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Study · Animal study (in vivo) · dog · 1979

5 results

Assessment of the effects of vasoactive intestinal peptide (VIP) on blood flow through and salivation of the dog salivary gland in comparison with those of secretin, glucagon and acetylcholine.

Shimizu T, Taira N

British journal of pharmacology1 Apr 1979Cited by 48 (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)Efficacy outcome

    In anaesthetised dogs, intra-arterial VIP produced a dose-dependent increase in blood flow through the submandibular gland artery (vasodilatation).

    In plain wordsIn dogs, VIP given into the gland artery widened the blood vessels and raised blood flow, more so at higher doses.

    Outcome
    IncreaseSubmandibular gland blood flow
    Study

    dogn: not reported in source

    perfused submandibular gland in situ, anesthetised dogs
    Outcome group
    Vascular function · Cardiovascular
    Studied dose
    Dose not stated · intra-arterialAs given in this study (dog).

    Source sentences

    Summary
    Vasoactive intestinal peptide (VIP), secretin and acetylcholine produced a dose-dependent increase in blood flow through the artery (vasodilatation) but glucagon was almost ineffective.
    2 context sentences
    Summary · context
    The vascular bed of the submandibular gland in situ was perfused with blood through the glandular artery at a constant pressure in anesthetized dogs.
    Summary · context
    All drugs were administered intra-arterially.
  2. 02AnimalAnimal study (in vivo)Activity measurement

    In dogs, the dose-blood flow curves for VIP and secretin were parallel, and VIP was about 100 times as potent as secretin on a molar basis.

    In plain wordsIn dogs, VIP was about 100 times more potent than secretin at raising blood flow in the gland.

    Outcome
    Not applicablePotency of VIP versus secretin on blood flow
    Study

    dogn: not reported in source

    perfused submandibular gland in situ, anesthetised dogs
    Comparator
    Secretin
    Outcome group
    Vascular function · Cardiovascular
    Studied dose
    Dose not stated · intra-arterialAs given in this study (dog).

    Measurements

    Relative molar potency versus secretin
    100 fold
    submandibular blood flow

    Source sentences

    Summary
    Dose-blood flow response curves for VIP and secretin were parallel, and VIP was about 100 times as potent as secretin on a molar basis.
    2 context sentences
    Summary · context
    The vascular bed of the submandibular gland in situ was perfused with blood through the glandular artery at a constant pressure in anesthetized dogs.
    Summary · context
    All drugs were administered intra-arterially.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In dogs, no tachyphylaxis developed to the vasodilator action of VIP.

    In plain wordsIn dogs, the blood vessel widening caused by VIP did not fade with repeated use.

    Outcome
    No significant changeTachyphylaxis to the vasodilator action of VIP
    Study

    dogn: not reported in source

    perfused submandibular gland in situ, anesthetised dogs
    Outcome group
    Vascular function · Cardiovascular
    Studied dose
    Dose not stated · intra-arterialAs given in this study (dog).

    Source sentences

    Summary
    No tachyphylaxis developed to the vasodilator action of VIP.
    2 context sentences
    Summary · context
    The vascular bed of the submandibular gland in situ was perfused with blood through the glandular artery at a constant pressure in anesthetized dogs.
    Summary · context
    All drugs were administered intra-arterially.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In dogs, the vasodilator response to VIP was scarcely modified by (-)-hyoscyamine, in doses that fully antagonized the response to acetylcholine.

    In plain wordsIn dogs, a drug that fully blocked acetylcholine's effect hardly changed the blood vessel widening caused by VIP.

    Outcome
    No significant changeEffect of (-)-hyoscyamine on the VIP vasodilator response
    Study

    dogn: not reported in source

    perfused submandibular gland in situ, anesthetised dogs
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated · intra-arterialAs given in this study (dog).

    Source sentences

    Summary
    The vasodilator responses to VIP and to electrical stimulation of the chordolingual nerve were scarcely modified by (-)-hyoscyamine in doses that fully antagonized the vasodilator response to acetylcholine.
    2 context sentences
    Summary · context
    The vascular bed of the submandibular gland in situ was perfused with blood through the glandular artery at a constant pressure in anesthetized dogs.
    Summary · context
    All drugs were administered intra-arterially.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In dogs, VIP was ineffective in eliciting salivary secretion from the submandibular gland.

    In plain wordsIn dogs, VIP did not cause the gland to make saliva.

    Outcome
    No significant changeSalivary secretion
    Study

    dogn: not reported in source

    perfused submandibular gland in situ, anesthetised dogs
    Outcome group
    Gastrointestinal protection · Gastrointestinal
    Studied dose
    Dose not stated · intra-arterialAs given in this study (dog).

    Source sentences

    Summary
    VIP, secretin and glucagon were ineffective in eliciting salivary secretion.
    2 context sentences
    Summary · context
    The vascular bed of the submandibular gland in situ was perfused with blood through the glandular artery at a constant pressure in anesthetized dogs.
    Summary · context
    All drugs were administered intra-arterially.

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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