Hisatomi A, Kimura M, Maeda M, Matsumoto M, Ohara K, Noguchi H
Toxicology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
J Toxicol Sci. 1993 Aug;18 Suppl 3:1-9. doi: 10.2131/jts.18.supplementiii_1.
HCO-60, a polyoxyethylene castor oil derivative, is used as a solubilizer in the injectable formulations of lipophilic agents. This study was performed to examine the toxicity of HCO-60 in various experimental animals including dogs, monkeys, rabbits, guinea pigs and rats. With 1.25 or 2.5 mg/kg of HCO-60 injected i.v. to dogs, blood pressure decreased, flush, swelling and itching appeared after injection, and with 10 mg/kg of HCO-60 there was additionally a decrease of spontaneous motility. In the two higher dose groups, these symptoms paralleled an increase of histamine levels. Since degranulation was observed after injection in the mast cells of the skin, but not in the liver of dogs, the histamine in the plasma was considered to be released from the mast cells of the skin. Pretreatment with diphenhydramine, a H1-receptor antagonist, suppressed the decrease of blood pressure induced by HCO-60. These findings show that the toxicity of HCO-60 is associated with histamine release from the mast cells. No symptoms occurred in monkeys, rabbits, guinea pigs or rats with 50 or 100 mg/kg of i.v. of HCO-60, and there was no change in plasma histamine levels. This study demonstrated that the toxicity of HCO-60 is species specific to dogs among the animals tested.
HCO - 60是一种聚氧乙烯蓖麻油衍生物,在亲脂性药物的注射剂配方中用作增溶剂。本研究旨在检测HCO - 60在包括狗、猴、兔、豚鼠和大鼠在内的各种实验动物中的毒性。给狗静脉注射1.25或2.5mg/kg的HCO - 60后,血压下降,注射后出现潮红、肿胀和瘙痒,而注射10mg/kg的HCO - 60时,自发活动还会减少。在两个较高剂量组中,这些症状与组胺水平的升高平行。由于在狗的皮肤肥大细胞注射后观察到脱颗粒现象,而在肝脏中未观察到,因此认为血浆中的组胺是从皮肤肥大细胞释放的。用H1受体拮抗剂苯海拉明预处理可抑制HCO - 60引起的血压下降。这些发现表明,HCO - 60的毒性与肥大细胞释放组胺有关。静脉注射50或100mg/kg的HCO - 60后,猴、兔、豚鼠或大鼠未出现任何症状,血浆组胺水平也没有变化。本研究表明,在受试动物中,HCO - 60的毒性对狗具有物种特异性。