Schneeloch Edda, Mies Günter, Busch Hans-Jörg, Buschmann Ivo R, Hossmann Konstantin-Alexander
Department of Experimental Neurology, Max Planck Institute for Neurological Research, Gleueler Strasse 50, 50931 Cologne, Germany.
Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12730-5. doi: 10.1073/pnas.0404880101. Epub 2004 Aug 11.
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a powerful arteriogenic factor in the hypoperfused rat brain. To test the pathophysiological relevance of this response, the influence of GM-CSF on brain energy state was investigated in a model of hemodynamic stroke. Sprague-Dawley rats were submitted to three-vessel (bilateral vertebral and unilateral common carotid artery) occlusion (3-VO) to induce unilaterally accentuated brain hypoperfusion. One week later, hemodynamic stroke was induced by additional lowering of arterial blood pressure. Experiments were terminated by in situ freezing of the brain. ATP was measured in cryostat sections by using a bioluminescence method. The use of 3-VO, in combination with 15 min of hypotension of 50, 40, or 30 mmHg, did not produce disturbances of energy metabolism, however, focal areas of ATP depletion were unilaterally detected after 3-VO, in combination with 15 min of hypotension of 20 mmHg. Treating such animals with GM-CSF (40 microg.kg(-1).d(-1)) during the 1-week interval between 3-VO and induced hypotension significantly reduced the hemispheric volume of energy depletion from 48.8 +/- 44.2% (untreated group, n = 10) to 15.8 +/- 17.4% (treated group, n = 8, P = 0.033). GM-CSF-induced arteriogenesis is another approach to protect the brain against ischemic injury.
粒细胞-巨噬细胞集落刺激因子(GM-CSF)是灌注不足的大鼠脑内一种强大的促动脉生成因子。为了检验这种反应的病理生理相关性,在血流动力学性脑卒中模型中研究了GM-CSF对脑能量状态的影响。将Sprague-Dawley大鼠进行三血管(双侧椎动脉和单侧颈总动脉)闭塞(3-VO)以诱导单侧加重的脑灌注不足。一周后,通过进一步降低动脉血压诱导血流动力学性脑卒中。实验通过脑原位冷冻终止。使用生物发光法在低温恒温器切片中测量三磷酸腺苷(ATP)。3-VO联合50、40或30 mmHg的15分钟低血压并未导致能量代谢紊乱,然而,在3-VO联合20 mmHg的15分钟低血压后,单侧检测到ATP耗竭的局灶区域。在3-VO和诱导低血压之间的1周间隔期间,用GM-CSF(40μg·kg⁻¹·d⁻¹)治疗此类动物,可使能量耗竭的半球体积从48.8±44.2%(未治疗组,n = 10)显著降低至15.8±17.4%(治疗组,n = 8,P = 0.033)。GM-CSF诱导的动脉生成是保护脑免受缺血性损伤的另一种方法。