Semrad S D, Rose M L, Adams J L
Department of Medical, University of Wisconsin School of Veterinary Medicine, Madison 53706.
Circ Shock. 1993 Aug;40(4):235-42.
The effects of a 21-aminosteroid, tirilazad mesylate (U74006F; The Upjohn Co., Kalamazoo, MI), developed for treatment of central nervous system trauma in human beings, on eicosanoid and tumor necrosis factor (TNF) generation were evaluated in both healthy and endotoxin-challenged neonatal calves. Endotoxemia was induced in 24 neonatal calves by intravenous infusion of Escherichia coli lipopolysaccharide (3.25 micrograms/kg) over 3 hr. Group I calves received the endotoxin infusion alone; group II calves received an infusion of 0.9% saline and were treated with tirilazad mesylate (1.5 mg/kg) 1 hr after the infusion was started, group III and IV calves were treated with tirilazad mesylate 1 hr after or before endotoxin infusion was started. Tirilazad mesylate effectively suppressed production of plasma prostacyclin (6-keto-PGF1 alpha) and TNF in endotoxin-challenged neonatal calves. In addition, production of thromboxane B2 was mitigated by treatment with tirilazad mesylate both 1 hr before and 1 hr after initiation of endotoxin infusion. It appears that tirilazad mesylate effectively suppresses eicosanoid and TNF generation induced by endotoxin, and thus may be beneficial in the treatment of endotoxemia and septicemia in neonatal calves.
为治疗人类中枢神经系统创伤而研发的一种21-氨基类固醇甲磺替拉扎特(U74006F;美国密歇根州卡拉马祖的普强公司),对健康和内毒素激发的新生小牛类花生酸和肿瘤坏死因子(TNF)生成的影响进行了评估。通过在3小时内静脉输注大肠杆菌脂多糖(3.25微克/千克),在24头新生小牛中诱导内毒素血症。I组小牛仅接受内毒素输注;II组小牛接受0.9%盐水输注,并在输注开始1小时后用甲磺替拉扎特(1.5毫克/千克)治疗,III组和IV组小牛在内毒素输注开始后或之前1小时用甲磺替拉扎特治疗。甲磺替拉扎特有效抑制了内毒素激发的新生小牛血浆前列环素(6-酮-PGF1α)和TNF的产生。此外,在内毒素输注开始前1小时和开始后1小时用甲磺替拉扎特治疗均减轻了血栓素B2的产生。甲磺替拉扎特似乎有效抑制内毒素诱导的类花生酸和TNF生成,因此可能有益于治疗新生小牛的内毒素血症和败血症。