Murphy D J, Joran M E
Department of Investigative Toxicology, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania.
Fundam Appl Toxicol. 1992 Feb;18(2):307-13. doi: 10.1016/0272-0590(92)90060-u.
SK&F 101926 is a synthetic octapeptide which was designed to promote free water excretion by antagonizing the action of antidiuretic hormone. The clinical and pathologic changes in rats resulting from lethal doses of SK&F 101926 have suggested that death is associated with respiratory failure and/or cardiovascular collapse. To define the relationships between respiratory failure, cardiovascular collapse, and death, respiratory and cardiovascular parameters were monitored in anesthetized rats following the intravenous administration of SK&F 101926 at a dosage (3 mg/kg) which resulted in 70% mortality. Within 5 min after receiving this dosage, mean arterial blood pressure was reduced to values between 30 and 40 mm Hg in all rats. This degree of hypotension was well tolerated by some rats and, consequently, was not considered to be the cause of death. Deaths occurred between 9 and 58 min after dosing and were preceded by respiratory depression involving marked reductions in respiratory rate and the lack of compensatory increases in tidal volume. At the time of respiratory arrest, heart rates remained above 200 beats/min, mean arterial blood pressure remained between 30 and 40 mm Hg, and there were no consistent changes in dynamic lung compliance or total pulmonary resistance. Pretreatment of rats with a mast cell stabilizing agent (disodium cromoglycate), a mast cell degranulating agent (compound 48/80), or a histamine/5-hydroxytryptamine blocking agent (cyproheptadine) prevented the reductions in respiratory rate and death caused by SK&F 101926. These pretreatments also reduced the effect of SK&F 101926 on blood pressure, but were not able to completely prevent the hypotension.(ABSTRACT TRUNCATED AT 250 WORDS)
SK&F 101926是一种合成八肽,其设计目的是通过拮抗抗利尿激素的作用来促进自由水排泄。致死剂量的SK&F 101926导致大鼠出现的临床和病理变化表明,死亡与呼吸衰竭和/或心血管衰竭有关。为了明确呼吸衰竭、心血管衰竭与死亡之间的关系,在麻醉大鼠静脉注射SK&F 101926(剂量为3毫克/千克,该剂量导致70%的死亡率)后,对其呼吸和心血管参数进行了监测。在接受该剂量后5分钟内,所有大鼠的平均动脉血压降至30至40毫米汞柱之间。一些大鼠对这种程度的低血压耐受性良好,因此,低血压不被认为是死亡原因。给药后9至58分钟出现死亡,死亡前有呼吸抑制,表现为呼吸频率显著降低且潮气量缺乏代偿性增加。在呼吸停止时,心率仍高于200次/分钟,平均动脉血压保持在30至40毫米汞柱之间,动态肺顺应性或总肺阻力没有一致变化。用肥大细胞稳定剂(色甘酸钠二钠)、肥大细胞脱颗粒剂(化合物48/80)或组胺/5-羟色胺阻断剂(赛庚啶)对大鼠进行预处理,可预防SK&F 101926引起的呼吸频率降低和死亡。这些预处理也降低了SK&F 101926对血压的影响,但不能完全预防低血压。(摘要截断于250字)