Brasitus T A, Dudeja P K, Dahiya R
J Clin Invest. 1986 Mar;77(3):831-40. doi: 10.1172/JCI112380.
Dimethylhydrazine (DMH) is a potent procarcinogen with selectivity for the colon. To determine whether alterations in the lipid composition and fluidity of rat colonic brush border membranes existed before the development of DMH-induced colon cancer, rats were injected s.c. with this agent (20 mg/kg body weight per wk) or diluent for 5, 10, and 15 wk. Animals were killed at these time periods and brush border membranes were prepared from proximal and distal colonocytes of each group. The "static" and "dynamic" components of fluidity of each membrane were then assessed, by steady-state fluorescence polarization techniques using limiting hindered fluorescence anisotropy and order parameter values of the fluorophore 1,6 diphenyl-1,3,5-hexatriene (DPH) and fluorescence anisotropy values of DL-2-(9-anthroyl) stearic acid and DL-12-(9-anthroyl) stearic acid, respectively. Membrane lipids were extracted and analyzed by thin-layer chromatography and gas-liquid chromatography. Phospholipid methylation activity in these membranes was also measured using S-adenosyl-L-methionine as the methyl donor. The results of these studies demonstrate that: the lipid composition and both components of fluidity of proximal DMH-treated and control membranes and their liposomes were similar at all time periods examined; at 5, 10, and 15 wk the "dynamic component of fluidity" of distal DMH-treated membranes and their liposomes was found to be higher, similar, and lower, respectively, than their control counterparts; the "static component of fluidity" of distal DMH-treated membranes and their liposomes, however, was similar to control preparations at all three time periods; and alterations in the lipid composition and phospholipid methylation activities appeared to be responsible for these differences in the "dynamic component of fluidity" at these various time periods.
二甲基肼(DMH)是一种对结肠具有选择性的强效致癌物前体。为了确定在DMH诱导的结肠癌发生之前大鼠结肠刷状缘膜的脂质组成和流动性是否存在改变,将大鼠皮下注射该试剂(每周20mg/kg体重)或稀释剂,持续5、10和15周。在这些时间段处死动物,并从每组的近端和远端结肠细胞制备刷状缘膜。然后通过稳态荧光偏振技术,分别使用荧光团1,6-二苯基-1,3,5-己三烯(DPH)的极限受阻荧光各向异性和有序参数值以及DL-2-(9-蒽基)硬脂酸和DL-12-(9-蒽基)硬脂酸的荧光各向异性值,评估每个膜流动性的“静态”和“动态”成分。提取膜脂质并通过薄层色谱和气-液色谱进行分析。还使用S-腺苷-L-甲硫氨酸作为甲基供体测量这些膜中的磷脂甲基化活性。这些研究结果表明:在所有检查的时间段,近端经DMH处理的膜及其脂质体与对照膜及其脂质体的脂质组成和流动性的两个成分相似;在5、10和15周时,远端经DMH处理的膜及其脂质体的“流动性动态成分”分别高于、相似于和低于其对照对应物;然而,远端经DMH处理的膜及其脂质体的“流动性静态成分”在所有三个时间段都与对照制剂相似;并且脂质组成和磷脂甲基化活性的改变似乎是这些不同时间段“流动性动态成分”差异的原因。