Yoshida Y, Dereski M O, Garcia J H, Hetzel F W, Chopp M
Department of Pathology (Neuropathology), Henry Ford Hospital, Detroit, Michigan 48202-2689.
J Neuropathol Exp Neurol. 1992 Jan;51(1):91-100. doi: 10.1097/00005072-199201000-00011.
Light activation of circulating hematoporphyrin derivatives has been used in the treatment of selected brain tumors. The effects of this photodynamic therapy on the non-neoplastic, adjacent brain tissue are incompletely characterized. We studied in adult Fisher rats the time-dependent (1 hour to 7 days) effects of photoactivated Photofrin II. Our protocol was comparable to that used in the treatment of human brain tumors. Structural and functional changes spread from the treatment surface and from the center to the periphery to involve the entire cerebral cortex exposed under a 5 mm craniectomy. The sequential changes spreading from the surface to the deepest cortical layer involve first astrocytes (1 hour), then endothelial cells and, ultimately, neurons. Thrombi were first noted in the microvasculature after 18 hours and coagulation necrosis of the entire area at risk occurred only after 48 hours. The results suggest that the photosensitizing agent crosses the intact blood-brain barrier and enters the astrocytic compartment where it becomes cytotoxic upon light activation. A comparison between the focal brain lesions of photodynamic therapy and those induced by middle cerebral artery occlusion suggests that cell damage evolves along different paths in these two forms of brain injury.
循环血卟啉衍生物的光激活已用于某些脑肿瘤的治疗。这种光动力疗法对非肿瘤性的相邻脑组织的影响尚未完全明确。我们在成年Fisher大鼠中研究了光激活的卟吩姆钠II的时间依赖性(1小时至7天)效应。我们的方案与用于治疗人类脑肿瘤的方案相当。结构和功能变化从治疗表面开始,从中心向周边扩散,累及5毫米颅骨切除术下暴露的整个大脑皮层。从表面到最深皮层的顺序变化首先涉及星形胶质细胞(1小时),然后是内皮细胞,最终是神经元。血栓在18小时后首次出现在微血管中,仅在48小时后才发生整个危险区域的凝固性坏死。结果表明,光敏剂穿过完整的血脑屏障并进入星形胶质细胞区室,在光激活后在该区室中产生细胞毒性。光动力疗法引起的局灶性脑损伤与大脑中动脉闭塞引起的损伤之间的比较表明,在这两种脑损伤形式中,细胞损伤沿着不同的路径发展。