Nishizawa M, Nakabayashi H, Uchida K, Nakagawa A, Niijima A
Department of Internal Medicine, Kanazawa Medical University, Uchinada, Japan.
J Auton Nerv Syst. 1996 Nov 6;61(2):149-54. doi: 10.1016/s0165-1838(96)00071-9.
To examine whether incretin hormones, truncated glucagon-like peptide-1 (tGLP-1) and glucose-dependent insulinotropic polypeptide (GIP), are recognized by the hepatic vagal nerve, changes of the impulse discharge rate in the afferent vagus upon their intraportal administrations were measured in situ in rats anesthetized with urethan and chloralose. One-min injection of tGLP-1 at a periphysiological dose of 0.2 pmol or a pharmacological dose of 4.0 pmol, but not of the vehicle, significantly facilitated the hepatic vagal afferents. However, the injection of GIP at either a physiological dose of 0.2 pmol, a periphysiological dose of 4.0 pmol, or an even much larger dose of 40.0 pmol did not change the afferents at all. The present results indicate that the hepatic vagus specifically recognizes an intraportal appearance of tGLP-1 in the hepatoportal area, suggesting that the vagal monitoring system for intraportal levels of the incretin hormone operates on ingestion of a mixed meal.
为了研究肠促胰岛素激素、截短的胰高血糖素样肽-1(tGLP-1)和葡萄糖依赖性促胰岛素多肽(GIP)是否能被肝迷走神经识别,在用乌拉坦和氯醛糖麻醉的大鼠中,原位测量门静脉内注射这些激素后传入迷走神经冲动发放率的变化。以生理剂量0.2 pmol或药理剂量4.0 pmol注射1分钟的tGLP-1(而非注射溶媒)可显著促进肝迷走神经传入。然而,以生理剂量0.2 pmol、生理周边剂量4.0 pmol或甚至更大剂量40.0 pmol注射GIP,对传入神经完全没有影响。目前的结果表明,肝迷走神经能特异性识别肝门区域门静脉内出现的tGLP-1,这表明肠促胰岛素激素门静脉水平的迷走神经监测系统在摄入混合餐时发挥作用。