Suzuki K, Niho T, Yamaguchi K, Ohnishi H
Agents Actions. 1984 Jun;14(5-6):699-706. doi: 10.1007/BF01978911.
The effect of protizinic acid (PRT), a non-steroidal antiinflammatory drug, on the in vivo leukokinin (LK) generation system using feline acute ischemia model, in vitro LK generation system and the LK-induced contraction of the isolated smooth muscle was investigated. When 3 mg/kg PRT was injected twice intravenously to cats with acute cardiac ischemia, increased blood acid protease activity was inhibited and significant inhibitory action on the decrease of leukokininogen, the precursor of LK, was observed. Simultaneously, ST-segment elevation on the electrocardiogram tended to be suppressed and the lowered mean aortic blood pressure was significantly restored. On the LK generation induced by rabbit kininogen and acid protease derived from mouse L-1210 leukemic cells or rabbit polymorphonuclear leukocytes, PRT showed a dose-dependent inhibition while indomethacin (IM) and ibuprofen (IB) at a concentration of 3 X 10(-4) M showed no effect. However, potencies of the inhibitory actions of PRT, IM and IB on the LK generation induced by bovine spleen cathepsin D were almost the same at a concentration of 3 X 10(-4) M. Furthermore, PRT as well as IM showed antagonistic action on the isolated rat uterine contraction induced by LK. These results suggest that PRT not only inhibits the in vitro and in vivo generation of LK but also antagonizes to it on the receptor site of LK.
研究了非甾体抗炎药原卟啉酸(PRT)对使用猫急性缺血模型的体内白细胞激肽(LK)生成系统、体外LK生成系统以及LK诱导的离体平滑肌收缩的影响。当对急性心脏缺血的猫静脉注射两次3mg/kg的PRT时,血液酸性蛋白酶活性的增加受到抑制,并且观察到对LK前体白细胞激肽原减少的显著抑制作用。同时,心电图上的ST段抬高趋于受到抑制,降低了的平均主动脉血压显著恢复。对于由兔激肽原和源自小鼠L-1210白血病细胞或兔多形核白细胞的酸性蛋白酶诱导的LK生成,PRT表现出剂量依赖性抑制,而浓度为3×10(-4)M的吲哚美辛(IM)和布洛芬(IB)则无作用。然而,在浓度为3×10(-4)M时,PRT、IM和IB对牛脾脏组织蛋白酶D诱导的LK生成的抑制作用强度几乎相同。此外,PRT以及IM对LK诱导的离体大鼠子宫收缩均表现出拮抗作用。这些结果表明,PRT不仅抑制LK的体外和体内生成,而且在LK的受体部位对其产生拮抗作用。