Konno S, Asano K, Gonokami Y, Kurokawa M, Kawazu K, Adachi M
First Department of Internal Medicine, School of Medicine, Showa University.
Arerugi. 1995 May;44(5):556-61.
We investigated the effect of IPD-1151T (Suplatast Tosilate, (+/-)-[2-[4-(3-ethoxy-2-hydroxypropoxy) phenyl-carbamoyl]-ethyl] dimethylsulfonium p-toluenesulfonate) against allergic bronchoconstriction induced by allergen and methacholine (MCh).BALB/c mice were sensitized by intraperitoneal injection of 0.5 microgram of keyhold limpet hemocyanin mixed with Al(OH)3. IPD-1151T was administered orally once a day for 5 or 14 days in doses of 10, 30 or 100 mg/kg body weight. Bronchoconstriction was measured 24 hrs after the final drug administration. IPD-1151T inhibited both antigen-mediated allergic bronchoconstriction and induction of bronchial hyperresponsiveness after sensitization or allergen challenge in actively sensitized mice. The degree of inhibition was proportional to the dose and frequency of oral administration of the agent.
我们研究了IPD - 1151T(托西拉酯,(+/-)-[2-[4-(3 - 乙氧基 - 2 - 羟基丙氧基)苯基 - 氨基甲酰基]-乙基]二甲苯磺酸铵)对变应原和乙酰甲胆碱(MCh)诱导的过敏性支气管收缩的影响。通过腹腔注射0.5微克与氢氧化铝混合的钥孔戚血蓝蛋白使BALB/c小鼠致敏。IPD - 1151T以10、30或100毫克/千克体重的剂量每天口服给药一次,持续5天或14天。在最后一次给药24小时后测量支气管收缩情况。IPD - 1151T抑制了主动致敏小鼠致敏或变应原激发后抗原介导的过敏性支气管收缩以及支气管高反应性的诱导。抑制程度与该药物口服给药的剂量和频率成正比。