Arnelo U, Reidelberger R, Adrian T E, Larsson J, Permert J
Department of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska 68178, USA.
Am J Physiol. 1998 Nov;275(5):R1537-42. doi: 10.1152/ajpregu.1998.275.5.R1537.
Our objective was to study whether islet amyloid polypeptide (IAPP) produces satiety by an endocrine mechanism. We used a rat model to determine whether postprandial plasma levels of IAPP are comparable to those required to inhibit feeding when IAPP is administered by continuous intravenous infusion. Food intake in rats with aortic catheters increased plasma IAPP levels from a fasting level of 10.8 +/- 0.5 pM to a peak level of 19.0 +/- 1.0 pM at 2.2 +/- 0.5 h. In rats with jugular vein and aortic catheters, the threshold intravenous dose for IAPP suppression of feeding was between 1 and 3 pmol . kg-1 . min-1. The 3 pmol . kg-1 . min-1 dose decreased 4-h intake by approximately 25% by decreasing meal frequency rather than meal size. This dose increased plasma IAPP by approximately 24 pM. These results suggest that postprandial plasma levels of IAPP are not quite sufficient to independently produce satiety.
我们的目的是研究胰岛淀粉样多肽(IAPP)是否通过内分泌机制产生饱腹感。我们使用大鼠模型来确定餐后血浆IAPP水平是否与通过持续静脉输注给予IAPP时抑制进食所需的水平相当。有主动脉导管的大鼠进食后,血浆IAPP水平从空腹时的10.8±0.5 pM升高至2.2±0.5小时时的峰值19.0±1.0 pM。在有颈静脉和主动脉导管的大鼠中,IAPP抑制进食的静脉注射阈值剂量在1至3 pmol·kg-1·min-1之间。3 pmol·kg-1·min-1的剂量通过减少进餐频率而非餐量使4小时摄入量减少了约25%。该剂量使血浆IAPP升高了约24 pM。这些结果表明,餐后血浆IAPP水平不足以独立产生饱腹感。