Yotis W W, Zeb M, Brennan P C, Kirchner F R, Glendenin L E, Wu-Yuan C D
Microbios. 1983;36(143):21-32.
The action of certain substances known to induce cellular alterations, or encounted in the oral cavity, on the accumulation of 18F by Streptococcus mutans GS-5 has been investigated. A 62-67% inhibition in the number of 18F atoms bound per mg dry weight of cells could be induced by a 15 min pretreatment with 2.7 X 10(-4) M cetyltrimethylammoniumbromide, 1 X 10(-1) M acetic anhydride, or 7 X 10(-2) M HCl. Plate counts indicated that alteration of the cellular composition rather than viability was responsible for this diminution in 18F accumulation. Prior exposure for 15 min of this organism to 1 M HCHO or 0.1 M NaOH did not alter 18F accumulation. Of the common salts encountered in the oral cavity, CaCl2 enhanced 18F binding. Pretreatment of the assay cells for 15-160 min with 0.1-10 mg/ml of trypsin, pronase, protease, alpha-glucosidase, dextranase, or lactoferrin had no significant effect on the accumulation of 18F. However, pre-exposure of cells for 60 min to 1-10 mg/ml of either amylase or lipase induced a 40-67% inhibition in the binding of 18F, while lysozyme enhanced the binding of 18F by the cells. It would appear then that the binding of 18F by S. mutans may be altered by certain substances encountered in the oral cavity.
已对某些已知能诱导细胞改变或在口腔中存在的物质对变形链球菌GS-5积累¹⁸F的作用进行了研究。用2.7×10⁻⁴M十六烷基三甲基溴化铵、1×10⁻¹M乙酸酐或7×10⁻²M盐酸预处理15分钟,可使每毫克细胞干重结合的¹⁸F原子数抑制62 - 67%。平板计数表明,¹⁸F积累减少是由于细胞组成的改变而非活力所致。将该生物体预先暴露于1M甲醛或0.1M氢氧化钠15分钟,并未改变¹⁸F的积累。在口腔中常见的盐类中,氯化钙可增强¹⁸F的结合。用0.1 - 10mg/ml的胰蛋白酶、链霉蛋白酶、蛋白酶、α - 葡萄糖苷酶、葡聚糖酶或乳铁蛋白对测定细胞预处理15 - 160分钟,对¹⁸F的积累没有显著影响。然而,将细胞预先暴露于1 - 10mg/ml的淀粉酶或脂肪酶60分钟,可使¹⁸F的结合抑制40 - 67%,而溶菌酶则增强细胞对¹⁸F的结合。因此,变形链球菌对¹⁸F的结合可能会被口腔中遇到的某些物质改变。