异。结果与SAH+溶剂组比较,黄体酮治疗显著降低了大鼠的死亡率、细胞凋亡程度以及caspase-3水平与MMP-9的表达水平,减轻了脑水肿和伊文思蓝的渗出,提高了神经功能评分。结论黄体酮可通过抑制细胞凋亡和稳定BBB减轻SAH后EBI。 Objective Toexplore the effect of progesterone on cell apoptosis,stability of the blood-brain barrier(BBB),brain edema,and mortality in male Sprague-Dawley rats subjected to subarachnoid hemorrhage(SAH)-induced early brain injury(EBI) by endovascular perforation.Methods Rats(n=66) were randomly assigned to sham,SAH+vehicle,and SAH+progesterone groups.Progesterone(16mg/kg) or an equal volume of vehicle was administered at 1h,6h and 12h after SAH.Mortality within 24h,neurological scores,brain edema,Evans blue dye extravasation,cell apoptosis,and the expression of caspase-3 and matrix metalloproteinase MMP-9 were assayed after 24h of SAH.Results Progesterone treatment significantly reduced mortality,brain edema,Evans blue dye extravasation,cell apoptosis,expression of caspase-3 and MMP-9,and improved neurologicalscores compared with the vehicle group.Conclusion Progesterone may reduce EBI after SAH by inhibiting cell apoptosis and stabilizing the BBB.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2013年第6期500-503,共4页 Journal of Apoplexy and Nervous Diseases
基金 卫生厅省部共建项目(No.WSJ2009-2-025)
关键词 蛛网膜下腔出血 早期脑损伤 黄体酮 细胞凋亡 血-脑屏障 Subarachnoid hemorrhage Early brain injury Progesterone Apoptosis Blood-brain barrier
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  • 1Jennett B. Epidemiology of head injury[J].Archives of Disease in Childhood,1998,(5):403-406.doi:10.1136/adc.78.5.403. 被引量:1
  • 2Kraus JF,Nourjah P. The epidemiology of mild,uncomplicated brain injury[J].Trauma,1988.1637-1643. 被引量:1
  • 3Djebaili M,Hoffman SW,Stein D. Allopregnanolone and progesterone decrease cell death and cognitive deficits after a contusion of the rat pre-frontal cortex[J].Neuroscience,2004,(2):349-359.doi:10.1016/j.neuroscience.2003.09.023. 被引量:1
  • 4Shear DA,Galani R,Hoffman SW. Progesterone protects against necrotic damage and behavioral abnormalities caused by traumatic brain injury[J].Experimental Neurology,2002.59-67. 被引量:1
  • 5O' Connor CA,Cernak I,Vink R. Both estrogen and progesterone attenuate edema formation following diffuse traumatic brain injury in rats[J].Brain Research,2005.171-174. 被引量:1
  • 6Ozacmak VH,Sayan H. The effects of 17beta estradiol,17alpha estradiol and progesterone on oxidative stress biomarkers in ovariectomized female rat brain subjected to global cerebral ischemia[J].Physiological Research,2009.909-912. 被引量:1
  • 7Sugawara T,Ayer R,Jadhav V. A new grading system evaluating bleeding scale in filament perforation subarachnoid hemorrhage rat model[J].Neuroscience Methods,2008.327-334. 被引量:1
  • 8Garcia JH,Wagner R,Liu KF. Neurological deficit and extent of neuronal necrosis attributable to middle cerebral artery occlusion in rats.Statistical validation[J].Stroke,1995.627-634. 被引量:1
  • 9Xi G,Hua Y,Keep PR. Brain edema after intracerebral hemorrhage:the effects of systemic complement depletion[J].Acta Neurochirungica Supplements(Wien),2002.253-256. 被引量:1
  • 10Sehba FA,Hou J,Pluta RM. The importance of early brain injury after subarachnoid hemorrhage[J].Progress in Neurobiology,2012.14-37. 被引量:1

同被引文献13

  • 1Stein D G. A clinical/translational perspective: can a developmen-tal hormone play a role in the treatment of traumatic brain injury[J].Horm Behav,2013,63(2):291-300. 被引量:1
  • 2Jiang W, Xia F, Han J, et al. Patterns of Nogo-A, NgR, and RhoAexpression in the brain tissues of rats with focal cerebral infarction[J], Transl Res,2009,154(1):40-48. 被引量:1
  • 3Huber A B.Weinmann 0,Brosamle C,et al. Patterns of Nogo mRNAand protein expression in the developing and adult rat and afterCNS lesions[J], J Neurosci,2002,22(9):3553-3567. 被引量:1
  • 4Ishrat T, Sayeed I, At if F, et a丨.Progesterone and allopregnanoloneattenuate blood-brain barrier dysfunction following permanentfocal ischemia by regulating the expression of matrix metallopro-teinases[J]. Exp Neurol,2010,226(1): 183-190. 被引量:1
  • 5De Nicola A F, Coronel F, Garay L I,et al. Therapeutic effects ofprogesterone in animal models of neurological disorders[J]. CNSNeurol Disord Drug Targets,2013,12(8): 1205-1218. 被引量:1
  • 6Leonelli E, Bianchi R, Cavaletti G, et al. Progesterone and itsderivatives are neuroprotective agents in experimental diabeticneuropathy: a multimodal analysis[J], Neuroscience, 2007,144(4):1293-1304. 被引量:1
  • 7Me付re D.Delespierre Z,Gou 6 zou M,et al. The membrane-asso-ciated progesterone-binding protein 25-Dx is expressed in brainregions involved in water homeostasis and is up-regulated aftertraumatic brain injury [J]. J Neurochem,2005,93(5): 1314-1326. 被引量:1
  • 8Ekmark-Lew 6 n S, Lewen A, Israelsson C, et al. Vimentin andGFAP responses in astrocytes after contusion trauma to themurine brain[J], Restor Neurol Neurosci,2010,28(3):311 -321. 被引量:1
  • 9Labombarda F, Gonz a 丨ez S,Lima A,et al. Progesterone attenu-4.ates astro- and microgliosis and enhances oligodendrocyte differentiation following spinal cord injury[J]. Exp Neurol, 2011, 231(1):135-146. 被引量:1
  • 10Torres Aleman I. Insulin-like growth factor-1 and central neu-rodegenerative diseases [J]. Endocrinol Metab Clin North Am,2012,41(2):395-408. 被引量:1

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