Tremel H, Strugala G, Forth W, Fichtl B
Arch Toxicol. 1985 Apr;57(1):74-5. doi: 10.1007/BF00286581.
T-2 toxin, a major trichothecene mycotoxin, was administered intravenously to rats. At a dose of 0.75 mg/kg two thirds of the animals died. In animals that received dexamethasone (1.6 mg/kg IV) either 30 min before or 1 h after the toxin, there was a more than fourfold reduction in lethality rate. Dexamethasone injected 3 h after the toxin was less effective. At a lethal dose of T-2 toxin (1 mg/kg IV) pretreatment with dexamethasone only delayed death, whereas lethality rate was barely affected (9/10 vs 10/10 in controls). Dexamethasone markedly reduced the incidence of lung edema and diarrhea. The incidence of hemorrhages, however, was not reduced by dexamethasone. Gastrointestinal bleeding was even more frequent in treated rats than in controls.
T-2毒素是一种主要的单端孢霉烯族霉菌毒素,通过静脉注射给予大鼠。剂量为0.75毫克/千克时,三分之二的动物死亡。在毒素注射前30分钟或注射后1小时接受地塞米松(1.6毫克/千克静脉注射)的动物中,致死率降低了四倍多。在毒素注射后3小时注射地塞米松效果较差。在T-2毒素的致死剂量(1毫克/千克静脉注射)下,用地塞米松预处理仅延迟了死亡,而致死率几乎未受影响(对照组为10/10,处理组为9/10)。地塞米松显著降低了肺水肿和腹泻的发生率。然而,地塞米松并未降低出血的发生率。接受治疗的大鼠胃肠道出血甚至比对照组更频繁。