Miner J L, Erlanson-Albertsson C, Paterson J A, Baile C A
Monsanto Company, St. Louis, MO 63198.
J Anim Sci. 1994 Jun;72(6):1578-82. doi: 10.2527/1994.7261578x.
Enterostatin, a peptide formed during the activation of pancreatic procolipase in the duodenum, is likely a mediator of satiety in the rat. The objective of this research was to determine whether administration of enterostatin into the lateral cerebral ventricle of sheep unfed for 2 h resulted in reduced feed intake. Bolus doses of 2 micrograms did reduce (P < .03) feed intake during the hour after injection by one- to two-thirds of control. Doses 20 micrograms or greater were not effective, and .2 microgram also did not have any statistically significant effect. This range of effective doses was similar to that observed in the rat, and the effective dose of 2 micrograms was approximately 10-fold greater on a per-animal basis, but less on a brain-size basis, than the amount needed to achieve a similar response in the rat. Therefore, enterostatin can reduce feed intake and thus may also be involved in satiety in sheep.
肠抑素是在十二指肠中胰原脂酶激活过程中形成的一种肽,它可能是大鼠饱腹感的一种介导物。本研究的目的是确定向禁食2小时的绵羊侧脑室注射肠抑素是否会导致采食量减少。2微克的大剂量注射确实使注射后一小时内的采食量减少(P <.03),减少量为对照组的三分之一到三分之二。20微克或更大剂量无效,0.2微克也没有任何统计学上的显著效果。这一有效剂量范围与在大鼠中观察到的相似,2微克的有效剂量按每只动物计算比在大鼠中产生类似反应所需的量大约10倍,但按脑大小计算则较少。因此,肠抑素可以减少采食量,从而也可能参与绵羊的饱腹感调节。