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Study · Animal study (in vivo) · pig · 2003

5 results

Effect of vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide on pancreatic, hepatic and duodenal mucosal bicarbonate secretion in the pig.

Glad H, Ainsworth MA, Svendsen P, Fahrenkrug J, Schaffalitzky de Muckadell OB

Digestion1 Jan 2003Cited by 16 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study5

5 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Pharmacokinetics

    In anaesthetized pigs, VIP infusion raised portal plasma VIP concentrations from 9 pM to 102, 220, 600, 850 and 3,795 pM at increasing doses.

    In plain wordsIn pigs, VIP infusion raised VIP levels in the portal blood in step with the dose.

    Outcome
    IncreasePortal plasma VIP concentration
    Study

    pign: not reported in source

    anaesthetized pigs
    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    250-6,000 pmol/kg x h · infusionAs given in this study (pig).

    Measurements

    Portal plasma VIP
    9 pM
    baseline
    Portal plasma VIP
    102 pM
    250 pmol/kg x h

    Source sentences

    Summary
    Infusion of VIP in these concentrations increased the portal plasma concentrations of VIP from 9 to 102, 220, 600, 850 and 3,795 pM, respectively.
    1 context sentence
    Summary · context
    The potency of pituitary adenylate cyclase-activating polypeptide (PACAP) and the related vasoactive intestinal peptide (VIP) on pancreaticobiliary and duodenal mucosal bicarbonate secretion (DMBS) was studied in anaesthetized pigs.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In anaesthetized pigs, VIP at 1,000 and 6,000 pmol/kg.h significantly stimulated pancreatic bicarbonate secretion.

    In plain wordsIn pigs, VIP infusion raised bicarbonate output from the pancreas.

    Outcome
    IncreasePancreatic bicarbonate secretion
    Study

    pign: not reported in source

    anaesthetized pigs
    Outcome group
    Gastrointestinal function · Gastrointestinal
    Studied dose
    250-6,000 pmol/kg x h · infusionAs given in this study (pig).

    Measurements

    Pancreatic bicarbonate secretion
    7.6 mmol/h
    6,000 pmol/kg.h

    Source sentences

    Summary
    At doses of 1,000 and 6,000 pmol/kg.h all three peptides significantly stimulated pancreatic bicarbonate secretion, VIP from 0.0 to 0.3 and 7.6 mmol/h, PACAP27 from 0.0 to 2.3 and 8.2 mmol/h, and PACAP38 from 0.0 to 0.2 and 7.4 mmol/h, respectively.
    1 context sentence
    Summary · context
    The potency of pituitary adenylate cyclase-activating polypeptide (PACAP) and the related vasoactive intestinal peptide (VIP) on pancreaticobiliary and duodenal mucosal bicarbonate secretion (DMBS) was studied in anaesthetized pigs.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In anaesthetized pigs, VIP increased hepatic bicarbonate output only at the highest dose, 6,000 pmol/kg.h.

    In plain wordsIn pigs, VIP raised bicarbonate output from the liver only at the highest dose.

    Outcome
    IncreaseHepatic bicarbonate output
    Study

    pign: not reported in source

    anaesthetized pigs
    Outcome group
    Gastrointestinal function · Liver
    Studied dose
    6,000 pmol/kg x h · infusionAs given in this study (pig).

    Measurements

    Hepatic bicarbonate output
    3.8 mmol/h
    6,000 pmol/kg.h

    Source sentences

    Summary
    Only during infusion of 6,000 pmol/kg.h did the three peptides elicit a significant increase in hepatic bicarbonate output. At this dose VIP increased hepatic bicarbonate output from 0.4 to 3.8 mmol/h, PACAP27 from 0.3 to 3.6 mmol/h, and PACAP38 from 0.1 to 1.4 mmol/h, respectively.
    1 context sentence
    Summary · context
    The potency of pituitary adenylate cyclase-activating polypeptide (PACAP) and the related vasoactive intestinal peptide (VIP) on pancreaticobiliary and duodenal mucosal bicarbonate secretion (DMBS) was studied in anaesthetized pigs.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In anaesthetized pigs, VIP dose-dependently and significantly increased duodenal mucosal bicarbonate secretion.

    In plain wordsIn pigs, VIP raised bicarbonate secretion from the duodenal lining in step with the dose.

    Outcome
    IncreaseDuodenal mucosal bicarbonate secretion
    Study

    pign: not reported in source

    anaesthetized pigs
    Outcome group
    Gastrointestinal function · Gastrointestinal
    Studied dose
    500-6,000 pmol/kg x h · infusionAs given in this study (pig).

    Measurements

    Duodenal mucosal bicarbonate secretion
    0.53 mmol/h
    6,000 pmol/kg.h

    Source sentences

    Summary
    Infusion of VIP (500, 1,000, 2,000 and 6,000 pmol/kg.h) dose-dependently and significantly enlarged DMBS from 0.09 to 0.19, 0.41, 0.54 and 0.53 mmol/h, respectively.
    1 context sentence
    Summary · context
    The potency of pituitary adenylate cyclase-activating polypeptide (PACAP) and the related vasoactive intestinal peptide (VIP) on pancreaticobiliary and duodenal mucosal bicarbonate secretion (DMBS) was studied in anaesthetized pigs.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In anaesthetized pigs at 6,000 pmol/kg.h, VIP-induced duodenal bicarbonate secretion was 4-fold higher than with PACAP27 and 8-fold higher than with PACAP38.

    In plain wordsIn pigs, VIP raised duodenal bicarbonate output more than the related peptides PACAP27 and PACAP38 did at the same dose.

    Outcome
    IncreaseDuodenal bicarbonate secretion versus PACAP
    Study

    pign: not reported in source

    anaesthetized pigs
    Comparator
    PACAP27, PACAP38
    Outcome group
    Gastrointestinal function · Gastrointestinal
    Studied dose
    6,000 pmol/kg x h · infusionAs given in this study (pig).

    Source sentences

    Summary
    A significant effect of PACAP27 and PACAP38 on DMBS was only obtained at a dose of 6,000 pmol/kg.h, and at this dose VIP-induced DMBS was 4- and 8-fold higher than that induced by PACAP27 and PACAP38, respectively.
    1 context sentence
    Summary · context
    The potency of pituitary adenylate cyclase-activating polypeptide (PACAP) and the related vasoactive intestinal peptide (VIP) on pancreaticobiliary and duodenal mucosal bicarbonate secretion (DMBS) was studied in anaesthetized pigs.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    12 Oct 2026, 12:58 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 12:41 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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