Chelikani Prasanth K, Haver Alvin C, Reidelberger Roger D
Department of Biomedical Sciences, Creighton University, Omaha, NE 68178, USA.
Peptides. 2006 Dec;27(12):3193-201. doi: 10.1016/j.peptides.2006.08.001. Epub 2006 Sep 7.
We used a conditioned taste aversion test to assess whether PYY(3-36) reduces food intake by producing malaise. Two-hour IV infusion of PYY(3-36) (8, 15, and 30 pmol/kg/min) at dark onset in non-food-deprived rats produced a dose-dependent inhibition of feeding and a conditioned aversion to the flavored chow paired with PYY(3-36) infusion. In food-deprived rats, PYY(3-36) at 2 and 4 pmol/kg/min inhibited intake of a flavored saccharin solution without producing conditioned taste aversion, whereas higher doses (8 and 15 pmol/kg/min) inhibited saccharin intake and produced taste aversion. These results suggest that anorexic doses of PYY(3-36) may produce a dose-dependent malaise in rats, which is similar to that reported for PYY(3-36) infusion in humans. Previous studies have shown that PYY(3-36) potently inhibits gastric emptying, and that gut distention can produce a conditioned taste aversion. Thus, PYY(3-36) may produce conditioned taste aversion in part by slowing gastric emptying.
我们使用条件性味觉厌恶测试来评估PYY(3-36)是否通过引起不适来减少食物摄入量。在非饥饿大鼠中,于黑暗开始时静脉输注两小时的PYY(3-36)(8、15和30 pmol/kg/分钟)会产生剂量依赖性的进食抑制,并对与PYY(3-36)输注配对的调味食物产生条件性厌恶。在饥饿大鼠中,2和4 pmol/kg/分钟的PYY(3-36)抑制了调味糖精溶液的摄入量,但未产生条件性味觉厌恶,而较高剂量(8和15 pmol/kg/分钟)则抑制了糖精摄入量并产生了味觉厌恶。这些结果表明,厌食剂量的PYY(3-36)可能在大鼠中产生剂量依赖性的不适,这与人类中PYY(3-36)输注的报道相似。先前的研究表明,PYY(3-36)能有效抑制胃排空,并且肠道扩张可产生条件性味觉厌恶。因此,PYY(3-36)可能部分通过减缓胃排空而产生条件性味觉厌恶。