Gabliks J
Infect Immun. 1972 Sep;6(3):364-9. doi: 10.1128/iai.6.3.364-369.1972.
Chlorinated hydrocarbon 2,2-bis(parachlorophenyl)-1,1,1-trichloroethane (DDT) and its derivative 2,2-bis(parachlorophenyl)-1,1-dichloroethane (o,p'-DDD) protected the cells of human embryonic intestine, Henle strain, against the cytotoxic effects induced by staphylococcal enterotoxin B (SEB). The hydrocarbons were incorporated in the culture medium, and the cytotoxicity of SEB was measured by cell destruction and by inhibition of cell growth during incubation for 48 hr. When DDT at nontoxic levels (4 to 25 mug/ml) was added to cultures, 24 or 4 hr prior to or 7 hr after the administration of toxin (100 mug/ml), the cells did not show the characteristic cytotoxicity. A therapeutic effect was also observed with o,p'-DDD added to cultures 9 hr after SEB. Because the cells treated with DDT for a period of 24 hr remained resistant to the toxin when DDT was removed from the cultures, it appears that DDT acts upon the cells rather then upon enterotoxin B. The protective effect of DDT was also observed against the toxin-induced skin erythemas and necrosis in guinea pigs treated with DDT.
氯代烃2,2-双(对氯苯基)-1,1,1-三氯乙烷(滴滴涕)及其衍生物2,2-双(对氯苯基)-1,1-二氯乙烷(邻,对'-滴滴滴)可保护人胚胎肠亨勒株细胞免受葡萄球菌肠毒素B(SEB)诱导的细胞毒性作用。将这些碳氢化合物加入培养基中,并通过细胞破坏和在48小时孵育期间对细胞生长的抑制来测量SEB的细胞毒性。当在给予毒素(100微克/毫升)前24小时或4小时或后7小时向培养物中加入无毒水平(4至25微克/毫升)的滴滴涕时,细胞未表现出特征性的细胞毒性。在SEB加入9小时后向培养物中加入邻,对'-滴滴滴也观察到了治疗效果。由于当从培养物中去除滴滴涕时,用滴滴涕处理24小时的细胞对毒素仍具有抗性,因此似乎滴滴涕作用于细胞而非肠毒素B。在用滴滴涕处理的豚鼠中也观察到了滴滴涕对毒素诱导的皮肤红斑和坏死的保护作用。