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Pancreatic polypeptide administration improves abnormal glucose metabolism in patients with chronic pancreatitis

Journal of Clinical Endocrinology and Metabolism 81(10): 3566-3572

Pancreatic polypeptide administration improves abnormal glucose metabolism in patients with chronic pancreatitis

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 obesitymatched 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 cntdot m-2 cntdot min-1), HGP fell 91 +- 5% in NL subjects but only 68 +- 8% in CP subjects (P lt 0.05). One month later, the clamp was repeated during the final 2 h of an 8-h infusion of bovine PP (2 pmol cntdot kg-1 cntdot 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 ( apprx - 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.

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Accession: 002914848

PMID: 8855802

DOI: 10.1210/jcem.81.10.8855802

Related references

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