Kubo M, Ochiai T, Kato J, Ishida R
Biological Research Laboratory, Tanabe Seiyaku Co., Ltd., Osaka, Japan.
Jpn J Pharmacol. 1991 Dec;57(4):517-26. doi: 10.1254/jjp.57.517.
The long-term oral administration of TA-6366 (5 mg/kg/day) from 4-weeks old impeded the genetic hypertension development with only a slight decrease in heart rate in spontaneously hypertensive rats (SHRs). However, the lower dose (1 mg/kg/day) of TA-6366 did not affect the development, but it lowered blood pressure after the development was almost accomplished. Concomitantly, relative heart weights in both the groups were markedly decreased to almost the same degree. The reduction of ACE activity in the aorta, brain and lung of both groups was found at 24 hr after the final administration, particularly at the 5 mg/kg/day dose; and that of the aorta was kept at almost the same low level even on the 9th day after withdrawal. After withdrawal of TA-6366 (5 mg/kg/day), the significant decrease in blood pressure was sustained at least for 10 weeks. The beneficial effect of TA-6366 on the hypertension development in SHRs seems to be related to its strong and long-lasting ACE inhibition, especially in the vasculature.
从4周龄起长期口服TA - 6366(5毫克/千克/天)可抑制自发性高血压大鼠(SHRs)的遗传性高血压发展,且心率仅有轻微下降。然而,较低剂量(1毫克/千克/天)的TA - 6366对高血压发展无影响,但在高血压发展基本完成后可降低血压。与此同时,两组大鼠的相对心脏重量均显著下降,且下降程度几乎相同。在末次给药后24小时,两组大鼠主动脉、脑和肺中的ACE活性均降低,尤其是5毫克/千克/天剂量组;即使在停药后第9天,主动脉中的ACE活性仍维持在几乎相同的低水平。停用TA - 6366(5毫克/千克/天)后,血压显著下降至少持续10周。TA - 6366对SHRs高血压发展的有益作用似乎与其强大且持久的ACE抑制作用有关,尤其是在血管系统中。