Zetler G, Mörsdorf K H
Naunyn Schmiedebergs Arch Pharmacol. 1984 Mar;325(3):209-13. doi: 10.1007/BF00495945.
Subcutaneous (SC) injections of ceruletide (caerulein diethylammonium hydrate, CER) and the octapeptide of cholecystokinin (CCK-8) reduced the intake of liquid food in male NMRI mice starved for 18 h. The corresponding ED50 values were 2 micrograms/kg for CER and 24 micrograms/kg for CCK-8; hence, on a molar basis, CER was 14 times more potent than CCK-8. Naloxone (0.2 and 1 mg/kg, SC) inhibited eating. (D-Ala)2(MePhe)4-(Met(O)-ol)5-enkephalin (FK 33-824; 0.3 and 1 mg/kg) was only stimulatory. Naloxone enhanced the effect of CER, whereas FK 33-824 antagonized it. It is concluded that concerning the inhibition of food intake, opioid peptides can be antagonists of CCK-like peptides. This is consistent with the current view of the regulation of appetitive behaviour.
皮下注射蛙皮素(蛙皮素二乙铵水合物,CER)和胆囊收缩素八肽(CCK - 8)可减少饥饿18小时的雄性NMRI小鼠的流食摄入量。相应的半数有效剂量(ED50)值,CER为2微克/千克,CCK - 8为24微克/千克;因此,按摩尔计算,CER的效力是CCK - 8的14倍。纳洛酮(0.2和1毫克/千克,皮下注射)抑制进食。(D - 丙氨酸)2(甲基苯丙氨酸)4 - (甲硫氨酸(氧) - 醇)5 - 脑啡肽(FK 33 - 824;0.3和1毫克/千克)仅具有刺激作用。纳洛酮增强了CER的作用,而FK 33 - 824则拮抗其作用。得出的结论是,关于食物摄入的抑制,阿片肽可以是CCK样肽的拮抗剂。这与当前对食欲行为调节的观点一致。