VIP and its homologous increase vascular conductance in certain endocrine and exocrine glands
- West Virginia Univ. Medical Center, Morgantown (USA)
The effects of vasoactive intestinal peptide (VIP) and related structural homologues on tissue vascular conductances were investigated in anesthetized male rats. VIP, peptide histidine isoleucine (PHI), secretin, growth hormone-releasing factor (GHRF), gastric inhibitory peptide (GIP), or saline was infused intravenously over 4 min. Tissue blood flows were measured during this time by use of {sup 141}Ce-labeled microspheres. Circulating thyrotropin (TSH), triiodothyronine (T{sub 3}), and thyroxine (T{sub 4}) levels were determined before and at 20 min and 2 h after treatment. Marked increases in thyroid, pancreatic, and salivary gland vascular Cs occurred during peptide infusion with the order of potency correlating with the degree of structural homology to VIP. PHI and secretin produced maximal increases in vascular Cs, which were the same as those obtained with VIP. Circulating TSH, T{sub 3}, and T{sub 4} levels were not different from values in saline-infused rats after peptide treatments that caused striking increases in thyroid vascular C. These observations indicate that the vascular beds of certain endocrine and exocrine glands are responsive to the vasodilatory action of VIP and related homologues with the order of potency corresponding to the degree of structural homology to VIP. These results are also consistent with the proposal that structural homologues of VIP act at the same vascular receptor as VIP. Alternative, the involvement of different vascular receptors, acting through the same mechanism at a level beyond the receptor site, cannot be excluded.
- OSTI ID:
- 6724927
- Journal Information:
- American Journal of Physiology; (USA), Vol. 254:4; ISSN 0002-9513
- Country of Publication:
- United States
- Language:
- English
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551001* - Physiological Systems- Tracer Techniques