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用脂质灌注大鼠小肠期间神经降压素的释放与降解

Release and degradation of neurotensin during perfusion of rat small intestine with lipid.

作者信息

Ferris C F, Carraway R E, Hammer R A, Leeman S E

出版信息

Regul Pept. 1985 Oct;12(2):101-11. doi: 10.1016/0167-0115(85)90191-0.

Abstract

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.

摘要

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。

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