In mouse aortic rings with healthy endothelium, VIP caused concentration-dependent relaxation of precontracted rings.
In plain wordsIn mouse aorta rings in the lab, VIP relaxed the blood vessel in a dose-dependent way.
- Outcome
- IncreaseVIP-induced relaxation of aortic rings
- Study
mousen: not reported in source
Thoracic aortic rings from adult male C57BL/6J mice, precontracted with phenylephrine- Outcome group
- Vascular function · Cardiovascular
- Studied dose
- Dose not stated
Measurements
- Maximum relaxation
- 65.1%
- VIP, endothelium intact
- -logEC50
- 8.29
- VIP, endothelium intact
Source sentences
Isoprenaline, acetylcholine, calcitonin gene-related peptide (CGRP), vasoactive intestinal peptide (VIP) and sodium nitroprusside all caused concentration-dependent relaxations in aortic rings possessing healthy endothelium and precontracted with phenylephrine.
2 context sentences(design, population, supporting numbers)
Maximum relaxations were 64.9+/-2.6%, 66.8+/-2.9%, 114.3+/-4.6%, 65.1+/-4.2% and 116.2+/-5.1% with -logEC(50) values of 6.76+/-0.14, 7.04+/-0.11, 8.53+/-0.14, 8.29+/-0.26 and 8.10+/-0.20 for isoprenaline, acetylcholine, CGRP, VIP and sodium nitroprusside, respectively.
We investigated the vasorelaxant responses on thoracic aortic rings from the adult male C57BL/6J mouse.