U.O.C., Endocrinologia e Diabetologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Istituto Patologia Speciale Medica, Università Cattolica del Sacro Cuore, Rome, Italy.
J Clin Endocrinol Metab. 2019 Jul 1;104(7):2685-2694. doi: 10.1210/jc.2018-02804.
Changes in bile flow after bariatric surgery may beneficially modulate secretion of insulin and incretins, leading to diabetes remission. However, the exact mechanism(s) involved is still unclear. Here, we propose an alternative method to investigate the relationship between alterations in physiological bile flow and insulin and incretin secretion by studying changes in gut-pancreatic function in extrahepatic cholestasis in nondiabetic humans.
To pursue this aim, 58 nondiabetic patients with recent diagnosis of periampullary tumors underwent an oral glucose tolerance test (OGTT), and a subgroup of 16 patients also underwent 4-hour mixed meal tests and hyperinsulinemic-euglycemic clamps.
The analysis of the entire cohort revealed a strong inverse correlation between total bilirubin levels and insulinogenic index. When subjects were divided on the basis of bilirubin levels, used as a marker of altered bile flow, subjects with high bilirubin levels displayed inferior glucose control and decreased insulin secretion during the OGTT. Altered bile flow elicited a markedly greater increase in glucagon and glucagon-like peptide 1 (GLP-1) secretion at fasting state, and following the meal, both glucagon and GLP-1 levels remained increased over time. Conversely, Glucose-dependent insulinotropic polypeptide (GIP) levels were comparable at the fasting state, whereas the increase following meal ingestion was significantly blunted with high bilirubin levels. We reveal strong correlations between total bilirubin and glucagon and GLP-1 levels.
Our findings suggest that acute extrahepatic cholestasis determines major impairment in enteroendocrine gut-pancreatic secretory function. The altered bile flow may determine a direct deleterious effect on β-cell function, perhaps mediated by the impairment of incretin hormone function.
减重手术后胆汁流量的变化可能通过调节胰岛素和肠促胰岛素的分泌而有益于糖尿病的缓解。然而,其涉及的确切机制仍不清楚。在这里,我们提出了一种替代方法,通过研究非糖尿病患者肝外胆汁淤积症中肠道-胰腺功能的变化来研究生理胆汁流量变化与胰岛素和肠促胰岛素分泌之间的关系。
为了达到这个目的,58 名近期诊断为壶腹周围肿瘤的非糖尿病患者接受了口服葡萄糖耐量试验(OGTT),其中 16 名患者还接受了 4 小时混合餐试验和高胰岛素-正常血糖钳夹试验。
对整个队列的分析显示总胆红素水平与胰岛素原指数呈强烈负相关。当根据胆红素水平(作为胆汁流量改变的标志物)对患者进行分组时,高胆红素水平的患者在 OGTT 中显示出较差的血糖控制和胰岛素分泌减少。改变的胆汁流量在空腹状态下引起胰高血糖素和胰高血糖素样肽 1(GLP-1)分泌的明显增加,并且在进食后,两者的 GLP-1 水平随着时间的推移而持续升高。相反,葡萄糖依赖性胰岛素释放肽(GIP)水平在空腹状态下相当,而在高胆红素水平下,进食后 GIP 水平的增加显著减弱。我们发现总胆红素与胰高血糖素和 GLP-1 水平之间存在强烈的相关性。
我们的发现表明,急性肝外胆汁淤积症会导致肠道胰腺内分泌功能的严重损害。改变的胆汁流量可能通过影响肠促胰岛素激素功能对β细胞功能产生直接的有害影响。