1994
DOI: 10.1111/j.1365-2885.1994.tb00236.x
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Equine coronary artery responds to 5‐hydroxytryptamine with relaxation in vitro

Abstract: Isolated equine coronary arteries responded to 5-hydroxytryptamine (5-HT) with relaxations in both endothelium-dependent and endothelium-independent mechanisms. Experiments were designed to characterize the 5-HT receptor subtype mediating these relaxations. Both 5-HT and alpha-methyl-5-HT (alpha-Me-5-HT; 5-HT2 agonist) produced concentration-dependent relaxations in equine coronary arteries precontracted with a thromboxane A2 derivative (ONO11113). The degree of the maximal relaxation induced by alpha-Me-5-HT … Show more

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Cited by 10 publications
(6 citation statements)
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“…, 1991). Equine coronary arteries have also been shown to relax in response to 5‐HT, partially mediated by endothelial 5‐HT 2 receptors (Obi et al. , 1994; Bailey, 1998).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…, 1991). Equine coronary arteries have also been shown to relax in response to 5‐HT, partially mediated by endothelial 5‐HT 2 receptors (Obi et al. , 1994; Bailey, 1998).…”
Section: Discussionmentioning
confidence: 99%
“…Secondly, 5-HT has also been shown to stimulate NO production by endothelial cells through activation of 5-HT 1 -like, 5-HT 2 and 5-HT 7 receptor subtypes on endothelial cells of blood vessel of differing origin from various species (Verbeuren et al, 1991). Equine coronary arteries have also been shown to relax in response to 5-HT, partially mediated by endothelial 5-HT 2 receptors (Obi et al, 1994;Bailey, 1998). Preconstricted isolated large equine digital arteries, on the other hand, failed to relax in response to 5-HT (Bailey, 1998).…”
Section: Discussionmentioning
confidence: 99%
“…There are examples in which 5-HT relaxant receptors are revealed without blockade of contractile 5-HT receptors. This includes the equine coronary artery (Obi et al, 1994) and dog coronary artery (Terrón, 1996). Although no antagonists of contractile 5-HT receptors were added in the equine coronary artery studies, Terrón (1996) showed that whereas 5-HT relaxation was present naturally in the dog coronary artery, the sensitivity to 5-HT and 5-carboxamidotryptamine (5-CT) as relaxants was increased when the 5-HT 1B/1D receptor antagonist N-[4-methoxy-3-(4-methyl-1-piperazinyl)phenyl]-2Ј-methyl-4Ј-(5-methyl-1,2,4-oxadiazol-3-yl)-1-1Ј-biphenyl-4-carboxamide (GR127935) was added.…”
Section: -Hydroxytryptamine Synthesis and Handlingmentioning
confidence: 99%
“…Serotonin reportedly induced basilar arterial contraction via the 5-HT 1 receptor in the Habu snake [18] and was involved in pulmonary vascular responses (a study with no receptor mediation) in the file snake (Acrochordus granulatus) [35]. Many vascular responses to serotonin are constrictive, but reported responses also include relaxation in the rat jugular vein [36,37], pig pulmonary artery [38,39], and equine coronary artery [40]. Although serotonin-induced relaxation responses vary between animal species and blood vessels, 5-HT 1 , 5-HT 2 , and 5-HT 7 receptors and endothelial cell-derived NO all appear to be involved [34,[36][37][38][39][40].…”
Section: Discussionmentioning
confidence: 99%
“…Many vascular responses to serotonin are constrictive, but reported responses also include relaxation in the rat jugular vein [36,37], pig pulmonary artery [38,39], and equine coronary artery [40]. Although serotonin-induced relaxation responses vary between animal species and blood vessels, 5-HT 1 , 5-HT 2 , and 5-HT 7 receptors and endothelial cell-derived NO all appear to be involved [34,[36][37][38][39][40]. In further experiments with antagonists and inhibitors that effectively yielded serotonin-induced relaxation, the combination of L-NNA, SB269970, methiothepin, or ketanserin inhibited serotonin-induced relaxation at low concentrations but not at high concentrations (Figure 5A).…”
Section: Discussionmentioning
confidence: 99%