Literature DB >> 2852361

Vasoactive intestinal peptide evokes endothelium-dependent relaxation and cyclic AMP accumulation in rat aorta.

T Sata1, J Linden, L W Liu, E Kubota, S I Said.   

Abstract

We have investigated VIP-induced relaxation and cyclic AMP accumulation in rat thoracic aorta strips, and the importance of endothelium to both actions. The relaxation was greatly attenuated by removal of endothelium, but was unaltered by cyclo-oxygenase or lipoxygenase inhibitors. Similarly, cyclic AMP formation was nearly abolished with loss of endothelium, but was largely unaffected by inhibitors of arachidonate pathways, cytochrome P450 or guanylate cyclase. VIP may stimulate the release of a diffusible factor from endothelium (an EDRF), which activates adenylate cyclase and relaxes aortic smooth muscle.

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Year:  1988        PMID: 2852361     DOI: 10.1016/0196-9781(88)90133-7

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  4 in total

1.  Adenoviral transfer of vasoactive intestinal peptide (VIP) gene inhibits rat aortic and pulmonary artery smooth muscle cell proliferation.

Authors:  Rose-Claire St Hilaire; Philip J Kadowitz; James R Jeter
Journal:  Peptides       Date:  2009-08-19       Impact factor: 3.750

2.  Nitric oxide-related vasodilator responses to parasympathetic stimulation of the submandibular gland in the cat.

Authors:  A V Edwards; J R Garrett
Journal:  J Physiol       Date:  1993-05       Impact factor: 5.182

3.  Effects of vasoactive neuropeptides on human saphenous vein.

Authors:  T N Luu; A H Chester; G S O'Neil; S Tadjkarimi; M H Yacoub
Journal:  Br Heart J       Date:  1992-06

4.  Adenylate cyclase-mediated vascular responses of rabbit aorta, mesenteric artery and skin microcirculation.

Authors:  A J Wilson; J B Warren
Journal:  Br J Pharmacol       Date:  1993-10       Impact factor: 8.739

  4 in total

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