Morse C C, Sigler C, Lock S, Hakkinen P J, Haschek W M, Witschi H P
Exp Mol Pathol. 1985 Apr;42(2):251-60. doi: 10.1016/0014-4800(85)90031-0.
The development of cyclophosphamide-induced pulmonary lesions over a 1-year period was studied in mice. Male BALB/c mice received a single intraperitoneal injection of 100 mg/kg of cyclophosphamide. Within 3 weeks there were scattered foci of intraalveolar foamy macrophages. With time, these foci increased in size and, 1 year later, occupied large areas in all lung lobes. There was also diffuse interstitial fibrosis. Chemical determination done 3, 12, 24, and 52 weeks after cyclophosphamide showed that lungs of animals treated with cyclophosphamide had significantly more hydroxyproline per lung than controls. One year after cyclophosphamide pressure-volume curves measured in vivo were shifted down and to the right and total lung volumes were decreased. A single injection of cyclophosphamide produced an irreversible and progressive pulmonary lesion.
研究了小鼠在1年时间内环磷酰胺诱导的肺部病变的发展情况。雄性BALB/c小鼠腹腔注射一次100 mg/kg的环磷酰胺。3周内出现散在的肺泡内泡沫状巨噬细胞灶。随着时间推移,这些病灶面积增大,1年后占据了所有肺叶的大片区域。还存在弥漫性间质纤维化。环磷酰胺注射后3、12、24和52周进行的化学测定表明,接受环磷酰胺治疗的动物肺部每肺的羟脯氨酸含量明显高于对照组。环磷酰胺注射1年后,体内测量的压力-容积曲线向下和向右移动,肺总体积减小。单次注射环磷酰胺会产生不可逆的进行性肺部病变。