Characterization of bradykinin-induced endothelium-independent contraction in equine basilar artery.
Abstract: We investigated the effect of bradykinin (BK) on isolated equine basilar arterial rings with and without endothelium. BK induced concentration-dependent contraction of resting arterial rings and no relaxation when the rings were precontracted by prostaglandin F(2alpha). The maximal response and pD(2) value were 161.2 +/- 28.1% (to 60 mm KCl-induced contraction) and 8.24 +/- 0.25 respectively. The cumulative concentration-response curve for BK was not shifted to the right by des-Arg(9)-[Leu(8)]-BK (a B(1)-receptor antagonist), HOE140 (a B(2)-receptor antagonist) or NPC567 (another B(2)-receptor antagonist). In four of six basilar arteries, NPC567 induced concentration-dependent contraction. Indomethacin (a cyclooxygenase inhibitor), nordihydroguaiaretic acid (a lipoxygenase inhibitor), quinacrine (a phospholipase A(2) inhibitor), tetrodotoxin (a selective blocker of Na(+) channels), guanethidine (a nor-adrenergic neuron blocking drug), phentolamine (an alpha-adrenoceptor antagonist), Nomega-nitro-L-arginine (L-NNA, a nitric oxide (NO) synthase inhibitor) and endothelial denudation did not affect the BK-induced contraction. L-NNA and indomethacin induced contraction and relaxation under resting vascular tone respectively. These results suggest that endothelial cells are not involved in BK-induced contraction and that the contraction is not mediated via activation of known B(1) and B(2) receptors. Arachidonic acid metabolites and neurotransmitters like norepinephrine and NO might not play a role in BK-induced contraction in equine basilar artery.
Publication Date: 2009-08-04 PubMed ID: 19646091DOI: 10.1111/j.1365-2885.2008.01037.xGoogle Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigates the impact of bradykinin, a peptide that promotes inflammation, on horse basilar artery rings with or without an endothelium, a thin layer of cells lining blood vessels. The researchers found that the presence of bradykinin lead to the contraction of these arterial rings regardless of the presence of endothelial cells, and the contractions were not mediated through known B1 and B2 receptors.
Study Design and Methods
- The researchers explored the effect of bradykinin (BK) on isolated horse basilar arterial rings.
- They conducted tests with and without the presence of endothelium, the tissue lining blood vessels.
- They examined the response of arterial rings under resting conditions and under a pre-contracted scenario through the use of prostaglandin F(2alpha).
- The impact and response of different receptor antagonists, inhibitors, and blocking drugs were analyzed in the presence of bradykinin.
Results
- Bradykinin led to a concentration-based contraction of the arterial rings.
- When the arterial rings were precontracted, there was no subsequent relaxation induced by bradykinin.
- The reaction to bradykinin was not altered by various B1- and B2-receptor antagonists like des-Arg(9)-[Leu(8)]-BK, HOE140, or NPC567.
- In a few instances, NPC567 led to concentration-based arterial ring contraction.
- Various inhibitors, blockers, and the process of endothelial denudation did not have an impact on the contraction instigated by bradykinin.
- Interestingly, nitric oxide synthase inhibitor (L-NNA) and cyclooxygenase inhibitor (indomethacin) led to contraction and relaxation of vessels respectively when under natural vascular tones.
Conclusions
- The study concluded that endothelial cells do not play a role in the contraction of equine basilar artery instigated by bradykinin.
- The arterial ring contraction induced by bradykinin was not mediated through the activation of known B1 or B2 receptors.
- Arachidonic acid by-products or neurotransmitters such as norepinephrine and nitric oxide were not believed to have a role in the bradykinin-induced contraction of the equine basilar artery.
Cite This Article
APA
Ueno D, Yabuki A, Obi T, Shiraishi M, Nishio A, Miyamoto A.
(2009).
Characterization of bradykinin-induced endothelium-independent contraction in equine basilar artery.
J Vet Pharmacol Ther, 32(3), 264-270.
https://doi.org/10.1111/j.1365-2885.2008.01037.x Publication
Researcher Affiliations
- Department of Veterinary Pharmacology, Faculty of Agriculture, Kagoshima University, Korimoto, Kagoshima, Japan.
MeSH Terms
- Abattoirs
- Analysis of Variance
- Animals
- Basilar Artery / drug effects
- Basilar Artery / physiology
- Bradykinin / pharmacology
- Dinoprost / administration & dosage
- Endothelium, Vascular / drug effects
- Endothelium, Vascular / physiology
- Female
- Horses / physiology
- Male
- Swine
- Vasodilator Agents / pharmacology
Citations
This article has been cited 4 times.- Islam MZ, Sawatari Y, Kojima S, Kiyama Y, Nakamura M, Sasaki K, Otsuka M, Obi T, Shiraishi M, Miyamoto A. Vasomotor effects of 5-hydroxytryptamine, histamine, angiotensin II, acetylcholine, noradrenaline, and bradykinin on the cerebral artery of bottlenose dolphin (Tursiops truncatus). J Vet Med Sci 2020 Oct 20;82(10):1456-1463.
- Islam MZ, Watanabe Y, Nguyen HT, Yamazaki-Himeno E, Obi T, Shiraishi M, Miyamoto A. Vasomotor effects of acetylcholine, bradykinin, noradrenaline, 5-hydroxytryptamine, histamine and angiotensin II on the mouse basilar artery. J Vet Med Sci 2014 Oct;76(10):1339-45.
- Radenković M, Stojanović M, Skorupan N, Prostran M. Pharmacological analysis of the rat femoral artery response to bradykinin. Sci Pharm 2013 Jul-Sep;81(3):749-61.
- Islam MZ, Wu S, Ootawa T, Smith H, Nguyen HTT, Harada E, Miyamoto A. Characteristics of Cerebrovascular Response to Intrinsic Vasoactive Substances in Sika Deer (Cervus nippon yesoensis) and the Possible Effects of Gravity on Adrenergic Responses. Animals (Basel) 2024 Dec 4;14(23).
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