Zhang Zibo, Jin Hongtao, Bao Jie, Fang Fang, Wei Jinfeng, Wang Aiping
Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Xian Nong Tan Street, Xuan Wu District, Beijing, 100050, China.
Photochem Photobiol Sci. 2006 Nov;5(11):1006-17. doi: 10.1039/b605516h. Epub 2006 Sep 28.
The purpose of the current study was to investigate the potential repeated-dose toxicity of ZnPcP2S2-based photodynamic therapy (ZnPc-PDT) in Wistar rats. The animals were administered ZnPcS2P2 intravenously ten times successively every 4 d and irradiated with a 670 nm laser light for 6 min at subsequent 48 h and 72 h. At the end of the treatment period, 10 rats/sex/group were sacrificed, while 5 rats/sex/group were sacrificed after a two-week recovery period. During the test period, clinical signs, mortality, body weights, food and water consumption, ophthalmoscopy, hematology, serum biochemistry, urinalysis, organ weights, gross findings and histopathology were examined. The association between the increased liver weight and hepatic spotty and lytic necrosis seen in high dose females corroborates the conclusion that high dose ZnPc-PDT could induce hepatic injury in Wistar rats and they are probably related to the abnormality of certain biochemical parameters of females in the high dose group. Furthermore, microscopic examination for the ZnPc-PDT groups shows the presence of some Kelly and khaki granules in Kupffer cells and endothelia of the livers, epithelia of the renal tubules, marginal sinus and medulla of the spleens, alveolar walls of the lungs, reticular cells and macrophages of the mesenteric lymph nodes, testicular Leydig cells, epididymal epithelial cells, endometrial stromal cells, and interstitial cells and corpora lutea of the ovaries from all or most of the animals. There were no adverse effects on mortality, clinical signs, food and water consumption, ophthalmoscopy, uranalysis, hematology, serum biochemistry, body weights and necropsy findings in control, low and mid dose groups. Based on these results, it was concluded that the intravenous repeated-dose of ZnPcP2S2-PDT induced the abnormalities of liver weights, hepatic biochemistry and histopathology, and pigmentation in the several important organs in Wistar rats at 4 mg kg(-1) d(-1). The target organ was determined to be liver (and spleen perhaps), but this was not so obvious in males. The no-observed-adverse-effect level (NOAEL) was considered to be 1.0 mg kg(-1) for both sexes.
本研究的目的是调查基于二硫化锌酞菁(ZnPcP2S2)的光动力疗法(ZnPc-PDT)对Wistar大鼠的潜在重复给药毒性。给动物每隔4天连续静脉注射10次ZnPcS2P2,并在随后的48小时和72小时用670nm激光照射6分钟。在治疗期结束时,每组处死10只/性别大鼠,而每组5只/性别大鼠在两周恢复期后处死。在试验期间,检查了临床体征、死亡率、体重、食物和水消耗、检眼镜检查、血液学、血清生物化学、尿液分析、器官重量、大体检查结果和组织病理学。高剂量雌性大鼠肝脏重量增加与肝脏斑点状和溶解性坏死之间的关联证实了高剂量ZnPc-PDT可诱导Wistar大鼠肝损伤的结论,且它们可能与高剂量组雌性大鼠某些生化参数异常有关。此外,对ZnPc-PDT组的显微镜检查显示,所有或大多数动物的肝脏库普弗细胞和内皮、肾小管上皮、脾脏边缘窦和髓质、肺肺泡壁、肠系膜淋巴结的网状细胞和巨噬细胞、睾丸间质细胞、附睾上皮细胞、子宫内膜基质细胞以及卵巢的间质细胞和黄体中存在一些凯利和卡其色颗粒。对照组、低剂量组和中剂量组在死亡率、临床体征、食物和水消耗、检眼镜检查、尿液分析、血液学、血清生物化学、体重和尸检结果方面均未出现不良反应。基于这些结果,得出结论:以4mg kg(-1) d(-1)的剂量静脉重复给药ZnPcP2S2-PDT可导致Wistar大鼠肝脏重量、肝脏生物化学和组织病理学异常以及几个重要器官出现色素沉着。确定的靶器官为肝脏(可能还有脾脏),但在雄性大鼠中不太明显。两性的无观察到不良反应水平(NOAEL)均被认为是1.0mg kg(-1)。