Endothelial modulation of α1‐adrenoceptor contractile responses in the tail artery of spontaneously hypertensive rats

1 Vascular contraction induced by phenylephrine was studied in tail artery rings from spontaneously hypertensive (SHR) and Wistar Kyoto rats (WKY) with particular focus on the role of endothelium. The influence of receptor reserve and the density of α1‐adrenoceptors on the possible differences obser...

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Veröffentlicht in:British journal of pharmacology 1996-10, Vol.119 (4), p.765-771
Hauptverfasser: Tabernero, Antonia, Giraldo, Jesús, Vivas, Nuria María, Badia, Albert, Vila, Elisabet
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creator Tabernero, Antonia
Giraldo, Jesús
Vivas, Nuria María
Badia, Albert
Vila, Elisabet
description 1 Vascular contraction induced by phenylephrine was studied in tail artery rings from spontaneously hypertensive (SHR) and Wistar Kyoto rats (WKY) with particular focus on the role of endothelium. The influence of receptor reserve and the density of α1‐adrenoceptors on the possible differences observed were also analysed. 2 Phenylephrine (0.01–100 μm) induced concentration‐dependent vasoconstrictions. The maximum response (α, P < 0.001) was greater but the pEC50 (P < 0.05) smaller in rings from SHR than from WKY rats irrespective of the presence or absence of endothelium. 3 Removal of endothelial cells resulted in a decrease of the maximum contraction with no modification in the pEC50 in arteries from both WKY and SHR. 4 The density of α1‐adrenoceptors (Bmax) and the dissociation constant (KD) were found to be the same for preparations from SHR and WKY rats in [3H]‐prazosin binding experiments. 5 The apparent affinity (pKA) determined by the nested hyperbolic method and the operational model was similar in tail arteries from the two rat strains, irrespective of the presence or absence of endothelium. However, in endothelium‐denuded rings, the pKA value was enhanced when compared with intact rings, in both SHR and WKY rats. 6 In rings from hypertensive rats, the operational parameter maximum possible effect (Em) was greater and the agonist efficacy (τ) was smaller than in rings from normotensive rats. When the endothelium was removed log τ and Em diminished in preparations from both rat strains. 7 In summary, the increased maximum responsiveness to phenylephrine in rings from SHR could be due to enhancement in Em. The log τ values indicate a deterioration in the transduction of the stimulus provided by the agonist in tail arteries from hypertensive animals. This study also suggests that the absence of endothelium modifies the α1‐adrenoceptor‐mediated vasocontriction probably by altering the transduction signalling mechanisms. The importance of analysing the degree of endothelium functionality when comparing results from different groups of rats is stated.
doi_str_mv 10.1111/j.1476-5381.1996.tb15738.x
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The influence of receptor reserve and the density of α1‐adrenoceptors on the possible differences observed were also analysed. 2 Phenylephrine (0.01–100 μm) induced concentration‐dependent vasoconstrictions. The maximum response (α, P &lt; 0.001) was greater but the pEC50 (P &lt; 0.05) smaller in rings from SHR than from WKY rats irrespective of the presence or absence of endothelium. 3 Removal of endothelial cells resulted in a decrease of the maximum contraction with no modification in the pEC50 in arteries from both WKY and SHR. 4 The density of α1‐adrenoceptors (Bmax) and the dissociation constant (KD) were found to be the same for preparations from SHR and WKY rats in [3H]‐prazosin binding experiments. 5 The apparent affinity (pKA) determined by the nested hyperbolic method and the operational model was similar in tail arteries from the two rat strains, irrespective of the presence or absence of endothelium. However, in endothelium‐denuded rings, the pKA value was enhanced when compared with intact rings, in both SHR and WKY rats. 6 In rings from hypertensive rats, the operational parameter maximum possible effect (Em) was greater and the agonist efficacy (τ) was smaller than in rings from normotensive rats. When the endothelium was removed log τ and Em diminished in preparations from both rat strains. 7 In summary, the increased maximum responsiveness to phenylephrine in rings from SHR could be due to enhancement in Em. The log τ values indicate a deterioration in the transduction of the stimulus provided by the agonist in tail arteries from hypertensive animals. This study also suggests that the absence of endothelium modifies the α1‐adrenoceptor‐mediated vasocontriction probably by altering the transduction signalling mechanisms. 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The influence of receptor reserve and the density of α1‐adrenoceptors on the possible differences observed were also analysed. 2 Phenylephrine (0.01–100 μm) induced concentration‐dependent vasoconstrictions. The maximum response (α, P &lt; 0.001) was greater but the pEC50 (P &lt; 0.05) smaller in rings from SHR than from WKY rats irrespective of the presence or absence of endothelium. 3 Removal of endothelial cells resulted in a decrease of the maximum contraction with no modification in the pEC50 in arteries from both WKY and SHR. 4 The density of α1‐adrenoceptors (Bmax) and the dissociation constant (KD) were found to be the same for preparations from SHR and WKY rats in [3H]‐prazosin binding experiments. 5 The apparent affinity (pKA) determined by the nested hyperbolic method and the operational model was similar in tail arteries from the two rat strains, irrespective of the presence or absence of endothelium. However, in endothelium‐denuded rings, the pKA value was enhanced when compared with intact rings, in both SHR and WKY rats. 6 In rings from hypertensive rats, the operational parameter maximum possible effect (Em) was greater and the agonist efficacy (τ) was smaller than in rings from normotensive rats. When the endothelium was removed log τ and Em diminished in preparations from both rat strains. 7 In summary, the increased maximum responsiveness to phenylephrine in rings from SHR could be due to enhancement in Em. The log τ values indicate a deterioration in the transduction of the stimulus provided by the agonist in tail arteries from hypertensive animals. This study also suggests that the absence of endothelium modifies the α1‐adrenoceptor‐mediated vasocontriction probably by altering the transduction signalling mechanisms. The importance of analysing the degree of endothelium functionality when comparing results from different groups of rats is stated.</description><subject>[3H]‐prazosin binding</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>endothelium</subject><subject>hypertension</subject><subject>Medical sciences</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Tail artery</topic><topic>Vascular wall</topic><topic>α1‐adrenoceptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tabernero, Antonia</creatorcontrib><creatorcontrib>Giraldo, Jesús</creatorcontrib><creatorcontrib>Vivas, Nuria María</creatorcontrib><creatorcontrib>Badia, Albert</creatorcontrib><creatorcontrib>Vila, Elisabet</creatorcontrib><collection>Pascal-Francis</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tabernero, Antonia</au><au>Giraldo, Jesús</au><au>Vivas, Nuria María</au><au>Badia, Albert</au><au>Vila, Elisabet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelial modulation of α1‐adrenoceptor contractile responses in the tail artery of spontaneously hypertensive rats</atitle><jtitle>British journal of pharmacology</jtitle><date>1996-10</date><risdate>1996</risdate><volume>119</volume><issue>4</issue><spage>765</spage><epage>771</epage><pages>765-771</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><coden>BJPCBM</coden><abstract>1 Vascular contraction induced by phenylephrine was studied in tail artery rings from spontaneously hypertensive (SHR) and Wistar Kyoto rats (WKY) with particular focus on the role of endothelium. The influence of receptor reserve and the density of α1‐adrenoceptors on the possible differences observed were also analysed. 2 Phenylephrine (0.01–100 μm) induced concentration‐dependent vasoconstrictions. The maximum response (α, P &lt; 0.001) was greater but the pEC50 (P &lt; 0.05) smaller in rings from SHR than from WKY rats irrespective of the presence or absence of endothelium. 3 Removal of endothelial cells resulted in a decrease of the maximum contraction with no modification in the pEC50 in arteries from both WKY and SHR. 4 The density of α1‐adrenoceptors (Bmax) and the dissociation constant (KD) were found to be the same for preparations from SHR and WKY rats in [3H]‐prazosin binding experiments. 5 The apparent affinity (pKA) determined by the nested hyperbolic method and the operational model was similar in tail arteries from the two rat strains, irrespective of the presence or absence of endothelium. However, in endothelium‐denuded rings, the pKA value was enhanced when compared with intact rings, in both SHR and WKY rats. 6 In rings from hypertensive rats, the operational parameter maximum possible effect (Em) was greater and the agonist efficacy (τ) was smaller than in rings from normotensive rats. When the endothelium was removed log τ and Em diminished in preparations from both rat strains. 7 In summary, the increased maximum responsiveness to phenylephrine in rings from SHR could be due to enhancement in Em. The log τ values indicate a deterioration in the transduction of the stimulus provided by the agonist in tail arteries from hypertensive animals. This study also suggests that the absence of endothelium modifies the α1‐adrenoceptor‐mediated vasocontriction probably by altering the transduction signalling mechanisms. The importance of analysing the degree of endothelium functionality when comparing results from different groups of rats is stated.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/j.1476-5381.1996.tb15738.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects [3H]‐prazosin binding
Biological and medical sciences
Cardiovascular system
endothelium
hypertension
Medical sciences
Pharmacology. Drug treatments
Tail artery
Vascular wall
α1‐adrenoceptors
title Endothelial modulation of α1‐adrenoceptor contractile responses in the tail artery of spontaneously hypertensive rats
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