Brunicardi F C, Chaiken R L, Ryan A S, Seymour N E, Hoffmann J A, Lebovitz H E, Chance R E, Gingerich R L, Andersen D K, Elahi D
Department of Surgery, State University of New York Health Science Center, Brooklyn, USA.
J Clin Endocrinol Metab. 1996 Oct;81(10):3566-72. doi: 10.1210/jcem.81.10.8855802.
Chronic pancreatitis (CP) is associated with lowered plasma levels and a blunted nutrient-induced release of pancreatic polypeptide (PP). To investigate the possible role of PP on glucose metabolism, we studied male patients with documented CP (n = 5) and obesity-matched control subjects (NL) (n = 6). Hepatic glucose production (HGP) and overall glucose disposal rates were determined by [3-3H]glucose infusion during a hyperinsulinemic-euglycemic clamp during three separate admissions. Basal rates of HGP were higher in CP patients. In response to an infusion of insulin (60 pmol.m-2.min-1), HGP fell 91 +/- 5% in NL subjects but only 68 +/- 8% in CP subjects (P < 0.05). One month later, the clamp was repeated during the final 2 h of an 8-h infusion of bovine PP (2 pmol.kg-1.min-1). HGP before the insulin infusion and its subsequent suppression (NL: 83 +/- 5%; CP: 86 +/- 15%) were nearly identical between groups. In follow-up studies 1 month after the PP infusion, HGP both basally and in response to insulin alone were similar to the first study. During oral glucose tolerance tests (OGTT) performed 18 h after the PP infusion, subjects with normal (n = 7) baseline OGTT responses showed no effect. All patients with diabetic (n = 3) or nondiagnostic (n = 1) OGTT responses, however, demonstrated lowered mean plasma glucose levels (approximately -2.3 mmol/L; range: -0.6 to -7.2 mmol/L). OGTTs repeated 1 month after the PP treatment showed a return to pretreatment responses. We conclude that chronic pancreatitis accompanied by PP deficiency is associated with partial hepatic resistance both in the basal state and in response to hyperinsulinemia. This impairment is reversed after iv PP administration. PP deficiency may therefore play a role in the development of pancreatogenic diabetes caused by pancreatic injury.
慢性胰腺炎(CP)与血浆中胰多肽(PP)水平降低以及营养物质诱导的PP释放减弱有关。为了研究PP对葡萄糖代谢的可能作用,我们对有记录的CP男性患者(n = 5)和肥胖匹配的对照受试者(NL)(n = 6)进行了研究。在三次单独住院期间,通过在高胰岛素-正常血糖钳夹期间输注[3-³H]葡萄糖来测定肝葡萄糖生成(HGP)和总体葡萄糖处置率。CP患者的基础HGP率较高。在输注胰岛素(60 pmol·m⁻²·min⁻¹)后,NL受试者的HGP下降了91±5%,而CP受试者仅下降了68±8%(P < 0.05)。一个月后,在8小时输注牛PP(2 pmol·kg⁻¹·min⁻¹)的最后2小时内重复进行钳夹。两组之间胰岛素输注前的HGP及其随后的抑制情况(NL:83±5%;CP:86±15%)几乎相同。在PP输注后1个月的随访研究中,基础HGP以及单独对胰岛素反应的HGP与第一项研究相似。在PP输注后18小时进行口服葡萄糖耐量试验(OGTT)时,基线OGTT反应正常的受试者(n = 7)未显示出影响。然而,所有糖尿病OGTT反应患者(n = 3)或非诊断性OGTT反应患者(n = 1)的平均血浆葡萄糖水平均降低(约-2.3 mmol/L;范围:-0.6至-7.2 mmol/L)。PP治疗后1个月重复进行的OGTT显示恢复到治疗前的反应。我们得出结论,伴有PP缺乏的慢性胰腺炎在基础状态和对高胰岛素血症的反应中均与部分肝脏抵抗有关。静脉注射PP后这种损害会得到逆转。因此,PP缺乏可能在胰腺损伤所致胰源性糖尿病的发生中起作用。