Abstract |
A recent study reported the vasoactive intestinal peptide (VIP) fragment VIP(10-28) inhibited the rise in skin blood flow during heat stress. Our laboratory has reported that the nitric oxide (NO) pathway and histamine receptor-1 (H1)-receptor activation is common to both exogenous VIP-mediated dilation and active vasodilation (AVD). The present study aimed to further examine the specific role for VIP in AVD by using VIP(10-28) to antagonize VIP-mediated dilation in the presence of NO synthase (NOS) inhibition and an H1 antagonist. Study 1 (n = 12) examined whether VIP(10-28) antagonizes vasodilation to exogenous VIP via inhibition of NO-dependent mechanisms. Study 2 (n = 6) investigated AVD in skin sites receiving VIP(10-28) alone and in combination with NOS inhibition. Study 3 (n = 6) examined AVD in sites receiving VIP(10-28) alone and combined VIP(10-28) and H1 antagonism. Due to differences in our findings and those previously published, study 4 (n = 6) investigated whether an increase in baseline skin blood flow could result in a diminished rise in AVD. Red blood cell flux was measured using laser Doppler flowmetry, and cutaneous vascular conductance (flux/mean arterial pressure) was normalized to maximal vasodilation (28 mM sodium nitroprusside). VIP(10-28) augmented vasodilation to exogenous VIP (P < 0.05 vs. control) and hyperthermia (P < 0.05 vs. control). NOS inhibition had no effect on the augmented dilation during exogenous VIP or hyperthermia (P > 0.05). Similarly, H1-receptor antagonists had no effect on the augmented dilation during hyperthermia (P > 0.05 vs. VIP(10-28)). In study 4, percentage of maximal cutaneous vascular conductance was attenuated when baseline skin blood flow was elevated before whole body heating. Our results suggest that VIP(10-28) may be an unsuitable antagonist for examining a role for VIP-mediated dilation in human skin.
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Authors | Brad W Wilkins, Brett J Wong, Nathan J Tublitz, Gregg R McCord, Christopher T Minson |
Journal | Journal of applied physiology (Bethesda, Md. : 1985)
(J Appl Physiol (1985))
Vol. 99
Issue 6
Pg. 2294-301
(Dec 2005)
ISSN: 8750-7587 [Print] United States |
PMID | 16109832
(Publication Type: Clinical Trial, Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Peptide Fragments
- Vasoactive Intestinal Peptide
- vasoactive intestinal peptide (10-28)
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Topics |
- Adult
- Blood Flow Velocity
(drug effects, physiology)
- Dose-Response Relationship, Drug
- Female
- Humans
- Injections, Subcutaneous
- Peptide Fragments
(administration & dosage)
- Skin
(blood supply, drug effects)
- Skin Physiological Phenomena
(drug effects)
- Vasoactive Intestinal Peptide
(administration & dosage)
- Vasodilation
(drug effects, physiology)
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