Ferris C F, Carraway R E, Hammer R A, Leeman S E
Regul Pept. 1985 Oct;12(2):101-11. doi: 10.1016/0167-0115(85)90191-0.
The levels of neurotensin (NT) and its metabolite, the N-terminal octapeptide (NT1-8), identified by HPLC and measured by RIA, were increased in the hepatic-portal circulation of the anesthetized rat during perfusion of the small intestine with a lipid solution, while levels of both peptides remained unchanged in the general circulation. There was no significant arteriovenous difference for NT or NT1-8 during saline perfusion of the small intestine. Plasma collected from the superior mesenteric vein during the infusion of [3H]NT into the superior mesenteric artery showed major peaks of radioactivity with the retention times of NT1-8 and NT1-11 on HPLC. Only 12% of the radioactivity recovered from plasma was intact NT. These studies demonstrate that chromatographically identified NT and its metabolite, NT1-8, are elevated in the portal circulation but not systemic circulation during lipid perfusion and that the small intestine may be both the site of release and metabolism of NT.
通过高效液相色谱法(HPLC)鉴定并用放射免疫分析法(RIA)测定,在给麻醉大鼠的小肠灌注脂质溶液期间,其肝门静脉循环中神经降压素(NT)及其代谢产物N端八肽(NT1-8)的水平升高,而在体循环中这两种肽的水平保持不变。在小肠灌注生理盐水期间,NT或NT1-8没有显著的动静脉差异。在将[3H]NT注入肠系膜上动脉期间,从肠系膜上静脉采集的血浆在HPLC上显示出放射性主峰,其保留时间与NT1-8和NT1-11一致。从血浆中回收的放射性中只有12%是完整的NT。这些研究表明,在脂质灌注期间,经色谱鉴定的NT及其代谢产物NT1-8在门静脉循环中升高,但在体循环中未升高,并且小肠可能是NT的释放和代谢部位。