Kiliç Kaya, Konya Deniz, Kurtkaya Ozlem, Sav Aydin, Pamir M Necmettin, Kiliç Türker
Laboratory of Molecular Neurosurgery, Marmara University Institute of Neurological Sciences, Istanbul, Turkey.
J Neurosurg. 2007 Mar;106(3):463-9. doi: 10.3171/jns.2007.106.3.463.
The authors studied the effect of Gamma Knife irradiation on angiogenesis induced by cerebral arteriovenous malformation (AVM) tissues implanted in the corneas of rats.
Ten AVM specimens obtained from tissue resections performed at Marmara University between 1998 and 2004 were used. A uniform amount of tissue was implanted into the micropocket between the two epithelial layers of the cornea. Gamma Knife irradiation was applied with dose prescriptions of 15 or 30 Gy to one cornea at 100% isodose. Dosing was adjusted so that the implanted cornea of one eye received 1.5 Gy when 15 Gy was applied to the other cornea. Similarly, one cornea received 3 Gy when 30 Gy was applied to the other cornea. Angiogenic activity was graded daily by biomicroscopic observations. Forty-eight other rats were used for microvessel counting and vascularendothelial growth factor (VEGF) staining portions of the experiment. Micropieces of the specimens were again used for corneal implantation. Rats from each group were killed on Days 5, 10, 15, and 20, and four corneas from each group were examined. Gamma Knife irradiation dose dependently decreased AVM-induced neovascularization in the rat cornea as determined by biomicroscopic grading of angiogenesis, microvessel count, and VEGF expression.
The results suggest that Gamma Knife irradiation inhibits angiogenesis induced by AVM tissue in the cornea angiogenesis model. The data are not directly related to understanding how Gamma Knife irradiation occludes existing AVM vasculature, but to understanding why properly treated AVMs do not recur and do not show neovascularization after Gamma Knife irradiation.
作者研究了伽玛刀照射对植入大鼠角膜的脑动静脉畸形(AVM)组织诱导的血管生成的影响。
使用1998年至2004年在马尔马拉大学进行组织切除获得的10个AVM标本。将均匀量的组织植入角膜两层上皮之间的微袋中。以15或30 Gy的剂量处方在100%等剂量下对一只角膜进行伽玛刀照射。调整剂量,使得当对另一只角膜施加15 Gy时,一只眼睛植入角膜接受1.5 Gy。同样,当对另一只角膜施加30 Gy时,一只角膜接受3 Gy。通过生物显微镜观察每天对血管生成活性进行分级。另外48只大鼠用于实验的微血管计数和血管内皮生长因子(VEGF)染色部分。标本的小片再次用于角膜植入。每组大鼠在第5、10、15和20天处死,并检查每组的四个角膜。通过血管生成的生物显微镜分级、微血管计数和VEGF表达确定,伽玛刀照射剂量依赖性地降低了大鼠角膜中AVM诱导的新生血管形成。
结果表明伽玛刀照射抑制了角膜血管生成模型中AVM组织诱导的血管生成。这些数据与理解伽玛刀照射如何闭塞现有的AVM血管系统没有直接关系,而是与理解为什么经过适当治疗的AVM在伽玛刀照射后不会复发且不会出现新生血管形成有关。