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Updated: Jan 17, 2026

Co-staining Blood Vessels and Nerve Fibers in Adipose Tissue
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Vasoactive Intestinal Peptide: Another Player in Adipose Tissue Blood Flow Regulation?

Richard Sotorník1, Julie Ménard2, Pascal Brassard1

  • 1Division of Endocrinology, Department of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.

Microcirculation (New York, N.Y. : 1994)
|September 14, 2025
PubMed
Summary

Vasoactive intestinal peptide (VIP) effectively increases adipose tissue blood flow (ATBF) in healthy individuals. However, some people show a reduced ATBF response to VIP, potentially linked to cardiometabolic risk.

Keywords:
133Xenon washoutadipose tissue blood flowgastrointestinal tractvasoactive intestinal peptide

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Area of Science:

  • Physiology
  • Metabolism
  • Cardiovascular Health

Background:

  • Adipose tissue blood flow (ATBF) normally increases after meals, but this response is impaired in about one-third of healthy individuals.
  • This impaired ATBF response is associated with prolonged postprandial lipemia and elevated cardiometabolic risk.
  • Vasoactive intestinal peptide (VIP), a gut neurotransmitter, possesses vasodilatory properties.

Purpose of the Study:

  • To investigate the role of VIP in regulating ATBF.
  • To determine if VIP contributes to the blunted postprandial ATBF response observed in some individuals.

Main Methods:

  • Assessed plasma VIP levels and ATBF using the 133Xenon washout technique after an oral glucose load in 16 healthy participants.
  • Measured ATBF during in situ microinfusion of varying VIP doses in 12 participants.

Main Results:

  • Oral glucose did not alter plasma VIP levels.
  • VIP microinfusion significantly increased ATBF in a dose-dependent manner (p < 0.0001).
  • Individuals with a blunted post-glucose ATBF response showed a trend towards a lower response to VIP.

Conclusions:

  • VIP demonstrates a potent vasodilatory effect on adipose tissue.
  • A diminished response to VIP may contribute to the blunted ATBF observed in certain individuals.
  • Further research in larger cohorts is needed to confirm the role of local VIP unresponsiveness in this non-responder status.