Mei J, Erlanson-Albertsson C
Department of Medical and Physiological Chemistry, University of Lund, Sweden.
Regul Pept. 1992 Oct 13;41(3):209-18. doi: 10.1016/0167-0115(92)90114-a.
The effect of enterostatin, the amino-terminal pentapeptide of pancreatic procolipase, on high-fat food intake has been investigated after intracerebroventricular as well as after intravenous injection. After an overnight fast enterostatin given i.c.v. at doses of 167 pmol and 333 pmol produced a significant and dose-dependent reduction in high-fat food intake, while a higher dose of 667 pmol had no effect. Following intravenous injection of enterostatin the intake of high-fat food was suppressed at doses of 8.3 nmol and 16.7 nmol, while no effect was observed at higher doses. The inhibition of feeding started 3 h after the initiation of feeding and persisted to the end of the test period (6 h). Enterostatin at a dose of 16.7 nmol gave no sign of aversion in an aversion test comparing the effect of enterostatin, lithium chloride and saline on liquid intake. The data suggest that enterostatin may exert its satiety effect on high-fat feeding by being absorbed into the bloodstream.
已对胰原脂酶的氨基末端五肽肠抑素经脑室注射及静脉注射后对高脂食物摄入量的影响进行了研究。禁食一夜后,以167皮摩尔和333皮摩尔的剂量经脑室注射肠抑素,可显著且剂量依赖性地降低高脂食物摄入量,而667皮摩尔的较高剂量则无此作用。静脉注射肠抑素后,8.3纳摩尔和16.7纳摩尔的剂量可抑制高脂食物的摄入,而较高剂量则未观察到作用。进食开始3小时后开始出现摄食抑制,并持续至试验期结束(6小时)。在一项比较肠抑素、氯化锂和生理盐水对液体摄入量影响的厌恶试验中,16.7纳摩尔剂量的肠抑素未表现出厌恶迹象。数据表明,肠抑素可能通过被吸收进入血液循环而对高脂喂养发挥其饱腹感作用。