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Effect of cholecystokinin-A receptor blockade on postprandial insulinaemia and gastric emptying in humans.

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  • معلومة اضافية
    • المصدر:
      Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 9432572 Publication Model: Print Cited Medium: Print ISSN: 1350-1925 (Print) Linking ISSN: 13501925 NLM ISO Abbreviation: Neurogastroenterol Motil Subsets: MEDLINE
    • بيانات النشر:
      Original Publication: Osney Mead, Oxford, UK : Blackwell Scientific Publications, c1994-
    • الموضوع:
    • نبذة مختصرة :
      Our aim was determine the relationship between cholecystokinin (CCK)-A receptor blockade, glucose levels, insulin secretion and gastric emptying in humans, and to assess the effect of CCK-A blockade on pancreatic polypeptide secretion. After a 12-h fast, six healthy volunteers were given [99mTc]iminodiacetic acid monosodium salt (IDA) intravenously (5 mCi). One hour later they were offered a 577 kcal liquid meal containing [99mTc]diethylenetriaminepentaacetic acid (DTPA) (2 mCi) and glucose (105 g). Scintigraphic gastric and gallbladder activity, and plasma glucose, insulin and pancreatic polypeptide responses were monitored. In a second experiment, a continuous intravenous infusion of loxiglumide (7.5 mg kg h(-1)) was started 60 min before and continued until 120 min after test meal ingestion to block the CCK-A receptors. Gallbladder emptying was blocked by loxiglumide. Loxiglumide accelerated gastric emptying, increased insulin secretion without alteration of glucose profiles, and abolished all phases of the postprandial pancreatic polypeptide response. Blockade of peripheral CCK-A receptors accelerates gastric emptying of liquids with an increase in postprandial insulin levels. The lack of changes in glycaemia suggests that alternative homeostatic mechanisms also control postprandial glucose levels. Inhibition of pancreatic polypeptide release may reflect an independent effect of loxiglumide on vagal control involved in pancreatic polypeptide release.
    • الرقم المعرف:
      0 (Blood Glucose)
      0 (Insulin)
      0 (Receptor, Cholecystokinin A)
      0 (Receptors, Cholecystokinin)
      77MPX3N42I (loxiglumide)
      EPL8W5565D (Proglumide)
    • الموضوع:
      Date Created: 20021003 Date Completed: 20030305 Latest Revision: 20191106
    • الموضوع:
      20240829
    • الرقم المعرف:
      10.1046/j.1365-2982.2002.00355.x
    • الرقم المعرف:
      12358680