Nair S C, Panikkar B, Akamanchi K G, Panikkar K R
Amala Cancer Research Centre, Kerala, India.
Cancer Lett. 1991 Dec 1;60(3):253-8. doi: 10.1016/0304-3835(91)90121-w.
Topical application of 100 mg/kg body weight of Ixora javanica flower extract inhibited the growth and delayed the onset of papilloma formation in mice initiated with 7,12-dimethylbenz[a]anthracene (DMBA) and promoted using croton oil. The extract at the same dose, when administered orally inhibited the growth of subcutaneously injected 20-methylcholanthrene (MCA)-induced soft tissue fibrosarcomas significantly. Oral administration of 200 mg/kg of the extract inhibited the growth of intraperitoneally transplanted sarcoma-180 and Ehrlich ascites carcinoma tumours besides showing an increase in the life span of the treated mice. Toxicity studies showed that the blood urea nitrogen levels were elevated post treatment. The active compounds responsible for the above inhibitory effects on tumour growth were identified as ferulic acid (4-hydroxy-3-methoxy cinnamic acid) and its regionmer 3-hydroxy-4-methoxy cinnamic acid.
以100毫克/千克体重的爪哇龙船花提取物进行局部应用,可抑制由7,12 - 二甲基苯并[a]蒽(DMBA)引发、巴豆油促进的小鼠乳头瘤形成,抑制其生长并延迟发病。相同剂量的提取物经口服,可显著抑制皮下注射20 - 甲基胆蒽(MCA)诱导的软组织纤维肉瘤的生长。口服200毫克/千克的提取物除了能延长受试小鼠的寿命外,还可抑制腹腔移植的肉瘤 - 180和艾氏腹水癌肿瘤的生长。毒性研究表明,治疗后血尿素氮水平升高。对肿瘤生长具有上述抑制作用的活性化合物被鉴定为阿魏酸(4 - 羟基 - 3 - 甲氧基肉桂酸)及其区域异构体3 - 羟基 - 4 - 甲氧基肉桂酸。