Moriyoshi Y, Shiratori K, Iwabe C, Watanabe S, Takeuchi T
Department of Internal Medicine, Tokyo Women's Medical College, Japan.
J Gastroenterol. 1996 Apr;31(2):249-53. doi: 10.1007/BF02389525.
We assessed the duration of the anti-cholecystokinin (CCK) action of FK480, a new non-peptide CCK-A receptor antagonist developed in Japan, in an in vivo study in rats, comparing it with CR 1505. Pancreatic exocrine secretion stimulated by intravenous infusion of CCK-8 (0.06 microgram/kg per h) was measured at intervals of 0-24 h after the oral administration of FK480 (1.5 mg/kg) and CR 1505 (30 mg/kg). FK480 significantly inhibited both CCK-stimulated pancreatic juice volume flow and amylase output 0, 4, 8, and 12 h after oral administration, whereas the inhibitory effect of CR 1505 had completely disappeared by 8 h after oral administration. It was concluded that orally administered FK480 has a prolonged anti-CCK action.
我们在大鼠体内研究中评估了日本研发的新型非肽类胆囊收缩素-A(CCK-A)受体拮抗剂FK480的抗胆囊收缩素(CCK)作用持续时间,并将其与CR 1505进行比较。在口服FK480(1.5mg/kg)和CR 1505(30mg/kg)后,于0至24小时的时间间隔测量静脉输注CCK-8(0.06微克/千克每小时)刺激的胰腺外分泌。口服FK480后0、4、8和12小时,FK480显著抑制了CCK刺激的胰液体积流量和淀粉酶分泌量,而CR 1505的抑制作用在口服后8小时完全消失。得出的结论是,口服FK480具有延长的抗CCK作用。